Özkınay F - Search Results

1

Coexistence of Gaucher Disease and severe congenital neutropenia.

Kose MD, Canda E, Kağnıcı M, Uçar SK, Onay H, Yıldırım Sozmen E, Karapınar D, Özkınay F, Çoker M. Kose MD, et al. Among authors: ozkinay f. Blood Cells Mol Dis. 2019 May;76:1-6. doi: 10.1016/j.bcmd.2018.07.001. Epub 2018 Aug 10. Blood Cells Mol Dis. 2019. PMID: 30473482

2

HDR (hypoparathyroidism, sensorineural deafness, renal dysplasia) syndrome presenting with hypocalcemia-induced generalized psoriasis.

Aksoylar S, Aydinok Y, Serdaroğlu E, Coker M, Ozdemir F, Ozkinay F. Aksoylar S, et al. Among authors: ozkinay f. J Pediatr Endocrinol Metab. 2004 Jul;17(7):1031-4. doi: 10.1515/jpem.2004.17.7.1031. J Pediatr Endocrinol Metab. 2004. PMID: 15301053

3

Evaluation of telomerase mRNA (hTERT) in childhood acute leukemia.

Cogulu O, Kosova B, Karaca E, Gunduz C, Ozkinay F, Aksoylar S, Gulen H, Kantar M, Oniz H, Karapinar D, Cetingul N, Erbay A, Vergin C, Ozkinay C. Cogulu O, et al. Among authors: ozkinay f, ozkinay c. Leuk Lymphoma. 2004 Dec;45(12):2477-80. doi: 10.1080/10428190400007508. Leuk Lymphoma. 2004. PMID: 15621763

4

Trigonocephaly and Wilson's disease in two siblings.

Cogulu O, Onay H, Ozgenc F, Karaca E, Gunduz C, Tzetis M, Cankaya T, Kanavakis E, Ozkinay F. Cogulu O, et al. Among authors: ozkinay f. Clin Dysmorphol. 2005 Jul;14(3):161-164. Clin Dysmorphol. 2005. PMID: 15930910

5

Unusual course of an acute lymphoblastic leukemia case with i(9q) as a sole cytogenetic abnormality.

Cogulu O, Karapinar DY, Karaca E, Aydinok Y, Ozkinay F. Cogulu O, et al. Among authors: ozkinay f. Leuk Res. 2006 Nov;30(11):1461-3. doi: 10.1016/j.leukres.2006.02.018. Epub 2006 Mar 24. Leuk Res. 2006. PMID: 16564090

6

Might there be a link between mannose binding lectin and vitiligo?

Onay H, Pehlivan M, Alper S, Ozkinay F, Pehlivan S. Onay H, et al. Among authors: ozkinay f. Eur J Dermatol. 2007 Mar-Apr;17(2):146-8. doi: 10.1684/ejd.2007.0128. Epub 2007 Mar 2. Eur J Dermatol. 2007. PMID: 17337399

7

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

8

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

9

The evaluation of hTERT mRNA expression in acute leukemia children and 2 years follow-up of 40 cases.

Cogulu O, Kosova B, Gunduz C, Karaca E, Aksoylar S, Erbay A, Karapinar D, Vergin C, Vural F, Tombuloglu M, Cetingul N, Ozkinay F. Cogulu O, et al. Among authors: ozkinay f. Int J Hematol. 2008 Apr;87(3):276-83. doi: 10.1007/s12185-008-0054-y. Epub 2008 Feb 22. Int J Hematol. 2008. PMID: 18293058

10

Rapid prenatal diagnosis of common aneuploidies in amniotic fluid using quantitative fluorescent polymerase chain reaction.

Onay H, Ugurlu T, Aykut A, Pehlivan S, Inal M, Tinar S, Ozkinay C, Ozkinay F. Onay H, et al. Among authors: ozkinay f, ozkinay c. Gynecol Obstet Invest. 2008;66(2):104-10. doi: 10.1159/000128598. Epub 2008 Apr 29. Gynecol Obstet Invest. 2008. PMID: 18446039

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

301 results

Search Page