Erdem H - Search Results

1

Autosomal recessive spastic ataxia of Charlevoix-Saguenay in two unrelated Turkish families.

Gücüyener K, Ozgül K, Paternotte C, Erdem H, Prud'homme JF, Ozgüç M, Topaloğlu H. Gücüyener K, et al. Among authors: erdem h. Neuropediatrics. 2001 Jun;32(3):142-6. doi: 10.1055/s-2001-16616. Neuropediatrics. 2001. PMID: 11521210

2

Clinical observations in autosomal recessive spastic paraplegia in childhood and further evidence for genetic heterogeneity.

Topaloğlu H, Pinarli G, Erdem H, Gücüyener K, Karaduman A, Topçu M, Akarsu AN, Ozgüç M. Topaloğlu H, et al. Among authors: erdem h. Neuropediatrics. 1998 Aug;29(4):189-94. doi: 10.1055/s-2007-973559. Neuropediatrics. 1998. PMID: 9762694

3

Allele distribution of D5S125, MAP1B5' and D5S679 microsatellite markers in Turkish spinal muscular atrophy families.

Erdem H, Pehlivan S, Topaloğlu H, Togan I, Ozgüç M. Erdem H, et al. Turk J Pediatr. 1997 Oct-Dec;39(4):447-52. Turk J Pediatr. 1997. PMID: 9433145

4

Deletion analysis in Turkish patients with spinal muscular atrophy.

Erdem H, Pehlivan S, Topaloglu H, Ozgüç M. Erdem H, et al. Brain Dev. 1999 Mar;21(2):86-9. doi: 10.1016/s0387-7604(98)00063-1. Brain Dev. 1999. PMID: 10206524

5

Prenatal diagnosis of spinal muscular atrophy in Turkish families.

Erdem H, Dayangaç D, Pehlivan S, Topaloglu H. Erdem H, et al. Cent Eur J Public Health. 2001 Feb;9(1):35-7. Cent Eur J Public Health. 2001. PMID: 11243588

6

Allele frequencies of Mp6D-9 and GATT markers in 32 Turkish cystic fibrosis families.

Ozgüç M, Yilmaz E, Erdem H, Coşkun T, Ozçelik U, Togan I, Göçmen A, Ayter S, Ozalp I. Ozgüç M, et al. Among authors: erdem h. Clin Genet. 1994 May;45(5):266-8. doi: 10.1111/j.1399-0004.1994.tb04153.x. Clin Genet. 1994. PMID: 8076413

7

Association between mutations and the variable number tandem repeat alleles in a sample of Turkish phenylketonuria patients.

Ozgüç M, Yilmaz E, Erdem H, Coşkun T, Tokatli A, Ozalp I. Ozgüç M, et al. Among authors: erdem h. J Inherit Metab Dis. 1994;17(3):373-4. doi: 10.1007/BF00711836. J Inherit Metab Dis. 1994. PMID: 7807959 No abstract available.

8

Deletion analysis of Duchenne muscular dystrophy.

Erdem H, Ayter S, Ozgüç M, Topçu M, Topaloğlu H, Renda Y. Erdem H, et al. Turk J Pediatr. 1993 Jan-Mar;35(1):15-21. Turk J Pediatr. 1993. PMID: 8236513

9

Mutation analysis in Turkish phenylketonuria patients.

Ozgüç M, Ozalp I, Coşkun T, Yilmaz E, Erdem H, Ayter S. Ozgüç M, et al. Among authors: erdem h. J Med Genet. 1993 Feb;30(2):129-30. doi: 10.1136/jmg.30.2.129. J Med Genet. 1993. PMID: 8445616 Free PMC article.

10

Study of 12 mutations in Turkish cystic fibrosis patients.

Yilmaz E, Erdem H, Ozgüç M, Coşkun T, Ozçelik U, Göçmen A, Ozalp I. Yilmaz E, et al. Among authors: erdem h. Hum Hered. 1995 May-Jun;45(3):175-7. doi: 10.1159/000154281. Hum Hered. 1995. PMID: 7542223

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