Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J C Turpin

Showing results (61-70 of 88) with videos related to

Pageof 9
Sort By:
Pediatrie|October 1, 1978
[Juvenile form of metachromatic leukodystrophy. Clinical variant of sulfatidosis]J C Turpin, J F Elchardus, J Morice, et al.
Developmental Neuroscience|January 1, 1991
Adult forms of metachromatic leukodystrophy: clinical and biochemical approachN Baumann, M Masson, V Carreau, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|January 6, 1983
[Study of thesaurismosis induced by perhexiline maleate. Confirmation of experimental data]J C Turpin, M Pluot, S Albouz, et al.
Presse Medicale (Paris, France : 1983)|December 19, 1992
[Prenatal diagnosis in a family affected by amyloid neuropathy]J C Turpin, S Berriche, F David, et al.
Revue Neurologique|January 1, 1991
[Type C Niemann-Pick disease: supranuclear ophthalmoplegia associated with deficient biosynthesis of cholesterol esters]J C Turpin, J Y Goas, M Masson, et al.
Revue Neurologique|April 1, 1997
[2 familial cases of metachromatic leukodystrophy of late onset]J L Brault, V Gielselmann, A Carpentier, et al.
Journal of Inherited Metabolic Disease|August 19, 2007
Psychiatric manifestations revealing inborn errors of metabolism in adolescents and adultsF Sedel, N Baumann, J-C Turpin, et al.
Journal of the Neurological Sciences|April 1, 1979
Analysis of the major lipid classes in human peripheral nerve biopsies. Age group differences and abnormalities of ganglioside level in perhexiline maleate therapyS Pollet, J J Hauw, J C Turpin, et al.
Pediatrie|September 1, 1981
[A+(8,13) translocation followed for 3 generations]J C Turpin, J P Duc, L Larget-Piet, et al.
Journal of Medical Genetics|February 1, 1993
A transthyretin variant (alanine 71) associated with familial amyloidotic polyneuropathy in a French familyM D Benson, J C Turpin, G Lucotte, et al.
Pageof 9

Showing results (61-70 of 88) with videos related to

Sort By:
Pageof 9
Pediatrie|October 1, 1978
[Juvenile form of metachromatic leukodystrophy. Clinical variant of sulfatidosis]J C Turpin, J F Elchardus, J Morice, et al.
Developmental Neuroscience|January 1, 1991
Adult forms of metachromatic leukodystrophy: clinical and biochemical approachN Baumann, M Masson, V Carreau, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|January 6, 1983
[Study of thesaurismosis induced by perhexiline maleate. Confirmation of experimental data]J C Turpin, M Pluot, S Albouz, et al.
Presse Medicale (Paris, France : 1983)|December 19, 1992
[Prenatal diagnosis in a family affected by amyloid neuropathy]J C Turpin, S Berriche, F David, et al.
Revue Neurologique|January 1, 1991
[Type C Niemann-Pick disease: supranuclear ophthalmoplegia associated with deficient biosynthesis of cholesterol esters]J C Turpin, J Y Goas, M Masson, et al.
Revue Neurologique|April 1, 1997
[2 familial cases of metachromatic leukodystrophy of late onset]J L Brault, V Gielselmann, A Carpentier, et al.
Journal of Inherited Metabolic Disease|August 19, 2007
Psychiatric manifestations revealing inborn errors of metabolism in adolescents and adultsF Sedel, N Baumann, J-C Turpin, et al.
Journal of the Neurological Sciences|April 1, 1979
Analysis of the major lipid classes in human peripheral nerve biopsies. Age group differences and abnormalities of ganglioside level in perhexiline maleate therapyS Pollet, J J Hauw, J C Turpin, et al.
Pediatrie|September 1, 1981
[A+(8,13) translocation followed for 3 generations]J C Turpin, J P Duc, L Larget-Piet, et al.
Journal of Medical Genetics|February 1, 1993
A transthyretin variant (alanine 71) associated with familial amyloidotic polyneuropathy in a French familyM D Benson, J C Turpin, G Lucotte, et al.
Pageof 9