Ozguc M - Search Results

1

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.

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

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

4

The effect of mannose-binding protein gene polymorphisms in recurrent respiratory system infections in children and lung tuberculosis.

Ozbaş-Gerçeker F, Tezcan I, Berkel AI, Ozkara S, Ozcan A, Ersoy F, Sanal O, Ozgüç M. Ozbaş-Gerçeker F, et al. Among authors: ozguc m. Turk J Pediatr. 2003 Apr-Jun;45(2):95-8. Turk J Pediatr. 2003. PMID: 12921293

5

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.

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

7

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

8

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

9

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.

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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