Peter M - Search Results

1

Prepubertal diagnosis of X-linked congenital adrenal hypoplasia presenting after infancy.

Loke KY, Larry KS, Lee YS, Peter M, Drop SL. Loke KY, et al. Among authors: peter m. Eur J Pediatr. 2000 Sep;159(9):671-5. doi: 10.1007/pl00008404. Eur J Pediatr. 2000. PMID: 11014466

2

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.

3

Thirteen novel mutations in the NR0B1 (DAX1) gene as cause of adrenal hypoplasia congenita.

Krone N, Riepe FG, Dörr HG, Morlot M, Rudorff KH, Drop SL, Weigel J, Pura M, Kreze A, Boronat M, de Luca F, Tiulpakov A, Partsch CJ, Peter M, Sippell WG. Krone N, et al. Among authors: peter m. Hum Mutat. 2005 May;25(5):502-3. doi: 10.1002/humu.9331. Hum Mutat. 2005. PMID: 15841486

4

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

5

Prenatal diagnosis of congenital adrenal hypoplasia.

Peter M, Partsch CJ, Dörr HG, Sippell WG. Peter M, et al. Horm Res. 1996 Jul;46(1):41-5. doi: 10.1159/000184976. Horm Res. 1996. PMID: 8854139

6

Comparison of complete and incomplete suppression of pituitary-gonadal activity in girls with central precocious puberty: influence on growth and predicted final height. The German-Dutch Precocious Puberty Study Group.

Partsch CJ, Hümmelink R, Peter M, Sippell WG, Oostdijk W, Odink RJ, Drop SL. Partsch CJ, et al. Among authors: peter m. Horm Res. 1993;39(3-4):111-7. doi: 10.1159/000182709. Horm Res. 1993. PMID: 8262471

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

Anorexia nervosa in congenital adrenal hyperplasia: long-term follow-up of 4 cases.

Brand M, Schoof E, Partsch C-J, Peter M, Hoepffner W, Dörr HG, Sippell WG. Brand M, et al. Among authors: peter m. Exp Clin Endocrinol Diabetes. 2000;108(6):430-5. doi: 10.1055/s-2000-8139. Exp Clin Endocrinol Diabetes. 2000. PMID: 11026757

9

X-linked congenital adrenal hypoplasia: new mutations and long-term follow-up in three patients.

Binder G, Wollmann H, Schwarze CP, Strom TM, Peter M, Ranke MB. Binder G, et al. Among authors: peter m. Clin Endocrinol (Oxf). 2000 Aug;53(2):249-55. doi: 10.1046/j.1365-2265.2000.01038.x. Clin Endocrinol (Oxf). 2000. PMID: 10931108

10

Improved test to identify heterozygotes for congenital adrenal hyperplasia without index case examination.

Peter M, Sippell WG, Lorenzen F, Willig RP, Westphal E, Grosse-Wilde H. Peter M, et al. Lancet. 1990 Jun 2;335(8701):1296-9. doi: 10.1016/0140-6736(90)91185-d. Lancet. 1990. PMID: 1971375

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

1,271 results

Search Page

Filters