Search research articles
Contact Us
Filters
Showing results (131-140 of 147) with videos related to
Page
of 15
Sort By:
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 1, 1993
Relief of akinesia by apomorphine and cerebral metabolic changes in Parkinson's disease
E Broussolle, L Cinotti, P Pollak, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 1, 1996
Hereditary neuropathy with liability to pressure palsies with a partial deletion of the region often duplicated in Charcot-Marie-Tooth disease, type 1A
F Chapon, P Diraison, B Lechevalier, et al.
Human Mutation
|
April 13, 1999
Missense mutation in exon 11 (Codon 378) of the presenilin-1 gene in a French family with early-onset Alzheimer's disease and transmission study by mismatch enhanced allele specific amplification. Mutations in brief no. 141. Online. besancon@rockefeller1.univ.lyon1.fr
R Besançon, A Lorenzi, M Cruts, et al.
Cytogenetics and Cell Genetics
|
January 1, 1994
Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP)
E Le Guern, F Sturtz, M Gugenheim, et al.
Archives of Neurology
|
January 1, 1996
Giant lambl excrescences. An unusual source of cerebral embolism
N Nighoghossian, L Derex, R Loire, et al.
European Neurology
|
January 1, 1996
Modelization of motor nerve conduction velocities for Charcot-Marie-Tooth (Type-1) patients. CMT-France Network
F G Sturtz, F Chauvin, E Ollagnon-Roman, et al.
Acta Neurologica Scandinavica
|
October 1, 1995
DNA analysis as a tool to confirm the diagnosis of asymptomatic hereditary neuropathy with liability to pressure palsies (HNPP) with further evidence for the occurrence of de novo mutations
P M Gonnaud, F Sturtz, Y Fourbil, et al.
Clinical Chemistry
|
July 1, 1996
Molecular diagnosis of Charcot-Marie-Tooth 1A disease and hereditary neuropathy with liability to pressure palsies by quantifying CMT1A-REP sequences: consequences of recombinations at variant sites on chromosomes 17p11.2-12
A Vandenberghe, P Latour, G Chauplannaz, et al.
Neurology
|
July 24, 2002
Prevalence and clinical characteristics of migraine in France
P Henry, J P Auray, A F Gaudin, et al.
Cephalalgia : an International Journal of Headache
|
March 11, 2004
Use and misuse of triptans in France: data from the GRIM2000 population survey
C Lucas, J-P Auray, A-F Gaudin, et al.
Page
of 15
Search research articles
Search
Showing results (131-140 of 147) with videos related to
Sort By:
Page
of 15
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 1, 1993
Relief of akinesia by apomorphine and cerebral metabolic changes in Parkinson's disease
E Broussolle, L Cinotti, P Pollak, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 1, 1996
Hereditary neuropathy with liability to pressure palsies with a partial deletion of the region often duplicated in Charcot-Marie-Tooth disease, type 1A
F Chapon, P Diraison, B Lechevalier, et al.
Human Mutation
|
April 13, 1999
Missense mutation in exon 11 (Codon 378) of the presenilin-1 gene in a French family with early-onset Alzheimer's disease and transmission study by mismatch enhanced allele specific amplification. Mutations in brief no. 141. Online. besancon@rockefeller1.univ.lyon1.fr
R Besançon, A Lorenzi, M Cruts, et al.
Cytogenetics and Cell Genetics
|
January 1, 1994
Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP)
E Le Guern, F Sturtz, M Gugenheim, et al.
Archives of Neurology
|
January 1, 1996
Giant lambl excrescences. An unusual source of cerebral embolism
N Nighoghossian, L Derex, R Loire, et al.
European Neurology
|
January 1, 1996
Modelization of motor nerve conduction velocities for Charcot-Marie-Tooth (Type-1) patients. CMT-France Network
F G Sturtz, F Chauvin, E Ollagnon-Roman, et al.
Acta Neurologica Scandinavica
|
October 1, 1995
DNA analysis as a tool to confirm the diagnosis of asymptomatic hereditary neuropathy with liability to pressure palsies (HNPP) with further evidence for the occurrence of de novo mutations
P M Gonnaud, F Sturtz, Y Fourbil, et al.
Clinical Chemistry
|
July 1, 1996
Molecular diagnosis of Charcot-Marie-Tooth 1A disease and hereditary neuropathy with liability to pressure palsies by quantifying CMT1A-REP sequences: consequences of recombinations at variant sites on chromosomes 17p11.2-12
A Vandenberghe, P Latour, G Chauplannaz, et al.
Neurology
|
July 24, 2002
Prevalence and clinical characteristics of migraine in France
P Henry, J P Auray, A F Gaudin, et al.
Cephalalgia : an International Journal of Headache
|
March 11, 2004
Use and misuse of triptans in France: data from the GRIM2000 population survey
C Lucas, J-P Auray, A-F Gaudin, et al.
Page
of 15