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

B Estournet

Showing results (41-50 of 59) with videos related to

Pageof 6
Sort By:
Radiology|March 12, 1998
Congenital muscular dystrophy: use of brain MR imaging findings to predict merosin deficiencyS Lamer, R Y Carlier, J M Pinard, et al.
Clinical Chemistry and Laboratory Medicine|April 29, 1999
Allele-specific amplification for the diagnosis of autosomal recessive spinal muscular atrophyC Ravard-Goulvestre, C Boucly, B Mathieu, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|April 1, 1994
Congenital muscular dystrophy with merosin deficiencyF M Tomé, T Evangelista, A Leclerc, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|December 1, 1995
Readjusting the localization of merosin (laminin alpha 2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2A Helbling-Leclerc, H Topaloglu, F M Tomé, et al.
Neuromuscular Disorders : NMD|November 2, 1999
Genetic heterogeneity of congenital muscular dystrophy with rigid spine syndromeB Moghadaszadeh, H Topaloglu, L Merlini, et al.
Annales De Medecine Interne|February 1, 1978
[Evaluation of the long term results of coronary surgery by the exercise electrocardiogram]B Estournet, M Baudet, S P Rosier, et al.
Nature Genetics|August 31, 2001
Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndromeB Moghadaszadeh, N Petit, C Jaillard, et al.
Neurology|October 10, 2001
Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular studyY He, K J Jones, N Vignier, et al.
Revue Neurologique|January 1, 1996
[Congenital muscular dystrophy with merosin deficiency: clinical, histopathological, immunocytochemical and genetic analysis]M Fardeau, F M Tomé, A Helbling-Leclerc, et al.
Neurology|May 27, 2006
A gene for an autosomal recessive lower motor neuron disease with childhood onset maps to 1p36I Maystadt, M Zarhrate, D Leclair-Richard, et al.
Pageof 6

Showing results (41-50 of 59) with videos related to

Sort By:
Pageof 6
Radiology|March 12, 1998
Congenital muscular dystrophy: use of brain MR imaging findings to predict merosin deficiencyS Lamer, R Y Carlier, J M Pinard, et al.
Clinical Chemistry and Laboratory Medicine|April 29, 1999
Allele-specific amplification for the diagnosis of autosomal recessive spinal muscular atrophyC Ravard-Goulvestre, C Boucly, B Mathieu, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|April 1, 1994
Congenital muscular dystrophy with merosin deficiencyF M Tomé, T Evangelista, A Leclerc, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|December 1, 1995
Readjusting the localization of merosin (laminin alpha 2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2A Helbling-Leclerc, H Topaloglu, F M Tomé, et al.
Neuromuscular Disorders : NMD|November 2, 1999
Genetic heterogeneity of congenital muscular dystrophy with rigid spine syndromeB Moghadaszadeh, H Topaloglu, L Merlini, et al.
Annales De Medecine Interne|February 1, 1978
[Evaluation of the long term results of coronary surgery by the exercise electrocardiogram]B Estournet, M Baudet, S P Rosier, et al.
Nature Genetics|August 31, 2001
Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndromeB Moghadaszadeh, N Petit, C Jaillard, et al.
Neurology|October 10, 2001
Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular studyY He, K J Jones, N Vignier, et al.
Revue Neurologique|January 1, 1996
[Congenital muscular dystrophy with merosin deficiency: clinical, histopathological, immunocytochemical and genetic analysis]M Fardeau, F M Tomé, A Helbling-Leclerc, et al.
Neurology|May 27, 2006
A gene for an autosomal recessive lower motor neuron disease with childhood onset maps to 1p36I Maystadt, M Zarhrate, D Leclair-Richard, et al.
Pageof 6