Zobrazeno 1 - 10
of 132
pro vyhledávání: '"F. Grahmann"'
Autor:
H. Buchner, F. Grahmann
Publikováno v:
Klinische Neurophysiologie. 40:155-158
We report on the case of a 44-year-old female patient with a history psychiatric alcohol and drug addiction, depression, motor function disorder and a polyneuropathic syndrome with progressive gait disorder. The motor functional disorder rapidly deve
Publikováno v:
DMW - Deutsche Medizinische Wochenschrift. 114:1658-1661
An acute polyneuropathy developed during intensive-care treatment of three young men who had sustained severe multiple traumas and of one woman with bacterial meningoencephalitis. In the first case there was a predominantly distal paraparesis of the
Autor:
Armin Wagner, Hans-Jochen Verlohren, F. Grahmann, Petra Baum, Wieland Hermann, Tobias Lohmann
Publikováno v:
Journal of Neurology. 250:682-687
Objective: In previous studies, a lower incidence of diabetes-related complications such as diabetic neuropathy has been reported in patients with early stages of type 1 diabetes compared with type 2 diabetes. The aim of this study was to compare the
Autor:
A. Wagner, Wieland Hermann, H. Kuhn, Swen Hesse, F. Grahmann, Thomas Villmann, Henryk Barthel
Publikováno v:
Journal of Neurology. 249:896-901
In Wilson's disease a disturbed glucose metabolism especially in striatal and cerebellar areas has been reported. This is correlated with the severity of extrapyramidal motor symptoms (EPS). These findings are only based on a small number of patients
Publikováno v:
Der Nervenarzt. 72:932-938
Die Wirksamkeit der repetitiven transkraniellen Magnetstimulation (rTMS) wurde bei 9 Parkinson-Patienten untersucht (Hoehn-und-Yahr-Stadium 1 oder 2). Primarer Zielparameter war die Verbesserung im motorischen Teil der Unified Parkinson's Disease Rat
Autor:
Thomas Mothes, Holm H. Uhlig, J. Karbe, Mona Amin, Manja Kamprad, Awad A. Osman, H. Hummelsheim, F. Grahmann
Publikováno v:
Scandinavian Journal of Immunology. 53:204-208
Screening a human small intestinal library with human serum yielded a clone which encoded a protein res4-22 the gene of which was highly homologous to a recently described gene located in the Huntington's disease locus. Autoantibodies against res4-22
Publikováno v:
Der Nervenarzt. 71:970-974
Bei 33 Patienten mit einem Morbus Wilson wurden auf der Grundlage eines standardisierten Scoresystems zur klinisch-neurologischen Schweregradbeurteilung Verlaufskontrollen zwischen Datum der Diagnosestellung und nach medikamentoser Behandlung zum akt
Publikováno v:
Klinische Neurophysiologie. 31:94-100
Autor:
M. Mück-Weymann, Detlef Claus, Josef G. Heckmann, M. J. Hilz, F. Grahmann, Bernhard Neundörfer
Publikováno v:
Aktuelle Neurologie. 24:79-83
Publikováno v:
Aktuelle Neurologie. 17:113-116