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Genes and Immunity|February 24, 2001
Chromosome 17q22-q24 and multiple sclerosis genetic susceptibility. American-French Multiple Sclerosis Genetic GroupB Fontaine, I Cournu, I Arnaud, et al.
Human Genetics|September 1, 1996
Recessive Schwartz-Jampel syndrome (SJS): confirmation of linkage to chromosome 1p, evidence of genetic homogeneity and reduction of the SJS locus to a 3-cM intervalB Fontaine, S Nicole, H Topaloglu, et al.
Neurology|September 22, 2010
Long-term follow-up of neuromyelitis optica with a pediatric onsetN Collongues, R Marignier, H Zéphir, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|December 8, 2009
Season of birth and not vitamin D receptor promoter polymorphisms is a risk factor for multiple sclerosisD A Fernandes de Abreu, M C Babron, M C I Babron, et al.
Conservation Biology : the Journal of the Society for Conservation Biology|December 22, 2006
Taxonomic considerations in listing subspecies under the U.S. Endangered Species ActSusan M Haig, Erik A Beever, Steven M Chambers, et al.
Nature Genetics|December 28, 1999
Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegiaJ Hazan, N Fonknechten, D Mavel, et al.
Scientific Reports|September 1, 2018
Subcontinental heat wave triggers terrestrial and marine, multi-taxa responsesKatinka X Ruthrof, David D Breshears, Joseph B Fontaine, et al.
European Journal of Neurology|March 20, 2010
EFNS guidelines on the molecular diagnosis of channelopathies, epilepsies, migraine, stroke, and dementiasJ-M Burgunder, J Finsterer, Z Szolnoki, et al.
European Journal of Neurology|May 28, 2009
EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington's disease, Parkinson's disease and dystoniasH F Harbo, J Finsterer, J Baets, et al.
European Journal of Neurology|May 27, 2010
EFNS guidelines for the molecular diagnosis of neurogenetic disorders: motoneuron, peripheral nerve and muscle disordersJ-M Burgunder, L Schöls, J Baets, et al.
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