Olek K - Search Results

1

Diagnostic difficulties in glucokinase hyperinsulinism.

Meissner T, Marquard J, Cobo-Vuilleumier N, Maringa M, Rodríguez-Bada P, García-Gimeno MA, Baixeras E, Weber J, Olek K, Sanz P, Mayatepek E, Cuesta-Muñoz AL. Meissner T, et al. Among authors: olek k. Horm Metab Res. 2009 Apr;41(4):320-6. doi: 10.1055/s-0028-1102922. Epub 2008 Dec 3. Horm Metab Res. 2009. PMID: 19053014 Free article.

2

Myotonic dystrophy and limb girdle muscular dystrophy in one family.

Schröder R, Beyenburg S, Weber J, Olek K, Zierz S. Schröder R, et al. Among authors: olek k. Clin Investig. 1994 May;72(5):409-13. doi: 10.1007/BF00252840. Clin Investig. 1994. PMID: 8086779

3

Cystic fibrosis: typing 89 German families with linked DNA probes.

Weber J, Aulehla-Scholz C, Kaiser R, Eigel A, Neugebauer M, Horst J, Olek K. Weber J, et al. Among authors: olek k. Hum Genet. 1988 Dec;81(1):54-6. doi: 10.1007/BF00283729. Hum Genet. 1988. PMID: 2904405

4

Microdissection and microcloning of human chromosome 7q22-32 region.

Weber J, Weith A, Kaiser R, Grzeschik KH, Olek K. Weber J, et al. Among authors: olek k. Somat Cell Mol Genet. 1990 Mar;16(2):123-8. doi: 10.1007/BF01233042. Somat Cell Mol Genet. 1990. PMID: 1969681

5

The frequency of the CF delta F508 deletion in CF chromosomes of different ethnic origin.

Aulehla-Scholz C, Kaiser R, Weber J, Pivetta O, Eigel A, Dworniczak B, Olek K, Horst J. Aulehla-Scholz C, et al. Among authors: olek k. Hum Genet. 1990 Sep;85(4):392-3. doi: 10.1007/BF02428269. Hum Genet. 1990. PMID: 2210740 No abstract available.

6

Maturity-onset diabetes of the young: an update.

Olek K. Olek K. Clin Lab. 2006;52(11-12):593-8. Clin Lab. 2006. PMID: 17175890 Review.

7

Mitochondrial DNA and the origins of the domestic horse.

Jansen T, Forster P, Levine MA, Oelke H, Hurles M, Renfrew C, Weber J, Olek K. Jansen T, et al. Among authors: olek k. Proc Natl Acad Sci U S A. 2002 Aug 6;99(16):10905-10. doi: 10.1073/pnas.152330099. Epub 2002 Jul 18. Proc Natl Acad Sci U S A. 2002. PMID: 12130666 Free PMC article.

8

Carnitine palmitoyltransferase II deficiency: molecular and biochemical analysis of 32 patients.

Wieser T, Deschauer M, Olek K, Hermann T, Zierz S. Wieser T, et al. Among authors: olek k. Neurology. 2003 Apr 22;60(8):1351-3. doi: 10.1212/01.wnl.0000055901.58642.48. Neurology. 2003. PMID: 12707442

9

Identification and DNA sequence analysis of 15 new alpha 1-antitrypsin variants, including two PI*Q0 alleles and one deficient PI*M allele.

Faber JP, Poller W, Weidinger S, Kirchgesser M, Schwaab R, Bidlingmaier F, Olek K. Faber JP, et al. Among authors: olek k. Am J Hum Genet. 1994 Dec;55(6):1113-21. Am J Hum Genet. 1994. PMID: 7977369 Free PMC article.

10

Sequence data of the rare deficient alpha 1-antitrypsin variant PI Zaugsburg.

Faber JP, Weidinger S, Olek K. Faber JP, et al. Among authors: olek k. Am J Hum Genet. 1990 Jun;46(6):1158-62. Am J Hum Genet. 1990. PMID: 2339709 Free PMC article.

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