Proceedings: Loss of noradrenergic and dopaminergic terminals in the chronically isolated cerebral cortex of the cat.

Por Hirsch, J C, Tassin, J P, Thierry, A M
Publicado em 1975

Autosomal dominant paroxysmal kinesigenic choreoathetosis: a clinical and genetic study of two families

Por PICARD, F, TASSIN, J, VIDAILHET, M, MARESCAUX, C, PICARD, F, AGID, Y, BRICE, A
Publicado em 1998

Anatomical study of the paraspinal approach to the lumbar spine

Por Vialle, Raphaël, Court, C., Khouri, N., Olivier, E., Miladi, L., Tassin, J. L., Defives, T., Dubousset, J.
Publicado em 2004

Noradrenaline and functional plasticity in kitten visual cortex: a re-examination.

Por Adrien, J, Blanc, G, Buisseret, P, Frégnac, Y, Gary-Bobo, E, Imbert, M, Tassin, J P, Trotter, Y
Publicado em 1985

Dopaminergic control of 125I-labeled neurotensin binding site density in corticolimbic structures of the rat brain.

Por Herve, D, Tassin, J P, Studler, J M, Dana, C, Kitabgi, P, Vincent, J P, Glowinski, J, Rostene, W
Publicado em 1986

The first de novo mutation of the connexin 32 gene associated with X linked Charcot-Marie-Tooth disease.

Por Meggouh, F, Benomar, A, Rouger, H, Tardieu, S, Birouk, N, Tassin, J, Barhoumi, C, Yahyaoui, M, Chkili, T, Brice, A, LeGuern, E
Publicado em 1998

A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3.

Por Bouhouche, A, Benomar, A, Birouk, N, Mularoni, A, Meggouh, F, Tassin, J, Grid, D, Vandenberghe, A, Yahyaoui, M, Chkili, T, Brice, A, LeGuern, E
Publicado em 1999

Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous...

Por Tassin, J, Dürr, A, de Broucker, T, Abbas, N, Bonifati, V, De Michele, G, Bonnet, A M, Broussolle, E, Pollak, P, Vidailhet, M, De Mari, M, Marconi, R, Medjbeur, S, Filla, A, Meco, G, Agid, Y, Brice, A
Publicado em 1998