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75 Possible Causes for krude

  • Septo-Optic Dysplasia

    McNay DE, Turton JP, Kelberman D, Woods KS, Brauner R, Papadimitriou A, Keller E, Keller A, Haufs N, Krude H, Shalet SM, Dattani MT.[ghr.nlm.nih.gov]

  • 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]

  • Pseudohypoparathyroidism

    Léger J, Olivieri A, Donaldson M, Torresani T, Krude H, van Vliet G, Polak M, Butler G; Congenital Hypothyroidism Consensus Conference Group: European Society for Paediatric[karger.com]

  • Obesity due to Congenital Leptin Deficiency

    Krude 2 Email author 1. Sozialpädiatrisches Zentrum (SPZ) Charité-Universitätsmedizin Berlin Berlin Deutschland 2.[link.springer.com] Krude geben an, dass kein Interessenkonflikt besteht. Dieser Beitrag beinhaltet keine Studien an Menschen oder Tieren. Literatur 1.[link.springer.com] Krude H, Biebermann H, Luck W et al (1998) Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans.[link.springer.com]

  • 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]

  • Genetic Combined Pituitary Hormone Deficiencies

    McNay DE, Turton JP, Kelberman D, Woods KS, Brauner R, Papadimitriou A, Keller E, Keller A, Haufs N, Krude H, Shalet SM, Dattani MT: HESX1 mutations are an uncommon cause[karger.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]

  • Triple A Syndrome

    Kleinau, Dirk Schnabel, Detlef Bockenhauer, Louise C Wilson, Ian Tully, Sarah Kiff, Patrick Scheerer, Monica Reyes, Sarah Paisdzior, John W Gregory, Jeremy Allgrove, Heiko Krude[readbyqxmd.com]

  • Hypothyroidism

    Macchia PE, Lapi P, Krude H, et al. PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis. Nat Genet . 1998 May. 19(1):83-6. [Medline] .[emedicine.medscape.com]

  • Allan-Herndon-Dudley Syndrome

    Friesema EC , Grueters A , Krude H , von Moers A , Reeser M et al.[nature.com] PubMed Central PubMed Google Scholar Krude H, Schutz B, Biebermann H, von Moers A, Schnabel D, Neitzel H, Tonnies H, Weise D, Lafferty A, Schwarz S, et al: Choreoathetosis[ojrd.biomedcentral.com] PubMed Google Scholar Al Taji E, Biebermann H, Limanova Z, Hnikova O, Zikmund J, Dame C, Gruters A, Lebl J, Krude H: Screening for mutations in transcription factors in a[ojrd.biomedcentral.com]

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