Zobrazeno 1 - 10
of 78
pro vyhledávání: '"W G Sippell"'
Autor:
W. G. Sippell, M Hermanussen
Publikováno v:
Clinical Genetics. 28:106-111
Kallmann's syndrome is a rare condition defined as a combination of hypogonadotropic hypogonadism and anosmia. The present study shows two genealogical tables. In the first family six male members in four generations had Kallmann's syndrome. All carr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4dfc69a926d90e59f911d72ac8a06e6
https://doi.org/10.1111/j.1399-0004.1985.tb00368.x
https://doi.org/10.1111/j.1399-0004.1985.tb00368.x
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 80:424-429
Corticosterone methyloxidase type I (CMO-I) deficiency is an autosomal recessively inherited disorder causing congenital hypoaldosteronism due to defects in aldosterone synthase (P450aldo), the enzyme that converts 11-deoxycorticosterone to corticost
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::524ca74ad871be394b64410f426a3367
https://doi.org/10.1210/jcem.80.2.7852500
https://doi.org/10.1210/jcem.80.2.7852500
Publikováno v:
Schilddrüse 2005: Henning-Symposium. 17. Konferenz über die menschliche Schilddrüse, Heidelberg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae99af73424199de589f05813626fc08
https://doi.org/10.1515/9783110919387.95
https://doi.org/10.1515/9783110919387.95
Autor:
K. W. Schmid, G. Kahaly, B. Wiedenma, G. K. Stalla, O.-A. Müller, Th. Thomas, H. Lehnert, Ch. Kasperk, A. Körner, F. G. Riepe, M. Reincke, J. Hensen, H. Dralle, D. Zehnder, J. Pfeilschifter, U. Plöckinger, Hendrik Lehnert, A. Steinmetz, M. Schott, K. Reschke, M. Blüher, W.J. Faßbender, M. B. Ranke, W. Kern, L. Wildt, B. Gallwitz, C. Sievers, Hans Hauner, J. Hebebrand, H. Mönig, D. Grammatopoulo, H. Börschmann, K. G. Parhofer, K. Müssig, M. Bidlingmaier, B. Koletzko, N. Begum, M. Hummel, R. Paschke, Martin Wabitsch, H.-P. Bruch, M. Buchfelder, E. Ritz, H. Siggelkow, M. Stumvoll, St. Schäfer, C.-J. Partsch, K. A. Iwen, G. Brabant, R. Gärtner, C. Bürk, H. J. Schneider, Th. Gudermann, M. Kalinowski, A.-G. Ziegler, R. Lobmann, W. Wuttke, O. Hiort, B. Hinney, S. H. Scharla, P.-M. Holterhus, Ch. Reiners, C. Schulz, W. G. Sippell, J. Schopohl, G. Emons, P. H. Kann, K. Mann, Ch. J. Strasbu, V. Mattle, A. Fritsche, N. Stefan, W. Karges, E. Nieschlag, A. Grüters-Kieslich, W. Kiess, F. Sayk, K.-J. Klose, F. Beuschlein
Publikováno v:
Rationelle Diagnostik und Therapie in Endokrinologie, Diabetologie und Stoffwechsel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1058a8067d8a52b448f0346849cf7459
https://doi.org/10.1055/b-002-13401
https://doi.org/10.1055/b-002-13401
Autor:
R Hümmelink, W G Sippell
Publikováno v:
Hormone and Metabolic Research. 22:101-108
The present study was designed to answer the following three questions: Is there any difference between the growth hormone (GH) response to i.v. injections of GHRH 1-44 by a slowly injecting hormone pump or to a s. s. or rapid i. v. injection by syri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62f116a1ef6000fa71de8d0d5a468438
https://doi.org/10.1055/s-2007-1004860
https://doi.org/10.1055/s-2007-1004860
Publikováno v:
Pädiatrie ISBN: 9783540718956
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0bddf37441afedf3f49a9e4bf31e473
https://doi.org/10.1007/978-3-540-76460-1_71
https://doi.org/10.1007/978-3-540-76460-1_71
Publikováno v:
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. 23(6)
Endoscopic third ventriculostomy (ETV) is a standard procedure for the treatment of obstructive hydrocephalus in children. Main part of the procedure is the perforation of the third ventricle floor (tuber cinereum). This structure is part of the hypo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a72b1f4975f981360a4a5452edc5595
https://pubmed.ncbi.nlm.nih.gov/17447075
https://pubmed.ncbi.nlm.nih.gov/17447075
Autor:
R, Fölster-Holst, F G, Riepe, W, Ahrens, M, Möller, J, Brasch, C-J, Partsch, O, Hiort, W G, Sippell
Publikováno v:
Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete. 57(10)
Albright hereditary osteodystrophy (AHO) is characterized by a symptom complex including short stature, brachymetacarpia, obesity, round facies, cutaneous osteomas, and mental retardation. AHO is caused by mutations in the GNAS-gene localized on chro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::787c32f39d540e0f8635081ab598fc7e
https://pubmed.ncbi.nlm.nih.gov/16270203
https://pubmed.ncbi.nlm.nih.gov/16270203
Publikováno v:
Journal of endocrinological investigation. 28(5)
Sodium loss in infants with salt wasting (SW) congenital adrenal hyperplasia (CAH) does usually not occur within the first week of life. We hypothesized that sufficient mineralocorticoid activity might by temporarily maintained by still appropriate c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b783fc415aef0bdd2f6569a493eb57a9
https://pubmed.ncbi.nlm.nih.gov/16075923
https://pubmed.ncbi.nlm.nih.gov/16075923
Autor:
W. G. Sippell
Publikováno v:
Pädiatrie ISBN: 9783662091777
Die Nebennieren setzen sich aus der vom Zolomepithel (Mesoderm) abstammenden Nebennierenrinde (NNR) und dem vom Sympathikus (Ektoderm) stammenden Nebennierenmark (NNM) zusammen. An der Rinde unterscheidet man von innen nach ausen 3 Zonen: Zona reticu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e5cbad41fb0dbd79b489e78000a2799
https://doi.org/10.1007/978-3-662-09176-0_67
https://doi.org/10.1007/978-3-662-09176-0_67