Author/Creator: Vandenberghe, A - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Vandenberghe, A

1. Axonal phenotype of Charcot-Marie-Tooth disease associated with a mutation in the myelin protein zero gene. Issue 6 (1st June 1999)

Authors:: Chapon, F; Latour, P; Diraison, P; Schaeffer, S; Vandenberghe, A
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 66:Issue 6(1999)
Page Start:: 779
Record Type:: Journal Article
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2. Frequency of mutations in the early growth response 2 gene associated with peripheral demyelinating neuropathies. Issue 12 (1st December 2002)

Authors:: Vandenberghe, N; Upadhyaya, M; Gatignol, A; Boutrand, L; Boucherat, M; Chazot, G; Vandenberghe, A; Latour, P
Journal:: Journal of medical genetics
Issue:: Volume 39:Issue 12(2002)
Page Start:: e81
Record Type:: Journal Article
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3. 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)

Authors:: Chapon, F; Diraison, P; Lechevalier, B; Chazot, G; Viader, F; Bonnebouche, C; Vandenberghe, A; Timmerman, V; Van Broeckhoven, C; Vandenberghe, A
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 61:Issue 5(1996)
Page Start:: 535
Record Type:: Journal Article
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4. Mild recurrent neuropathy in CMT1B with a novel nonsense mutation in the extracellular domain of the MPZ gene. Issue 2 (1st February 2001)

Authors:: Lagueny, A; Latour, P; Vital, A; Le Masson, G; Rouanet, M; Ferrer, X; Vital, C; Vandenberghe, A
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 70:Issue 2(2001)
Page Start:: 232
Record Type:: Journal Article
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