Diagnosis of Charcot-Marie-Tooth disease

Journal of Biomedicine and Biotechnology

Volumn 2009, Issue , 2009, Pages

  Banchs, Isabel ^a   Casasnovas, Carlos ^b   Albertí, Antonia ^b   De Jorge, Laura ^a   Povedano, Mnica ^b   Montero, Jordi ^b   Martínez Matos, Juan Antonio ^b   Volpini, Victor ^a  

^a BELLVITGE BIOMEDICAL RESEARCH INSTITUTE IDIBELL   (Spain)

^b HOSPITAL UNIVERSITARI DE BELLVITGE   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ASCORBIC ACID; CORTICOSTEROID; MYELIN PROTEIN; MYELIN ZERO PROTEIN; PERIPHERAL MYELIN PROTEIN 22; UNCLASSIFIED DRUG;

BRAIN ELECTROPHYSIOLOGY; CLINICAL FEATURE; CLINICAL PROTOCOL; CLINICAL TRIAL; DIAGNOSTIC TEST; DISEASE CLASSIFICATION; DISEASE COURSE; DISEASE SEVERITY; DRUG MEGADOSE; EPIDEMIOLOGICAL DATA; GENE EXPRESSION; GENE MUTATION; GENETIC ANALYSIS; HEREDITARY MOTOR SENSORY NEUROPATHY; HEREDITARY MOTOR SENSORY NEUROPATHY 1; HEREDITARY MOTOR SENSORY NEUROPATHY 1A; HEREDITARY MOTOR SENSORY NEUROPATHY 1B; HEREDITARY MOTOR SENSORY NEUROPATHY 2; HEREDITY; HISTOPATHOLOGY; HUMAN; MOLECULAR GENETICS; NERVE BIOPSY; NEUROPATHY; PHENOTYPE; POLYMERASE CHAIN REACTION; PROGNOSIS; PROSPECTIVE STUDY; REFSUM DISEASE; REVIEW; RISK FACTOR; ANIMAL; CHROMOSOME MAP; CLASSIFICATION; ELECTROPHYSIOLOGY; GENE EXPRESSION PROFILING; GENETICS; METHODOLOGY; MOUSE; NEUROLOGIC DISEASE; PATHOLOGY; PERIPHERAL NERVE; PREVALENCE;

ANIMALS; CHARCOT-MARIE-TOOTH DISEASE; CHROMOSOME MAPPING; ELECTROPHYSIOLOGY; GENE EXPRESSION PROFILING; HUMANS; MICE; NERVOUS SYSTEM DISEASES; PERIPHERAL NERVES; PREVALENCE;

EID: 71149111852     PISSN: 11107243     EISSN: 11107251     Source Type: Journal    
DOI: 10.1155/2009/985415     Document Type: Review

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