Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis. - Wikidata - awgldk - TriplyDB

Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.

Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.

http://www.wikidata.org/entity/Q39722890

about

What causes amyotrophic lateral sclerosis?Gene discovery in amyotrophic lateral sclerosis: implications for clinical management.Common polymorphisms of chemokine (C-X3-C motif) receptor 1 gene modify amyotrophic lateral sclerosis outcome: A population-based study.An association study between SCFD1 rs10139154 variant and amyotrophic lateral sclerosis in a Chinese cohort.Beyond disease susceptibility-Leveraging genome-wide association studies for new insights into complex disease biology.Stage at which riluzole treatment prolongs survival in patients with amyotrophic lateral sclerosis: a retrospective analysis of data from a dose-ranging study.Long-term effects of edaravone on survival of patients with amyotrophic lateral sclerosis.The multistep hypothesis of ALS revisited: The role of genetic mutations

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P2860

Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.

http://www.wikidata.org/entity/Q39722890

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Association of a Locus in the ...... Amyotrophic Lateral Sclerosis.

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Association of a Locus in the ...... Amyotrophic Lateral Sclerosis.

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Association of a Locus in the ...... Amyotrophic Lateral Sclerosis.

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Association of a Locus in the ...... Amyotrophic Lateral Sclerosis.

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Association of a Locus in the ...... Amyotrophic Lateral Sclerosis.

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Association of a Locus in the ...... Amyotrophic Lateral Sclerosis.

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JAMANEUROL.2016.1114

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Association of a Locus in the ...... Amyotrophic Lateral Sclerosis.

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Antonia Ratti

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Bryan J Traynor

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Cinzia Gellera

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Cinzia Tiloca

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Frank P Diekstra

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Gianni Sorarù

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John E Landers

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John Powell

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Jonathan D Glass

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Judith Melki

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P2860

Prolonged survival in motor neuron disease: a descriptive study of the King's database 1990-2002

Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

Natural history and clinical features of the flail arm and flail leg ALS variants

Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance

Ataxia and Purkinje cell degeneration in mice lacking the CAMTA1 transcription factor

Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis

A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis.

METAL: fast and efficient meta-analysis of genomewide association scans

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10.1001/JAMANEUROL.2016.1114

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7

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Philip Van Damme

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Cristina Cereda

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2016-05-31T00:00:00Z

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amyotrophic lateral sclerosis

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