Unveiling the SOD1-mediated ALS phenotype: insights from a comprehensive meta-analysis
Published 2023 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Unveiling the SOD1-mediated ALS phenotype: insights from a comprehensive meta-analysis
Authors
Keywords
-
Journal
JOURNAL OF NEUROLOGY
Volume -, Issue -, Pages -
Publisher
Springer Science and Business Media LLC
Online
2023-11-06
DOI
10.1007/s00415-023-12074-6
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- The HFE p.H63D (p.His63Asp) Polymorphism Is a Modifier of ALS Outcome in Italian and French Patients with SOD1 Mutations
- (2023) Antonio Canosa et al. Biomedicines
- Emerging Trends in the Field of Inflammation and Proteinopathy in ALS/FTD Spectrum Disorder
- (2023) Fabiola De Marchi et al. Biomedicines
- Clinical and genetic features of amyotrophic lateral sclerosis patients with C9orf72 mutations
- (2023) Maximilian Wiesenfarth et al. Brain Communications
- Amyotrophic lateral sclerosis with SOD1 mutations shows distinct brain metabolic changes
- (2022) Antonio Canosa et al. EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING
- Genetic epidemiology of amyotrophic lateral sclerosis in Norway – a 2-year population based study
- (2022) Cathrine Goberg Olsen et al. NEUROEPIDEMIOLOGY
- Genetic factors for survival in amyotrophic lateral sclerosis: an integrated approach combining a systematic review, pairwise and network meta-analysis
- (2022) Wei-Ming Su et al. BMC Medicine
- Fast versus slow disease progression in amyotrophic lateral sclerosis–clinical and genetic factors at the edges of the survival spectrum
- (2022) Simon Witzel et al. NEUROBIOLOGY OF AGING
- Behavioral and Cognitive Phenotypes of Patients With Amyotrophic Lateral Sclerosis Carrying SOD1 Variants
- (2022) Eleonora Dalla Bella et al. NEUROLOGY
- Trial of Antisense Oligonucleotide Tofersen for SOD1 ALS
- (2022) Timothy M. Miller et al. NEW ENGLAND JOURNAL OF MEDICINE
- Immunotherapy in advanced kidney cancer: an alternative meta-analytic method using reconstructed survival data in case of proportional hazard assumption violation
- (2022) Luigi Nocera et al. Frontiers in Oncology
- The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration
- (2022) Sarah Opie-Martin et al. Nature Communications
- Targeted sequencing panels in Italian ALS patients support different etiologies in the ALS/FTD continuum
- (2021) Anna Bartoletti-Stella et al. JOURNAL OF NEUROLOGY
- Familial clustering of primary lateral sclerosis and amyotrophic lateral sclerosis: Supplementary evidence for a continuum
- (2021) Philippe Corcia et al. EUROPEAN JOURNAL OF NEUROLOGY
- Mutation spectrum of amyotrophic lateral sclerosis in Central South China
- (2021) Zhen Liu et al. NEUROBIOLOGY OF AGING
- Genotype-phenotype correlations in a chinese population with familial amyotrophic lateral sclerosis
- (2021) WenChao Liu et al. NEUROLOGICAL RESEARCH
- Structural MRI Signatures in Genetic Presentations of the Frontotemporal Dementia-Motor Neuron Disease Spectrum
- (2021) Edoardo Gioele Spinelli et al. NEUROLOGY
- Assessing treatment effects and publication bias across different specialties in medicine: a meta-epidemiological study
- (2021) Simon Schwab et al. BMJ Open
- Clinical and genetic features of patients with amyotrophic lateral sclerosis in southern China
- (2020) W. Chen et al. EUROPEAN JOURNAL OF NEUROLOGY
- Genetics and Sex in the Pathogenesis of Amyotrophic Lateral Sclerosis (ALS): Is There a Link?
- (2020) Francesca Trojsi et al. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
- Clinical features and outcomes of the flail arm and flail leg and pure lower motor neuron MND variants: a multicentre Italian study
- (2020) Paride Schito et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Phenotypes and malignancy risk of different FUS mutations in genetic amyotrophic lateral sclerosis
- (2019) Marcel Naumann et al. Annals of Clinical and Translational Neurology
- Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction model
- (2018) Henk-Jan Westeneng et al. LANCET NEUROLOGY
- The multistep hypothesis of ALS revisited
- (2018) Adriano Chiò et al. NEUROLOGY
- Comparison of the clinical and cognitive features of genetically positive ALS patients from the largest tertiary center in Serbia
- (2017) Ivan V. Marjanović et al. JOURNAL OF NEUROLOGY
- Genetic epidemiology of amyotrophic lateral sclerosis: a systematic review and meta-analysis
- (2017) Zhang-Yu Zou et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Genetic epidemiology of motor neuron disease-associated variants in the Scottish population
- (2017) Holly A. Black et al. NEUROBIOLOGY OF AGING
- Genetics of Amyotrophic Lateral Sclerosis
- (2017) Mehdi Ghasemi et al. Cold Spring Harbor Perspectives in Medicine
- Amyotrophic lateral sclerosis
- (2017) Orla Hardiman et al. Nature Reviews Disease Primers
- Mutant SOD1 mediated pathogenesis of Amyotrophic Lateral Sclerosis
- (2016) Simran J. Kaur et al. GENE
- Defining SOD1 ALS natural history to guide therapeutic clinical trial design
- (2016) Taha Bali et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Genotype-phenotype correlations of amyotrophic lateral sclerosis
- (2016) Hong-Fu Li et al. Translational Neurodegeneration
- Screening of SOD1, FUS and TARDBP genes in patients with amyotrophic lateral sclerosis in central-southern China
- (2016) Lihua Hou et al. Scientific Reports
- Genetic studies of Russian patients with amyotrophic lateral sclerosis
- (2015) Elena V. Lysogorskaia et al. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
- Phenotype difference between ALS patients with expanded repeats inC9ORF72and patients with mutations in other ALS-related genes
- (2012) Stéphanie Millecamps et al. JOURNAL OF MEDICAL GENETICS
- Endogenous female reproductive hormones and the risk of amyotrophic lateral sclerosis
- (2012) Sonja Jong et al. JOURNAL OF NEUROLOGY
- Genetic analysis and SOD1 mutation screening in Iranian amyotrophic lateral sclerosis patients
- (2012) Afagh Alavi et al. NEUROBIOLOGY OF AGING
- Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease
- (2012) S. Lattante et al. NEUROLOGY
- Extensive genetics of ALS: A population-based study in Italy
- (2012) A. Chio et al. NEUROLOGY
- Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutations
- (2012) P. Corcia et al. NEUROLOGY
- Proposed criteria for familial amyotrophic lateral sclerosis
- (2011) Susan Byrne et al. Amyotrophic Lateral Sclerosis
- Global gene expression profiling of somatic motor neuron populations with different vulnerability identify molecules and pathways of degeneration and protection
- (2011) Eva Hedlund et al. BRAIN
- Preferred reporting items for systematic reviews and meta-analyses: The PRISMA statement
- (2010) David Moher et al. International Journal of Surgery
- SOD1 A4V familial ALS in North America: Can understanding the past lead to a better future?
- (2009) C. Armon NEUROLOGY
- SOD1 gene mutations in ALS patients from British Columbia, Canada: Clinical features, neurophysiology and ethical issues in management
- (2008) Andrew Eisen et al. Amyotrophic Lateral Sclerosis
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreAdd your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload Now