CARASIL: Identification of the clinical concept

Clinical Neurology

Volumn 50, Issue 11, 2010, Pages 849-851

  Fukutake, Toshio ^a  

^a KAMEDA MEDICAL CENTER   (Japan)

Author keywords

Alopecia; Binswanger's disease; CARASIL; HTRA1 gene; Spondylosis deformans

Indexed keywords

ALOPECIA; CADASIL; CHROMOSOME 10Q; CLINICAL FEATURE; CONFERENCE PAPER; CONSANGUINITY; HAPLOTYPE; HUMAN; JAPAN; LOW BACK PAIN; NEUROIMAGING; NEURORADIOLOGY; WHITE MATTER;

ADOLESCENT; ADULT; BRAIN; CADASIL; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MUTATION; PATHOLOGY, MOLECULAR; SERINE ENDOPEPTIDASES; YOUNG ADULT;

EID: 84856373611     PISSN: 0009918X     EISSN: None     Source Type: Journal    
DOI: 10.5692/clinicalneurol.50.849     Document Type: Conference Paper

References (10)

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5. Fukutake T, Shimoe Y, Hattori T. Differences in MRI lesions of two hereditary vascular leukoencephalopathies: CADASIL and CARASIL. J Stroke Cerebrovasc Dis 2000;9(suppl 1):263-264.
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