Gürsel T - Search Results

1

Association of xeroderma pigmentosum with thrombasthenia.

Hasanoğlu A, Gücüyener K, Tümer L, Gürsel T. Hasanoğlu A, et al. Among authors: gursel t. Turk J Pediatr. 1996 Apr-Jun;38(2):261-4. Turk J Pediatr. 1996. PMID: 8701496

2

Bernard-Soulier-like functional platelet defect in myelodysplastic syndrome and in acute myeloblastic leukemia associated with trilineage myelodysplasia.

Hiçsönmez G, Gümrük F, Cetin M, Ozbek N, Tuncer M, Gürsel T. Hiçsönmez G, et al. Among authors: gursel t. Turk J Pediatr. 1995 Oct-Dec;37(4):425-9. Turk J Pediatr. 1995. PMID: 8560614

3

Bone marrow hemophagocytosis and immunological abnormalities in a patient with lysinuric protein intolerance.

Gürsel T, Koçak U, Tümer L, Hasanoğlu A. Gürsel T, et al. Acta Haematol. 1997;98(3):160-2. doi: 10.1159/000203612. Acta Haematol. 1997. PMID: 9352748

4

Assessment of brain perfusion by 99mTc-HMPAO SPECT in akinetic mutism due to high-dose intravenous methotrexate therapy.

Karabacak NI, Ozturk G, Gucuyener K, Gokcora N, Gursel T. Karabacak NI, et al. Among authors: gursel t. Childs Nerv Syst. 1997 Oct;13(10):560-2. doi: 10.1007/s003810050138. Childs Nerv Syst. 1997. PMID: 9403207

5

Evaluation of clinical characteristics, diagnosis and management in childhood immune thrombocytopenic purpura: a single center's experience.

Koçak U, Aral YZ, Kaya Z, Oztürk G, Gürsel T. Koçak U, et al. Among authors: gursel t. Turk J Pediatr. 2007 Jul-Sep;49(3):250-5. Turk J Pediatr. 2007. PMID: 17990576

6

Fatal Epstein-Barr virus infection in a case of familial hemophagocytic lymphohistiocytosis with syntaxin-11 mutation.

Albayrak M, Kaya Z, Yilmaz-Keskin E, Stadt UZ, Koçak U, Gürsel T. Albayrak M, et al. Among authors: gursel t. Turk J Pediatr. 2009 Jul-Aug;51(4):371-4. Turk J Pediatr. 2009. PMID: 19950846

7

Hematologic Findings of Inherited Metabolic Disease: They are More Than Expected.

Sal E, Yenicesu I, Okur I, Kaya Z, Ezgu FS, Kocak U, Tumer L, Gursel T, Hasanoglu A. Sal E, et al. Among authors: gursel t. J Pediatr Hematol Oncol. 2018 Jul;40(5):355-359. doi: 10.1097/MPH.0000000000001206. J Pediatr Hematol Oncol. 2018. PMID: 29746437

8

An unusual ocular manifestation in Fanconi anemia: congenital glaucoma.

Aslan D, Ozdogan S, Onol M, Kaya Z, Gursel T. Aslan D, et al. Among authors: gursel t. Am J Hematol. 2005 Jan;78(1):64-6. doi: 10.1002/ajh.20232. Am J Hematol. 2005. PMID: 15609293 Free article.

9

Severe Myelotoxicity Associated with Thiopurine S-Methyltransferase*3A/*3C Polymorphisms in a Patient with Pediatric Leukemia and the Effect of Steroid Therapy.

Belen BF, Gürsel T, Akyürek N, Albayrak M, Kaya Z, Koçak Ü. Belen BF, et al. Among authors: gursel t. Turk J Haematol. 2014 Dec 5;31(4):276-85. doi: 10.4274/tjh.2013.0082. Turk J Haematol. 2014. PMID: 25541649 Free PMC article.

10

Bilateral knee and right ankle osteonecrosis in an adolescent girl with acute lymphoblastic leukemia.

Koçak Ü, Kaya Z, Albayrak M, Şenköylü A, Akyürek N, Gürsel T. Koçak Ü, et al. Among authors: gursel t. Turk J Haematol. 2009 Mar 5;26(1):34-7. Turk J Haematol. 2009. PMID: 27265108

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