Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Michael M. Ritter"'
Autor:
Elke Kaminsky, Judith Gerards, Andreas Gal, Michael M. Ritter, Wolfgang Hoeppner, Marcus Quinkler
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports
Summary DAX1 (NR0B1) is an orphan nuclear receptor, which plays an important role in development and function of the adrenal glands and gonads. Mutations in DAX1 cause X-linked adrenal hypoplasia congenita (X-linked AHC), which is characterized by ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7aa8ac3cc41c132140a89ac63ebd3b6
https://doi.org/10.1530/edm-17-0054
https://doi.org/10.1530/edm-17-0054
Publikováno v:
Journal of Lipid Research, Vol 41, Iss 5, Pp 727-733 (2000)
Epidemiologic studies and in vitro experiments indicate that low density lipoprotein (LDL) subtypes differ concerning their atherogenic potential. Small, dense LDL are more atherogenic than large, buoyant LDL. LDL apheresis is a potent therapeutic mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5de5702c359d04ecc027cb63b25d28c6
https://doi.org/10.1016/s0022-2275(20)32381-6
https://doi.org/10.1016/s0022-2275(20)32381-6
Autor:
J. Müller-Höcker, A. Stäbler, H. Fürst, R. Tiling, Michael M. Ritter, E. Laubach, A. Geier, Peter Schwandt
Publikováno v:
Der Internist. 40:311-315
Eine 60jahrige Patientin mit einem 9 Monate zuvor resezierten Nebenschilddrusen-Karzinom wurde mit Muskelschwache, Polyurie, Polydipsie und unstillbarem Erbrechen in somnolentem Zustand stationar aufgenommen. Bei der klinischen Untersuchung imponiert
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77ae4980071895c9829a4fce8d90fe94
https://doi.org/10.1007/s001080050340
https://doi.org/10.1007/s001080050340
Autor:
Robert A. Wahl, Oliver Gimm, Wolfgang Höppner, Bernd Koch, Siegfried Walgenbach, Michael M. Ritter, Günter Görtz, Fritz Spelsberg, Rainer Hampel, A. Heiss, Henning Dralle, Dietmar Simon, Raoul Hinze, Karin Frank-Raue, Bruno Niederle
Publikováno v:
World Journal of Surgery. 22:744-751
When mutations of the RETproto-oncogene were found in 1993 to account for hereditary medullary thyroid carcinoma (MTC), surgeons obtained the opportunity to operate on patients prophylactically (i. e., at a clinically asymptomatic stage). Whether thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a656e31e06529b9f63cc1c49984af892
https://doi.org/10.1007/s002689900463
https://doi.org/10.1007/s002689900463
Autor:
P. Groth, Friedhelm Raue, Karin Frank-Raue, Marlene Reuter, Michael M. Ritter, Wolfgang Höppner, M. Grußendorf, B. Saller, Ilona Berndt
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 83:770-774
One hundred and eighty-one families with multiple endocrine neoplasia type 2A (MEN-2A) or familial medullary thyroid carcinoma (FMTC) have been investigated for mutations in the ret protooncogene in Germany. In 8 families with FMTC or MEN-2A, no muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aadc5ff4280251d887c81cefb8073e7d
https://doi.org/10.1210/jcem.83.3.4619
https://doi.org/10.1210/jcem.83.3.4619
Autor:
Cecilia Giunta, H.C. Geiss, Andrea Superti-Furga, E. Laubach, Beat Steinmann, E. Hiller, Michael M. Ritter, Peter Schwandt
Publikováno v:
Der Internist. 38:1225-1230
Aufgrund des klinischen Bildes einer familiaren Blutungsneigung sowie mehrerer Komplikationen (spontane A. carotis-Sinus cavernosus-Fistel, Arteriendissektion bei einer Angiographie, Nierenarterienaneurysmata, spontane Peritoneumeinrisse) wurde bei d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0c68cbdf1b0c64eb057da9cf1fa652e
https://doi.org/10.1007/s001080050134
https://doi.org/10.1007/s001080050134
Autor:
Wolfgang Hoeppner, Dieter Engelhardt, Hendrik Jähnig, Michael M. Ritter, Fritz Spelsberg, Hiltrud Brauch, Thorsten Wöhl
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 82:4101-4104
Pheochromocytoma is a tumor that may occur sporadically or may be a manifestation of a hereditary disease, such as von Hippel-Lindau disease (VHL) and multiple endocrine neoplasia (MEN) type 2. As patients with VHL or MEN type 2 are at risk to develo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48dc4730fd138006e40e25030268594c
https://doi.org/10.1210/jcem.82.12.4454
https://doi.org/10.1210/jcem.82.12.4454
Autor:
Michael M. Ritter, Wolfgang Höppner
Publikováno v:
Human Molecular Genetics. 6:587-590
Activating germline mutations in the cysteine-rich domain of the RET proto-oncogene are found in >92% of the cases of multiple endocrine neoplasia type 2A (MEN2A) and 85% of familial medullary thyroid carcinoma (FMTC). In virtually 100% of patients w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0dc23954e159ff73e2a807389af543f
https://doi.org/10.1093/hmg/6.4.587
https://doi.org/10.1093/hmg/6.4.587
Publikováno v:
Hepatology. 24:1334-1337
High serum concentrations of lipoprotein (a) [Lp(a)] are considered a risk factor for premature atherosclerosis. Besides apolipoprotein B-100, Lp(a) consists of apolipoprotein (a) [apo(a)], which shows a remarkable size polymorphism. The serum concen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cae52d632627b8cb513387c3394987af
https://doi.org/10.1002/hep.510240602
https://doi.org/10.1002/hep.510240602