Found: 26
Select item for more details and to access through your institution.
Memantine administration prevented chorea movement in Huntington's disease: a case report.
- Published in:
- 2023
- By:
- Publication type:
- Case Study
Clinical Application of the FoundationOne CDx Assay to Therapeutic Decision‐Making for Patients with Advanced Solid Tumors.
- Published in:
- Oncologist, 2021, v. 26, n. 4, p. e588, doi. 10.1002/onco.13639
- By:
- Publication type:
- Article
Effect of expression alteration in flanking genes on phenotypes of St8sia2-deficient mice.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-50006-5
- By:
- Publication type:
- Article
A comparative study of curated contents by knowledge-based curation system in cancer clinical sequencing.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-47673-9
- By:
- Publication type:
- Article
Longitudinal study of primary progressive aphasia in a patient with pathologically diagnosed Alzheimer's disease: a case report.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Neutral Lipid Storage Disease Associated with the PNPLA2 Gene: Case Report and Literature Review.
- Published in:
- European Neurology, 2020, v. 83, n. 3, p. 317, doi. 10.1159/000508346
- By:
- Publication type:
- Article
Chondroitin beta-1,4-N-acetylgalactosaminyltransferase-1 missense mutations are associated with neuropathies.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 2, p. 143, doi. 10.1038/jhg.2010.148
- By:
- Publication type:
- Article
Regional gray matter-dedicated SUVR with 3D-MRI detects positive amyloid deposits in equivocal amyloid PET images.
- Published in:
- Annals of Nuclear Medicine, 2020, v. 34, n. 11, p. 856, doi. 10.1007/s12149-020-01513-3
- By:
- Publication type:
- Article
CANVAS-related RFC1 mutations in patients with immune-mediated neuropathy.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-45011-8
- By:
- Publication type:
- Article
CANVAS-related RFC1 mutations in patients with immune-mediated neuropathy.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-45011-8
- By:
- Publication type:
- Article
CANVAS-related RFC1 mutations in patients with immune-mediated neuropathy.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-45011-8
- By:
- Publication type:
- Article
A New Mouse Allele of Glutamate Receptor Delta 2 with Cerebellar Atrophy and Progressive Ataxia.
- Published in:
- PLoS ONE, 2014, v. 9, n. 9, p. 1, doi. 10.1371/journal.pone.0107867
- By:
- Publication type:
- Article
Corrigendum: Lamin B1 duplications cause autosomal dominant leukodystrophy.
- Published in:
- 2007
- By:
- Publication type:
- Correction notice
Lamin B1 duplications cause autosomal dominant leukodystrophy.
- Published in:
- Nature Genetics, 2006, v. 38, n. 10, p. 1114, doi. 10.1038/ng1872
- By:
- Publication type:
- Article
Intragenic deletion in the gene encoding ubiquitin carboxy-terminal hydrolase in gad mice.
- Published in:
- Nature Genetics, 1999, v. 23, n. 1, p. 47, doi. 10.1038/12647
- By:
- Publication type:
- Article
Clinical practice guideline for chronic headache 2013.
- Published in:
- Neurology & Clinical Neuroscience, 2019, v. 7, n. 5, p. 231, doi. 10.1111/ncn3.12322
- By:
- Publication type:
- Article
Novel mutation in the SOD1 gene in a patient with early-onset, rapidly progressive amyotrophic lateral sclerosis.
- Published in:
- Neurology & Clinical Neuroscience, 2017, v. 5, n. 6, p. 189, doi. 10.1111/ncn3.12153
- By:
- Publication type:
- Article
Fremanezumab for Episodic Migraine Prevention in Japanese Patients: Subgroup Analysis from Two International Trials.
- Published in:
- Journal of Pain Research, 2023, v. 16, p. 1673, doi. 10.2147/jpr.s393854
- By:
- Publication type:
- Article
Fremanezumab for Chronic Migraine Prevention in Japanese Patients: Subgroup Analysis from Two International Trials.
- Published in:
- Journal of Pain Research, 2023, v. 16, p. 1311, doi. 10.2147/JPR.S393854
- By:
- Publication type:
- Article
Lung carcinoma–associated cognitive impairment in a patient with Alzheimer's disease pathology: A case report.
- Published in:
- Clinical Case Reports, 2021, v. 9, n. 7, p. 1, doi. 10.1002/ccr3.4482
- By:
- Publication type:
- Article
Phenotypic and molecular diversities of spinocerebellar ataxia type 2 in Japan.
- Published in:
- Journal of Neurology, 2021, v. 268, n. 8, p. 2933, doi. 10.1007/s00415-021-10467-z
- By:
- Publication type:
- Article
Functional consequences of a CKIdmutation causing familial advanced sleep phase syndrome.
- Published in:
- Nature, 2005, v. 434, n. 7033, p. 640, doi. 10.1038/nature03453
- By:
- Publication type:
- Article
PSP-Phenotype in SCA8: Case Report and Systemic Review.
- Published in:
- Cerebellum, 2019, v. 18, n. 1, p. 76, doi. 10.1007/s12311-018-0955-0
- By:
- Publication type:
- Article
Progressive amnestic cognitive impairment in a middle-aged patient with developmental language disorder: a case report.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Time Course of Radiological Imaging and Variable Interindividual Symptoms in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Associated with p.Arg487His Mutation in the VCP Gene.
- Published in:
- European Neurology, 2017, v. 78, n. 1/2, p. 78, doi. 10.1159/000478906
- By:
- Publication type:
- Article
Oxidation and interaction of DJ-1 with 20S proteasome in the erythrocytes of early stage Parkinson's disease patients.
- Published in:
- Scientific Reports, 2016, p. 30793, doi. 10.1038/srep30793
- By:
- Publication type:
- Article