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1. Brain glucose utilisation in a patient with "athymhormia" from a family with autosomal dominant parkinsonism and psychic disturbances. Issue 8 (August 1994)

2. Familial cavernous malformations in a large French kindred: mapping of the gene to the CCM1 locus on chromosome 7q. Issue 1 (1st July 1997)

4. Hereditary neuropathy with liability to pressure palsies with a partial deletion of the region often duplicated in Charcot-Marie-Tooth disease, type 1A. Issue 5 (November 1996)