Familial hemiplegic migraine, nystagmus, and cerebellar atrophy

Annals of Neurology

Volumn 39, Issue 1, 1996, Pages 100-106

  Elliott, Michael A ^a,b   Peroutka, S J ^c   Welch, S ^c   May, Eugene F ^a,b  

^a Neurology   (United States)

^b MADIGAN ARMY MEDICAL CENTER   (United States)

^c Spectra Biomedical Inc   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CEREBELLUM ATROPHY; CEREBELLUM DEGENERATION; CEREBELLUM VERMIS; CHROMOSOME 19; CLINICAL ARTICLE; EYE MOVEMENT; FAMILIAL DISEASE; FEMALE; GENETIC LINKAGE; HEMIPLEGIA; HUMAN; MALE; MIGRAINE; NUCLEAR MAGNETIC RESONANCE IMAGING; NYSTAGMUS; PEDIGREE; PRIORITY JOURNAL; SCHOOL CHILD;

ADOLESCENT; ADULT; AGED; ATROPHY; CEREBELLUM; CHILD; CHROMOSOMES, HUMAN, PAIR 19; DNA; FEMALE; HEMIPLEGIA; HUMANS; LOD SCORE; MAGNETIC RESONANCE IMAGING; MALE; MIGRAINE DISORDERS; NYSTAGMUS, PATHOLOGIC; PEDIGREE;

EID: 0030052699     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.410390115     Document Type: Article

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