Found: 5
Select item for more details and to access through your institution.
Adult-type metachromatic leukodystrophy with compound heterozygous ARSA mutations: A case report and phenotypic comparison with a previously reported case.
- Published in:
- Psychiatry & Clinical Neurosciences, 2011, v. 65, n. 1, p. 105, doi. 10.1111/j.1440-1819.2010.02169.x
- By:
- Publication type:
- Article
Sleep Disorders in Four Patients With Myotonic Dystrophy Type 1.
- Published in:
- Frontiers in Neurology, 2020, v. 11, p. 1, doi. 10.3389/fneur.2020.00012
- By:
- Publication type:
- Article
Association of auditory Charles Bonnet syndrome with increased blood flow in the nondominant Brodmann area 22.
- Published in:
- Psychiatry & Clinical Neurosciences Reports, 2023, v. 2, n. 2, p. 1, doi. 10.1002/pcn5.92
- By:
- Publication type:
- Article
Different Clinical Phenotypes in Siblings with a Presenilin-1 P264L Mutation.
- Published in:
- Dementia & Geriatric Cognitive Disorders, 2012, v. 33, n. 2/3, p. 132, doi. 10.1159/000338394
- By:
- Publication type:
- Article
Familial Semantic Dementia with P301L Mutation in the Tau Gene.
- Published in:
- Dementia & Geriatric Cognitive Disorders, 2011, v. 31, n. 5, p. 334, doi. 10.1159/000328412
- By:
- Publication type:
- Article