Braun A - Search Results

1

Predicting phenotype in steroid 21-hydroxylase deficiency? Comprehensive genotyping in 155 unrelated, well defined patients from southern Germany.

Krone N, Braun A, Roscher AA, Knorr D, Schwarz HP. Krone N, et al. Among authors: braun a. J Clin Endocrinol Metab. 2000 Mar;85(3):1059-65. doi: 10.1210/jcem.85.3.6441. J Clin Endocrinol Metab. 2000. PMID: 10720040 Clinical Trial.

2

Comprehensive analytical strategy for mutation screening in 21-hydroxylase deficiency.

Krone N, Roscher AA, Schwarz HP, Braun A. Krone N, et al. Among authors: braun a. Clin Chem. 1998 Oct;44(10):2075-82. Clin Chem. 1998. PMID: 9761237 Clinical Trial.

3

A novel frameshift mutation (141delT) in exon 1 of the 21-hydroxylase gene (CYP21) in a patient with the salt wasting form of congenital adrenal hyperplasia. Mutation in brief no. 255. Online.

Krone N, Braun A, Roscher AA, Schwarz HP. Krone N, et al. Among authors: braun a. Hum Mutat. 1999;14(1):90-1. doi: 10.1002/(sici)1098-1004(1999)14:1<90::aid-humu20>3.0.co;2-h. Hum Mutat. 1999. PMID: 10447270

4

Multiplex minisequencing of the 21-hydroxylase gene as a rapid strategy to confirm congenital adrenal hyperplasia.

Krone N, Braun A, Weinert S, Peter M, Roscher AA, Partsch CJ, Sippell WG. Krone N, et al. Among authors: braun a. Clin Chem. 2002 Jun;48(6 Pt 1):818-25. Clin Chem. 2002. PMID: 12028996

5

Identification of polymorphic sites of the human bradykinin B2 receptor gene.

Braun A, Kammerer S, Böhme E, Müller B, Roscher AA. Braun A, et al. Biochem Biophys Res Commun. 1995 Jun 6;211(1):234-40. doi: 10.1006/bbrc.1995.1801. Biochem Biophys Res Commun. 1995. PMID: 7779090

6

A novel sequence polymorphism in the promoter region of the human B2-bradykinin receptor gene.

Braun A, Maier E, Kammerer S, Müller B, Roscher AA. Braun A, et al. Hum Genet. 1996 May;97(5):688-9. doi: 10.1007/BF02281884. Hum Genet. 1996. PMID: 8655154

7

Polymorphisms in the gene for the human B2-bradykinin receptor. New tools in assessing a genetic risk for bradykinin-associated diseases.

Braun A, Kammerer S, Maier E, Böhme E, Roscher AA. Braun A, et al. Immunopharmacology. 1996 Jun;33(1-3):32-5. doi: 10.1016/0162-3109(96)00079-3. Immunopharmacology. 1996. PMID: 8856111

8

Rapid and simple diagnosis of the two common alpha 1-proteinase inhibitor deficiency alleles Pi*Z and Pi*S by DNA analysis.

Braun A, Meyer P, Cleve H, Roscher AA. Braun A, et al. Eur J Clin Chem Clin Biochem. 1996 Sep;34(9):761-4. doi: 10.1515/cclm.1996.34.9.761. Eur J Clin Chem Clin Biochem. 1996. PMID: 8891530

9

Characterization of a novel mutation in exon 10 of the adrenoleukodystrophy gene.

Holzinger A, Maier E, Stöckler-Ipsiroglu S, Braun A, Roscher AA. Holzinger A, et al. Among authors: braun a. Clin Genet. 1998 Jun;53(6):482-7. doi: 10.1111/j.1399-0004.1998.tb02600.x. Clin Genet. 1998. PMID: 9712540

10

Analysis of the two common alpha-1-antitrypsin deficiency alleles PiMS and PiMZ as modifiers of Pseudomonas aeruginosa susceptibility in cystic fibrosis.

Meyer P, Braun A, Roscher AA. Meyer P, et al. Among authors: braun a. Clin Genet. 2002 Oct;62(4):325-7. doi: 10.1034/j.1399-0004.2002.620413.x. Clin Genet. 2002. PMID: 12372062

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