অনুসন্ধান ফলাফলগুলি - Annick Labarre‐Vila
- প্রদর্শন 1 - 2 ফলাফল এর 2
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1
A homozygous splicing mutation causing a depletion of skeletal muscle RYR1 is associated with multi-minicore disease congenital myopathy with ophthalmoplegia অনুযায়ী Nicole Monnier, Ana Ferreiro, Isabelle Marty, Annick Labarre‐Vila, Paulette Mezin, Joël Lunardi
প্রকাশিত 2003Artigo -
2
Generalised sensory system abnormalities in amyotrophic lateral sclerosis: a European multicentre study অনুযায়ী Kirsten Pugdahl, Anders Fuglsang‐Frederiksen, Mamede de Carvalho, Birger Johnsen, P R W Fawcett, Annick Labarre‐Vila, Rocco Liguori, W. Nix, IS Schofield
প্রকাশিত 2006Artigo
অনুসন্ধান সাধনীগুলি:
সম্পর্কিত বিষয়
Internal medicine
Medicine
Pathology
Amyotrophic lateral sclerosis
Biology
Biopsy
Central core disease
Congenital myopathy
Disease
Dorsal root ganglion
Electrophysiology
Endocrinology
Endoplasmic reticulum
Gene
Genetics
Malignant hyperthermia
Missense mutation
Muscle biopsy
Mutation
Myopathy
Neuroscience
Polyneuropathy
Psychology
RYR1
Ryanodine receptor
Sensory nerve
Sensory system
Skeletal muscle