Autosomal dominant limb-girdle muscular dystrophy type 1H
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Universitäts NeuroMuskuläres Centrum am Universitätsklinikum Dresden
Universitätsklinikum Carl Gustav Carus Dresden UniversitätsCentrum für Seltene Erkrankungen Dresden (USE)
Fetscherstr. 74
01307 Dresden
0351 4583876
0351 4585802
Website
- Juvenile myasthenia gravis
- Limb-girdle muscular dystrophy
- Duchenne and Becker muscular dystrophy
- Dermatomyositis
- Lambert-Eaton myasthenic syndrome
- Amyotrophic lateral sclerosis
- Myotonic dystrophy
- Guillain-Barré syndrome
- Rhabdomyosarcoma
- Botulism
- Charcot-Marie-Tooth disease type 1
- Malignant hyperthermia of anesthesia
Zentrum für neuromuskuläre Erkrankungen im Kindesalter am Universitätsklinikum Freiburg
Universitätsklinikum Freiburg Freiburg Zentrum für Seltene Erkrankungen (FZSE)
Mathildenstraße 1
79106 Freiburg
- Motor neuron disease
- Autosomal dominant slowed nerve conduction velocity
- Distal hereditary motor neuropathy type 1
- Muscular dystrophy
- Bulbospinal muscular atrophy
- Distal myopathy
- Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome
- Microcephaly-complex motor and sensory axonal neuropathy syndrome
- Limb-girdle muscular dystrophy
- Spinocerebellar ataxia with axonal neuropathy type 1
- Becker muscular dystrophy
- Amyotrophic lateral sclerosis
- Proximal spinal muscular atrophy
- Duchenne muscular dystrophy
- Emery-Dreifuss muscular dystrophy