Topic: Adult
Journal: Neuromuscular Disorders : Nmd
Documents
A list of abstracts that contain a topic of "Adult" and a journal name of "Neuromuscular Disorders : Nmd".
Dermatomyositis, Lobar Panniculitis and Inflammatory Myopathy with Abundant Macrophages.
PMID: 16809038
A Second Pedigree with Autosomal Dominant Nemaline Myopathy Caused by Tpm3 Mutation: a Clinical and Pathological Study.
PMID: 17376686
Pompe Disease (Glycogen Storage Disease Type Ii) in Argentineans: Clinical Manifestations and Identification of 9 Novel Mutations.
PMID: 17056254
Severe Phenotype in Infantile Facioscapulohumeral Muscular Dystrophy.
PMID: 16934468
Muscle Cell and Motor Protein Function in Patients with a Iia Myosin Missense Mutation (Glu-706 to Lys).
PMID: 17005402
High Erythropoietin and Low Vascular Endothelial Growth Factor Levels in Cerebrospinal Fluid from Hypoxemic Als Patients Suggest an Abnormal Response to Hypoxia.
PMID: 17142042
The 577x Allele of the Actn3 Gene is Associated with Improved Exercise Capacity in Women with Mcardle's Disease.
PMID: 17560787
A Comparative Analysis of Collagen Vi Production in Muscle, Skin and Fibroblasts from 14 Ullrich Congenital Muscular Dystrophy Patients with Dominant and Recessive Col6a Mutations.
PMID: 16935502
Clinical Spectrum of Cmt4c Disease in Patients Homozygous for the P.arg1109x Mutation in Sh3tc2.
PMID: 16806930
Mri in Dnm2-related Centronuclear Myopathy: Evidence for Highly Selective Muscle Involvement.
PMID: 17134899
Inherited Neuromyotonia: a Clinical and Genetic Study of a Family.
PMID: 17140792
Sleep Disorders in Childhood-onset Myotonic Dystrophy Type 1.
PMID: 16934465
Relationship Between Cardiac Arrhythmias and Sleep Apnoea in Permanently Paced Patients with Type I Myotonic Dystrophy.
PMID: 17360183