Egbert Schulze

MVZ Labor Dr. Limbach & Kollegen GbR
Heidelberg, BW, Germany

Last Updated: 09/26/2026

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Found 8 publications

Distinct clinical phenotypes in a family with a novel truncating MEN1 frameshift mutation.

Distinct clinical phenotypes in a family with a novel truncating MEN1 frameshift mutation.

Journal: BMC endocrine disorders

Published: September 07, 2021

Cross-oncopanel study reveals high sensitivity and accuracy with overall analytical performance depending on genomic regions.

Cross-oncopanel study reveals high sensitivity and accuracy with overall analytical performance depending on genomic regions.

Journal: Genome biology

Published: July 28, 2020

Typical characteristics of children with congenital adrenal hyperplasia due to 11β-hydroxylase deficiency: a single-centre experience and review of the literature.

Typical characteristics of children with congenital adrenal hyperplasia due to 11β-hydroxylase deficiency: a single-centre experience and review of the literature.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: July 09, 2018

Clinical Features and Response to Treatment of Prolactinomas in Children and Adolescents: A Retrospective Single-Centre Analysis and Review of the Literature.

Clinical Features and Response to Treatment of Prolactinomas in Children and Adolescents: A Retrospective Single-Centre Analysis and Review of the Literature.

Journal: Hormone research in paediatrics

Published: November 02, 2017

Evaluation of a Recently Established Test for Familial Hyperaldosteronism Type 1.

Evaluation of a Recently Established Test for Familial Hyperaldosteronism Type 1.

Journal: Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme

Published: December 07, 2016

Heterozygous inactivating CaSR mutations causing neonatal hyperparathyroidism: function, inheritance and phenotype.

Heterozygous inactivating CaSR mutations causing neonatal hyperparathyroidism: function, inheritance and phenotype.

Journal: European journal of endocrinology

Published: March 14, 2016

Amino alcohol- (NPS-2143) and quinazolinone-derived calcilytics (ATF936 and AXT914) differentially mitigate excessive signalling of calcium-sensing receptor mutants causing Bartter syndrome Type 5 and autosomal dominant hypocalcemia.

Amino alcohol- (NPS-2143) and quinazolinone-derived calcilytics (ATF936 and AXT914) differentially mitigate excessive signalling of calcium-sensing receptor mutants causing Bartter syndrome Type 5 and autosomal dominant hypocalcemia.

Journal: PloS one

Published: May 23, 2014

Prevalence and clinical spectrum of nonsecretory medullary thyroid carcinoma in a series of 839 patients with sporadic medullary thyroid carcinoma.

Prevalence and clinical spectrum of nonsecretory medullary thyroid carcinoma in a series of 839 patients with sporadic medullary thyroid carcinoma.

Journal: Thyroid : official journal of the American Thyroid Association

Published: September 06, 2012

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Last Updated: 09/26/2026