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

T Darras

Showing results (101-110 of 303) with videos related to

Pageof 31
Sort By:
Journal Belge De Radiologie|December 1, 1993
Absence of the left pulmonary arteryJ Jaucot, J M Bailly, T Darras, et al.
Muscle & Nerve|December 31, 2013
Referral and diagnostic trends in pediatric electromyography in the molecular eraIoannis Karakis, Wendy Liew, Basil T Darras, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 24, 2014
Inter-session reliability of electrical impedance myography in children in a clinical trial settingTom R Geisbush, Nicole Visyak, Lavanya Madabusi, et al.
Annals of Neurology|March 25, 2022
Reply to: The 4-Copy Conundrum in the Treatment of Infants with Spinal Muscular AtrophyCrystal J J Yeo, Zachary Simmons, Darryl C De Vivo, et al.
Muscle & Nerve|March 6, 2013
Clinical correlates of Charcot-Marie-Tooth disease in patients with pes cavus deformitiesIoannis Karakis, Matt Gregas, Basil T Darras, et al.
Pediatric Neurology|March 7, 2018
Electrophysiologic Features of Radial Neuropathy in Childhood and AdolescenceIoannis Karakis, Sofia Georghiou, H Royden Jones, et al.
Nature Reviews. Disease Primers|August 4, 2022
Spinal muscular atrophyEugenio Mercuri, Charlotte J Sumner, Francesco Muntoni, et al.
Clinical Genetics|June 7, 2003
XL PCR for the detection of large trinucleotide expansions in juvenile Huntington's diseaseJ M Milunsky, T A Maher, B A Loose, et al.
Gene|February 14, 1990
Novel use of a chimpanzee pseudogene for chromosomal mapping of human cytochrome c oxidase subunit IVM I Lomax, M D Welch, B T Darras, et al.
American Journal of Human Genetics|July 1, 1989
Brother/sister pairs affected with early-onset, progressive muscular dystrophy: molecular studies reveal etiologic heterogeneityU Francke, B T Darras, J H Hersh, et al.
Pageof 31

Showing results (101-110 of 303) with videos related to

Sort By:
Pageof 31
Journal Belge De Radiologie|December 1, 1993
Absence of the left pulmonary arteryJ Jaucot, J M Bailly, T Darras, et al.
Muscle & Nerve|December 31, 2013
Referral and diagnostic trends in pediatric electromyography in the molecular eraIoannis Karakis, Wendy Liew, Basil T Darras, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 24, 2014
Inter-session reliability of electrical impedance myography in children in a clinical trial settingTom R Geisbush, Nicole Visyak, Lavanya Madabusi, et al.
Annals of Neurology|March 25, 2022
Reply to: The 4-Copy Conundrum in the Treatment of Infants with Spinal Muscular AtrophyCrystal J J Yeo, Zachary Simmons, Darryl C De Vivo, et al.
Muscle & Nerve|March 6, 2013
Clinical correlates of Charcot-Marie-Tooth disease in patients with pes cavus deformitiesIoannis Karakis, Matt Gregas, Basil T Darras, et al.
Pediatric Neurology|March 7, 2018
Electrophysiologic Features of Radial Neuropathy in Childhood and AdolescenceIoannis Karakis, Sofia Georghiou, H Royden Jones, et al.
Nature Reviews. Disease Primers|August 4, 2022
Spinal muscular atrophyEugenio Mercuri, Charlotte J Sumner, Francesco Muntoni, et al.
Clinical Genetics|June 7, 2003
XL PCR for the detection of large trinucleotide expansions in juvenile Huntington's diseaseJ M Milunsky, T A Maher, B A Loose, et al.
Gene|February 14, 1990
Novel use of a chimpanzee pseudogene for chromosomal mapping of human cytochrome c oxidase subunit IVM I Lomax, M D Welch, B T Darras, et al.
American Journal of Human Genetics|July 1, 1989
Brother/sister pairs affected with early-onset, progressive muscular dystrophy: molecular studies reveal etiologic heterogeneityU Francke, B T Darras, J H Hersh, et al.
Pageof 31