Gunduz M - Search Results

1

An infantile case of Zellweger syndrome presented with Kabuki-like phenotype.

Ezgu F, Eminoglu T, Okur I, Gunduz M, Tumer L, Hasanoglu A, Dalgic B. Ezgu F, et al. Among authors: gunduz m. Genet Couns. 2011;22(2):217-20. Genet Couns. 2011. PMID: 21848015

2

Severe renal tubulopathy in a newborn due to BCS1L gene mutation: effects of different treatment modalities on the clinical course.

Ezgu F, Senaca S, Gunduz M, Tumer L, Hasanoglu A, Tiras U, Unsal R, Bakkaloglu SA. Ezgu F, et al. Among authors: gunduz m. Gene. 2013 Oct 10;528(2):364-6. doi: 10.1016/j.gene.2013.07.007. Epub 2013 Jul 26. Gene. 2013. PMID: 23892085

3

Effect of enteral and parenteral nutrition on growth parameters of hospitalized Turkish children.

Ezgu FS, Tumer L, Cinasal G, Hasanoglu A, Gunduz M. Ezgu FS, et al. Among authors: gunduz m. Indian Pediatr. 2005 May;42(5):469-72. Indian Pediatr. 2005. PMID: 15923694

4

Cholesteryl ester storage disease in a young child presenting as isolated hepatomegaly treated with simvastatin.

Dalgiç B, Sari S, Gündüz M, Ezgü F, Tümer L, Hasanoğlu A, Akyol G. Dalgiç B, et al. Among authors: gunduz m. Turk J Pediatr. 2006 Apr-Jun;48(2):148-51. Turk J Pediatr. 2006. PMID: 16848116

5

Vitamin D intoxication and hypercalcaemia in an infant treated with pamidronate infusions.

Ezgu FS, Buyan N, Gündüz M, Tümer L, Okur I, Hasanoglu A. Ezgu FS, et al. Among authors: gunduz m. Eur J Pediatr. 2004 Mar;163(3):163-5. doi: 10.1007/s00431-003-1387-4. Epub 2004 Jan 9. Eur J Pediatr. 2004. PMID: 14714183

6

Endothelial activation and inflammation in prepubertal obese Turkish children.

Süheyl Ezgü F, Hasanoğlu A, Tümer L, Ozbay F, Aybay C, Gündüz M. Süheyl Ezgü F, et al. Among authors: gunduz m. Metabolism. 2005 Oct;54(10):1384-9. doi: 10.1016/j.metabol.2005.05.003. Metabolism. 2005. PMID: 16154440

7

Neonates with inborn errors of metabolism: spectrum and short-term outcomes at a tertiary care hospital.

Gündüz M, Ünal S, Okur İ, Ayrancı Sucaklı İ, Güzel F, Koç N. Gündüz M, et al. Turk J Pediatr. 2015 Jan-Feb;57(1):45-52. Turk J Pediatr. 2015. PMID: 26613220

8

Neonatal form of biotin-thiamine-responsive basal ganglia disease. Clues to diagnosis.

Değerliyurt A, Gündüz M, Ceylaner S, Ünal Ö, Ünal S. Değerliyurt A, et al. Among authors: gunduz m. Turk J Pediatr. 2019;61(2):261-266. doi: 10.24953/turkjped.2019.02.016. Turk J Pediatr. 2019. PMID: 31951338 Free article.

Degerliyurt A, Gunduz M, Ceylaner S, Unal O, Unal S. Neonatal form of biotin-thiamine-responsive basal ganglia disease. ...

9

Dysmorphic Facial Features and Other Clinical Characteristics in Two Patients with PEX1 Gene Mutations.

Gunduz M, Unal O. Gunduz M, et al. Case Rep Pediatr. 2016;2016:5175709. doi: 10.1155/2016/5175709. Epub 2016 Nov 2. Case Rep Pediatr. 2016. PMID: 27882258 Free PMC article.

10

Mutation spectrum of fumarylacetoacetase gene and clinical aspects of tyrosinemia type I disease.

Dursun A, Ozgül RK, Sivri S, Tokatlı A, Güzel A, Mesci L, Kılıç M, Aliefendioglu D, Ozçay F, Gündüz M, Coşkun T. Dursun A, et al. Among authors: gunduz m. JIMD Rep. 2011;1:17-21. doi: 10.1007/8904_2011_10. Epub 2011 Jun 22. JIMD Rep. 2011. PMID: 23430822 Free PMC article.

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