E. Plassart

发表

Apolipoprotein E Polymorphism in Multiple Sclerosis

B. Fontaine, A. Gervais, E. Schuller, 1998, Annals of clinical biochemistry.

Isolation of new genes in distal Xq28: transcriptional map and identification of a human homologue of the ARD1 N-acetyl transferase of Saccharomyces cerevisiae.

C. Tribioli, S. Rivella, S. Bione, 1994, Human molecular genetics.

Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31–32 in three European families

J. Weissenbach, N. Baumann, A. Elbaz, 1994, Nature Genetics.

Paramyotonia congenita: genotype to phenotype correlations in two families and report of a new mutation in the sodium channel gene

J. Hauw, B. Eymard, B. Fontaine, 1996, Journal of the Neurological Sciences.

Apolipoprotein E and multiple sclerosis: A biochemical and genetic investigation

J. Delattre, B. Fontaine, A. Gervais, 1998, Journal of the Neurological Sciences.

Periodic paralysis and voltage-gated ion channels.

Bertrand Fontaine, B. Fontaine, N. Tabti, 1996, Kidney international.

Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP)

J. Weissenbach, A. Elbaz, F. Lehmann-Horn, 1994, Human Genetics.

Mutations in the Muscle Sodium Channel Gene (SCN4A) in 13 French Families with Hyperkalemic Periodic Paralysis and Paramyotonia Congenita: Phenotype to Genotype Correlations and Demonstration of the Predominance of Two Mutations

G. Serratrice, F. Chapon, C. Confavreux, 1994, European journal of human genetics : EJHG.

Genes with triplet repeats: a new class of mutations causing neurological diseases.

B. Fontaine, E. Plassart, 1994, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

Charcot‐Marie‐Tooth disease with intermediate motor nerve conduction velocities: Characterization of 14 C×32 mutations in 35 families

Y. Agid, A. Brice, N. Birouk, 1997, Human mutation.

Respiratory and motor events in sleeping infants: their correlation with thoracico-abdominal respiratory relationships.

L. Curzi-Dascalova, E. Plassart, L. Curzi‐Dascalova, 1978, Early human development.

Charcot‐Marie‐Tooth disease with intermediate motor nerve conduction velocities: Characterization of 14 C×32 mutations in 35 families

Y. Agid, A. Brice, N. Birouk, 1997, Human mutation.