Publications by authors named "Peter Heidemann"

Claim this Profile
S
Sex chromosome DSD individuals with mosaic 45,X0 and aberrant Y chromosomes in 46,XY cells: distinct gender phenotypes and germ cell tumour risks.
Peter H Vogt, Banu Besikoglu, Markus Bettendorf, Petra Frank-Herrmann, Jutta Zimmer, Peter H Heidemann

Syst Biol Reprod Med· August 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical and functional characterization of a patient carrying a compound heterozygous pericentrin mutation and a heterozygous IGF1 receptor mutation.
Eva Müller, Desiree Dunstheimer, Jürgen Klammt, Daniela Friebe, Wieland Kiess, Peter H Heidemann

PLoS One· October 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Activating mutations in the calcium-sensing receptor: genetic and clinical spectrum in 25 patients with autosomal dominant hypocalcaemia - a German survey.
Friedhelm Raue, Josef Pichl, Helmuth-G Dörr, Dirk Schnabel, Peter Heidemann

Clin Endocrinol (Oxf)· December 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical and molecular profile of a new series of patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome: inconsistent correlation between forkhead box protein 3 expression and disease severity.
Eleonora Gambineri, Lucia Perroni, Laura Passerini, Lucia Bianchi, Claudio Doglioni, Peter H Heidemann

J Allergy Clin Immunol· December 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Five novel mutations in steroidogenic factor 1 (SF1, NR5A1) in 46,XY patients with severe underandrogenization but without adrenal insufficiency.
Birgit Köhler, Lin Lin, Bruno Ferraz-de-Souza, Peter Wieacker, Peter Heidemann

Hum Mutat· January 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Insulin tolerance test causes hypokalaemia and can provoke cardiac arrhythmias.
Gerhard Binder, Axel Bosk, Matthias Gass, Michael B Ranke, Peter H Heidemann

Horm Res· February 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
W
Wide phenotypic variability in families with holoprosencephaly and a sonic hedgehog mutation.
Ute Hehr, Claudia Gross, Uta Diebold, Dagmar Wahl, Ulrike Beudt, Peter Heidemann

Eur J Pediatr· July 2004

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
Bi-allelic inactivation of the MEN1 tumor suppressor gene in human grade II astrocytoma.
Wolfram Karges, Beate Karges, Leopold Ludwig, Peter H Heidemann

Cancer Lett· June 2003

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId.
Bengt Hansske, Christian Thiel, Torben Lübke, Martin Hasilik, Stefan Höning, Peter H Heidemann

J Clin Invest· March 2002

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis