PROF EKREM UNAL compressed

Professeur Ekrem Ünal, docteur en médecine

Hôpital MedicalPoint Gaziantep
Hématologie et oncologie pédiatriques

Demande de rappel

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Nom

Formation et expertise

  • 1995-2001 : docteur en médecine, université de Selçuk, faculté de médecine de Meram

  • 2001-2007 : Médecin assistant de recherche, Université de Selçuk, Faculté de médecine de Meram

  • 2007-2012 : Médecin spécialiste, Université d’Erciyes, Faculté de médecine, Département de santé et maladies pédiatriques, hématologie et oncologie

  • 2012-2015 : Professeur adjoint, Université d’Erciyes, Faculté de médecine, Département de santé et maladies pédiatriques, hématologie et oncologie

  • 2015-2021 : Professeur associé, Université d’Erciyes, Faculté de médecine, Département de santé et maladies pédiatriques, hématologie et oncologie

  • 2021-2023 : Professeur, Université Erciyes, Faculté de médecine, Département de santé et maladies pédiatriques, hématologie et oncologie

Expertise clinique

  • Lymphome

  • Leucémie

Expérience professionnelle

  • 1995-2001 : docteur en médecine, université de Selçuk, faculté de médecine de Meram

  • 2001-2007 : Médecin assistant de recherche, Université de Selçuk, Faculté de médecine de Meram

  • 2007-2012 : Médecin spécialiste, Université d’Erciyes, Faculté de médecine, Département de santé et maladies pédiatriques, hématologie et oncologie

  • 2012-2015 : Professeur adjoint, Université d’Erciyes, Faculté de médecine, Département de santé et maladies pédiatriques, hématologie et oncologie

  • 2015-2021 : Professeur associé, Université d’Erciyes, Faculté de médecine, Département de santé et maladies pédiatriques, hématologie et oncologie

  • 2021-2023 : Professeur, Université Erciyes, Faculté de médecine, Département de santé et maladies pédiatriques, hématologie et oncologie

Affiliations professionnelles

  • Association turque d’hématologie

  • Association turque d’hématologie pédiatrique

  • Association européenne d’hématologie (EHA)

  • Société internationale d’oncologie pédiatrique (SIOP)

  • Groupe européen pour la transplantation de sang et de moelle (EBMT)

Recherche et publications

  • Atabek ME, Pirgon O, Unal E. Refractory cutaneous leishmaniasis in an adolescent : initial manifestation of type 1 diabetes. J Infect. 2006 Oct;53(4):290-1.

  • Unal E, Oran B, Baysal T, Baspinar O, Keser M, Karaarslan S, Arbag H. Pulmonary arterial pressure in infants with laryngomalacia. Int J Pediatr Otorhinolaryngol. 2006 Dec;70(12):2067-71.

  • Unal E. The real incidence of thyroid carcinoma in childhood. Laryngoscope. 2006 Nov;116(11):2095.

  • Koksal Y, Unal E, Aribas OK, Oran B. An uncommon extrapulmonary sequestration located in the upper posterior mediastinum associated with the azygos lobe in a child. J Thorac Cardiovasc Surg. 2007 Apr;133(4):1110-1.

  • Atabek ME, Pirgon O, Pituitary-adrenal axis suppression due à l’administration de stéroïdes topiques chez un nourrisson. Pediatr Int. 2007 Apr;49(2):242-4.

  • Koksal Y, Sahin M, Koksal H, Orhan D, Unal E, Alagoz E. Thyroid medullary carcinoma in a teenager with Cowden syndrome. Laryngoscope. 2007 Jul;117(7):1180-2.

  • Unal E, Koksal Y, Baysal T, Energin Ml, Aydin K, Caliskan U. Le syndrome de Kluver-Bucy chez un garçon atteint d’un lymphome non hodgkinien. Pediatr Hematol Oncol. 2007 Mar;24(2):149-52.

  • Unal E, Yazar A, Oran B. The importance of troponin-I as a predictor of cardiac injury caused by carbon monoxide poisoning. Inhal Toxicol. 2007 mai;19(6-7):587.

  • Koksal Y, Toy H, Unal E, Baysal T, Esen H, Paksoy Y, Ustun ME. Astrocytome pilocytique se développant sur le site d’un médulloblastome précédemment traité chez un enfant. Childs Nerv Syst. 2008 Mar;24(3):289-92.

  • Unal E, Kaya U, Aydin K. Fatal valproate overdose in a newborn baby. Hum Exp Toxicol. 2007 mai;26(5):453-6.

  • Elmaci MA, Unal E, Peru H. Le vrai diagnostic de la cystinurie. Urol Int. 2007;78(4):363.

  • Unal E, Koksal Y, Vajtai I, Toy H, Kocaogullar Y, Paksoy Y. Astroblastome chez un enfant. Childs Nerv Syst. 2008 Feb;24(2):165-8.

  • Unal E, Yazar A, Koksal Y, Caliskan U, Paksoy Y, Kalkan E. Thrombose du sinus veineux cérébral chez un adolescent atteint d’un sarcome d’Ewing. Childs Nerv Syst. 2008 Sep;24(9):983-6.

  • Unal E, Koksal Y, Cimen O, Paksoy Y, Tavli L. Transformation glioblastomateuse maligne d’un gliome de bas grade chez un enfant. Childs Nerv Syst. 2008 Dec;24(12):1385-9.

  • Unal E, Koksal Y, Energin VM, Reisli I. Importance de la chimioprophylaxie et des vaccins dans la prévention de la méningite récurrente. Pediatr Int. 2008 Jun;50(3):416.

  • Unal E, Koksal Y, Akcoren Z, Tavl L, Gunel E, Kerimoglu U. Mesenchymal hamartoma of the liver mimicking hepatoblastoma. J Pediatr Hematol Oncol. 2008 Jun;30(6):458-60.

  • Koksal Y, Caliskan U, Unal E. Hypothermia in a child with Hodgkin disease. J Pediatr Hematol Oncol. 2009 Feb;31(2):136-8.

  • Köksal Y, Toy H, Talim B, Unal E, Akçören Z, Cengiz M. Merkel cell carcinoma in a child. J Pediatr Hematol Oncol. 2009 Mai;31(5):359-61.

  • Patiroglu T, Unal E, Yikilmaz A, Koker MY, Ozturk MK. Présentation atypique de la maladie granulomateuse chronique chez un adolescent présentant un abcès à Aspergillus localisé au niveau du lobe frontal et imitant une tumeur intracrânienne. Childs Nerv Syst. 2010 Feb;26(2):149-54.

  • Cimen O, Oran B, Cimen D, Baysal T, Karaaslan S, Unal E, Başarili K, Büyükbaş S. Release of N-terminal pro-brain natriuretic peptide in children with acute rheumatic carditis. Cardiol Young. 2010 Jun;20(3):297-301.

  • Baysal T, Koksal Y, Oran B, Sen M, Unal E, Cimen D. Fonctions cardiaques évaluées avec l’imagerie Doppler tissulaire dans les cancers de l’enfant traités avec des anthracyclines. Pediatr Hematol Oncol. 2010 Feb;27(1):13-23.

  • Unal E, Koksal Y, Toy H, Gunel E, Acikgozoglu S. Neuroblastoma arising from an unresected sacrococcygeal teratoma in a child. J Pediatr Hematol Oncol. 2010 Apr;32(3):233-5.

  • Patiroglu T, Ozcan A, Karakukcu M, Ozdemir MA, Poyrazoglu G, Canpolat M, Unal E. Mycophenolate mofetil-induced pseudotumor cerebri in a boy with autoimmune lymphoproliferative disease. Childs Nerv Syst. 2011 May;27(5):853-5.

  • Qaddoumi I, Unal E, Diez B, Kebudi R, Quintana Y, Bouffet E, Chantada G. Enquête en ligne sur les ressources pour le traitement et le suivi à long terme des enfants atteints de tumeurs cérébrales dans les pays en développement. Childs Nerv Syst. 2011 Nov;27(11):1957-61.

  • Patiroglu T, Ozdemir MA, Unal E, Altuner Torun Y, Coskun A, Menku A, Mutlu FT, Karakukcu M. Intracranial hemorrhage in children with congenital factor deficiencies. Childs Nerv Syst. 2011 Nov;27(11):1963-6.

  • Patiroglu T, Unal E, Kardas F, Ozdemir MA, Karakukcu M, Sayilmaz O. Phenylketonuria with Acute Myeloblastic Leukemia in a 9-year-old Boy : Reporting a Rare Case. J Pediatr Hematol Oncol. 2011 Aug;33(6):e256-7.

  • Ozdemir MA, Karakukcu M, Per H, Unal E, Gumus H, Patiroglu T. Late-type vitamin K deficiency bleeding : experience from 120 patients. Childs Nerv Syst. 2012 Feb;28(2):247-51.

  • Patiroglu T, Unal E, Ozdemir MA, Karakukucu M, Mutlu FT. Administration accidentelle d’une surdose intramusculaire de vincristine. Drug Chem Toxicol. 2012 Apr;35(2):232-4.

  • Kondolot M, Unal E, Poyrazoglu G, Kara A, Yikilmaz A, Kumandas S, Arslan D. Orbital myositis associated with focal active colitis in a teenage girl. Childs Nerv Syst. 2012 Apr;28(4):641-3.

  • Unal E, Mutlu FT, Karakukcu M. The importance of MTHFR polymorphisms in pediatric cerebral stroke. Childs Nerv Syst. 2012 Jan;28(1):13.

  • Sezer S, Baykan A, Yilmaz E, Unal E, Onan SH, Yikilmaz A, Uzum K, Ozdemir MA, Narin N. Atrial fibrillation as an uncommon presentation in a large pleomorphic xanthoastrocytoma. Childs Nerv Syst. 2012 Mar;28(3):475-9.

  • van de Vijver E, Maddalena A, Sanal ., Holland SM, Uzel G, Madkaikar M, de Boer M, van Leeuwen K, K.ker MY, Parvaneh N, Fischer A, Law SK, Klein N, Tezcan FI, Unal E, Patiroglu T, Belohradsky BH, Schwartz K, Somech R, Kuijpers TW, Roos D. Hematologically important mutations : leukocyte adhesion deficiency (first update). Blood Cells Mol Dis. 2012 Jan 15;48(1):53-61.

  • Karakukcu C, Karakukcu M, Unal E, Patiroglu T, Ozdemir MA, Torun YA, Tang PH. Coenzyme Q10 levels in β-thalassemia and its association with ferritin levels and chelation therapy. Hemoglobin. 2012;36(3):219-29.

  • Kardas F, Patiroglu T, Unal E, Chiang SC, Bryceson YT, Kendirci M. Hemophagocytic syndrome in a 4-month-old infant with biotinidase deficiency. Pediatr Blood Cancer. 2012 Jul 15;59(1):191-3.

  • Patiroglu T, Gungor HE, Unal E, Kurtoglu S, Yikilmaz A, Patiroglu T. Hashimoto thyroiditis associated with ataxia telangiectasia. J Pediatr Endocrinol Metab. 2012;25(3-4):349-52.

  • Patiroglu T, Unal E, Karakukcu M, Ozdemir MA, Tucer B, Yikilmaz A, Deniz K. Multiple fungal brain abscesses in a child with acute lymphoblastic leukemia. Mycopathologia. 2012 Dec;174(5-6):505-9.

  • Patiroglu T, Tunc A, Eke Gungor H, Unal E. The efficacy of Pelargonium sidoides in the treatment of upper respiratory tract infections in children with transient hypogammaglobulinemia of infancy. Phytomedicine. 2012 Aug 15;19(11):958-61.

  • Patiroglu T, Sarici D, Unal E, Yikilmaz A, Tucer B, Karakukcu M, Ozdemir MA, Canoz O, Akcakus M. Cerebellar hemangioblastoma associated with diffuse neonatal hemangiomatosis in an infant. Childs Nerv Syst. 2012 Oct;28(10):1801-5.

  • Patiroglu T, Gungor HE, Unal E. Autoimmune diseases detected in children with primary immunodeficiency diseases : results from a reference centre at middle anatolia. Acta Microbiol Immunol Hung. 2012 Sep;59(3):343-53.

  • Sav H, Atalay MA, Unal E, Koç N. Galactomannan, 1,3-ß-D-Glucan et tests PCR : L’importance des échantillons de lavage broncho-alvéolaire. Mikrobiyol Bul. 2012 Oct;46(4):695-701.

  • Patiroglu T, Eke Gungor H, Arslan D, Deniz K, Unal E, Coskun A. Gastric signet ring carcinoma in a patient with ataxia-telangiectasia : a case report and review of the literature. J Pediatr Hematol Oncol. 2013 Nov;35(8):e341-3.

  • Chiang SC, Theorell J, Entesarian M, Meeths M, Mastafa M, Al-Herz W, Frisk P, Gilmour KC, Ifversen M, Langenskiöld C, Machaczka M, Naqvi A, Payne J, Perez-Martinez A, Sabel M, Unal E, Unal S, Winiarski J, Nordenskjöld M, Ljunggren HG, Henter JI, Bryceson YT. Comparison of primary human cytotoxic T-cell and natural killer cell responses reveal similar molecular requirements for lytic granule exocytosis but differences in cytokine production. Blood. 2013 Feb 21;121(8):1345-56.

  • Patiroglu T, Unal E, Yildirim S. Infantile tremor syndrome associated with cobalamin therapy : a case report. Clin Neurol Neurosurg. 2013 Sep;115(9):1903-5.

  • Patiroglu T, Gungor HE, Lazaroski S, Unal E. Chronic granulomatous disease with markedly elevated IgE levels mimicking hyperimmunoglobulin E syndrome. Acta Microbiol Immunol Hung. 2013 Jun;60(2):155-62.

  • Ozdemir MA, Yilmaz K, Abdulrezzak U, Muhtaroglu S, Patiroglu T, Karakukcu M, Unal E. The efficacy of vitamin K2 and calcitriol combination on thalassemic osteopathy. J Pediatr Hematol Oncol. 2013 Nov;35(8):623-7.

  • Canpolat M, Per H, Gumus H, Yikilmaz A, Unal E, Patiroglu T, Cinar L, Kurtsoy A, Kumandas S. Rapamycin has a beneficial effect on controlling epilepsy in children with tuberous sclerosis complex : results of 7 children from a cohort of 86. Childs Nerv Syst. 2014 Feb;30(2):227-40.

  • Patiroglu T, Haluk Akar H, van den Burg M, Unal E, Akyildiz BN, Tekerek NU, Yilmaz E. X-linked severe combined immunodeficiency due to a novel mutation complicated with hemophagocytic lymphohistiocytosis and presented with invagination : A case report. Eur J Microbiol Immunol (Bp). 2014 Sep;4(3):174-6.

  • Kose D, Paksoy Y, Koksal Y, Unal E. Complication neurologique du lymphome non hodgkinien chez l’enfant : expérience d’un seul centre en Turquie. Childs Nerv Syst. 2014 Apr;30(4):639-45.

  • Per H, Unal E, Poyrazoglu HG, Ozdemir MA, Donmez H, Gumus H, Uzum K, Canpolat M, Akyildiz BN, Coskun A, Kurtsoy A, Kumandas S. Childhood stroke : results of 130 children from a reference center in Central Anatolia, Turkey. Pediatr Neurol. 2014 Jun;50(6):595-600.

  • Kutuk MS, Croisille L, Gorkem SB, Yilmaz E, Korkmaz L, Bierling P, Unal E. Fetal intracranial hemorrhage related to maternal autoimmune thrombocytopenic purpura. Childs Nerv Syst. 2014 Dec;30(12):2147-50.

  • Kilic SC, Alaygut D, Unal E, Koç E, Patiroglu T. Intoxication aiguë à la colchicine compliquée d’une hématopoïèse extramédullaire due au filgrastim chez un enfant. J Pediatr Hematol Oncol. 2014 Oct;36(7):e460-2.

  • Kutuk MS, Balta B, Kodera H, Matsumoto N, Saitsu H, Doganay S, Canpolat M, Dolanbay M, Unal E, Dundar M. Existe-t-il une relation entre les mutations COL4A1/A2 et l’hémorragie intraventriculaire fœtale détectée en anténatal ? Childs Nerv Syst. 2014 Mar;30(3):419-24.

  • Patiroglu T, Gungor HE, Triot A, Unal E. Severe congenital neutropenia in two siblings related to HAX1 mutation without neurodevelopmental disorders. Genet Couns. 2013;24(3):253-8.

  • Patiroglu T, Gungor HE, Unal E, Koker Y. Les caractéristiques cliniques et les mutations génétiques de la maladie granulomateuse chronique : résultats d’un centre de référence en Anatolie moyenne. Genet Couns. 2013;24(3):327-35.

  • Patıroğlu T, Eke Güngör H, Belohradsky JS, Unal E, Klein C. Myeloperoxidase deficiency : the secret under the flag of unstained cell. Turk J Haematol. 2013 Jun;30(2):232-3.

  • Sassi A, Lazaroski S, Wu G, Haslam SM, Fliegauf M, Mellouli F, Patiroglu T, Unal E, Ozdemir MA, Jouhadi Z, Khadir K, Ben-Khemis L, Ben-Ali M, Ben-Mustapha I, Borchani L, Pfeifer D, Jakob T, Khemiri M, Asplund AC, Gustafsson MO, Lundin KE, Falk-Sörqvist E, Moens LN, Gungor HE, Engelhardt KR, Dziadzio M, Stauss H, Fleckenstein B, Meier R, Prayitno K, Maul-Pavicic A, Schaffer S, Rakhmanov M, Henneke P, Kraus H, Eibel H, Kölsch U, Nadifi S, Nilsson M, Bejaoui M, Schäffer AA, Smith CI, Dell A, Barbouche MR, Grimbacher B. Les mutations homozygotes hypomorphes de la phosphoglucomutase 3 (PGM3) altèrent l’immunité et augmentent les niveaux d’IgE sériques. J Allergy Clin Immunol. 2014 May;133(5):1410-9.

  • Patiroglu T, Isik B, Unal E, Canoz O, Deniz K, Kosemehmetoglu K, Karakukcu M, Ozdemir MA. Rhabdomyosarcome alvéolaire métastatique crânien imitant une tumeur maligne hématologique chez un adolescent. Childs Nerv Syst. 2014 Oct;30(10):1737-41. doi : 10.1007/s00381-014-2443-2.

  • Ünal E, Özsoylu S, Bayram A, Özdemir MA, Yılmaz E, Canpolat M, Tümtürk A, Per H. "L’hémorragie intracrânienne chez les nourrissons comme conséquence grave et évitable d’une forme tardive de carence en vitamine K : une image selfie de la Turquie, des stratégies pour demain". Childs Nerv Syst. 2014 Aug;30(8):1375-82.

  • Triot A, Järvinen PM, Arostegui JI, Murugan D, Kohistani N, Dapena Díaz JL, Racek T, Puchałka J, Gertz EM, Schäffer AA, Kotlarz D, Pfeifer D, Díaz de Heredia Rubio C, Özdemir MA, Patıroglu T, Karakükcü M, Sánchez de Toledo Codina J, Yagüe J, Touw IP, Ünal E, Klein C.
    "Inherited biallelic CSF3R mutations in severe congenital neutropenia"
    Blood. 2014 Jun 12;123(24):3811-7.

  • Patıroglu T, Akar HH, Gilmour K, Özdemir MA, Bibi S, Henriquez F, Burns SO, Ünal E.
    « Déficit immunitaire combiné sévère atypique causé par une nouvelle mutation homozygote du gène Rag1 chez une fillette présentant un pyoderma gangrenosum : rapport de cas et revue de la littérature. »
    J Clin Immunol. Oct. 2014 ; 34(7) : 792-5. doi : 10.1007/s10875-014-0077-5. Publication en ligne le 8 août 2014. PMID : 25104208.

  • Bayram AK, Yılmaz E, Per H, Ito M, Uchino H, Doğanay S, Houkin K, Ünal E.
    "Familial moyamoya disease in two Turkish siblings with same polymorphism in RNF213 gene but different clinical features."
    Childs Nerv Syst. 2016 Mar;32(3):569-73.

  • Patıroglu T, Akar HH, van der Burg M, Ünal E.
    "Autosomal recessive hyper IgM syndrome associated with activation-induced cytidine deaminase gene in three Turkish siblings presented with tuberculosis lymphadenitis - Case report."
    Acta Microbiol Immunol Hung. 2015 Sep;62(3):267-74.

  • Doğan MS, Doğanay S, Koç G, Görkem SB, Ünal E, Öztürk F, Coşkun A.
    "Inflammatory Myofibroblastic Tumor of the Kidney and Bilateral Lung Nodules in a Child Mimicking Wilms Tumor With Lung Metastases"
    JPediatr Hematol Oncol. 2015 Aug;37(6):e390-3.

  • Karakükcü M, Karakükcü C, Ünal E, Öztürk A, Çıraçı Z, Patıroglu T, Özdemir MA.
    "The Importance of Nucleated Red Blood Cells in Patients with Beta Thalassemia Major and Comparison of Two Automated Systems with Manual Microscopy and Flow Cytometry."
    Clin Lab. 2015;61(9):1289-95.

  • Hazar V, Kesik V, Aksoylar S, Karakükcü M, Öztürk G, Küpesiz A, Atas E, Öniz H, Kansoy S, Ünal E, Tanyeli A, Erbey F, Elli M, Taçyıldız N, Karasu GT, Koçak U, Anak S, Yılmaz Bengoa S, Sezgin G, Atay D, Ünal E, Uygun V, Kurucu N, Kaya Z, Yesilipek A ; Groupe d’étude turc sur la transplantation de moelle osseuse pédiatrique (TPBMT-SG).
    "Outcome of autologous hematopoietic stem cell transplantation in children and adolescents with relapsed or refractory Hodgkin’s lymphoma"
    PediatrTransplant. 2015 Nov;19(7):745-52.

  • Patıroglu T, Haluk Akar H, Gilmour K, Ünal E, Akif Özdemir M, Bibi S, Burns S, Chiang SC, Schlums H, Bryceson YT, Karakükcü M.
    "A case of XMEN syndrome presented with severe auto-immune disorders mimicking autoimmune lymphoproliferative disease."
    Clin Immunol. 2015 Jul;159(1):58-62.

  • Engelhardt KR, Gertz ME, Keles S, Schäffer AA, Sigmund EC, Glocker C, Saghafi S, Pourpak Z, Ceja R, Sassi A, Graham LE, Massaad MJ, Mellouli F, Ben-Mustapha I, Khemiri M, Kilic SS, Etzioni A, Freeman AF, Thiel J, Schulze I, Al-Herz W, Metin A, Sanal Ö, Tezcan I, Yeganeh M, Niehues T, Dueckers G, Weinspach S, Patıroglu T, Ünal E, Dasouki M, Yılmaz M, Genel F, Aytekin C, Kutukculer N, Somer A, Kilic M, Reisli I, Camcioglu Y, Gennery AR, Cant AJ, Jones A, Gaspar BH, Arkwright PD, Pietrogrande MC, Baz Z, Al-Tamemi S, Lougaris V, Lefranc G, Megarbane A, Boutros J, Galal N, Bejaoui M, Barbouche MR, Geha RS, Chatila TA, Grimbacher B.
    "Le phénotype clinique étendu de 64 patients atteints d’un déficit du dédicateur de la cytokinèse 8.
    J Allergy Clin Immunol. 2015 Aug;136(2):402-12.

  • Canpolat M, Ceylan O, Per H, Koç G, Tümtürk A, Kumandaş S, Patıroglu T, Doğanay S, Gümüş H, Ünal E, Köse M, Görkem SB, Kurtsoy A, Öztürk MK.
    "Brain abscesses in children : results of 24 children from a reference center in Central Anatolia, Turkey"
    JChild Neurol. 2015 Mar;30(4):458-67.

  • Özdemir MA, Işık B, Patıroglu T, Karakükcü M, Mutlu FT, Yılmaz E, Ünal E.
    "A case of congenital afibrinogenemia complicated with thromboembolic events that required repeated amputations"
    Blood Coagul Fibrinolysis. 2015 Apr;26(3):354-6.

  • Tesi B, Lagerstedt-Robinson K, Chiang SC, Ben Bdira E, Abboud M, Belen B, Devecioğlu O, Fadoo Z, Yeoh AE, Erichsen HC, Möttönen M, Akar HH, Hästbacka J, Kaya Z, Nunes S, Patıroglu T, Sabel M, Sarıbeyoğlu ET, Tvedt TH, Ünal E, Ünal S, Ünuvar A, Meeths M, Henter JI, Nordenskjöld M, Bryceson YT.
    "Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosis"
    Genome Med. 2015 Dec 18;7:130.

  • Tümtürk A, Kaya Özcora G, Kaçar Bayram A, Kabaklıoğlu M, Doğanay S, Canpolat M, Gümüş H, Kumandaş S, Ünal E, Kurtsoy A, Per H.
    "Torticollis in children : an alert symptom not to be turned away."
    Childs Nerv Syst. 2015 Sep;31(9):1461-70.

  • Karakükcü M, Ünal E.
    "Stem cell mobilization and collection from pediatric patients and healthy children".
    Transfus Apher Sci. 2015 Aug;53(1):17-22.

  • Kesik V, Ataş E, Karakükcü M, Aksoylar S, Erbey F, Taçyıldız N, Küpesiz A, Öniz H, Ünal E, Kansoy S, Öztürk G, Elli M, Kaya Z, Ünal E, Hazar V, Yılmaz Bengoa Ş, Karasu G, Atay D, Dağdemir A, Ören H, Koçak Ü, Yeşilipek MA.
    "Facteurs pronostiques et nouveau modèle d’indice pronostique pour les enfants et les adolescents atteints de lymphome de Hodgkin ayant subi une transplantation autologue de cellules souches hématopoïétiques : A Multicenter Study of the Turkish Pediatric Bone Marrow Transplantation Study Group"
    Turk J Haematol. 2016 Dec 1;33(4):265-272.

  • Tümtürk A, Özdemir MA, Per H, Ünal E, Küçük A, Ulutabanca H, Karakükcü M, Canoz O, Gümüş H, Coşkun A, Kurtsoy A.
    "Pediatric central nervous system tumors in the first 3 years of life : pre-operative mean platelet volume, neutrophil/lymphocyte count ratio, and white blood cell count correlate with the presence of a central nervous system tumor"
    Childs Nerv Syst. 2017 Feb;33(2):233-238.

  • Lévy R, Okada S, Béziat V, Moriya K, Liu C, Chai LY, Migaud M, Hauck F, Al Ali A, Cyrus C, Vatte C, Patıroglu T, Ünal E, Ferneiny M, Hyakuna N, Nepesov S, Oleastro M, Ikinciogullari A, Doğu F, Asano T, Ohara O, Yun L, Della Mina E, Bronnimann D, Itan Y, Gothe F, Bustamante J, Boisson-Dupuis S, Tahuil N, Aytekin C, Salhi A, Al Muhsen S, Kobayashi M, Toubiana J, Abel L, Li X, Camcıoğlu Y, Celmeli F, Klein C, AlKhater SA, Casanova JL, Puel A.
    "Caractéristiques génétiques, immunologiques et cliniques des patients atteints d’infections bactériennes et fongiques dues à un déficit héréditaire en IL-17RA".
    Proc Natl Acad Sci U S A. 2016 Dec 20;113(51):E8277-E8285. doi : 10.1073/pnas.1618300114. Epub 2016 Dec 7. PMID : 27930337 ; PMCID : PMC5187691.

  • Özcan A, Patıroglu T, Acer H, Gümüş H, Şenol S, Karakükcü M, Özdemir MA, Ünal E.
    "Fibromuscular Dysplasia Complicated With Cerebral Stroke in a Child With Congenital Dyserythropoietic Anemia Type II"
    JPediatr Hematol Oncol. 2016 Nov;38(8):e333-e335.

  • Patıroglu T, Akar HH, Ünal E, Özdemir MA, Karakükcü M.
    "Hematopoietic Stem Cell Transplant for Primary Immunodeficiency Diseases : A Single-Center Experience"
    Exp Clin Transplant. 2017 Jun;15(3):337-343.

  • Çıraçı S, Özcan A, Özdemir MM, Chiang SCC, Tesi B, Özdemir AM, Karakükcü M, Patıroglu T, Acipayam C, Doğanay S, Gümüş H, Ünal E.
    "A Case of Familial Hemophagocytic Lymphohistiocytosis Type 4 With Involvement of the Central Nervous System Complicated With Infarct"
    JPediatr Hematol Oncol. 2017 Aug;39(6):e321-e324.

  • Özdemir A, Güneş T, Chiang SCC, Ünal E.
    "A Newborn With Familial Hemophagocytic Lymphohistiocytosis Complicated With Transfusion Associated Graft Versus Host Disease"
    JPediatr Hematol Oncol. 2017 Aug;39(6):e309-e311.

  • Yılmaz E, Bayram Kaçar A, Bozpolat A, Zararsız G, Görkem BS, Karakükcü M, Patıroglu T, Gümüş H, Özdemir MA, Özcan A, Per H, Ünal E.
    "The relationship between hematological parameters and prognosis of children with acute ischemic stroke"
    Childs Nerv Syst. 2018 Apr;34(4):655-661.

  • Tüfekçi Ö, Koçak Ü, Kaya Z, Yenicesu İ, Albayrak C, Albayrak D, Yılmaz Bengoa Ş, Patıroğlu T, Karakükçü M, Ünal E, Ünal İnce E, İleri T, Ertem M, Celkan T, Özdemir GN, Sarper N, Kaçar D, Yaralı N, Özbek NY, Küpesiz A, Karapınar T, Vergin C, Çalışkan Ü, Tokgöz H, Sezgin Evim M, Baytan B, Güneş AM, Yılmaz Karapınar D, Karaman S, Uygun V, Karasu G, Yeşilipek MA, Koç A, Erduran E, Atabay B, Öniz H, Ören H.
    "Leucémie myélomonocytaire juvénile en Turquie : A Retrospective Analysis of Sixty-five Patients"
    Turk J Haematol. 2018 Mar 1;35(1):27-34.

  • Zitouni S, Koç G, Doğanay S, Saraçoğlu S, Gümüş KZ, Çıraçı S, Coşkun A, Ünal E, Per H, Kurtsoy A, Kontaş O.
    "Apparent diffusion coefficient in differentiation of pediatric posterior fossa tumors"
    Jpn JRadiol. 2017 Aug;35(8):448-453.

  • Sav H, Atalay MA, Koç AN, Ünal E, Demir G, Zararsız G.
    "Utility of the Aspergillus galactomannan antigen testing for neutropenic paediatric patients"
    Infez Med. 2017 Mar 1;25(1):38-44.

  • Kim AR, Ulirsch JC, Wilmes S, Ünal E, Moraga I, Karakükcü M, Yuan D, Kazerounian S, Abdulhay NJ, King DS, Gupta N, Gabriel SB, Lander ES, Patıroglu T, Özcan A, Özdemir MA, Garcia KC, Piehler J, Gazda HT, Klein DE, Sankaran VG.
    "Functional Selectivity in Cytokine Signaling Revealed Through a Pathogenic EPO Mutation"
    Cell. 2017 Mar 9;168(6):1053-1064.

  • Özcan A, Canpolat M, Doğanay S, Ünal E, Karakükcü M, Özdemir MA, Patıroglu T.
    "Cerebral Sinus Venous Thrombosis and Prothrombotic Risk Factors in Children : A Single-Center Experience From Turkey"
    JPediatr Hematol Oncol. 2018 Aug;40(6):e369-e372.

  • Patıroğlu T, Erdoğ Şahin N, Ünal E, Kendirci M, Karakükcü M, Özdemir MA.
    "Effectiveness of Ankaferd BloodStopper in Prophylaxis and Treatment of Oral Mucositis in Childhood Cancers Evaluated with Plasma Citrulline Levels."
    Turk J Haematol. 2018 Mar 1;35(1):85-86.

  • Somekh I, Marquardt B, Liu Y, Rohlfs M, Hollizeck S, Karakükcü M, Ünal E, Yılmaz E, Patıroğlu T, Cansever M, Frizinsky S, Vishnvenska-Dai V, Rechavi E, Stauber T, Simon AJ, Lev A, Klein C, Kotlarz D, Somech R.
    "Novel Mutations in RASGRP1 are Associated with Immunodeficiency, Immune Dysregulation, and EBV-Induced Lymphoma"
    JClin Immunol. 2018 Aug;38(6):699-710.

  • Özcan A, Arslanoglu C, Ünal E, Patıroğlu T, Özdemir MA, Deniz K, Özcan SS, Karakükcü M.
    "Evaluation of childhood solid pseudopapillary tumors of the pancreas"
    North Clin Istanbul. 2018 Sep;5(3):207-210.

  • İçöz K, Gerçek T, Murat A, Özcan S, Ünal E.
    "Capturing B type acute lymphoblastic leukemia cells using two types of antibodies"
    Biotechnol Prog. 2019 Jan;35(1):e2737.

    Bozpolat A, Ünal E, Topaloğlu T, Taheri S, Bayram AK, Özcan A, Karakükçü M, Özdemir MA, Per H. The relationship between the prognosis of children with acute arterial stroke and polymorphisms of CDKN2B, HDAC9, NINJ2, NAA25 genes. J Thromb Thrombolysis. 2019 May;47(4):578-584.

  • Eken A, Cansever M, Somekh I, Mizoguchi Y, Ziętara N, Okus FZ, Erdem S, Canatan H, Akyol S, Özcan A, Karakükçü M, Hollizeck S, Rohlfs M, Ünal E, Klein C, Patiroğlu T. Genetic Deficiency and Biochemical Inhibition of ITK Affect Human Th17, Treg, and Innate Lymphoid Cells. J Clin Immunol. 2019 Mai;39(4):391-400.

  • Özcan A, Saraçoğlu S, Verboon JM, Karakükçü M, Patiroğlu T, Coşkun A, Sankaran VG, Ünal E. A mummy emerges from the grave : Scurvy confounding the clinical presentation of a child with Fanconi anemia. Am J Hematol. 2019 Apr;94(4):506-507.

  • Farmer JR, Foldvari Z, Ujhazi B, De Ravin SS, Chen K, Bleesing JJH, Schuetz C, Al-Herz W, Abraham RS, Joshi AY, Costa-Carvalho BT, Buchbinder D, Booth C, Reiff A, Ferguson PJ, Aghamohammadi A, Abolhassani H, Puck JM, Adeli M, Cancrini C, Palma P, Bertaina A, Locatelli F, Di Matteo G, Geha RS, Kanariou MG, Lycopoulou L, Tzanoudaki M, Sleasman JW, Parikh S, Pinero G, Fischer BM, Dbaibo G, Ünal E, Patiroğlu T, Karakükçü M, Al-Saad KK, Dilley MA, Pai SY, Dutmer CM, Gelfand EW, Geier CB, Eibl MM, Wolf HM, Henderson LA, Hazen MM, Bonfim C, Wolska-Kuśnierz B, Butte MJ, Hernandez JD, Nicholas SK, Stepensky P, Chandrakasan S, Miano M, Westermann-Clark E, Goda V, Kriván G, Holland SM, Fadugba O, Henrickson SE, Özen A, Karakoc-Aydıner E, Barış S, Kıyıkım A, Bredius R, Hoeger B, Boztug K, Pashchenko O, Neven B, Moshous D, Villartay JP, Bousfiha AA, Hill HR, Notarangelo LD, Walter JE. Outcomes and Treatment Strategies for Autoimmunity and Hyperinflammation in Patients with RAG Deficiency (Résultats et stratégies de traitement de l’auto-immunité et de l’hyperinflammation chez les patients présentant un déficit en RAG). J Allergy Clin Immunol Pract. 2019 Jul-Aug;7(6):1970-1985.e4.

  • Grabowski P, Hesse S, Hollizeck S, Rohlfs M, Behrends U, Sherkat R, Tamary H, Ünal E, Somech R, Patiroğlu T, Canzar S, van der Werff Ten Bosch J, Klein C, Rappsilber J. Proteome Analysis of Human Neutrophil Granulocytes From Patients With Monogenic Disease Using Data-independent Acquisition. Mol Cell Proteomics. 2019 Apr;18(4):760-772.

  • Çelkan T, Kızıloçak H, Evim M, Meral Güneş A, Özbek NY, Yaraşlı N, Ünal E, Patiroğlu T, Yılmaz Karapınar D, Sarper N, Zengin E, Karaman S, Koçak Ü, Kürekçi E, Özdemir C, Tuğcu D, Uysalol E, Dikme G, Adaletli İ, Kuruoğlu S, Kebudi R. Infections fongiques hépatospléniques chez les enfants atteints de leucémie - Facteurs de risque et résultats : A Multicentric Study. J Pediatr Hematol Oncol. 2019 May;41(4):256-260.

  • Alhashem F, Yılmaz E, Özdemir MA, Deniz K, Yıkılmaz A, Patiroğlu T, Karakükçü M, Ünal E. Biliary Rhabdomyosarcoma in an Infant Male With Neurofibromatosis Type 1. J Pediatr Hematol Oncol. 2019 Jan;41(1):e24-e26.

  • Belen Apak FB, Ümit EG, Zengin Y, Sezgin Evim M, Ünal E, Özbaş HM, Acıpayam C. Assessment of Patients with von Willebrand Disease with ISTH/BAT and PBQ Scores. Turk J Haematol. 2020 Feb 20;37(1):57-58.

  • Magg T, Shcherbina A, Arslan D, Desai MM, Wall S, Mitsialis V, Conca R, Ünal E, Karacabey N, Mukhina A, Rodina Y, Taur PD, Illig D, Marquardt B, Hollizeck S, Jeske T, Gothe F, Schober T, Rohlfs M, Koletzko S, Lurz E, Muise AM, Snapper SB, Hauck F, Klein C, Kotlarz D. CARMIL2 Deficiency Presenting as Very Early Onset Inflammatory Bowel Disease (déficit en CARMIL2 se manifestant par une maladie inflammatoire de l’intestin très précoce). Inflamm Bowel Dis. 2019 Oct 18;25(11):1788-1795.

  • Eken A, Cansever M, Okus FZ, Erdem S, Nain E, Azizoglu ZB, Haliloglu Y, Karakükçü M, Özcan A, Devecioglu O, Aksu G, Arikan Ayyildiz Z, Topal E, Karakoc Aydiner E, Kıyıkım A, Metin A, Cipe F, Kaya A, Artac H, Reisli I, Guner SN, Uygun V, Karasu G, Dönmez Altuntaş H, Canatan H, Oukka M, Özen A, Chatila TA, Keleş S, Barış S, Ünal E, Patiroğlu T. Déficit en ILC3 et anomalies généralisées des ILC chez les patients déficients en DOCK8. Allergy. 2020 Apr;75(4):921-932.

  • Hangul M, Köse M, Özcan A, Ünal E. Propranolol treatment for chylothorax due to diffuse lymphangiomatosis. Pediatr Blood Cancer. 2019 May;66(5):e27592.

  • Somekh I, Thian M, Medgyesi D, Gülez N, Magg T, Gallón Duque A, Stauber T, Lev A, Genel F, Ünal E, Simon AJ, Lee YN, Kalinichenko A, Dmytrus J, Kraakman MJ, Schiby G, Rohlfs M, Jacobson JM, Özer E, Akcal Ö, Conca R, Patiroğlu T, Karakükçü M, Özcan A, Shahin T, Appella E, Tatematsu M, Martinez-Jaramillo C, Chinn IK, Orange JS, Trujillo-Vargas CM, Franco JL, Hauck F, Somech R, Klein C, Boztug K. Le déficit en CD137 provoque une dysrégulation immunitaire avec prédisposition à la lymphomagénèse. Blood. 2019 Oct 31;134(18):1510-1516.

  • Altay D, Özcan A, Ünal E, Deniz K, Özkan KU, Patiroğlu T, Arslan D. Une cause rare de vomissements chez un adolescent : le lymphome de Burkitt gastrique. Turk J Pediatr. 2019;61(3):431-435.

  • Cansever M, Ziętara N, Chiang SCC, Özcan A, Yılmaz E, Karakükçü M, Rohlfs M, Somekh I, Canoz O, Abdulrezzak U, Bryceson Y, Klein C, Ünal E, Patiroğlu T. A Rare Case of Activated Phosphoinositide 3-Kinase Delta Syndrome (APDS) Presenting With Hemophagocytosis Complicated with Hodgkin Lymphoma. J Pediatr Hematol Oncol. 2020 Mar;42(2):156-159.

  • Hazar V, Karasu GT, Uygun V, Özbek N, Karakükçü M, Öztürk G, Daloğlu H, Kılıç SÇ, Aksu T, Ünal E, Koçak Ü, Yeşilipek A, Akçay A, Gürsel O, Küpesiz A, Okur FV, İleri T, Kansoy S, Bayram İ, Karagün BŞ, Gökçe M, Kaya Z, Ok Bozkaya İ, Patiroğlu T, Aksoylar S. Rôle d’une deuxième transplantation pour les enfants atteints de leucémie aiguë après une rechute posttransplantation : une étude du groupe d’étude turc sur la transplantation de moelle osseuse. Leuk Lymphoma. 2020 Jun;61(6):1465-1474.

  • Atik T, Işık E, Onay H, Akgün B, Shamsali M, Kavaklı K, Evim M, Tüysüz G, Özbek NY, Şahin F, Salcıoğlu Z, Albayrak C, Oymak Y, Ünal E, Belen FB, Yılmaz Keskin E, Balkan C, Baytan B, Küpesiz A, Culha V, Tahtakesen Güçer TN, Güneş AM, Özkınay F. Factor8 Gene Mutation Spectrum of 270 Patients with Hemophilia A : Identification of 36 Novel Mutations (Spectre des mutations du gène du facteur 8 chez 270 patients atteints d’hémophilie A : identification de 36 nouvelles mutations). Turk J Haematol. 2020 Aug 28;37(3):145-153.

  • Akyol S, Özcan A, Sekine T, Chiang SCC, Yılmaz E, Karakükçü M, Patiroğlu T, Bryceson Y, Ünal E. Different Clinical Presentation of 3 Children With Familial Hemophagocytic Lymphohistiocytosis With 2 Novel Mutations. J Pediatr Hematol Oncol. 2020 Oct;42(7):e627-e629.

  • İçöz K, Akar Ü, Ünal E. Microfluidic Chip based direct triple antibody immunoassay for monitoring patient comparative response to leukemia treatment. Biomed Microdevices. 2020 Jul 13;22(3):48.

  • Ünal E, Yılmaz E, Özcan A, Işık B, Karakükçü M, Turan C, Akgün H, Öztürk F, Coşkun A, Özdemir MA, Patiroğlu T. Twenty children with non-Wilms renal tumors from a reference center in Central Anatolia, Turkey. Turk J Med Sci. 2020 Feb 13;50(1):18-24.

  • Łyszkiewicz M, Ziętara N, Frey L, Pannicke U, Stern M, Liu Y, Fan Y, Puchałka J, Hollizeck S, Somekh I, Rohlfs M, Yilmaz T, Ünal E, Karakükçü M, Patiroğlu T, Kellerer C, Karasu E, Sykora KW, Lev A, Simon A, Somech R, Roesler J, Hoenig M, Keppler OT, Schwarz K, Klein C. Le déficit en FCHO1 humain révèle le rôle de l’endocytose médiée par la clathrine dans le développement et la fonction des cellules T. Nat Commun. 2020 Feb 25;11(1):1031.

  • Simon AJ, Golan AC, Lev A, Stauber T, Barel O, Somekh I, Klein C, AbuZaitun O, Eyal E, Kol N, Ünal E, Amariglio N, Rechavi G, Somech R. Whole exome sequencing (WES) approach for diagnosing primary immunodeficiencies (PIDs) in a highly consanguineous community. Clin Immunol. 2020 May;214:108376.

  • Özcan A, Ünal E, Karakükçü M, Coşkun A, Özdemir MA, Patiroğlu T. Vena cava superior syndrome in the children with mediastinal tumors : Single-center experience. North Clin Istanbul. 2020 Apr 9;7(3):255-259.

  • Özcan A, Samur B, Akyol Ş, Erdoğmuş NA, Patiroğlu T, Karakükçü M, Ünal E. Congenital afibrinogenemia in a 4-year-old girl complicated with acute lymphoblastic leukemia. Turk J Pediatr. 2020;62(2):289-292.

  • Ravell JC, Matsuda-Lennikov M, Chauvin SD, Zou J, Biancalana M, Deeb SJ, Price S, Su HC, Notarangelo G, Jiang P, Morawski A, Kanellopoulou C, Binder K, Mukherjee R, Anibal JT, Sellers B, Zheng L, He T, George AB, Pittaluga S, Powers A, Kleiner DE, Kapuria D, Ghany M, Hunsberger S, Cohen JI, Uzel G, Bergerson J, Wolfe L, Toro C, Gahl W, Folio LR, Matthews H, Angelus P, Chinn IK, Trujillo-Vargas CM, Franco JL, Orrego-Arango J, Gutiérrez-Hincapié S, Patel NC, Raymond K, Patiroğlu T, Ünal E, Karakükçü M, Day AG, Mehta P, Masutani E, De Ravin SS, Malech HL, Altan-Bonnet G, Rao VK, Mann M, Lenardo MJ. Une glycosylation défectueuse et des anomalies multisystémiques caractérisent l’immunodéficience primaire XMEN. J Clin Invest. 2020 Jan 2;130(1):507-522.

    Ejaz A, Özcan A, Ünal E, Karakükçü M, Sankaran VG. Long-Term Patient-Customized Therapy for a Pathogenic EPO (Thérapie à long terme adaptée au patient pour une EPO pathogène). Med. 2021 Jan 15;2(1):33-37.e1.

  • Altay D, Yılmaz E, Özcan A, Karakükçü M, Ünal E, Arslan D. Hepatitis-associated aplastic anemia in pediatric patients : single center experience. Transfus Apher Sci. 2020 Dec;59(6):102900.

  • Ghosh S, Köstel Bal S, Edwards ESJ, Pillay B, Jiménez Heredia R, Erol Cipe F, Rao G, Salzer E, Zoghi S, Abolhassani H, Momen T, Gostick E, Price DA, Zhang Y, Oler AJ, Gonzaga-Jauregui C, Erman B, Metin A, İlhan I, Haskoloğlu S, İslamoğlu C, Baskin K, Ceylaner S, Yılmaz E, Ünal E, Karakükçü M, Berghuis D, Cole T, Gupta AK, Hauck F, Kogler H, Hoepelman AIM, Barış S, Karakoc-Aydiner E, Özen A, Kager L, Holzinger D, Paulussen M, Krüger R, Meisel R, Oommen PT, Morris E, Neven B, Worth A, van Montfrans J, Fraaij PLA, Choo S, Doğu F, Davies EG, Burns S, Dückers G, Becker RP, von Bernuth H, Latour S, Faraci M, Gattorno M, Su HC, Pan-Hammarström Q, Hammarström L, Lenardo MJ, Ma CS, Niehues T, Aghamohammadi A, Rezaei N, İkinciogulları A, Tangye SG, Lankester AC, Boztug K. Phénotype clinique et immunologique étendu et résultats de la transplantation dans les déficits en CD27 et CD70. Blood. 2020 Dec 3;136(23):2638-2655.

  • Paç Kısaarslan A, Witzel M, Ünal E, Rohlfs M, Akyıldız B, Doğan ME, Poyrazoğlu H, Klein C, Patiroğlu T. Refractory and Fatal Presentation of Severe Autoimmune Hemolytic Anemia in a Child With the DNASE1L3 Mutation Complicated with an Additional DOCK8 Variant (Présentation réfractaire et fatale d’une anémie hémolytique auto-immune sévère chez un enfant porteur de la mutation DNASE1L3 compliquée par un variant DOCK8 supplémentaire). J Pediatr Hematol Oncol. 2021 Apr 1;43(3):e452-e456.

  • Yılmaz E, Kühn HS, Odakir E, Niemela JE, Özcan A, Eken A, Rohlfs M, Cansever M, Gök V, Aydın F, Karakükçü M, Hauck F, Klein C, Ünal E, Rosenzweig SD, Patiroğlu T. Common Variable Immunodeficiency, Autoimmune Hemolytic Anemia, and Pancytopenia Associated With a Defect in IKAROS. J Pediatr Hematol Oncol. 2021 Apr 1;43(3):e351-e357.

  • Ozkaya M, Baykan A, Cakir M, Vural C, Sunkak S, Unal E, Eken A.

  • Le nombre et l’activité des cellules CD3+TCR Vα7.2+CD161+ sont augmentés chez les enfants atteints de fièvre rhumatismale aiguë.

  • Int J Cardiol. 2021 Jun 15;333:174-183. doi : 10.1016/j.ijcard.2021.02.020. Epub 2021 Feb 22. PMID : 33631279.

  • Hangul M, Tuzuner AB, Somekh I, Klein C, Patiroglu T, Unal E, Kose M.
    Type 1 Plasminogen Deficiency With Pulmonary Involvement : Novel Treatment and Novel Mutation.
    J Pediatr Hematol Oncol. 2021 May 1;43(4):e558-e560.

  • Frede N, Rojas-Restrepo J, Caballero Garcia de Oteyza A, Buchta M, Hübscher K, Gámez-Díaz L, Proietti M, Saghafi S, Chavoshzadeh Z, Soler-Palacin P, Galal N, Adeli M, Aldave-Becerra JC, Al-Ddafari MS, Ardenyz Ö, Atkinson TP, Kut FB, Çelmeli F, Rees H, Kilic SS, Kirovski I, Klein C, Kobbe R, Korganow AS, Lilic D, Lunt P, Makwana N, Metin A, Özgür TT, Karakas AA, Seneviratne S, Sherkat R, Sousa AB, Unal E, Patiroglu T, Wahn V, von Bernuth H, Whiteford M, Doffinger R, Jouhadi Z, Grimbacher B.
    Analyse génétique d’une cohorte de 275 patients atteints de syndromes d’hyper-IgE et/ou de candidoses cutanées chroniques.
    J Clin Immunol. 2021 Nov;41(8):1804-1838.

  • Capo V, Penna S, Merelli I, Barcella M, Scala S, Basso-Ricci L, Draghici E, Palagano E, Zonari E, Desantis G, Uva P, Cusano R, Sergi Sergi L, Crisafulli L, Moshous D, Stepensky P, Drabko K, Kaya Z, Unal E, Gezdirici A, Menna G, Serafini M, Aiuti A, Locatelli SL, Carlo-Stella C, Schulz AS, Ficara F, Sobacchi C, Gentner B, Villa A.
    Expanded circulating hematopoietic stem/progenitor cells as novel cell source for the treatment of TCIRG1 osteopetrosis.
    Haematologica. 2021 Jan 1;106(1):74-86.

  • Casini A, von Mackensen S, Santoro C, Djambas Khayat C, Belhani M, Ross C, Dorgalaleh A, Naz A, Ünal E, Abdelwahab M, Lozeron ED, Trillot N, Susen S, Peyvandi F, de Moerloose P ; QualyAfib Study Group.
    Phénotype clinique, supplémentation en fibrinogène et qualité de vie liée à la santé chez les patients atteints d’afibrinogénémie.
    Blood. 2021 Jun 3;137(22):3127-3136.

  • Canpolat M, Kaya Özçora GD, Poyrazoğlu H, Per H, Çoşkun A, Gümüş H, Arslan D, Ünal E, Karakükçü M, Patıroğlu T, Kumandaş S.
    Long-Term Follow-Up of Patients with a Diagnosis of Posterior Reversible Encephalopathy Syndrome.
    Turk Arch Pediatr. 2021 Nov;56(6):569-575.

  • Celik N, Sahin F, Ruzi M, Yay M, Unal E, Onses MS.
    Blood repellent superhydrophobic surfaces constructed from nanoparticle-free and biocompatible materials.
    Colloids Surf B Biointerfaces. 2021 Sep;205:111864.

  • Tumturk A, Gorkem SB, Ozmansur EN, Peduk Y, Arslan U, Gok V, Dogan H, Cetin BS, Sahin A, Gumus H, Guney A, Unal E, Kurtsoy A, Per H.
    The Spectrum of Underlying Diseases in Children with Torticollis.
    Turk Neurosurg. 2021;31(3):389-398.

  • Solmaz I, Ozdemir MA, Unal E, Abdurrezzak U, Muhtaroglu S, Karakukcu M.
    Effet de la vitamine K2 et de la vitamine D3 sur la densité minérale osseuse chez les enfants atteints de leucémie lymphoblastique aiguë : une étude de cohorte prospective.
    J Pediatr Endocrinol Metab. 2021 Feb 25;34(4):441-447.

  • Karaman S, Kebudi R, Kizilocak H, Karakas Z, Demirag B, Evim MS, Yarali N, Kaya Z, Karagun BS, Aydogdu S, Caliskan U, Ayhan AC, Bahadir A, Cakir B, Guner BT, Albayrak C, Karapinar DY, Kazanci EG, Unal E, Turkkan E, Akici F, Bor O, Vural S, Yilmaz S, Apak H, Baytan B, Tahta NM, Güzelkucuk Z, Kocak U, Antmen B, Tokgöz H, Fisgin T, Özdemir N, Gunes AM, Vergin C, Unuvar A, Ozbek N, Tugcu D, Bay SB, Tanyildiz HG, Celkan T.
    Infections fongiques du système nerveux central chez les enfants atteints de leucémie et subissant une transplantation de cellules souches hématopoïétiques : Une étude rétrospective multicentrique.
    J Pediatr Hematol Oncol. 2022 Nov 1;44(8):e1039-e1045.

  • Gül F, Gonen ZB, Jones OY, Taşlı NP, Zararsız G, Ünal E, Özdarendeli A, Şahin F, Eken A, Yılmaz S, Karakukçu M, Kırbaş OK, Gökdemir NS, Bozkurt BT, Özkul Y, Oktay BD, Uygut MA, Cinel I, Çetin M.
    Une étude pilote pour le traitement de la pneumonie sévère COVID-19 par une formulation aérosolisée d’exosomes de plasma immunitaire humain convalescent (ChipEXO™).
    Front Immunol. 2022 Nov 9;13:963309.

  • Haliloglu Y, Ozcan A, Erdem S, Azizoglu ZB, Bicer A, Ozarslan OY, Kilic O, Okus FZ, Demir F, Canatan H, Karakukcu M, Uludag SZ, Kutuk MS, Unal E, Eken A.
    Characterization of cord blood CD3+TCRVα7.2+ CD161high T and innate lymphoid cells in the pregnancies with gestational diabetes, morbidly adherent placenta, and pregnancy hypertension diseases.
    Am J Reprod Immunol. 2022 Jul;88(1):e13555.

  • Goktas S, Azizoglu ZB, Petersheim D, Erdogan M, Eke Gungor H, Bisgin A, Tuğ Bozdoğan S, Eken A, Unal E, Klein C, Patiroglu T.
    A Novel Intronic Mutation Reduces HAX1 Level and is Associated with Severe Congenital Neutropenia.
    J Pediatr Hematol Oncol. 2022 Jan 1;44(1):e62-e67.

  • Samur BM, Samur TG, Çiflikli FE, Özcan A, Gök V, Soykan R, Soytürk F, Kiliç Ö, Kandur M, Kandemir R, Zararsiz G, Karakükcü M, Patiroglu T, Ünal E.
    Evaluation of primary care physicians’ approaches to hemophilia and bleeding disorders : a questionnaire survey.
    Blood Coagul Fibrinolysis. 2022 Oct 1;33(7):381-388.

  • Gok V, Ozcan A, Ozer S, Karaman F, Aykutlu E, Yilmaz E, Karakukcu M, Bisgin A, Unal E.
    Aceruloplasminemia presenting with microcytic anemia in a Turkish boy due to a novel pathogenic variant.
    Pediatr Hematol Oncol. 2022 Oct 29:1-9.

  • Gok V, Tada H, Ensar Dogan M, Alakus Sari U, Aslan K, Ozcan A, Yilmaz E, Kardas F, Karakukcu M, Canatan H, Karakukcu C, Dundar M, Inazu A, Unal E.
    A teenager boy with a novel variant of Sitosterolemia presented with pancytopenia.
    Clin Chim Acta. 2022 Apr 1;529:61-66.

  • Efe YS, Özbey H, Caner N, Erdem E, Kuzucu EG, Karakükçü M, Patıroğlu T, Ünal E, Yılmaz E, Özcan A.
    Social exclusion and behavior problems in adolescents with cancer and healthy counterparts.
    J Pediatr Nurs. 2022 May-Jun;64:e95-e101.

  • Yilmaz E, Azizoglu ZB, Aslan K, Erdem S, Haliloglu Y, Suna PA, Yay AH, Deniz K, Tasdemir A, Per S, Unal E, Karakukcu M, Patiroglu T.
    Therapeutic effects of vitamin D and IL-22 on methotrexate-induced mucositis in mice.
    Anticancer Drugs. 2022 Jan 1;33(1):11-18.

  • Taşlı NP, Gönen ZB, Kırbaş OK, Gökdemir NS, Bozkurt BT, Bayrakcı B, Sağraç D, Taşkan E, Demir S, Ekimci Gürcan N, Bayındır Bilgiç M, Bayrak ÖF, Yetişkin H, Kaplan B, Pavel STI, Dinç G, Serhatlı M, Çakırca G, Eken A, Aslan V, Yay M, Karakukcu M, Unal E, Gül F, Basaran KE, Ozkul Y, Şahin F, Jones OY, Tekin Ş, Özdarendeli A, Cetin M.
    Études précliniques sur l’exosome dérivé du plasma immunitaire humain convalescent : Omics and Antiviral Properties to SARS-CoV-2.
    Front Immunol. 2022 Mar 24;13:824378.

  • Alsavaf MB, Verboon JM, Dogan ME, Azizoglu ZB, Okus FZ, Ozcan A, Dundar M, Eken A, Donmez-Altuntas H, Sankaran VG, Unal E.
    A novel missense mutation outside the DNAJ domain of DNAJC21 is associated with Shwachman-Diamond syndrome.
    Br J Haematol. 2022 Jun;197(6):e88-e93. doi : 10.1111/bjh.18112. Epub 2022 Mar 17. PMID : 35298850.

  • Kolukisa B, Baser D, Akcam B, Danielson J, Bilgic Eltan S, Haliloglu Y, Sefer AP, Babayeva R, Akgun G, Charbonnier LM, Schmitz-Abe K, Kendir Demirkol Y, Zhang Y, Gonzaga-Jauregui C, Jimenez Heredia R, Kasap N, Kiykim A, Ozek Yucel E, Gok V, Unal E, Pac Kisaarslan A, Nepesov S, Baysoy G, Onal Z, Yesil G, Celkan TT, Cokugras H, Camcioglu Y, Eken A, Boztug K, Lo B, Karakoc-Aydiner E, Su HC, Ozen A, Chatila TA, Baris S.
    Evolution and long-term outcomes of combined immunodeficiency due to CARMIL2 deficiency.
    Allergy. 2022 Mar;77(3):1004-1019.

  • Köse D, Güzelçiçek A, Öz Ö, Erdem AY, Haliloğlu Y, Witzel M, Klein C, Ünal E.
    The Mutation of CD27 Deficiency Presented With Familial Hodgkin Lymphoma and a Review of the Literature.
    J Pediatr Hematol Oncol. 2022 May 1;44(4):e833-e843.

  • Samur BM, Karakukcu C, Ozcan A, Unal E, Yilmaz E, Karakukcu M.
    Assessment of extracorporeal photopheresis related cell damage.
    Transfus Apher Sci. 2022 Dec;61(6):103472.

  • Lévy R, Gothe F, Momenilandi M, Magg T, Materna M, Peters P, Raedler J, Philippot Q, Rack-Hoch AL, Langlais D, Bourgey M, Lanz AL, Ogishi M, Rosain J, Martin E, Latour S, Vladikine N, Distefano M, Khan T, Rapaport F, Schulz MS, Holzer U, Fasth A, Sogkas G, Speckmann C, Troilo A, Bigley V, Roppelt A, Dinur-Schejter Y, Toker O, Bronken Martinsen KH, Sherkat R, Somekh I, Somech R, Shouval DS, Kühl JS, Ip W, McDermott EM, Cliffe L, Ozen A, Baris S, Rangarajan HG, Jouanguy E, Puel A, Bustamante J, Alyanakian MA, Fusaro M, Wang Y, Kong XF, Cobat A, Boutboul D, Castelle M, Aguilar C, Hermine O, Cheminant M, Suarez F, Yildiran A, Bousfiha A, Al-Mousa H, Alsohime F, Cagdas D, Abraham RS, Knutsen AP, Fevang B, Bhattad S, Kiykim A, Erman B, Arikoglu T, Unal E, Kumar A, Geier CB, Baumann U, Neven B ; Consortium CARMIL2 ; Rohlfs M, Walz C, Abel L, Malissen B, Marr N, Klein C, Casanova JL, Hauck F, Béziat V.
    Le déficit en CARMIL2 humain est à l’origine d’un phénotype immunologique et clinique plus large que le déficit en CD28.
    J Exp Med. 2023 Feb 6;220(2):e20220275.

  • Kondolot M, Yilmaz E, Erdog Sahin N, Ozcan A, Kaynar L, Unal E, Karakukcu M.
    Antibody Response against Vaccine Antigens in Children after TCRαβ-Depleted Haploidentical Stem Cell Transplantation : Is It Similar to That in Recipients with Fully Matched Donors ?
    Transplant Cell Ther. 2023 Feb;29(2):128.e1-128.e9.

  • Linder MI, Mizoguchi Y, Hesse S, Csaba G, Tatematsu M, Łyszkiewicz M, Ziȩtara N, Jeske T, Hastreiter M, Rohlfs M, Liu Y, Grabowski P, Ahomaa K, Maier-Begandt D, Schwestka M, Pazhakh V, Isiaku AI, Briones Miranda B, Blombery P, Saito MK, Rusha E, Alizadeh Z, Pourpak Z, Kobayashi M, Rezaei N, Unal E, Hauck F, Drukker M, Walzog B, Rappsilber J, Zimmer R, Lieschke GJ, Klein C.
    Les défauts génétiques humains de SRP19 et SRPRA provoquent une neutropénie congénitale sévère avec des changements protéomiques distincts.
    Blood. 2023 Feb 9;141(6):645-658.

  • Cekic S, Aydin F, Karali Y, Sevinir BB, Canoz O, Boztug K, Unal E, Kilic SS.
    T-cell/histiocyte-rich large B-cell lymphoma in a patient with a novel frameshift MSH6 mutation.
    Pediatr Blood Cancer. 2023 Mar;70(3):e30008.

  • Gök V, Erdem Ş, Haliloğlu Y, Bişgin A, Belkaya S, Başaran KE, Canatan MF, Özcan A, Yılmaz E, Acıpayam C, Karakükcü M, Canatan H, Per H, Patıroğlu T, Eken A, Ünal E.
    Immunodeficiency associated with a novel functionally defective variant of SLC19A1 benefits from folinic acid treatment.
    Genes Immun. 2023 Feb;24(1):12-20.

  • Erdem S, Haskologlu S, Haliloglu Y, Celikzencir H, Arik E, Keskin O, Eltan SB, Yucel E, Canatan H, Avcilar H, Yilmaz E, Ozcan A, Unal E, Karakukcu M, Celiksoy MH, Kilic SS, Demir A, Genel F, Gulez N, Koker MY, Ozen AO, Baris S, Metin A, Guner SN, Reisli I, Keles S, Dogu EF, Ikinciogullari KA, Eken A.
    Defective Treg generation and increased type 3 immune response in leukocyte adhesion deficiency 1.
    Clin Immunol. 2023 Jul 9;253:109691. doi : 10.1016/j.clim.2023.109691. Epub ahead of print. PMID : 37433423.

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