<--- Back to Details
First PageDocument Content
Genetic genealogy / TREAT-NMD / Limb-girdle muscular dystrophy / Duchenne muscular dystrophy / Centronuclear myopathy / Spinal muscular atrophy / Neuromuscular disease / Congenital muscular dystrophy / Myopathy / Health / Muscular dystrophy / Medicine
Date: 2014-05-20 04:36:22
Genetic genealogy
TREAT-NMD
Limb-girdle muscular dystrophy
Duchenne muscular dystrophy
Centronuclear myopathy
Spinal muscular atrophy
Neuromuscular disease
Congenital muscular dystrophy
Myopathy
Health
Muscular dystrophy
Medicine

ECRD 2014 TREAT-NMD as a funded network and new funding opportunities Kate Bushby Newcastle University @bushbykate

Add to Reading List

Source URL: www.rare-diseases.eu

Download Document from Source Website

File Size: 2,24 MB

Share Document on Facebook

Similar Documents

Mutations in BICD2 Cause Dominant Congenital Spinal Muscular Atrophy and Hereditary Spastic Paraplegia

Mutations in BICD2 Cause Dominant Congenital Spinal Muscular Atrophy and Hereditary Spastic Paraplegia

DocID: 1uWce - View Document

Fostering Health and Growth for Spinal Muscular Atrophy  SMA CARE SERIES Nutrition Basics

Fostering Health and Growth for Spinal Muscular Atrophy SMA CARE SERIES Nutrition Basics

DocID: 1trbw - View Document

TRAINING IMPROVES OXIDATIVE CAPACITY, BUT NOT FUNCTION, IN SPINAL MUSCULAR ATROPHY TYPE III

TRAINING IMPROVES OXIDATIVE CAPACITY, BUT NOT FUNCTION, IN SPINAL MUSCULAR ATROPHY TYPE III

DocID: 1tqwe - View Document

Resistance Strength Training Exercise in Children with Spinal Muscular Atrophy  Aga Lewelt, MD, MS1; Kristin J. Krosschell, PT, DPT, MA, PCS2; Gregory J. Stoddard, MS3; Cindy Weng, MS3; Mei Xue, MS4; Robin L. Marcus, PT,

Resistance Strength Training Exercise in Children with Spinal Muscular Atrophy Aga Lewelt, MD, MS1; Kristin J. Krosschell, PT, DPT, MA, PCS2; Gregory J. Stoddard, MS3; Cindy Weng, MS3; Mei Xue, MS4; Robin L. Marcus, PT,

DocID: 1tqop - View Document

Dear Primary Care Provider, Spinal Muscular Atrophy (SMA) is a genetic neuromuscular disease characterized by weakness of the skeletal and respiratory muscles. SMA is a rare disorder occurring approximately 1 in 10,000 b

DocID: 1tkD5 - View Document