Ozguc M - Search Results

1

Mutation frequency of Familial Mediterranean Fever and evidence for a high carrier rate in the Turkish population.

Yilmaz E, Ozen S, Balci B, Duzova A, Topaloglu R, Besbas N, Saatci U, Bakkaloglu A, Ozguc M. Yilmaz E, et al. Among authors: ozguc m. Eur J Hum Genet. 2001 Jul;9(7):553-5. doi: 10.1038/sj.ejhg.5200674. Eur J Hum Genet. 2001. PMID: 11464248

2

MEFV gene mutations in familial Mediterranean fever phenotype II patients with renal amyloidosis in childhood: a retrospective clinicopathological and molecular study.

Balci B, Tinaztepe K, Yilmaz E, Guçer S, Ozen S, Topaloğlu R, Beşbaş N, Ozguç M, Bakkaloğlu A. Balci B, et al. Among authors: ozguc m. Nephrol Dial Transplant. 2002 Nov;17(11):1921-3. doi: 10.1093/ndt/17.11.1921. Nephrol Dial Transplant. 2002. PMID: 12401847

3

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: ozguc m. Hum Hered. 1995 May-Jun;45(3):175-7. doi: 10.1159/000154281. Hum Hered. 1995. PMID: 7542223

4

Frequency of the IVS-10nt546 mutation in 44 Turkish phenylketonuria patients.

Ozgüç M, Ozalp I, Coşkun T, Yilmaz E, Erdem H, Ayter S. Ozgüç M, et al. Turk J Pediatr. 1993 Jan-Mar;35(1):11-4. Turk J Pediatr. 1993. PMID: 7901929

5

Mutation analysis in Turkish phenylketonuria patients.

Ozgüç M, Ozalp I, Coşkun T, Yilmaz E, Erdem H, Ayter S. Ozgüç M, et al. 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.

6

Is there a heterozygote advantage for familial Mediterranean fever carriers against tuberculosis infections: speculations remain?

Ozen S, Balci B, Ozkara S, Ozcan A, Yilmaz E, Besbas N, Ozguc M, Kastner DL, Bakkaloglu A. Ozen S, et al. Among authors: ozguc m. Clin Exp Rheumatol. 2002 Jul-Aug;20(4 Suppl 26):S57-8. Clin Exp Rheumatol. 2002. PMID: 12371639 No abstract available.

7

Mutations of the CFTR gene in Turkish patients with congenital bilateral absence of the vas deferens.

Dayangaç D, Erdem H, Yilmaz E, Sahin A, Sohn C, Ozgüç M, Dörk T. Dayangaç D, et al. Among authors: ozguc m. Hum Reprod. 2004 May;19(5):1094-100. doi: 10.1093/humrep/deh223. Epub 2004 Apr 7. Hum Reprod. 2004. PMID: 15070876

8

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. J Inherit Metab Dis. 1994;17(3):373-4. doi: 10.1007/BF00711836. J Inherit Metab Dis. 1994. PMID: 7807959 No abstract available.

9

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. Clin Genet. 1994 May;45(5):266-8. doi: 10.1111/j.1399-0004.1994.tb04153.x. Clin Genet. 1994. PMID: 8076413

10

Sodium chloride deficiency in cystic fibrosis patients.

Ozçelik U, Göçmen A, Kiper N, Coşkun T, Yilmaz E, Ozgüç M. Ozçelik U, et al. Among authors: ozguc m. Eur J Pediatr. 1994 Nov;153(11):829-31. doi: 10.1007/BF01972892. Eur J Pediatr. 1994. PMID: 7843198

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