Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Hermann Dieter Schworm"'
Autor:
K.-P. Boergen, Thomas Berninger, Günther Rudolph, Alfons Meindl, Hermann-Dieter Schworm, Martin Bechmann, Thomas Meitinger, Helene Achatz, Anselm Kampik
Publikováno v:
Graefe's Archive for Clinical and Experimental Ophthalmology. 239:167-172
Background: Mutations in the OA1 gene on the short arm of the X chromosome are known to cause X-linked ocular albinism (xlOA) in males. A four-generation family with this disorder, including asymptomatic carrier females, was investigated by molecular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::893ba48ab02e1ec830416423f6391053
https://doi.org/10.1007/s004170000234
https://doi.org/10.1007/s004170000234
Publikováno v:
Der Ophthalmologe. 97:557-560
BACKGROUND In silicone intubation of the nasolacrimal duct for congenital obstruction, retrieval of the guide thread behind the inferior turbinate can be difficult and time consuming. To facilitate this maneuver a modification of the conventional tec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3631e58b6aadfeda3889d66dd760da1d
https://doi.org/10.1007/s003470070065
https://doi.org/10.1007/s003470070065
Autor:
Hans-Jürgen Heberling, Christine Spitzweg, Tina Mühlberg, Werner Joba, Armin E. Heufelder, Hermann-Dieter Schworm
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 85:734-742
Recent data have indicated that orbital fibroblasts (OF) can be stimulated to produce marked quantities of interleukin-1 receptor antagonist (IL-1RA), a powerful inhibitor of the proinflammatory activities of interleukin-1 in the orbital tissues in G
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6dfa7b99617b702c40faa0239f697ccf
https://doi.org/10.1210/jcem.85.2.6192
https://doi.org/10.1210/jcem.85.2.6192
Autor:
Donald Zimmermann, Lorenz C Hofbauer, Armin E. Heufelder, Tomas Jelinek, Hermann-Dieter Schworm, Alicja Mrozek-Lasota
Publikováno v:
Medizinische Klinik. 92:528-533
Patienten mit angeborenen oder in fruher Kindheit erworbenen gastrointestinalen und hepatobiliaren Erkrankungen haben ein hohes Risiko fur diverse endokrinologische und metabolische Storungen. Eine 27jahrige Frau mit bekanntem Alagille-Syndrom stellt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6ff47844fde408a5e2d786bb4302c7a
https://doi.org/10.1007/bf03044928
https://doi.org/10.1007/bf03044928
Autor:
Armin E. Heufelder, Tina Mühlberg, August König, Gabriela Heufelder, Lorenz C Hofbauer, Hermann-Dieter Schworm
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 82:2244-2247
Interleukin-1 (IL-1) plays an important role in the pathogenesis of Graves’ ophthalmopathy (GO). Impaired antagonism of the proinflammatory cytokine IL-1 by the naturally occurring IL-1 receptor antagonist (IL-1RA) has been implicated in the initia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca7232d2f3615e44ac7f3dc12213394f
https://doi.org/10.1210/jcem.82.7.4068
https://doi.org/10.1210/jcem.82.7.4068
Autor:
Günther Rudolph, K.-P. Boergen, Hermann-Dieter Schworm, P. Kalpadakis, Christos Haritoglou, Oliver Ehrt
Publikováno v:
Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus. 6(2)
The essential feature of the Parry-Romberg syndrome is atrophy of the subcutaneous tissues on one side of the face. It is a progressive, rather self-limiting disease whose pathogenesis is still unknown. Ocular manifestations include enophthalmos, eye
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e59b9065a39233a0ed4e418b59e3597
https://pubmed.ncbi.nlm.nih.gov/11997811
https://pubmed.ncbi.nlm.nih.gov/11997811
Autor:
K. B. Jedele, Anselm Kampik, Hermann-Dieter Schworm, Thomas Meitinger, Gerda Rudolph, E. Holinski, Konstanze Hörtnagel, K.-P. Boergen
Publikováno v:
Europe PubMed Central
Scopus-Elsevier
Scopus-Elsevier
The Schimmelpenning-Feuerstein-Mims syndrome (SFM), characterized by linear nevus sebaceous and ocular and neurologic abnormalities, is a sporadic condition without known familial cases or etiology. We report the occurrence of SFM in only one of two
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa5b34c95e997c0bb3f19c4c5db7d30f
http://europepmc.org/abstract/med/9007330
http://europepmc.org/abstract/med/9007330
