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

Nigel G Laing

Showing results (11-20 of 203) with videos related to

Pageof 21
Sort By:
Brain Pathology (Zurich, Switzerland)|July 1, 2009
Actinopathies and myosinopathiesHans H Goebel, Nigel G Laing
Neuromuscular Disorders : NMD|November 5, 2021
Genetic neuromuscular disorders: what is the best that we can do?Nigel G Laing, Royston W Ong, Gianina Ravenscroft
Brain : a Journal of Neurology|January 2, 2015
Pathophysiological concepts in the congenital myopathies: blurring the boundaries, sharpening the focusGianina Ravenscroft, Nigel G Laing, Carsten G Bönnemann
Handbook of Clinical Neurology|September 24, 2008
Congenital myopathiesNigel G Laing, Caroline A Sewry, Phillipa Lamont
Acta Neuropathologica|July 25, 2012
Skeletal muscle α-actin diseases (actinopathies): pathology and mechanismsKristen J Nowak, Gianina Ravenscroft, Nigel G Laing
The New England Journal of Medicine|February 26, 2025
Nationwide, Couple-Based Genetic Carrier Screening. ReplyMartin B Delatycki, Edwin P Kirk, Nigel G Laing
Current Opinion in Neurology|September 13, 2005
Distal myopathiesFrank L Mastaglia, Phillipa J Lamont, Nigel G Laing
Plos One|October 3, 2012
Nemaline myopathy-related skeletal muscle α-actin (ACTA1) mutation, Asp286Gly, prevents proper strong myosin binding and triggers muscle weaknessJulien Ochala, Gianina Ravenscroft, Nigel G Laing, et al.
Neuromuscular Disorders : NMD|May 11, 2006
Novel slow-skeletal myosin (MYH7) mutation in the original myosin storage myopathy kindredDanielle E Dye, Biagio Azzarelli, Hans H Goebel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 14, 2024
Genetics of inherited peripheral neuropathies and the next frontier: looking backwards to progress forwardsJevin M Parmar, Nigel G Laing, Marina L Kennerson, et al.
Pageof 21

Showing results (11-20 of 203) with videos related to

Sort By:
Pageof 21
Brain Pathology (Zurich, Switzerland)|July 1, 2009
Actinopathies and myosinopathiesHans H Goebel, Nigel G Laing
Neuromuscular Disorders : NMD|November 5, 2021
Genetic neuromuscular disorders: what is the best that we can do?Nigel G Laing, Royston W Ong, Gianina Ravenscroft
Brain : a Journal of Neurology|January 2, 2015
Pathophysiological concepts in the congenital myopathies: blurring the boundaries, sharpening the focusGianina Ravenscroft, Nigel G Laing, Carsten G Bönnemann
Handbook of Clinical Neurology|September 24, 2008
Congenital myopathiesNigel G Laing, Caroline A Sewry, Phillipa Lamont
Acta Neuropathologica|July 25, 2012
Skeletal muscle α-actin diseases (actinopathies): pathology and mechanismsKristen J Nowak, Gianina Ravenscroft, Nigel G Laing
The New England Journal of Medicine|February 26, 2025
Nationwide, Couple-Based Genetic Carrier Screening. ReplyMartin B Delatycki, Edwin P Kirk, Nigel G Laing
Current Opinion in Neurology|September 13, 2005
Distal myopathiesFrank L Mastaglia, Phillipa J Lamont, Nigel G Laing
Plos One|October 3, 2012
Nemaline myopathy-related skeletal muscle α-actin (ACTA1) mutation, Asp286Gly, prevents proper strong myosin binding and triggers muscle weaknessJulien Ochala, Gianina Ravenscroft, Nigel G Laing, et al.
Neuromuscular Disorders : NMD|May 11, 2006
Novel slow-skeletal myosin (MYH7) mutation in the original myosin storage myopathy kindredDanielle E Dye, Biagio Azzarelli, Hans H Goebel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 14, 2024
Genetics of inherited peripheral neuropathies and the next frontier: looking backwards to progress forwardsJevin M Parmar, Nigel G Laing, Marina L Kennerson, et al.
Pageof 21