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

I J Butler

Showing results (71-80 of 89) with videos related to

Pageof 9
Sort By:
Annals of Neurology|July 1, 1988
Neurological basis of respiratory complications in achondroplasiaF W Nelson, J T Hecht, W A Horton, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|November 1, 1990
Proton magnetic resonance of exercise-induced water changes in gastrocnemius muscleL K Fotedar, J M Slopis, P A Narayana, et al.
Magnetic Resonance Imaging|March 1, 1989
In vivo muscle magnetic resonance spectroscopy in a family with mitochondrial cytopathy: a defect in fat metabolismP A Narayana, J M Slopis, E F Jackson, et al.
Surgical Neurology|June 1, 1982
Cervical myelopathy due to dural compression in mucopolysaccharidosisH H Kaufman, H S Rosenberg, C I Scott, et al.
Nature Genetics|April 16, 1998
Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathiesL E Warner, P Mancias, I J Butler, et al.
Annals of Neurology|January 1, 1989
Cerebrospinal fluid biogenic amines and biopterin in Rett syndromeH Y Zoghbi, S Milstien, I J Butler, et al.
Pediatric Neurology|February 1, 1994
D-2-hydroxyglutaric aciduria in neonate with seizures and CNS dysfunctionW J Craigen, C Jakobs, E A Sekul, et al.
Genomics|May 18, 1999
Human bHLH transcription factor gene myogenin (MYOG): genomic sequence and negative mutation analysis in patients with severe congenital myopathiesB S Tseng, S T Cavin, E P Hoffman, et al.
Advances in Neurology|September 29, 1998
Rapid-onset dystonia-parkinsonism: a report of clinical, biochemical, and genetic studies in two familiesA Brashear, I J Butler, L J Ozelius, et al.
European Journal of Pediatrics|December 1, 1986
Foramen magnum stenosis in homozygous achondroplasiaJ T Hecht, W A Horton, I J Butler, et al.
Pageof 9

Showing results (71-80 of 89) with videos related to

Sort By:
Pageof 9
Annals of Neurology|July 1, 1988
Neurological basis of respiratory complications in achondroplasiaF W Nelson, J T Hecht, W A Horton, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|November 1, 1990
Proton magnetic resonance of exercise-induced water changes in gastrocnemius muscleL K Fotedar, J M Slopis, P A Narayana, et al.
Magnetic Resonance Imaging|March 1, 1989
In vivo muscle magnetic resonance spectroscopy in a family with mitochondrial cytopathy: a defect in fat metabolismP A Narayana, J M Slopis, E F Jackson, et al.
Surgical Neurology|June 1, 1982
Cervical myelopathy due to dural compression in mucopolysaccharidosisH H Kaufman, H S Rosenberg, C I Scott, et al.
Nature Genetics|April 16, 1998
Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathiesL E Warner, P Mancias, I J Butler, et al.
Annals of Neurology|January 1, 1989
Cerebrospinal fluid biogenic amines and biopterin in Rett syndromeH Y Zoghbi, S Milstien, I J Butler, et al.
Pediatric Neurology|February 1, 1994
D-2-hydroxyglutaric aciduria in neonate with seizures and CNS dysfunctionW J Craigen, C Jakobs, E A Sekul, et al.
Genomics|May 18, 1999
Human bHLH transcription factor gene myogenin (MYOG): genomic sequence and negative mutation analysis in patients with severe congenital myopathiesB S Tseng, S T Cavin, E P Hoffman, et al.
Advances in Neurology|September 29, 1998
Rapid-onset dystonia-parkinsonism: a report of clinical, biochemical, and genetic studies in two familiesA Brashear, I J Butler, L J Ozelius, et al.
European Journal of Pediatrics|December 1, 1986
Foramen magnum stenosis in homozygous achondroplasiaJ T Hecht, W A Horton, I J Butler, et al.
Pageof 9