Zenciroğlu A - Search Results

1

A novel mutation of laminin β-2 gene in Pierson syndrome manifested with nephrotic syndrome in the early neonatal period.

Aydin B, Ipek MS, Ozaltin F, Zenciroğlu A, Dilli D, Beken S, Okumuş N, Hoşağasi N, Saygili-Karagöl B, Kundak A, Renda R, Aydog O. Aydin B, et al. Among authors: zenciroglu a. Genet Couns. 2013;24(2):141-7. Genet Couns. 2013. PMID: 24032283

2

An uncommon association of vacterl complex with hypertrophic pyloric stenosis and horseshoe lung.

Ipek MS, Zenciroglu A, Aydin M, Okumus N, Orun UA, Uner C. Ipek MS, et al. Among authors: zenciroglu a. Genet Couns. 2010;21(3):289-92. Genet Couns. 2010. PMID: 20964119

3

A novel WT1 gene mutation in a newborn infant diagnosed with Denys-Drash syndrome.

Hakan N, Aydin M, Erdogan O, Cavusoglu YH, Aycan Z, Ozaltin F, Zenciroglu A, Apaydin S, Gunes R, Sahin G, Cinar G, Okumus N. Hakan N, et al. Among authors: zenciroglu a. Genet Couns. 2012;23(2):255-61. Genet Couns. 2012. PMID: 22876585

4

Crisponi syndrome: a new mutation in CRLF1 gene associated with moderate outcome.

Uzunalic N, Zenciroglu A, Beken S, Piras R, Dilli D, Aydin B, Chiappe F, Okumus N, Crisponi L. Uzunalic N, et al. Among authors: zenciroglu a. Genet Couns. 2013;24(2):161-6. Genet Couns. 2013. PMID: 24032286

5

Papillorenal syndrome with de novo reciprocal translocation t(2;15) (q31; q26).

Aydin B, Dilli D, Beken S, Zenciroglu A, Uzunalic N, Yuksekkaya P, Akyuz SG, Aydog O, Okumus N. Aydin B, et al. Among authors: zenciroglu a. Genet Couns. 2013;24(2):201-5. Genet Couns. 2013. PMID: 24032291

6

Apparent Lenz microphthalmia syndrome: a patient with unusual manifestations.

Okumus N, Zenciroglu A, Demirel N, Bas AY, Ceylaner S. Okumus N, et al. Among authors: zenciroglu a. Genet Couns. 2008;19(2):177-82. Genet Couns. 2008. PMID: 18618992

7

Calcified thrombosis of the inferior vena cava extending to renal veins in a newborn with homozygous MTHFR a1298c mutation.

Aydin B, Dilli D, Uzunaliç N, Zenciroğlu A, Okumuş N, Cinar HG, Aydin M, Ipek MS. Aydin B, et al. Among authors: zenciroglu a. Genet Couns. 2012;23(4):523-7. Genet Couns. 2012. PMID: 23431755 No abstract available.

8

Treacher Collins syndrome with multiple congenital heart defects after paroxetine exposure: case report.

Dinlen N, Zenciroğlu A, Dilli D, Aydin B, Beken S, Okumuş N. Dinlen N, et al. Among authors: zenciroglu a. Genet Couns. 2014;25(1):7-11. Genet Couns. 2014. PMID: 24783649

9

Hyperparathyroidism secondary to maternal hypoparathyroidism and vitamin D deficiency: an uncommon cause of neonatal respiratory distress.

Demirel N, Aydin M, Zenciroglu A, Okumus N, Cetinkaya S, Yildiz YT, Ipek MS. Demirel N, et al. Among authors: zenciroglu a. Ann Trop Paediatr. 2009 Jun;29(2):149-54. doi: 10.1179/146532809X440770. Ann Trop Paediatr. 2009. PMID: 19460269

10

Neonatal thrombo-embolism: risk factors, clinical features and outcome.

Demirel N, Aydin M, Zenciroglu A, Bas AY, Yarali N, Okumus N, Cinar G, Ipek MS. Demirel N, et al. Among authors: zenciroglu a. Ann Trop Paediatr. 2009 Dec;29(4):271-9. doi: 10.1179/027249309X12547917868961. Ann Trop Paediatr. 2009. PMID: 19941750

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