Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Stephan Neudecker"'
Autor:
Maren Winkler, Karin Kappes-Horn, Christina von Landenberg, Cornelia Kornblum, Stephan Neudecker, Jens Reimann
Publikováno v:
Journal of Neuropathology & Experimental Neurology.
To review our diagnostic and treatment approaches concerning sporadic inclusion body myositis (sIBM) and polymyositis with mitochondrial pathology (PM-Mito), we conducted a retrospective analysis of clinical and histological data of 32 patients diagn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df88b69cfe5b540f18b9b9b68091f28f
https://doi.org/10.1093/jnen/nlab101
https://doi.org/10.1093/jnen/nlab101
Publikováno v:
Acta Ophthalmologica Scandinavica. 84:415-418
Purpose: To explain the rare phenomenon of acute transient bilateral blindness without additional ophthalmological or neurological symptoms and signs. Methods: Six patients with isolated bilateral visual loss lasting 1–15 mins and occurring simulta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29f2dedc6b160e97fbfbeb13d111a9de
https://doi.org/10.1111/j.1600-0420.2006.00635.x
https://doi.org/10.1111/j.1600-0420.2006.00635.x
Publikováno v:
Obstetrics & Gynecology. 107:446-449
BACKGROUND:The postpartum angiopathy (Call-Fleming syndrome) is a rare, reversible cerebral vasoconstriction syndrome. Unlike in eclampsia, neither proteinuria nor hypertension have been observed in the Call-Fleming syndrome.CASE:A 17-year-old woman
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33b314e623513d823d1b6d97f04e30ab
https://doi.org/10.1097/01.aog.0000187945.61146.e6
https://doi.org/10.1097/01.aog.0000187945.61146.e6
Publikováno v:
Klinische Monatsblätter für Augenheilkunde. 221:509-512
Background: Central retinal artery occlusion with persistent amaurosis as the only focal symptom caused by dissection of the internal carotid artery has occasionally been reported. Central retinal artery occlusion due to a common carotid artery disse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::648fe5af9566b4b12b98b9f58685145e
https://doi.org/10.1055/s-2004-813138
https://doi.org/10.1055/s-2004-813138
Autor:
Michael Krasnianski, Wolfgang Hirsch, Rolf Peter Spielmann, Mirko Krivokuca, Andreas Schluter, Stephan Neudecker
Publikováno v:
Clinical Neurology and Neurosurgery. 106:110-113
Vasculitits of the central nervous system (CNS) is a known complication of chronic inflammatory bowel diseases. We report the case of a female patient with Crohn's disease, developing vasculitis of the CNS with evidence of pathological vessel depicti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cedf9431ab62331e4bb4571aa6c9bec7
https://doi.org/10.1016/j.clineuro.2003.09.004
https://doi.org/10.1016/j.clineuro.2003.09.004
Autor:
Stephan Neudecker
Publikováno v:
psychoneuro. 29:86-93
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c33df5354682642737b396305094f66
https://doi.org/10.1055/s-2003-38709
https://doi.org/10.1055/s-2003-38709
Publikováno v:
Der Nervenarzt. 74:151-158
Although the gene for facioscapulohumeral muscular dystrophy (FSHD) has not been identified so far, 4q35 deletion represents a diagnostic marker of the disease. In the present study, 46 consecutive symptomatic patients with 4q35 FSHD deletions or typ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89fd9bbd1c8ef715731402561913508f
https://doi.org/10.1007/s00115-002-1455-4
https://doi.org/10.1007/s00115-002-1455-4
Autor:
Stephan Zierz, Manfred Wehnert, Frank Hanisch, Michal Vytopil, Pascale Richard, Roberta Ricotti, Stephan Neudecker, Enzo Ricci, Daniela Toniolo, Luciano Merlini, L. Demay, Gisèle Bonne, Antonio Dello Russo
Publikováno v:
Neuromuscular Disorders. 12:958-963
Emery Dreifuss muscular dystrophy is a genetically heterogeneous disorder characterized by the clinical triad of early onset contractures, progressive muscular wasting and weakness with humeroperoneal distribution and cardiac conduction defects. Muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::026b4740bd8be82e2d48e0020be11acb
https://doi.org/10.1016/s0960-8966(02)00178-5
https://doi.org/10.1016/s0960-8966(02)00178-5
Die Hauptmann-Thannhauser-Muskeldystrophie und Differenzialdiagnosen von Myopathien mit Kontrakturen
Publikováno v:
Der Nervenarzt. 73:1004-1011
Die Hauptmann-Thannhauser-Muskeldystrophie ist durch die klinische Trias sich in den ersten 2 Dekaden manifestierender Kontrakturen von Halswirbelsaule, Ellbogen- und Sprunggelenk, langsam progredienter humeroperonealer Atrophien und Paresen sowie ei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f273edf4a124e51d08ebd6a2f32bfe1d
https://doi.org/10.1007/s00115-002-1388-y
https://doi.org/10.1007/s00115-002-1388-y
Publikováno v:
Neuromuscular Disorders. 9:305-307
The mitochondrial mutation A-->G at nucleotide position 3243 is associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) and other mitochondrial encephalomyopathies. We found this mutation in a 61-year-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e66ded707c55f6e96994111b14176d64
https://doi.org/10.1016/s0960-8966(99)00019-x
https://doi.org/10.1016/s0960-8966(99)00019-x