Coker M - Search Results

1

Glutaric aciduria type 1: Insights into diagnosis and neurogenetic outcomes.

Yoldas Celik M, Canda E, Yazici H, Erdem F, Yuksel Yanbolu A, Atik Altınok Y, Eraslan C, Aykut A, Durmaz A, Habif S, Kalkan Ucar S, Coker M. Yoldas Celik M, et al. Among authors: coker m. Eur J Pediatr. 2024 Dec 10;184(1):72. doi: 10.1007/s00431-024-05907-7. Eur J Pediatr. 2024. PMID: 39658645

2

Renal involvement as a rare complication of Dorfman-Chanarin syndrome: a case report.

Aksu G, Kalkan Ucar S, Bulut Y, Aydinok Y, Sen S, Anal O, Simsek Gosen D, Darcan S, Coker M, Kutukculer N. Aksu G, et al. Among authors: coker m. Pediatr Dermatol. 2008 May-Jun;25(3):326-31. doi: 10.1111/j.1525-1470.2008.00675.x. Pediatr Dermatol. 2008. PMID: 18577036

3

A monocentric pilot study of an antioxidative defense and hsCRP in pediatric patients with glycogen storage disease type IA and III.

Kalkan Ucar S, Coker M, Sözmen E, Goksen Simsek D, Darcan S. Kalkan Ucar S, et al. Among authors: coker m. Nutr Metab Cardiovasc Dis. 2009 Jul;19(6):383-90. doi: 10.1016/j.numecd.2008.09.005. Epub 2008 Dec 13. Nutr Metab Cardiovasc Dis. 2009. PMID: 19073362

4

Clinical overview of children with mucopolysaccharidosis type III A and effect of Risperidone treatment on children and their mothers psychological status.

Kalkan Ucar S, Ozbaran B, Demiral N, Yuncu Z, Erermis S, Coker M. Kalkan Ucar S, et al. Among authors: coker m. Brain Dev. 2010 Feb;32(2):156-61. doi: 10.1016/j.braindev.2008.12.010. Epub 2009 Feb 12. Brain Dev. 2010. PMID: 19217229 Clinical Trial.

5

Titration of betaine therapy to optimize therapy in an infant with 5,10-methylenetetrahydrofolate reductase deficiency.

Ucar SK, Koroğlu OA, Berk O, Yalaz M, Kültürsay N, Blom HJ, Coker M. Ucar SK, et al. Among authors: coker m. Eur J Pediatr. 2010 Feb;169(2):241-3. doi: 10.1007/s00431-009-0997-x. Epub 2009 May 12. Eur J Pediatr. 2010. PMID: 19434424

6

The first use of N-carbamylglutamate in a patient with decompensated maple syrup urine disease.

Kalkan Ucar S, Coker M, Habif S, Saz EU, Karapinar B, Ucar H, Kitis O, Duran M. Kalkan Ucar S, et al. Among authors: coker m. Metab Brain Dis. 2009 Sep;24(3):409-14. doi: 10.1007/s11011-009-9155-4. Epub 2009 Aug 18. Metab Brain Dis. 2009. PMID: 19688253

7

An association among iron, copper, zinc, and selenium, and antioxidative status in dyslipidemic pediatric patients with glycogen storage disease types IA and III.

Kalkan Ucar S, Coker M, Sözmen E, Goksen Simsek D, Darcan S. Kalkan Ucar S, et al. Among authors: coker m. J Trace Elem Med Biol. 2010 Jan;24(1):42-5. doi: 10.1016/j.jtemb.2009.10.004. Epub 2009 Nov 24. J Trace Elem Med Biol. 2010. PMID: 20122579

8

Salla disease in Turkish children: severe and conventional type.

Coker M, Kalkan-Uçar S, Kitiş O, Uçar H, Gökşen-Simşek D, Darcan S, Gökben S. Coker M, et al. Turk J Pediatr. 2009 Nov-Dec;51(6):605-9. Turk J Pediatr. 2009. PMID: 20196397

9

Alpha-galactosidase A activity levels in Turkish male hemodialysis patients.

Kalkan Uçar S, Sozmen E, Duman S, Başçi A, Çoker M. Kalkan Uçar S, et al. Among authors: coker m. Ther Apher Dial. 2012 Dec;16(6):560-5. doi: 10.1111/j.1744-9987.2012.01092.x. Epub 2012 Aug 13. Ther Apher Dial. 2012. PMID: 23190516

10

Analysis of the β-glucocerebrosidase gene in Turkish Gaucher disease patients: mutation profile and description of a novel mutant allele.

Karaca E, Kalkan S, Onay H, Aykut A, Coker M, Ozkinay F. Karaca E, et al. Among authors: coker m. J Pediatr Endocrinol Metab. 2012;25(9-10):957-62. doi: 10.1515/jpem-2012-0155. J Pediatr Endocrinol Metab. 2012. PMID: 23426826

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