Emerging pathways for hereditary axonopathies

Journal of Molecular Medicine

Volumn 83, Issue 12, 2005, Pages 935-943

  Züchner, Stephan ^a   Vance, Jeffery M ^a,b  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

^b DUKE UNIVERSITY   (United States)

Author keywords

ALS; Charcot Marie Tooth disease; Hereditary spastic paraplegia; Motor neuron disease; Spinal muscular atrophy

Indexed keywords

ADENOSINE TRIPHOSPHATASE; ALPHA CRYSTALLIN; CHAPERONIN; COPPER ZINC SUPEROXIDE DISMUTASE; DYNAMIN; DYNAMIN II; GENE PRODUCT; GUANOSINE TRIPHOSPHATASE; HEAT SHOCK PROTEIN; HEAT SHOCK PROTEIN 22; HEAT SHOCK PROTEIN 27; MITOFUSIN 2; NEUROFILAMENT PROTEIN; PROTEIN; RAB PROTEIN; SNARE PROTEIN; SPASTIN; UNCLASSIFIED DRUG;

AMYOTROPHIC LATERAL SCLEROSIS; APOPTOSIS; CELL LOSS; GENETICS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MICROTUBULE; MITOCHONDRION; MOTONEURON; MOTOR NEUROPATHY; NERVE FIBER; NEUROFILAMENT; NEUROPATHY; OXIDATIVE STRESS; PATHOLOGY; PREFRONTAL CORTEX; PROTEIN DOMAIN; REVIEW; SPINAL CORD; SPINAL MUSCULAR ATROPHY;

AMYOTROPHIC LATERAL SCLEROSIS; ANIMALS; CHARCOT-MARIE-TOOTH DISEASE; HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES; HUMANS; MOTOR NEURONS; MUSCULAR ATROPHY, SPINAL; PENETRANCE;

EID: 28544441744     PISSN: 09462716     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00109-005-0694-9     Document Type: Review

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