User profiles for Heinrich Schmidt

Heinrich (Heinz) Wilhelm Schmidt

Computer Science, RMIT University & Innovation Software Advisory
Verified email at rmit.edu.au
Cited by 3794

[HTML][HTML] Germ-line mutations in nonsyndromic pheochromocytoma

…, A Klein-Franke, P Klose, H Schmidt… - … England Journal of …, 2002 - Mass Medical Soc
Background The group of susceptibility genes for pheochromocytoma that included the proto-oncogene
RET (associated with multiple endocrine neoplasia type 2 [MEN-2]) and the …

Impact of nanoscale roughness of titanium thin film surfaces on bacterial retention

…, CC Berndt, RT Jones, II Yusuf, I Peake, HW Schmidt… - Langmuir, 2010 - ACS Publications
Two human pathogenic bacteria, Staphylococcus aureus CIP 68.5 and Pseudomonas
aeruginosa ATCC 9025, were adsorbed onto surfaces containing Ti thin films of varying thickness …

Reduced final height outcome in congenital adrenal hyperplasia under prednisone treatment: deceleration of growth velocity during puberty

W Bonfig, S Bechtold, H Schmidt… - The Journal of …, 2007 - academic.oup.com
Context: Normal to decreased final height (FH) has been reported in patients with congenital
adrenal hyperplasia (CAH). Objective: The objective was to determine FH outcome and …

Mutational Analysis of the SOX9 Gene in Campomelic Dysplasia and Autosomal Sex Reversal: Lack of Genotype/Phenotype Correlations

…, RA Pfeiffer, A Schinzel, H Schmidt… - Human molecular …, 1997 - academic.oup.com
It has previously been shown that, in the heterozygous state, mutations in the SOX9 gene
cause campomelic dysplasia (CD) and the often associated autosomal XY sex reversal. In 12 …

Hydrocortisone dosing during puberty in patients with classical congenital adrenal hyperplasia: an evidence-based recommendation

W Bonfig, SB Dalla Pozza, H Schmidt… - The Journal of …, 2009 - academic.oup.com
Context: Patients with congenital adrenal hyperplasia (CAH) are at risk for early pubertal
development and diminished pubertal growth. Liberal treatment with glucocorticoids will …

Chromatin-remodeling factor SMARCD2 regulates transcriptional networks controlling differentiation of neutrophil granulocytes

…, MR Schneider, E Wolf, HP Horny, H Schmidt… - Nature …, 2017 - nature.com
We identify SMARCD2 (SWI/SNF-related, matrix-associated, actin-dependent regulator of
chromatin, subfamily D, member 2), also known as BAF60b (BRG1/Brahma-associated factor …

Clinical and genetic heterogeneity of hypochondroplasia.

…, J Bonaventure, L Legeai-Mallet, H Schmidt… - Journal of Medical …, 1996 - jmg.bmj.com
Hypochondroplasia (HCH) is an autosomal dominant condition characterised by short stature,
micromelia, and lumbar lordosis. In a series of 29 HCH probands (13 sporadic cases, 16 …

Testicular adrenal rest tumors develop independently of long-term disease control: a longitudinal analysis of 50 adult men with congenital adrenal hyperplasia due to …

…, A Greifenstein, N Krone, H Schmidt… - The Journal of …, 2013 - academic.oup.com
Context: Testicular adrenal rest tumors (TARTs) and hypogonadotropic hypogonadism are
the two most common causes for male infertility in classic 21-hydroxylase deficiency. Current …

Children with classic congenital adrenal hyperplasia experience salt loss and hypoglycemia: evaluation of adrenal crises during the first 6 years of life

…, U Nennstiel-Ratzel, HG Dörr, H Schmidt… - European journal of …, 2016 - academic.oup.com
Objective To evaluate adrenal crises after the start of treatment up to the age of 6 years in
children with classic congenital adrenal hyperplasia (CAH). Design Analysis of data extracted …

[HTML][HTML] The effect of cardiovascular risk factors on the longitudinal evolution of the carotid intima medial thickness in children with type 1 diabetes mellitus

…, C Weissenbacher, H Netz, H Schmidt… - Cardiovascular …, 2011 - Springer
Background Type 1 diabetes mellitus is a generally accepted atherogenic risk factor. The
aim of this prospective longitudinal study was to evaluate changes in carotid intima media …