| Neuromuscular Home Page: Comprehensive professional resource at Washington University School of Medicine |
| Advancement of Research for Myopathies: A non-profit organization with the primary goal of speeding up bio-medical research on IBM2, the Autosomal Recessive form of Hereditary Inclusion Body Myopathies (HIBM). Includes a message board. |
| Centronuclear & Myotubular Myopathy: British information point for sufferers and their families of these disorders and associated muscle abnormalities. |
| Familial Desminopathy: Desmin related myopathy is a disorder characterized by accumulation of desmin in the muscle cells. It can be dominantly inherited or occur spontaneously, its effects can range from mild to severe. |
| Multicore Myopathy: Offers an informational and support site for all myopathies. |
| Myopathy: Information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS). |
| Myopathy and neuromuscular junction disorders: Detailed information on some of the muscle diseases. |
| Myotubular Myopathy Resource Group: Information and support for parents and medical professionals about x-linked, autosomal recessive, and autosomal dominant forms of MTM. Includes a web-based discussion group, newsletter, FAQs, articles, tips, current research, and family stories. |
| Nemaline Myopathy: Information and contacts regarding Nemaline Myopathy |
| NINDS: Inclusion Body Myositis: Also known as inflammatory myopathy, an information sheet compiled by National Institute of Neurological Disorders and Stroke. |
| Periodic Paralyses: Information sheet compiled by NINDS, the National Institute of Neurological Disorders and Stroke. |
| Rhabdomyolysis: Comprehensive information about the medical condition rhabdomyolysis, complete with tables, pictures, and diagrams. |
Classical
