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50 Possible Causes for biebermann

  • Nephrogenic Diabetes Insipidus

    Karger AG, Basel References Schliebe N, Strotmann R, Busse K, Mitschke D, Biebermann H, Schomburg L, et al: V2 vasopressin receptor deficiency causes changes in expression[karger.com] Schöneberg T, Schulz A, Biebermann H, Grüters A, Grimm T, Hübschmann K, et al: V2 vasopressin receptor dysfunction in nephrogenic diabetes insipidus caused by different molecular[karger.com]

  • Metformin

    The first cases of POMC mutation were documented by Krude et al. in 1998 [Krude H, Biebermann H, Luck W, Horn R, Brabant G, et al.[ncbi.nlm.nih.gov]

  • Sporadic Goitrous Cretinism

    Krude H, Schütz B, Biebermann H et al. (2002) Choreoathetosis, hypothyroidism and pulmonary alterations due to human NKX2–1 haploinsufficiency.[link.springer.com] Ambrugger P, Stoeva I, Biebermann H et al. (2001) Novel mutations of the thyroid peroxidase gene in patients with permanent congenital hypothyroidism.[link.springer.com] Gruters A, Krude H, Biebermann H (2004) Molecular genetic defects in congenital hypothyroidism. Eur J Endocrinol 151: 39–44 CrossRef Google Scholar 13.[link.springer.com]

  • 46,XX Gonadal Dysgenesis

    Journal of Medical Genetics; 52:240-247 (2015) Köhler B, Lin L, Ferraz-de-Souza B, Wieacker P, Heidemann P, Schröder V, Biebermann H, Schnabel D, Grüters A, Achermann JC:[klinikum.uni-muenster.de] Human Mutation, 29:59-64, 2008 Köhler B, Biebermann H, Friedsam V, Gellermann J, Maier R, Korth-Schütz S, Pohl M, Wieacker P, Hiort O, Grüters, A: Analysis of the Wilms’ tumor[klinikum.uni-muenster.de]

  • 46,XY Disorder of Sex Development

    Journal of Medical Genetics; 52:240-247 (2015) Köhler B, Lin L, Ferraz-de-Souza B, Wieacker P, Heidemann P, Schröder V, Biebermann H, Schnabel D, Grüters A, Achermann JC:[klinikum.uni-muenster.de] Human Mutation, 29:59-64, 2008 Köhler B, Biebermann H, Friedsam V, Gellermann J, Maier R, Korth-Schütz S, Pohl M, Wieacker P, Hiort O, Grüters, A: Analysis of the Wilms’ tumor[klinikum.uni-muenster.de]

  • Female Infertility due to Gonadal Dysgenesis

    Journal of Medical Genetics; 52:240-247 (2015) Köhler B, Lin L, Ferraz-de-Souza B, Wieacker P, Heidemann P, Schröder V, Biebermann H, Schnabel D, Grüters A, Achermann JC:[klinikum.uni-muenster.de] Human Mutation, 29:59-64, 2008 Köhler B, Biebermann H, Friedsam V, Gellermann J, Maier R, Korth-Schütz S, Pohl M, Wieacker P, Hiort O, Grüters, A: Analysis of the Wilms’ tumor[klinikum.uni-muenster.de]

  • Isoproterenol

    Kleinau G, Pratzka J, Nürnberg D, Grüters A, Führer-Sakel D, Krude H, Köhrle J, Schöneberg T, Biebermann H (October 2011).[en.wikipedia.org]

  • Gonadal Dysgenesis

    Journal of Medical Genetics; 52:240-247 (2015) Köhler B, Lin L, Ferraz-de-Souza B, Wieacker P, Heidemann P, Schröder V, Biebermann H, Schnabel D, Grüters A, Achermann JC:[ukm.de] Human Mutation, 29:59-64, 2008 Köhler B, Biebermann H, Friedsam V, Gellermann J, Maier R, Korth-Schütz S, Pohl M, Wieacker P, Hiort O, Grüters, A: Analysis of the Wilms’ tumor[ukm.de]

  • Triple A Syndrome

    March 2018: La Tunisie Médicale # 3 Heike Biebermann, Gunnar Kleinau, Dirk Schnabel, Detlef Bockenhauer, Louise C Wilson, Ian Tully, Sarah Kiff, Patrick Scheerer, Monica Reyes[readbyqxmd.com]

  • Spondylo-Megaepiphyseal-Metaphyseal Dysplasia

    Authors Heiko Krude, Barbara Schütz, Heike Biebermann, Arpad von Moers, Dirk Schnabel, Heidi Neitzel, Holger Tönnies, Dagmar Weise, Antony Lafferty, Siegfried Schwarz, Mario[jci.org]

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