Review
Published on 22 Sep 2014
Motoneuron firing in amyotrophic lateral sclerosis (ALS)
in Motor Neuroscience
Frontiers in Human Neuroscience
doi 10.3389/fnhum.2014.00719
- 25,159 views
- 39 citations
24 articles related to "Muscular Weakness"
Articles
Systematic Review
Published on 21 Oct 2022
Inflammatory myopathy following coronavirus disease 2019 vaccination: A systematic review
in Infectious Diseases: Epidemiology and Prevention
Frontiers in Public Health
doi 10.3389/fpubh.2022.1007637
- 19,141 views
- 20 citations
Case Report
Published on 04 Jan 2023
Case report: p.Glu134del SOD1 mutation in two apparently unrelated ALS patients with mirrored phenotype
in Dementia and Neurodegenerative Diseases
Frontiers in Neurology
doi 10.3389/fneur.2022.1052341
- 2,781 views
- 2 citations
Case Report
Published on 25 May 2022
Guillain-Barré Syndrome in Patient With SARS-CoV-2 PCR Positivity Treated Successfully With Therapeutic Exchange Plasma: A First Case Report From Vietnam
in Neuroinfectious Diseases
Frontiers in Neurology
doi 10.3389/fneur.2022.868667
- 3,805 views
- 5 citations
Case Report
Published on 29 Apr 2024
Effect of nutritional therapy in Emery–Dreifuss muscular dystrophy: a case report
in Clinical Nutrition
Frontiers in Nutrition
doi 10.3389/fnut.2024.1343548
- 2,716 views
- 1 citation
Case Report
Published on 20 Nov 2023
A novel splicing mutation identified in a DMD patient: a case report
in Genetics of Common and Rare Diseases
Frontiers in Pediatrics
doi 10.3389/fped.2023.1261318
- 3,645 views
- 1 citation
Case Report
Published on 14 Oct 2020
Unusual Presentation of Polyautoimmunity and Renal Tubular Acidosis in an Adolescent With Hashimoto's Thyroiditis and Central Pontine Myelinolysis
in Pediatric Endocrinology
Frontiers in Endocrinology
doi 10.3389/fendo.2020.548877
- 5,252 views
- 6 citations
Original Research
Published on 07 Feb 2022
Phenotype of VCP Mutations in Chinese Amyotrophic Lateral Sclerosis Patients
in Dementia and Neurodegenerative Diseases
Frontiers in Neurology
doi 10.3389/fneur.2022.790082
- 4,263 views
- 10 citations
Case Report
Published on 08 Nov 2022
Case report: Unusual episodic myopathy in a patient with novel homozygous deletion of first coding exon of MICU1 gene
in Neurogenetics
Frontiers in Neurology
doi 10.3389/fneur.2022.1008937
- 2,838 views
- 6 citations
Brief Research Report
Published on 24 Sep 2019
Ataxia in Patients With Bi-Allelic NFASC Mutations and Absence of Full-Length NF186
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2019.00896
- 5,023 views
- 9 citations
Case Report
Published on 21 Mar 2023
Case report: Homozygous variants of NEB and KLHL40 in two Arab patients with nemaline myopathy
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2023.1098102
- 4,479 views
- 2 citations
Original Research
Published on 22 Jul 2021
Serum Metabolic Profile in Patients With Long-Covid (PASC) Syndrome: Clinical Implications
in Geriatric Medicine
Frontiers in Medicine
doi 10.3389/fmed.2021.714426
- 29,698 views
- 89 citations
Case Report
Published on 26 Sep 2023
A homozygous missense variant in the YG box domain in an individual with severe spinal muscular atrophy: a case report and variant characterization
in Cellular Neuropathology
Frontiers in Cellular Neuroscience
doi 10.3389/fncel.2023.1259380
- 4,749 views
- 3 citations
Original Research
Published on 29 Nov 2024
Detection of gene variants associated with recessive limb–girdle muscular weakness and Pompe disease in a global cohort of patients through the application of next-generation sequencing analysis
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2024.1477291
- 5,380 views
- 2 citations
Review
Published on 06 May 2022
Adaptations in Muscular Strength for Individuals With Multiple Sclerosis Following Robotic Rehabilitation: A Scoping Review
in Rehabilitation in Neurological Conditions
Frontiers in Rehabilitation Sciences
doi 10.3389/fresc.2022.882614
- 4,160 views
- 6 citations
Review
Published on 09 Jul 2015
Muscle wasting in myotonic dystrophies: a model of premature aging
in Neuroinflammation and Neuropathy
Frontiers in Aging Neuroscience
doi 10.3389/fnagi.2015.00125
- 23,322 views
- 92 citations