Results for Query ‹ Alpha-b crystalin-related fatal infantile hypertonic myofibrillar myopathy medication

Desmin-related myofibrillar myopathy – Treatment

Hereditary inclusion body myopathy – Treatment

Centronuclear myopathy – Treatment

Myopathy – Treatments

Alexander disease – Treatment

Hereditary inclusion body myopathy – Research

Acquired non-inflammatory myopathy – Treatment

Glycogen storage disease type II – Treatment

Congenital myopathy – Treatment

Neuronal ceroid lipofuscinosis – Treatment | Enzyme replacement therapy

Neuronal ceroid lipofuscinosis – Treatment | Stem cells

Cerebrotendineous xanthomatosis – Treatment

Nemaline myopathy – Outcome

Inclusion body myositis – Treatment

Glycogen storage disease type II – Prognosis

Infantile neuronal ceroid lipofuscinosis – Treatment

Fucosidosis – Treatment

Nemaline myopathy – Treatment

Metachromatic leukodystrophy – Treatment

Equine polysaccharide storage myopathy – Management | Diet

Desmin-related myofibrillar myopathy – Prognosis

Mitochondrial DNA depletion syndrome – Research

Sandhoff disease – Treatment

Infantile Refsum disease – Management/prognosis

Mitochondrial DNA depletion syndrome – Treatment