Ozkinay C - Search Results

1

Molecular analysis and clinical findings of Griscelli syndrome patients.

Durmaz A, Ozkinay F, Onay H, Tombuloglu M, Atay A, Gursel O, Peker E, Atmaca M, Genel F, Bozabali S, Akin H, Ozkinay C. Durmaz A, et al. Among authors: ozkinay c. J Pediatr Hematol Oncol. 2012 Oct;34(7):541-4. doi: 10.1097/MPH.0b013e31826781ad. J Pediatr Hematol Oncol. 2012. PMID: 22983416

2

Griscelli syndrome: report of a case and review of the literature.

Kurugöl Z, Ozkinay F, Vardar F, Karaçali S, Kutukçuler N, Deveci R, Ozkinay C. Kurugöl Z, et al. Among authors: ozkinay f, ozkinay c. Pediatr Int. 2001 Jun;43(3):298-301. doi: 10.1046/j.1442-200x.2001.01383.x. Pediatr Int. 2001. PMID: 11380929 No abstract available.

3

Reasons for adult referrals for genetic counseling at a genetics center in Izmir, Turkey: analysis of 8965 cases over an eleven-year period.

Cogulu O, Ozkinay F, Akin H, Onay H, Karaca E, Durmaz AA, Durmaz B, Aykut A, Pariltay E, Kirbiyik O, Gunduz C, Ozkinay C. Cogulu O, et al. Among authors: ozkinay c. J Genet Couns. 2011 Jun;20(3):287-93. doi: 10.1007/s10897-010-9342-9. Epub 2011 Jan 8. J Genet Couns. 2011. PMID: 21221751

4

Two cases of macrocephaly and immune deficiency.

Cogulu O, Aykut A, Kutukculer N, Ozkinay C, Ozkinay F. Cogulu O, et al. Among authors: ozkinay f, ozkinay c. Clin Dysmorphol. 2007 Apr;16(2):81-84. doi: 10.1097/MCD.0b013e3280464ee6. Clin Dysmorphol. 2007. PMID: 17351349

5

Evidence of an association between mannose binding lectin codon 54 polymorphism and adenoidectomy and/or tonsillectomy in children.

Koturoglu G, Onay H, Midilli R, Pehlivan S, Eren E, Itirli G, Kurugol Z, Apaydin F, Ozkinay C, Ozkinay F. Koturoglu G, et al. Among authors: ozkinay f, ozkinay c. Int J Pediatr Otorhinolaryngol. 2007 Aug;71(8):1157-61. doi: 10.1016/j.ijporl.2007.05.004. Epub 2007 Jun 7. Int J Pediatr Otorhinolaryngol. 2007. PMID: 17559949

6

Purine nucleoside phosphorylase deficiency in a patient with spastic paraplegia and recurrent infections.

Ozkinay F, Pehlivan S, Onay H, van den Berg P, Vardar F, Koturoglu G, Aksu G, Unal D, Tekgul H, Can S, Ozkinay C. Ozkinay F, et al. Among authors: ozkinay c. J Child Neurol. 2007 Jun;22(6):741-3. doi: 10.1177/0883073807302617. J Child Neurol. 2007. PMID: 17641261

7

Role of angiotensin-converting enzyme gene polymorphisms in children with sepsis and septic shock.

Cogulu O, Onay H, Uzunkaya D, Gunduz C, Pehlivan S, Vardar F, Atlihan F, Ozkinay C, Ozkinay F. Cogulu O, et al. Among authors: ozkinay c. Pediatr Int. 2008 Aug;50(4):477-80. doi: 10.1111/j.1442-200X.2008.02583.x. Pediatr Int. 2008. PMID: 19143971

8

Interferon-gamma gene and interferon-gamma receptor-1 gene polymorphisms in children with tuberculosis from Turkey.

Onay H, Ekmekci AY, Durmaz B, Sayin E, Cosar H, Bayram N, Can D, Akin H, Ozkinay C, Ozkinay F. Onay H, et al. Among authors: ozkinay c. Scand J Infect Dis. 2010;42(1):39-42. doi: 10.3109/00365540903253502. Scand J Infect Dis. 2010. PMID: 20055726

9

Chromosomal rearrangements in children with idiopathic mental retardation using subtelomeric fluorescent in situ hybridization.

Cogulu O, Gunduz C, Karaca E, Onay H, Ozkinay C, Ozkinay F. Cogulu O, et al. Among authors: ozkinay f, ozkinay c. Genet Couns. 2006;17(3):321-31. Genet Couns. 2006. PMID: 17100201

10

Association between mannose binding lectin polymorphisms and predisposition to bacterial meningitis.

Vardar F, Pehlivan S, Onay H, Atlihan F, Güliz N, Ozkinay C, Ozkinay F. Vardar F, et al. Among authors: ozkinay f, ozkinay c. Turk J Pediatr. 2007 Jul-Sep;49(3):270-3. Turk J Pediatr. 2007. PMID: 17990579

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