Peter M - Search Results

1

Birthweight Differences in Monozygotic Twins Influence Pubertal Maturation and Near Final Height.

Schulte S, Wölfle J, Schreiner F, Stoffel-Wagner B, Peter M, Bartmann P, Gohlke B. Schulte S, et al. Among authors: peter m. J Pediatr. 2016 Mar;170:288-94.e1-2. doi: 10.1016/j.jpeds.2015.12.020. Epub 2016 Jan 12. J Pediatr. 2016. PMID: 26794471

2

Functional glucocorticoid receptor gene variants do not underlie the high variability of 17-hydroxyprogesterone screening values in healthy newborns.

Schreiner F, Tozakidou M, Maslak R, Holtkamp U, Peter M, Gohlke B, Woelfle J. Schreiner F, et al. Among authors: peter m. Eur J Endocrinol. 2009 Apr;160(4):667-73. doi: 10.1530/EJE-08-0639. Epub 2009 Jan 27. Eur J Endocrinol. 2009. PMID: 19174530

3

Serum leptin levels in patients with progressive central precocious puberty.

Heger S, Partsch CJ, Peter M, Blum WF, Kiess W, Sippell WG. Heger S, et al. Among authors: peter m. Pediatr Res. 1999 Jul;46(1):71-5. doi: 10.1203/00006450-199907000-00012. Pediatr Res. 1999. PMID: 10400137 Clinical Trial.

4

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

5

Changes in the concentrations of dehydroepiandrosterone sulfate and estriol in maternal plasma during pregnancy: a longitudinal study in healthy women throughout gestation and at term.

Peter M, Dörr HG, Sippell WG. Peter M, et al. Horm Res. 1994;42(6):278-81. doi: 10.1159/000184209. Horm Res. 1994. PMID: 7698724

6

Evidence for genetic heterogeneity of pseudohypoaldosteronism type 1: identification of a novel mutation in the human mineralocorticoid receptor in one sporadic case and no mutations in two autosomal dominant kindreds.

Viemann M, Peter M, López-Siguero JP, Simic-Schleicher G, Sippell WG. Viemann M, et al. Among authors: peter m. J Clin Endocrinol Metab. 2001 May;86(5):2056-9. doi: 10.1210/jcem.86.5.7449. J Clin Endocrinol Metab. 2001. PMID: 11344206

7

Rapid quantification of conjugated and unconjugated bile acids and C27 precursors in dried blood spots and small volumes of serum.

Janzen N, Sander S, Terhardt M, Das AM, Sass JO, Kraetzner R, Rosewich H, Peter M, Sander J. Janzen N, et al. Among authors: peter m. J Lipid Res. 2010 Jun;51(6):1591-8. doi: 10.1194/jlr.D003814. Epub 2010 Jan 21. J Lipid Res. 2010. PMID: 20093478 Free PMC article.

8

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

9

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

10

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

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