Brief Research Report
Published on 04 Aug 2021
Clinical and Genetic Analysis of Costa Rican Patients With Parkinson's Disease
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2021.656342
- 5,207 views
- 4 citations
- Frontiers in Neurology
- Neurogenetics
- Articles
Type at least 3 characters
305 articles
Articles
Case Report
Published on 02 Aug 2021
Stormorken Syndrome Caused by a Novel STIM1 Mutation: A Case Report
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2021.522513
- 3,493 views
- 4 citations
Editorial
Published on 22 Jul 2021
Editorial: Overlapping Phenotypes and Genetic Heterogeneity of Rare Neurodevelopmental Disorders
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2021.711288
- 2,729 views
- 4 citations
Editorial
Published on 07 Jul 2021
Editorial: Application of Omics Approaches to the Diagnosis of Genetic Neurological Disorders
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2021.712010
- 2,013 views
- 2 citations
Mini Review
Published on 24 Jun 2021
Exploring the Genotype–Phenotype Correlation in GBA-Parkinson Disease: Clinical Aspects, Biomarkers, and Potential Modifiers
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2021.694764
- 11,551 views
- 47 citations
Review
Published on 22 Jun 2021
Genetic Defects and Pro-inflammatory Cytokines in Parkinson's Disease
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2021.636139
- 7,749 views
- 30 citations
Case Report
Published on 17 Jun 2021
Case Report: Clinical Features of Childhood Leukoencephalopathy With Cerebral Calcifications and Cysts Due to SNORD118 Variants
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2021.585606
- 2,688 views
- 2 citations
Review
Published on 14 Jun 2021
Targeting of Lysosomal Pathway Genes for Parkinson's Disease Modification: Insights From Cellular and Animal Models
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2021.681369
- 7,731 views
- 14 citations
Original Research
Published on 11 Jun 2021
High PYGL Expression Predicts Poor Prognosis in Human Gliomas
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2021.652931
- 4,705 views
- 15 citations
Original Research
Published on 10 Jun 2021
A Novel Variation in the Mitochondrial Complex I Assembly Factor NDUFAF5 Causes Isolated Bilateral Striatal Necrosis in Childhood
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2021.675616
- 3,386 views
- 9 citations
Original Research
Published on 19 May 2021
Novel Compound Missense and Intronic Splicing Mutation in ALDH18A1 Causes Autosomal Recessive Spastic Paraplegia
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2021.627531
- 3,934 views
- 3 citations
Original Research
Published on 19 May 2021
Down-Regulation of Inpp5e Associated With Abnormal Ciliogenesis During Embryonic Neurodevelopment Under Inositol Deficiency
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2021.579998
- 3,460 views
- 7 citations
Original Research
Published on 19 May 2021
Novel Optineurin Frameshift Insertion in a Family With Frontotemporal Dementia and Parkinsonism Without Amyotrophic Lateral Sclerosis
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2021.645913
- 3,995 views
- 9 citations
Original Research
Published on 07 May 2021
MELAS/LS Overlap Syndrome Associated With Mitochondrial DNA Mutations: Clinical, Genetic, and Radiological Studies
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2021.648740
- 5,939 views
- 12 citations
Original Research
Published on 05 May 2021
Circulating hsa-miR-323b-3p in Huntington's Disease: A Pilot Study
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2021.657973
- 3,396 views
- 15 citations
Original Research
Published on 04 May 2021
The Value of NOTCH2NLC Gene Detection and Skin Biopsy in the Diagnosis of Neuronal Intranuclear Inclusion Disease
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2021.624321
- 4,256 views
- 16 citations