June B12 deficiency Churg-Strauss MG: Ocular SPG 17 (Silver syndrome) |
May Ataxia: CoQ10 deficiency b-Enolase Bulbo-spinal muscular atrophy Cardiomyopathy CMH6 Hypertrophic CIDP: Variants Distal motor axons EMG: Partial denervation Goldberg-Shprintzen HMG CoA synthase deficiency HNPP Hypo-K+ periodic paralysis K+ channels: KCNJ2 Macrophagic myofasciitis MAG neuropathy Migrant sensory neuritis Muscle-Eye-Brain disorders Muscles: Focal enlargement Myopathy + Excess autophagy Neuralgic amyotrophy Neuroacanthocytosis Periodic paralysis Andersen syndrome Comparative features POEMS syndrome Neuropathy + Respiratory failure Lethal neonatal axonal Infantile axonal Rod myopathy: Pathology Receptors Adenosine ATP Purine (P2) Sensory neuronopathy: Anti-Hu SPG15 Tangier disease VLCAD, myopathic type |
April Adrenomyeloneuropathy Ataxia + Intellectual deterioration Cl- channels: Disorders Congenital MD + rigid spine Connective tissue disease Scleroderma Vasculitis Episodic ataxia 2 Erythromelalgia Ethylene glycol Motor neuron Disorders Differential Diagnosis Distal HMN 7 HIBM + Respiratory failure Immunomodulation Treatment strategies LGMD 2A Miller Fisher syndrome Multifocal motor neuropathy Neuralgic amyotrophy POEMS syndrome Potassium channels: KCNK type Scapular winging Search SPG2 Sports & Occupations Strychnine Tomaculae Wallerian degeneration l 1996-2001 Revisions |