Results 211 to 220 of about 12,015 (253)

Clinical and genetic determinants of survival in amyotrophic lateral sclerosis patients from North India. [PDF]

Brain Commun
Khurana S, Gourie-Devi M, Vats Y, Verma S, Ganguly NK, Chugh P, Sharma A, Khanna L, Dhawan U, Taneja V.   +9 more
europepmc   +1 more source

Upregulated miR-10b-5p as a potential miRNA signature in amyotrophic lateral sclerosis patients. [PDF]

Front Cell Neurosci
Dash BP, Freischmidt A, Helferich AM, Ludolph AC, Andersen PM, Weishaupt JH, Hermann A.   +6 more
europepmc   +1 more source

Inverting the logic in amyotrophic lateral sclerosis. [PDF]

Brain
Turner MR.
europepmc   +1 more source

Proteomic analysis of brain and spinal cord tissue reveals distinct immune and mitochondrial processes between human and mouse ALS models. [PDF]

Sci Rep
Spiteri AG, Steele JR, Lee HC, Zhang H, Sun J, Schittenhelm RB, Yu CH, McLean C, Masters CL, Goudey B, Jin L, Pan Y.   +11 more
europepmc   +1 more source

Analysis of the presence of mutation in TARDBP gene in patients with frontotemporal lobar degeneration and implementation of APOE gene methodology for polymorphism determination in patients with Alzheimer\'s disease in São Paulo - SP

, 2012
Thaís Thaianara Oliveira da Costa
openalex   +1 more source

Multi-modal comparative phenotyping of knock-in mouse models of frontotemporal dementia/amyotrophic lateral sclerosis.

Dis Model Mech
Boyanova S, Banks G, Lipina TV, Bains RS, Forrest H, Stewart M, Carcolé M, Milioto C, Isaacs AM, Wells SE, Wiseman FK.   +10 more
europepmc   +1 more source

Integrative analysis of transcriptomics and drug-target networks identifies SMN1 as a novel biomarker and therapeutic target for amyotrophic lateral sclerosis. [PDF]

J Genet Eng Biotechnol
Eshak D, Arumugam M.
europepmc   +1 more source

Screening for TARDBP mutations in Japanese familial amyotrophic lateral sclerosis

Screening for TARDBP mutations in Japanese familial amyotrophic lateral sclerosis
openaire