Original Research
Published on 23 Jun 2020
Screening for REEP1 Mutations in 31 Chinese Hereditary Spastic Paraplegia Families
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2020.00499
- 3,216 views
- 5 citations
- Frontiers in Neurology
- Neurogenetics
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315 articles
Perspective
Published on 19 Jun 2020
Parkinson's Disease Research on the African Continent: Obstacles and Opportunities
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2020.00512
- 10,721 views
- 24 citations
Study Protocol
Published on 18 Jun 2020
Genetic Architecture of Parkinson's Disease in the Indian Population: Harnessing Genetic Diversity to Address Critical Gaps in Parkinson's Disease Research
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2020.00524
- 19,873 views
- 37 citations
Mini Review
Published on 29 May 2020
Olfactory Dysfunction in Familial and Sporadic Parkinson's Disease
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2020.00447
- 6,135 views
- 29 citations
Original Research
Published on 15 May 2020
Evidence of a Recessively Inherited CCN3 Mutation as a Rare Cause of Early-Onset Parkinsonism
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2020.00331
- 2,779 views
- 3 citations
Original Research
Published on 05 May 2020
Identification and Clinical Analysis of the First Nonsense Mutation in the PSEN1 Gene in a Family With Acute Encephalopathy and Retinitis Pigmentosa
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2020.00319
- 2,901 views
- 4 citations
Review
Published on 17 Apr 2020
The Regulation of microRNAs in Alzheimer's Disease
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2020.00288
- 13,445 views
- 95 citations
Systematic Review
Published on 25 Feb 2020
A Meta-Analytic Review of the Value of miRNA for Multiple Sclerosis Diagnosis
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2020.00132
- 5,838 views
- 22 citations
Systematic Review
Published on 18 Feb 2020
A Scoping Review of Inborn Errors of Metabolism Causing Progressive Intellectual and Neurologic Deterioration (PIND)
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2019.01369
- 6,935 views
- 27 citations
Case Report
Published on 14 Feb 2020
Hereditary Spastic Paraplegia and Intellectual Disability: Clinicogenetic Lessons From a Family Suggesting a Dual Genetics Diagnosis
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2020.00041
- 6,277 views
- 2 citations
Case Report
Published on 07 Feb 2020
A Novel CCM2 Gene Mutation Associated With Cerebral Cavernous Malformation
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2020.00070
- 6,061 views
- 8 citations
Original Research
Published on 17 Jan 2020
Four-Year Longitudinal Study of Motor and Non-motor Symptoms in LRRK2-Related Parkinson's Disease
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2019.01379
- 3,467 views
- 5 citations
Case Report
Published on 15 Jan 2020
Mutations of MACF1, Encoding Microtubule-Actin Crosslinking-Factor 1, Cause Spectraplakinopathy
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2019.01335
- 7,825 views
- 8 citations
Case Report
Published on 15 Jan 2020
A Novel Homozygous Variant in the Fork-Head-Associated Domain of Polynucleotide Kinase Phosphatase in a Patient Affected by Late-Onset Ataxia With Oculomotor Apraxia Type 4
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2019.01331
- 3,317 views
- 5 citations
Original Research
Published on 17 Dec 2019
Novel Alanyl-tRNA Synthetase 2 Pathogenic Variants in Leukodystrophies
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2019.01321
- 4,379 views
- 12 citations
Original Research
Published on 13 Dec 2019
The Role of Rare Coding Variants in Parkinson's Disease GWAS Loci
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2019.01284
- 7,088 views
- 23 citations