Peter M - Search Results

1

Amino acid substitution R384P in aldosterone synthase causes corticosterone methyloxidase type I deficiency.

Geley S, Jöhrer K, Peter M, Denner K, Bernhardt R, Sippell WG, Kofler R. Geley S, et al. Among authors: peter m. J Clin Endocrinol Metab. 1995 Feb;80(2):424-9. doi: 10.1210/jcem.80.2.7852500. J Clin Endocrinol Metab. 1995. PMID: 7852500

2

Multisteroid analysis in children with terminal aldosterone biosynthesis defects.

Peter M, Partsch CJ, Sippell WG. Peter M, et al. J Clin Endocrinol Metab. 1995 May;80(5):1622-7. doi: 10.1210/jcem.80.5.7745009. J Clin Endocrinol Metab. 1995. PMID: 7745009

3

CYP11B1 mutations causing congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency.

Geley S, Kapelari K, Jöhrer K, Peter M, Glatzl J, Vierhapper H, Schwarz S, Helmberg A, Sippell WG, White PC, Kofler R. Geley S, et al. Among authors: peter m. J Clin Endocrinol Metab. 1996 Aug;81(8):2896-901. doi: 10.1210/jcem.81.8.8768848. J Clin Endocrinol Metab. 1996. PMID: 8768848

4

Evidence for endocrinological abnormalities in heterozygotes for adrenal 11 beta-hydroxylase deficiency of a family with the R448H mutation in the CYP11B1 gene.

Peter M, Sippell WG. Peter M, et al. J Clin Endocrinol Metab. 1997 Oct;82(10):3506-8. doi: 10.1210/jcem.82.10.4051. J Clin Endocrinol Metab. 1997. PMID: 9329393

5

Hereditary defect in biosynthesis of aldosterone: aldosterone synthase deficiency 1964-1997.

Peter M, Fawaz L, Drop SL, Visser HK, Sippell WG. Peter M, et al. J Clin Endocrinol Metab. 1997 Nov;82(11):3525-8. doi: 10.1210/jcem.82.11.4399. J Clin Endocrinol Metab. 1997. PMID: 9360501

6

Congenital hypoaldosteronism: the Visser-Cost syndrome revisited.

Peter M, Sippell WG. Peter M, et al. Pediatr Res. 1996 Mar;39(3):554-60. doi: 10.1203/00006450-199603000-00027. Pediatr Res. 1996. PMID: 8929880

7

Mutation THR-185 ILE is associated with corticosterone methyl oxidase deficiency type II.

Peter M, Bünger K, Sólyom J, Sippell WG. Peter M, et al. Eur J Pediatr. 1998 May;157(5):378-81. doi: 10.1007/s004310050833. Eur J Pediatr. 1998. PMID: 9625333

8

Molecular genetic study in two patients with congenital hypoaldosteronism (types I and II) in relation to previously published hormonal studies.

Peter M, Bünger K, Drop SL, Sippell WG. Peter M, et al. Eur J Endocrinol. 1998 Jul;139(1):96-100. doi: 10.1530/eje.0.1390096. Eur J Endocrinol. 1998. PMID: 9703385 Review.

9

Homozygous deletion of arginine-173 in the CYP11B2 gene in a girl with congenital hypoaldosteronism. Corticosterone methyloxidase deficiency type II.

Peter M, Nikischin W, Heinz-Erian P, Fussenegger W, Kapelari K, Sippell WG. Peter M, et al. Horm Res. 1998;50(4):222-5. doi: 10.1159/000023278. Horm Res. 1998. PMID: 9838244

10

Disorders of the aldosterone synthase and steroid 11beta-hydroxylase deficiencies.

Peter M, Dubuis JM, Sippell WG. Peter M, et al. Horm Res. 1999;51(5):211-22. doi: 10.1159/000023374. Horm Res. 1999. PMID: 10559665 Review.

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