Alexander disease
Author:
Publisher
Elsevier
Reference55 articles.
1. Progressive fibrinoid degeneration of fibrillary astrocytes associated with mental retardation in a hydrocephalic infant;Alexander;Brain,1949
2. The clinical spectrum of late-onset Alexander disease: a systematic literature review;Balbi;J Neurol,2010
3. Focal central white matter lesions in Alexander disease;Barreau;J Child Neurol,2011
4. Alpha-B crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans;Berry;Am J Hum Genet,2001
5. Identification and characterization of GFAP k, a novel glial fibrillary acidic protein isoform;Blechingberg;Glia,2007
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1. Gene therapy for the leukodystrophies: From preclinical animal studies to clinical trials;Neurotherapeutics;2024-07
2. Oral findings in a patient with Alexander disease: A case report;Pediatric Dental Journal;2024-07
3. A retrospective observational cohort study of the anesthetic management and outcomes of pediatric patients with Alexander disease undergoing lumbar puncture or magnetic resonance imaging;Pediatric Anesthesia;2024-05-31
4. Brainstem Chipmunk Sign: A Diagnostic Imaging Clue across All Subtypes of Alexander Disease;American Journal of Neuroradiology;2024-05-02
5. Megalencephaly: Classification, Genetic Causes, and Related Syndromes;Journal of Pediatric Neurology;2024-04
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