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Neurology

Volumn 77, Issue 12, 2011, Pages 1205-1206

Clinical/scientific notes

(5) Basu, A a,f Horvath, R b,e Esisi, B g Birchall, D c Chinnery, P F d,e

a Departments of Paediatric Neurology (United Kingdom)

b Departments of Genetics (United Kingdom)

c Departments of Neuroradiology (United Kingdom)

d NEWCASTLE UPON TYNE HOSPITALS NHS FOUNDATION TRUST (United Kingdom)

e NEWCASTLE UNIVERSITY (United Kingdom)

f NEWCASTLE UNIVERSITY (United Kingdom)

g DARLINGTON MEMORIAL HOSPITAL (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLSALICYLIC ACID; CONNEXIN 32; DIPYRIDAMOLE; GAP JUNCTION PROTEIN;

ADULT; ARM WEAKNESS; BRAIN ISCHEMIA; BRAIN RADIOGRAPHY; CASE REPORT; CORPUS CALLOSUM; DIFFUSION WEIGHTED IMAGING; DYSARTHRIA; FAMILY HISTORY; GENETIC SCREENING; HEMIPARESIS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MAGNETIC RESONANCE ANGIOGRAPHY; MALE; NONSENSE MUTATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PERCEPTION DEAFNESS; PERIPHERAL NEUROPATHY; PRIORITY JOURNAL; RECURRENT DISEASE; SHORT SURVEY; ARTICLE; FOLLOW UP; GENETICS; STROKE; X CHROMOSOMAL INHERITANCE;

CHARCOT-MARIE-TOOTH DISEASE; CONNEXINS; FOLLOW-UP STUDIES; GENES, X-LINKED; HUMANS; MALE; RECURRENCE; STROKE; YOUNG ADULT;

EID: 80555125086 PISSN: 00283878 EISSN: 1526632X Source Type: Journal
DOI: 10.1212/WNL.0b013e31822f046e Document Type: Short Survey

Times cited : (19)

References (7)

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