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C Turpin

Showing results (21-30 of 117) with videos related to

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Biomedicine / [Publiee Pour L'A.A.I.C.I.G.]|October 1, 1977
Metachromatic leukodystrophy and arylsulphatase A: relations and discrepanciesG Dubois, J C Turpin, N Baumann
Journal of Neurology, Neurosurgery, and Psychiatry|December 17, 1998
Lack of mutation G209A in the alpha-synuclein gene in French patients with familial and sporadic Parkinson's diseaseG Lucotte, G Mercier, J C Turpin
Developmental Neuroscience|January 1, 1991
Clinical aspects of Niemann-Pick type C disease in the adultJ C Turpin, M Masson, N Baumann
Journal of Neurology|February 13, 1999
Variable number tandem repeat dopamine transporter gene polymorphism and Parkinson's disease: no association foundG Mercier, J C Turpin, G Lucotte
Human Genetics|April 1, 1993
A recombinant Friedreich's ataxia familyG Lucotte, S Berriche, J C Turpin
Comptes Rendus Hebdomadaires Des Seances De L'Academie Des Sciences. Serie D: Sciences Naturelles|May 27, 1974
[Characterization of a new type of metachromatic leukodystrophy]J C Turpin, G Dubois, N Baumann
Comptes Rendus Hebdomadaires Des Seances De L'Academie Des Sciences. Serie D: Sciences Naturelles|March 4, 1974
[Use of electrophoresis for the detection of metachromatic leukodystrophy from human leukocytes]G Dubois, J C Turpin, N Baumann
La Nouvelle Presse Medicale|June 3, 1972
[Laboratory diagnosis of Gaucher's disease. Value of leukocyte beta-glucosidase determination]J C Turpin, N Bauman, P Castaigne
Revue Neurologique|November 23, 2007
[Neurological presentations of lysosomal diseases in adult patients]F Sedel, J-C Turpin, N Baumann
La Presse Medicale|January 30, 1971
[Diagnostic value of the determination of intraleukocytic arylsulfatase for the early detection of metachromatic leukodystrophy]N Baumann, J C Turpin, P Castaigne
Pageof 12

Showing results (21-30 of 117) with videos related to

Sort By:
Pageof 12
Biomedicine / [Publiee Pour L'A.A.I.C.I.G.]|October 1, 1977
Metachromatic leukodystrophy and arylsulphatase A: relations and discrepanciesG Dubois, J C Turpin, N Baumann
Journal of Neurology, Neurosurgery, and Psychiatry|December 17, 1998
Lack of mutation G209A in the alpha-synuclein gene in French patients with familial and sporadic Parkinson's diseaseG Lucotte, G Mercier, J C Turpin
Developmental Neuroscience|January 1, 1991
Clinical aspects of Niemann-Pick type C disease in the adultJ C Turpin, M Masson, N Baumann
Journal of Neurology|February 13, 1999
Variable number tandem repeat dopamine transporter gene polymorphism and Parkinson's disease: no association foundG Mercier, J C Turpin, G Lucotte
Human Genetics|April 1, 1993
A recombinant Friedreich's ataxia familyG Lucotte, S Berriche, J C Turpin
Comptes Rendus Hebdomadaires Des Seances De L'Academie Des Sciences. Serie D: Sciences Naturelles|May 27, 1974
[Characterization of a new type of metachromatic leukodystrophy]J C Turpin, G Dubois, N Baumann
Comptes Rendus Hebdomadaires Des Seances De L'Academie Des Sciences. Serie D: Sciences Naturelles|March 4, 1974
[Use of electrophoresis for the detection of metachromatic leukodystrophy from human leukocytes]G Dubois, J C Turpin, N Baumann
La Nouvelle Presse Medicale|June 3, 1972
[Laboratory diagnosis of Gaucher's disease. Value of leukocyte beta-glucosidase determination]J C Turpin, N Bauman, P Castaigne
Revue Neurologique|November 23, 2007
[Neurological presentations of lysosomal diseases in adult patients]F Sedel, J-C Turpin, N Baumann
La Presse Medicale|January 30, 1971
[Diagnostic value of the determination of intraleukocytic arylsulfatase for the early detection of metachromatic leukodystrophy]N Baumann, J C Turpin, P Castaigne
Pageof 12