Durmaz A - Search Results

1

Propolis Extract Regulates microRNA Expression in Glioblastoma and Brain Cancer Stem Cells.

C Yilmaz U, Bagca BG, Karaca E, Durmaz A, Durmaz B, Aykut A, Kayalar H, Avci CB, Susluer SY, Pariltay E, Gunduz C, Cogulu O. C Yilmaz U, et al. Among authors: durmaz a, durmaz b. Anticancer Agents Med Chem. 2022;22(2):378-389. doi: 10.2174/1871520621666210504082528. Anticancer Agents Med Chem. 2022. PMID: 33949939

2

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. J Pediatr Hematol Oncol. 2009 Aug;31(8):592-4. doi: 10.1097/MPH.0b013e3181a71855. J Pediatr Hematol Oncol. 2009. PMID: 19636270

3

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: durmaz b. 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

4

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: durmaz aa, durmaz b. 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

5

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: durmaz b. 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

6

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: durmaz a, durmaz b. 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

7

Demonstration of uniparental-isodisomy on chromosome 22q11.2 in a patient with childhood schizophrenia and facial dysmorphology by whole-genome analysis.

Cogulu O, Pariltay E, Durmaz AA, Aykut A, Gunduz C, Ozbaran B, Aydin HH, Erermis S, Aydin C, Ozkinay F. Cogulu O, et al. Among authors: durmaz aa. J Neuropsychiatry Clin Neurosci. 2012 Winter;24(1):E13-4. doi: 10.1176/appi.neuropsych.11010027. J Neuropsychiatry Clin Neurosci. 2012. PMID: 22450627 No abstract available.

8

A new clinical presentation associated with pontine clefting, hyperpigmentation and short stature in addition to craniofacial, cardiac and developmental anomalies.

Cogulu O, Durmaz B, Wollnik B, Durmaz A, Darcan S, Ozkinay F. Cogulu O, et al. Among authors: durmaz a, durmaz b. Genet Couns. 2012;23(2):281-7. Genet Couns. 2012. PMID: 22876588

9

The association of RANK gene C421T and C575T polymorphisms with bone mineral density in postmenopausal Turkish women.

Işleten B, Durmaz B, Durmaz B, Onay H, Ozkınay F, Durmaz A, Turan V, Oztekin K. Işleten B, et al. Among authors: durmaz a, durmaz b. Arch Gynecol Obstet. 2013 Oct;288(4):917-23. doi: 10.1007/s00404-013-2831-y. Epub 2013 Apr 5. Arch Gynecol Obstet. 2013. PMID: 23553199

10

Subtelomeric rearrangements in patients with idiopathic intellectual disabilitiy/ multiple congenital anomalies and recurrent miscarriages: seven years' experience.

Durmaz B, Karaca E, Durmaz A, Atik T, Akin H, Cogulu O, Ozkinay F. Durmaz B, et al. Among authors: durmaz a. Genet Couns. 2013;24(2):167-77. Genet Couns. 2013. PMID: 24032287

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