Gürsel T - Search Results

1

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

2

Acute lymphoblastic leukemia and toxoplasmosis.

Hiçsönmez G, Kanra G, Gürsel T, Yetkin S, Altintaş K. Hiçsönmez G, et al. Among authors: gursel t. Turk J Pediatr. 1979 Jan;21(1):24-7. Turk J Pediatr. 1979. PMID: 296859 No abstract available.

3

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

4

Gastric angiodysplasia in a child with Bernard-Soulier syndrome: efficacy of octreotide in long-term management.

Kaya Z, Gürsel T, Dalgic B, Aslan D. Kaya Z, et al. Among authors: gursel t. Pediatr Hematol Oncol. 2005 Apr-May;22(3):223-7. doi: 10.1080/08880010590921568. Pediatr Hematol Oncol. 2005. PMID: 16020106

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

Transcobalamin II Deficiency in Four Cases with Novel Mutations.

Ünal Ş, Rupar T, Yetgin S, Yaralı N, Dursun A, Gürsel T, Çetin M. Ünal Ş, et al. Among authors: gursel t. Turk J Haematol. 2015 Dec;32(4):317-22. doi: 10.4274/tjh.2014.0154. Epub 2015 Apr 27. Turk J Haematol. 2015. PMID: 25914105 Free PMC article.

7

Guillain-Barré syndrome in a child with acute lymphoblastic leukemia.

Aral YZ, Gursel T, Ozturk G, Serdaroglu A. Aral YZ, et al. Among authors: gursel t. Pediatr Hematol Oncol. 2001 Jul-Aug;18(5):343-6. doi: 10.1080/088800101300312618. Pediatr Hematol Oncol. 2001. PMID: 11452406

8

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

9

Thrombosis during all-trans-retinoic acid therapy in a child with acute promyelocytic leukemia and factor VQ 506 mutation.

Koçak U, Gürsel T, Oztürk G, Kantarci S. Koçak U, et al. Among authors: gursel t. Pediatr Hematol Oncol. 2000 Mar;17(2):177-80. doi: 10.1080/088800100276541. Pediatr Hematol Oncol. 2000. PMID: 10734661

10

The frequency of menorrhagia and bleeding disorders in university students.

Gursel T, Biri A, Kaya Z, Sivaslıoglu S, Albayrak M. Gursel T, et al. Pediatr Hematol Oncol. 2014 Aug;31(5):467-74. doi: 10.3109/08880018.2014.886316. Epub 2014 Mar 31. Pediatr Hematol Oncol. 2014. PMID: 24684279 Clinical Trial.

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