Permanent diabetes without serological evidence of autoimmunity after transient neonatal diabetes.

Autor: Gottschalk, Michael E., Schatz, Desmond A., Clare-Salzler, Michael, Kaufman, Daniel L., Ting, Grace S. P., Geffner, Mitchell E., Gottschalk, M E, Schatz, D A, Clare-Salzler, M, Kaufman, D L, Ting, G S, Geffner, M E

Publikováno v: Diabetes Care; Oct1992, Vol. 15 Issue 10, p1273-1276, 4p, 2 Charts

The emergency management of hyperglycemic-hyperosmolar nonketotic coma in the pediatric patient.

Autor: Gottschalk, Michael E., Ros, Simon P., Zeller, W Patrick, Gottschalk, M E, Ros, S P, Zeller, W P

Publikováno v: Pediatric Emergency Care; Feb1996, Vol. 12 Issue 1, p48-51, 4p

Genotype-Phenotype Analysis in Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency

Autor: Krone, Nils, Reisch, Nicole, Idkowiak, Jan, Dhir, Vivek, Ivison, Hannah E., Hughes, Beverly A., Rose, Ian T., O'Neil, Donna M., Vijzelaar, Raymon, Smith, Matthew J., MacDonald, Fiona, Cole, Trevor R., Adolphs, Nicolai, Barton, John S., Blair, Edward M., Braddock, Stephen R., Collins, Felicity, Cragun, Deborah L., Dattani, Mehul T., Day, Ruth, Dougan, Shelley, Feist, Miriam, Gottschalk, Michael E., Gregory, John W., Haim, Michaela, Harrison, Rachel, Olney, Ann Haskins, Hauffa, Berthold P., Hindmarsh, Peter C., Hopkin, Robert J., Jira, Petr E., Kempers, Marlies, Kerstens, Michiel N., Khalifa, Mohamed M., Koehler, Birgit, Maiter, Dominique, Nielsen, Shelly, O'Riordan, Stephen M., Roth, Christian L., Shane, Kate P., Silink, Martin, Stikkelbroeck, Nike M. M. L., Sweeney, Elizabeth, Szarras-Czapnik, Maria, Waterson, John R., Williamson, Lori, Hartmann, Michaela F., Taylor, Norman F., Wudy, Stefan A., Malunowicz, Ewa M., Shackleton, Cedric H. L., Arlt, Wiebke, Smith, M.J.

Publikováno v: The Journal of Clinical Endocrinology & Metabolism; Vol 97
Journal of Clinical Endocrinology and Metabolism, 97(2), E257-E267. ENDOCRINE SOC
Journal of Clinical Endocrinology and Metabolism, 97, E257-67
Journal of Clinical Endocrinology and Metabolism, 97, 2, pp. E257-67

Context: P450 oxidoreductase deficiency (PORD) is a unique congenital adrenal hyperplasia variant that manifests with glucocorticoid deficiency, disordered sex development (DSD), and skeletal malformations. No comprehensive data on genotype-phenotype

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1befea8debd4fcc1e3cfd4902412f00e
https://hdl.handle.net/11370/45890e26-6095-43e3-8feb-cf88d01a1f8d

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Resistance to Thyrotropin Caused by Mutations in the Thyrotropin-Receptor Gene.

Autor: Sunthornthepvarakul, Thongkum, Gottschalk, Michael E., Hayashi, Yoshitaka, Refetoff, Samuel

Publikováno v: New England Journal of Medicine. 1/19/95, Vol. 332 Issue 3, p155-160. 1p.