PAPER Costales MG, Rzuczek SG, Disney MD27117425
PAPER Bourke SC, Steer J
Practical respiratory management in amyotrophic lateral sclerosis: evidence, controversies and recent advances.Neurodegener Dis Manag. 2016 Apr;6(2):147-60. PubMed: 27033240
PAPER Shen J, Cartwright MS27035248
PAPER Deng L, Hou L, Zhang J, Tang X, Cheng Z, Li G, Fang X, Xu J, Zhang X, Xu R
Polymorphism of rs3737597 in DISC1 Gene on Chromosome 1q42.2 in sALS Patients: a Chinese Han Population Case-Control Study.Mol Neurobiol. 2016 Apr 7; PubMed: 27052956
PAPER Jiang T, Zhang YD, Tan L, Yu JT27042960
PAPER Vrijsen B, Testelmans D, Belge C, Vanpee G, Van Damme P, Buyse B27077786
COMMUNITY NEWS 2016-05-06 Community News Two British charities have teamed up with the Medical Research Council to fund a new research institute for the study of dementia in the United Kingdom. The Dementia Research Institute will receive £150 million from the British government, ...
PAPER Beer AM, Cooper-Knock J, Fletcher S, Brown-Wright SH, Nandakumar TP, Shaw PJ
Case report of concurrent Fabry disease and amyotrophic lateral sclerosis supports a common pathway of pathogenesis.Amyotroph Lateral Scler Frontotemporal Degener. 2016 Apr 20;:1-3. PubMed: 27094629
PAPER Mompeán M, Chakrabartty A, Buratti E, Laurents DV27096426
PAPER E M, Yu S, Dou J, Jin W, Cai X, Mao Y, Zhu D, Yang R
Association between alcohol consumption and amyotrophic lateral sclerosis: a meta-analysis of five observational studies.Neurol Sci. 2016 Apr 21; PubMed: 27103621
COMMENT The PS1 gene appears to be a FAD mutation hot spot: More than 200 mutations have been identified (PSEN1 mutations). Does anyone know why? The age of onset varies from 30 to 60. In comparison, the number of APP mutations is smaller (APP mutations), ...
JOB 2016-05-06 Employer The Biodesign Institute, Neurodegenerative Research Center Principal Investigator Salvatore Oddo Description The research associate will conduct research in molecular and behavioral alterations in animal models of Alzheimer's disease and ...
COMMENT In this paper, Dr. Lui and co-workers demonstrated that progranulin (PGRN) deficiency facilitated synaptic pruning resulting from increased C1qa production in cultured microglia and in mice. PGRN haploinsufficiency, resulting from a heterozygous mutation ...
RESEARCH NEWS 2016-05-06 Research News Scientists and clinicians gathered at the University of Southern California in Los Angeles on April 15, 2016, for a day jam-packed with a dozen presentations. It was the third annual Zilkha Symposium on Alzheimer Disease & Related ...
PAPER von Schantz C, Kielar C, Hansen SN, Pontikis CC, Alexander NA, Kopra O, Jalanko A, Cooper JD
Progressive thalamocortical neuron loss in Cln5 deficient mice: Distinct effects in Finnish variant late infantile NCL.Neurobiol Dis. 2009 May;34(2):308-19. PubMed: 19385065
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