Clinical and genetic studies of a family from Peru affected by spinocerebellar ataxia type 7;Investigación clínica y genética de una familia peruana afectada por ataxia espinocerebelosa tipo 7.

Revista de neurologia

Volumn 31, Issue 10, 2000, Pages 923-928

  Castaneda M A ^a   Avalos, C ^a   Jeri F R ^a  

^a HOSPITAL NACIONAL DOS DE MAYO   (Peru)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; ATROPHY; BRAIN STEM; CASE REPORT; CEREBELLUM; CHROMOSOME 3; COGNITIVE DEFECT; COMPUTER ASSISTED TOMOGRAPHY; FEMALE; GENETICS; HEMISPHERIC DOMINANCE; HOSPITALIZATION; HUMAN; MAGNETIC RESONANCE ANGIOGRAPHY; MALE; MIDDLE AGED; OPTIC NERVE; PATHOLOGY; PATHOPHYSIOLOGY; PEDIGREE; PERU; PHYSIOLOGY; SPINOCEREBELLAR DEGENERATION; TRINUCLEOTIDE REPEAT; VISUAL DISORDER; WECHSLER INTELLIGENCE SCALE;

ADULT; AGED; ATROPHY; BRAIN STEM; CEREBELLUM; CHROMOSOMES, HUMAN, PAIR 3; COGNITION DISORDERS; FEMALE; FUNCTIONAL LATERALITY; HUMANS; MAGNETIC RESONANCE ANGIOGRAPHY; MALE; MIDDLE AGED; OPTIC NERVE; PEDIGREE; PERU; SEVERITY OF ILLNESS INDEX; SPINOCEREBELLAR ATAXIAS; TOMOGRAPHY, X-RAY COMPUTED; TRINUCLEOTIDE REPEAT EXPANSION; VISION DISORDERS; WECHSLER SCALES;

MLCS; MLOWN;

EID: 0034676589     PISSN: 02100010     EISSN: None     Source Type: Journal    
DOI: 10.33588/rn.3110.2000351     Document Type: Article

References (0)