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

D Fontan

Showing results (71-80 of 82) with videos related to

Pageof 9
Sort By:
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 1, 1996
[Superior sagittal sinus thrombosis in children during the first year of life: clinical aspects, imaging and development]J M Pedespan, J F Chateil, L Pedespan-Joly, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 20, 1999
Childhood demyelinating diseases with a prolonged remitting course and their relation to Schilder's disease: report of two casesV Leuzzi, G Lyon, M R Cilio, et al.
Pediatrie|June 1, 1977
[Tomodensitometric examinations in infantile cerebral pathology. Apropos of 205 cases]J P Hehunstre, A Dop, P Constant, et al.
Archives Francaises De Pediatrie|May 1, 1975
[Proceedings: Enlarged kidneys in infants less than 3 months old]D Laisne, J M Bondonny, M Rémi, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Merrf family with 8344 mutation in tRNA (lys). Evidence of a mitochondrial vasculopathy in muscle biopsiesM Coquet, F Degoul, A Vital, et al.
Journal of the Neurological Sciences|August 1, 1986
Congenital muscular dystrophy and cerebral CT scan anomalies. Results of a collaborative study of the Société de Neurologie InfantileB Echenne, M Arthuis, C Billard, et al.
Human Genetics|May 1, 1994
Skewed inactivation of an X chromosome deleted at the dystrophin gene in an asymptomatic mother and her affected daughterF Tihy, N Vogt, D Recan, et al.
Neuromuscular Disorders : NMD|May 23, 2001
X-linked myopathy with excessive autophagy: a clinicopathological study of five new familiesB Chabrol, D Figarella-Branger, M Coquet, et al.
Human Genetics|June 1, 1997
Biochemical and genetic studies of four patients with pyruvate dehydrogenase E1 alpha deficiencyC Marsac, C Benelli, I Desguerre, et al.
Annals of Neurology|November 18, 2000
Multi-minicore disease--searching for boundaries: phenotype analysis of 38 casesA Ferreiro, B Estournet, D Chateau, et al.
Pageof 9

Showing results (71-80 of 82) with videos related to

Sort By:
Pageof 9
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 1, 1996
[Superior sagittal sinus thrombosis in children during the first year of life: clinical aspects, imaging and development]J M Pedespan, J F Chateil, L Pedespan-Joly, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 20, 1999
Childhood demyelinating diseases with a prolonged remitting course and their relation to Schilder's disease: report of two casesV Leuzzi, G Lyon, M R Cilio, et al.
Pediatrie|June 1, 1977
[Tomodensitometric examinations in infantile cerebral pathology. Apropos of 205 cases]J P Hehunstre, A Dop, P Constant, et al.
Archives Francaises De Pediatrie|May 1, 1975
[Proceedings: Enlarged kidneys in infants less than 3 months old]D Laisne, J M Bondonny, M Rémi, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Merrf family with 8344 mutation in tRNA (lys). Evidence of a mitochondrial vasculopathy in muscle biopsiesM Coquet, F Degoul, A Vital, et al.
Journal of the Neurological Sciences|August 1, 1986
Congenital muscular dystrophy and cerebral CT scan anomalies. Results of a collaborative study of the Société de Neurologie InfantileB Echenne, M Arthuis, C Billard, et al.
Human Genetics|May 1, 1994
Skewed inactivation of an X chromosome deleted at the dystrophin gene in an asymptomatic mother and her affected daughterF Tihy, N Vogt, D Recan, et al.
Neuromuscular Disorders : NMD|May 23, 2001
X-linked myopathy with excessive autophagy: a clinicopathological study of five new familiesB Chabrol, D Figarella-Branger, M Coquet, et al.
Human Genetics|June 1, 1997
Biochemical and genetic studies of four patients with pyruvate dehydrogenase E1 alpha deficiencyC Marsac, C Benelli, I Desguerre, et al.
Annals of Neurology|November 18, 2000
Multi-minicore disease--searching for boundaries: phenotype analysis of 38 casesA Ferreiro, B Estournet, D Chateau, et al.
Pageof 9