Cogulu O - Search Results

1

Human immune disorder associated with homozygous hypomorphic mutation affecting MALT1B splice variant.

Kutukculer N, Seeholzer T, O'Neill TJ, Graß C, Aykut A, Karaca NE, Durmaz A, Cogulu O, Aksu G, Gehring T, Gewies A, Krappmann D. Kutukculer N, et al. Among authors: o neill tj, cogulu o. J Allergy Clin Immunol. 2021 Feb;147(2):775-778.e8. doi: 10.1016/j.jaci.2020.07.034. Epub 2020 Aug 25. J Allergy Clin Immunol. 2021. PMID: 32858082 Free PMC article. No abstract available.

2

Celiac disease in children with Down syndrome: importance of follow-up and serologic screening.

Cogulu O, Ozkinay F, Gunduz C, Cankaya T, Aydogdu S, Ozgenc F, Kutukculer N, Ozkinay C. Cogulu O, et al. Pediatr Int. 2003 Aug;45(4):395-9. doi: 10.1046/j.1442-200x.2003.01755.x. Pediatr Int. 2003. PMID: 12911473

3

Two cases of macrocephaly and immune deficiency.

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

4

An additional manifestation in acrocallosal syndrome: temporal lobe hypoplasia.

Aykut A, Cogulu O, Ekmekci AY, Ozkinay F. Aykut A, et al. Among authors: cogulu o. Genet Couns. 2008;19(2):237-40. Genet Couns. 2008. PMID: 18618999

5

Pachyonychia congenita type 2, N92S mutation of keratin 17 gene: clinical features, mutation analysis and pathological view.

Cogulu O, Onay H, Aykut A, Wilson NJ, Smith FJ, Dereli T, Ozkinay F. Cogulu O, et al. Eur J Pediatr. 2009 Oct;168(10):1269-72. doi: 10.1007/s00431-008-0908-6. Epub 2008 Dec 24. Eur J Pediatr. 2009. PMID: 19107515

6

A severe alpha thalassemia case compound heterozygous for Hb Adana in alpha1 gene and 20.5 kb double gene deletion.

Durmaz AA, Akin H, Ekmekci AY, Onay H, Durmaz B, Cogulu O, Aydinok Y, Ozkinay F. Durmaz AA, et al. Among authors: cogulu o. J Pediatr Hematol Oncol. 2009 Aug;31(8):592-4. doi: 10.1097/MPH.0b013e3181a71855. J Pediatr Hematol Oncol. 2009. PMID: 19636270

7

Interview with parents of children with Down syndrome: their perceptions and feelings.

Durmaz A, Cankaya T, Durmaz B, Vahabi A, Gunduz C, Cogulu O, Ozkinay F. Durmaz A, et al. Among authors: cogulu o. Indian J Pediatr. 2011 Jun;78(6):698-702. doi: 10.1007/s12098-010-0315-7. Epub 2010 Dec 17. Indian J Pediatr. 2011. PMID: 21165714

8

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. 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

9

The Association of minor congenital anomalies and childhood cancer.

Durmaz A, Durmaz B, Kadioglu B, Aksoylar S, Karapinar D, Koturoglu G, Orman MN, Ozkinay F, Cogulu O. Durmaz A, et al. Among authors: cogulu o. Pediatr Blood Cancer. 2011 Jul 1;56(7):1098-102. doi: 10.1002/pbc.23049. Epub 2011 Feb 25. Pediatr Blood Cancer. 2011. PMID: 21360657

10

The rate of sex chromosome aneuploidies in prenatal diagnosis and subsequent decisions in Western Turkey.

Ataman E, Cogulu O, Durmaz A, Karaca E, Durmaz B, Akin H, Ozkinay F. Ataman E, et al. Among authors: cogulu o. Genet Test Mol Biomarkers. 2012 Feb;16(2):150-3. doi: 10.1089/gtmb.2011.0130. Epub 2011 Oct 6. Genet Test Mol Biomarkers. 2012. PMID: 21977968

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