Showing results (1-10 of 13) with videos related to
Sort By:
Pageof 2
Psychiatrie, Neurologie, Und Medizinische Psychologie|March 1, 1990
[Is there a "temporal psychosyndrome (Landolt)"?]E Lange, U ReunerPsychiatrie, Neurologie, Und Medizinische Psychologie|September 1, 1990
[Psychopathology and criminal personality changes in patients with frontal lobe injuries]E Lange, U ReunerBritish Journal of Haematology|November 13, 2001
Early recognition of hereditary motor and sensory neuropathy type 1 can avoid life-threatening vincristine neurotoxicityR Naumann, J Mohm, U Reuner, et al.Neuropediatrics|August 12, 2003
The Kleine-Levin syndrome - effects of treatment with lithium -M Poppe, D Friebel, U Reuner, et al.Proceedings of the National Academy of Sciences of the United States of America|September 27, 2001
Myokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K+ channelK Dedek, B Kunath, C Kananura, et al.Journal of Neurology, Neurosurgery, and Psychiatry|July 20, 2004
Familial ALS in Germany: origin of the R115G SOD1 mutation by a founder effectS Niemann, H Joos, T Meyer, et al.Medizinische Klinik (Munich, Germany : 1983)|April 12, 1996
[Noninvasive nocturnal nasal mask ventilation (NIPPV) in childhood and adolescence. Dresden experiences with 11 patients]E Paditz, G Reitemeier, W Leupold, et al.Disease Markers|April 1, 1997
Direct molecular genetic diagnosis and heterozygote identification in X-linked Emery-Dreifuss muscular dystrophy by heteroduplex analysisK Wulff, U Ebener, C S Wehnert, et al.Medizinische Klinik (Munich, Germany : 1983)|April 28, 1997
[Noninvasive ventilation of a 4-year-old boy with severe central late onset hypoventilation syndrome]E Paditz, J Dinger, G Reitemeier, et al.American Journal of Medical Genetics|October 9, 1995
Systematic screening for mutations in the promoter and the coding region of the 5-HT1A geneJ Erdmann, D Shimron-Abarbanell, S Cichon, et al.Pageof 2