Frequent misdiagnosis of adult polyglucosan body disease

Deep IntronicGBE1Mutation in Manifesting Heterozygous Patients With Adult Polyglucosan Body Disease

(2015) H. Orhan Akman et al.   JAMA Neurology

Specific pattern of gadolinium enhancement in spondylotic myelopathy

(2014) Eoin P. Flanagan et al.   ANNALS OF NEUROLOGY

Primary progressive multiple sclerosis: progress and challenges

(2013) Claire M Rice et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Branching Enzyme Deficiency

(2013) Carmen Paradas et al.   JAMA Neurology

Adult polyglucosan body disease: Natural History and Key Magnetic Resonance Imaging Findings

(2012) Fanny Mochel et al.   ANNALS OF NEUROLOGY

The adult polyglucosan body disease mutation GBE1 c.1076A>C occurs at high frequency in persons of Ashkenazi Jewish background

(2012) Abrar Hussain et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Acute but transient neurological deterioration revealing adult polyglucosan body disease

(2012) Ségolène Billot et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Cerebral small vessel disease: from pathogenesis and clinical characteristics to therapeutic challenges

(2010) Leonardo Pantoni   LANCET NEUROLOGY

A 63-year-old woman with urinary incontinence and progressive gait disorder

(2009) A. Lossos et al.   NEUROLOGY