Pages that link to "Q58170990"
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The following pages link to Proposed criteria for familial amyotrophic lateral sclerosis (Q58170990):
Displaying 50 items.
- Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72 (Q24630288) (← links)
- Risk factors for amyotrophic lateral sclerosis (Q26827642) (← links)
- Oligoclonal bands in the cerebrospinal fluid of amyotrophic lateral sclerosis patients with disease-associated mutations. (Q34336785) (← links)
- The epidemiology of ALS: a conspiracy of genes, environment and time (Q34377698) (← links)
- Genetic architecture of ALS in Sardinia (Q34613626) (← links)
- Amyotrophic lateral sclerosis onset is influenced by the burden of rare variants in known amyotrophic lateral sclerosis genes. (Q34945003) (← links)
- Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72. (Q35776923) (← links)
- Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study (Q35859698) (← links)
- C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population (Q36024669) (← links)
- Extensive genetics of ALS: a population-based study in Italy (Q36359631) (← links)
- Designing an Internationally Accessible Web-Based Questionnaire to Discover Risk Factors for Amyotrophic Lateral Sclerosis: A Case-Control Study (Q36442254) (← links)
- OPTN 691_692insAG is a founder mutation causing recessive ALS and increased risk in heterozygotes. (Q36638834) (← links)
- Delineating the genetic heterogeneity of ALS using targeted high-throughput sequencing (Q37267700) (← links)
- Clinical neurogenetics: amyotrophic lateral sclerosis (Q37274526) (← links)
- De novo nonsense mutation of the FUS gene in an apparently familial amyotrophic lateral sclerosis case (Q37652972) (← links)
- Clinical genetics of amyotrophic lateral sclerosis: what do we really know? (Q37944428) (← links)
- Clinical diagnosis and management of amyotrophic lateral sclerosis (Q37944429) (← links)
- Familial amyotrophic lateral sclerosis in Alberta, Canada (Q38071377) (← links)
- Clinical and genetic heterogeneity of amyotrophic lateral sclerosis (Q38078984) (← links)
- Genetic counselling in ALS: facts, uncertainties and clinical suggestions (Q38119935) (← links)
- Clinical phenotypes and radiological findings in frontotemporal dementia related to TARDBP mutations. (Q38269451) (← links)
- Motor neuron disease-frontotemporal dementia: a clinical continuum (Q38417288) (← links)
- Genetic and constitutional factors are major contributors to substantia nigra hyperechogenicity (Q38645895) (← links)
- New ALS-Related Genes Expand the Spectrum Paradigm of Amyotrophic Lateral Sclerosis (Q38701291) (← links)
- Amyotrophic lateral sclerosis: moving towards a new classification system (Q38959347) (← links)
- Incidence of amyotrophic lateral sclerosis in the province of Novara, Italy, and possible role of environmental pollution (Q38983784) (← links)
- Predictive genetic testing for amyotrophic lateral sclerosis and frontotemporal dementia: genetic counselling considerations. (Q39354046) (← links)
- Amyotrophic lateral sclerosis: A higher than expected incidence in people over 80 years of age. (Q40736147) (← links)
- TBK1 mutations in Italian patients with amyotrophic lateral sclerosis: genetic and functional characterisation (Q42275954) (← links)
- Fast course ALS presenting with vocal cord paralysis: clinical features, bioinformatic and modelling analysis of the novel SOD1 Gly147Ser mutation (Q43447233) (← links)
- Truncating mutations in FUS/TLS give rise to a more aggressive ALS-phenotype than missense mutations: a clinico-genetic study in Germany (Q45254148) (← links)
- Constructional apraxia in frontotemporal dementia associated with the C9orf72 mutation: broadening the clinical and neuropsychological phenotype (Q45279455) (← links)
- Aggregation of neurologic and neuropsychiatric disease in amyotrophic lateral sclerosis kindreds: a population-based case-control cohort study of familial and sporadic amyotrophic lateral sclerosis (Q45855781) (← links)
- Genetic screening in sporadic ALS and FTD. (Q45958206) (← links)
- Association of NFE2L2 and KEAP1 haplotypes with amyotrophic lateral sclerosis. (Q46022971) (← links)
- Risk factors in Swedish young men for amyotrophic lateral sclerosis in adulthood. (Q47559952) (← links)
- Association of the New Variant Tyr424Asp at TBK1 Gene with Amyotrophic Lateral Sclerosis and Cognitive Decline (Q47657944) (← links)
- No association between VAPB mutations and familial or sporadic ALS in Sweden, Portugal and Iceland (Q47716521) (← links)
- Six SQSTM1 mutations in a Chinese amyotrophic lateral sclerosis cohort (Q48313563) (← links)
- Motor neuron disease: Common genetic variants and the heritability of ALS. (Q48556792) (← links)
- Familial Amyotrophic Lateral Sclerosis. (Q54158931) (← links)
- A novel phosphorylation site mutation in profilin 1 revealed in a large screen of US, Nordic, and German amyotrophic lateral sclerosis/frontotemporal dementia cohorts. (Q55056826) (← links)
- PFN1 mutations are also rare in the Catalan population with amyotrophic lateral sclerosis. (Q55058560) (← links)
- Determining the incidence of familiality in ALS: A study of temporal trends in Ireland from 1994 to 2016. (Q55378327) (← links)
- Screening for CCNF Mutations in a Chinese Amyotrophic Lateral Sclerosis Cohort. (Q55634425) (← links)
- Amyotrophic lateral sclerosis (Q56531747) (← links)
- Amyotrophic Lateral Sclerosis: An Aging-Related Disease (Q56839346) (← links)
- The El Escorial criteria: Strengths and weaknesses (Q57911703) (← links)
- A 50 bp deletion in the SOD1 promoter lowers enzyme expression but is not associated with ALS in Sweden (Q58125282) (← links)
- The multistep hypothesis of ALS revisited: The role of genetic mutations (Q58780876) (← links)