Pediatric Hematology & Oncology
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 to topical steroid administration in an infant. 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. Kluver-Bucy syndrome in a boy with non-Hodgkin lymphoma. 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 May;19(6-7):587.
Koksal Y, Toy H, Unal E, Baysal T, Esen H, Paksoy Y, Ustun ME. Pilocytic astrocytoma developing at the site of a previously treated medulloblastoma in a child. 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 May;26(5):453-6.
Elmaci MA, Unal E, Peru H. The real diagnosis of cystinuria. Urol Int. 2007;78(4):363.
Unal E, Koksal Y, Vajtai I, Toy H, Kocaogullar Y, Paksoy Y. Astroblastoma in a child. Childs Nerv Syst. 2008 Feb;24(2):165-8.
Unal E, Yazar A, Koksal Y, Caliskan U, Paksoy Y, Kalkan E. Cerebral venous sinus thrombosis in an adolescent with Ewing sarcoma. Childs Nerv Syst. 2008 Sep;24(9):983-6.
Unal E, Koksal Y, Cimen O, Paksoy Y, Tavli L. Malignant glioblastomatous transformation of a low-grade glioma in a child. Childs Nerv Syst. 2008 Dec;24(12):1385-9.
Unal E, Koksal Y, Energin VM, Reisli I. Importance of chemoprophylaxis and vaccines in the prevention of recurrent meningitis. 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 May;31(5):359-61.
Patiroglu T, Unal E, Yikilmaz A, Koker MY, Ozturk MK. Atypical presentation of chronic granulomatous disease in an adolescent boy with frontal lobe located Aspergillus abscess mimicking intracranial tumor. 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. Cardiac functions evaluated with tissue Doppler imaging in childhood cancers treated with 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. Web-based survey of resources for treatment and long-term follow-up for children with brain tumors in developing countries. 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. Accidental intramuscular overdose administration of 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 and PCR Tests: The importance of bronchoalveolar lavage samples. 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. Neurological complication of non Hodgkin lymphoma in childhood: experience from a single center in Turkey. 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. Acute colchicine intoxication complicated with extramedullary hematopoiesis due to filgrastim in a child. 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. Is there relation between COL4A1/A2 mutations and antenatally detected fetal intraventricular hemorrhage? 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. The clinical features and genetic mutations of chronic granulomatous disease: results from a reference centre at middle Anatolia. 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. Hypomorphic homozygous mutations in phosphoglucomutase 3 (PGM3) impair immunity and increase serum IgE levels. 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. Cranial metastatic alveolar rhabdomyosarcoma mimicking hematological malignancy in an adolescent boy. 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. “Intracranial hemorrhage in infants as a serious, and preventable consequence of late form of vitamin K deficiency: a selfie picture of Turkey, strategies for tomorrow.” 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.
“Atypical severe combined immunodeficiency caused by a novel homozygous mutation in Rag1 gene in a girl who presented with pyoderma gangrenosum: a case report and literature review.”
J Clin Immunol. 2014 Oct;34(7):792-5. doi: 10.1007/s10875-014-0077-5. Epub 2014 Aug 8. 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.”
J Pediatr 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; Turkish Pediatric Bone Marrow Transplantation Study Group (TPBMT-SG).
“Outcome of autologous hematopoietic stem cell transplantation in children and adolescents with relapsed or refractory Hodgkin’s lymphoma.”
Pediatr Transplant. 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.
“The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency.”
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.”
J Child 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.
“Prognostic Factors and a New Prognostic Index Model for Children and Adolescents with Hodgkin’s Lymphoma Who Underwent Autologous Hematopoietic Stem Cell Transplantation: 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.
“Genetic, immunological, and clinical features of patients with bacterial and fungal infections due to inherited IL-17RA deficiency.”
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.”
J Pediatr 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.”
J Pediatr 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.”
J Pediatr 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.
“Juvenile Myelomonocytic Leukemia in Turkey: 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 J Radiol. 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.”
J Pediatr 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.”
J Clin 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 May;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. 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. Hepatosplenic Fungal Infections in Children With Leukemia—Risk Factors and Outcome: 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. 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. ILC3 deficiency and generalized ILC abnormalities in DOCK8-deficient patients. 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. CD137 deficiency causes immune dysregulation with predisposition to lymphomagenesis. Blood. 2019 Oct 31;134(18):1510-1516.
Altay D, Özcan A, Ünal E, Deniz K, Özkan KU, Patiroğlu T, Arslan D. A rare cause of vomiting in an adolescent: gastric Burkitt`s lymphoma. 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. Role of a second transplantation for children with acute leukemia following posttransplantation relapse: a study by the Turkish Bone Marrow Transplantation Study Group. 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. 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. Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells. 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 Istanb. 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. Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease. 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. 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. Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency. 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. 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.
The number and activity of CD3+TCR Vα7.2+CD161+ cells are increased in children with acute rheumatic fever.
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.
Genetic Analysis of a Cohort of 275 Patients with Hyper-IgE Syndromes and/or Chronic Mucocutaneous Candidiasis.
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.
Clinical phenotype, fibrinogen supplementation, and health-related quality of life in patients with afibrinogenemia.
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.
Effect of vitamin K2 and vitamin D3 on bone mineral density in children with acute lymphoblastic leukemia: a prospective cohort study.
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.
Central Nervous System Fungal Infections in Children With Leukemia and Undergoing Hematopoietic Stem Cell Transplantation: A Retrospective Multicenter Study.
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.
A pilot study for treatment of severe COVID-19 pneumonia by aerosolized formulation of convalescent human immune plasma exosomes (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.
Preclinical Studies on Convalescent Human Immune Plasma-Derived Exosome: 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; CARMIL2 Consortium; Rohlfs M, Walz C, Abel L, Malissen B, Marr N, Klein C, Casanova JL, Hauck F, Béziat V.
Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency.
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.
Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes.
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.
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