Long term follow-up of cerebrovascular abnormalities in late onset Pompe disease (LOPD)

Journal of Neurology

Volumn 264, Issue 3, 2017, Pages 589-590

  Garibaldi, Matteo ^a,b   Sacconi, Sabrina ^a   Antonini, Giovanni ^b   Desnuelle, Claude ^a  

^a UNIVERSITY HOSPITAL OF NICE   (France)

^b SAPIENZA UNIVERSITY OF ROME   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; BRAIN HEMORRHAGE; CAROTID ARTERY ANOMALY; CEREBRAL ARTERY DISEASE; CEREBROVASCULAR DISEASE; CLINICAL ARTICLE; DISEASE DURATION; ENZYME REPLACEMENT; FEMALE; FOLLOW UP; GLYCOGEN STORAGE DISEASE TYPE 2; HEART PACING; HUMAN; INTERNAL CAROTID ECTASIA; LATE ONSET DISORDER; LATE ONSET POMPE DISEASE; LETTER; MAGNETIC RESONANCE ANGIOGRAPHY; MALE; PHENOTYPE; PRIORITY JOURNAL; RADIODIAGNOSIS; VERTEBROBASILAR DOLICHOECTASIA; X-RAY COMPUTED TOMOGRAPHY; ABNORMALITIES; AGED; BRAIN ARTERY; DIAGNOSTIC IMAGING; MIDDLE AGED; ONSET AGE; PATHOLOGY; TIME FACTOR;

ADULT; AGE OF ONSET; AGED; CEREBRAL ARTERIES; FEMALE; FOLLOW-UP STUDIES; GLYCOGEN STORAGE DISEASE TYPE II; HUMANS; MALE; MIDDLE AGED; TIME FACTORS;

EID: 85010764370     PISSN: 03405354     EISSN: 14321459     Source Type: Journal    
DOI: 10.1007/s00415-017-8396-0     Document Type: Letter

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