Search Results - "Liberczuk, Cynthia"
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Identification of PSEN2 mutation p.N141I in Argentine pedigrees with early-onset familial Alzheimer's disease
Published in Neurobiology of aging (01-10-2015)“…Abstract Presenilin 2 gene ( PSEN2) mutations account for <5% of all early-onset familial Alzheimer's disease (EOFAD) cases and only 13 have strong evidence…”
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Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer’s disease
Published in Translational psychiatry (31-01-2019)“…Rare coding variants in TREM2 , PLCG2 , and ABI3 were recently associated with the susceptibility to Alzheimer’s disease (AD) in Caucasians. Frequencies and…”
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RARE VARIANTS IN PLCG2, ABI3, AND TREM2 GENES ARE ASSOCIATED WITH ALZHEIMER’S DISEASE IN AN ARGENTINIAN SAMPLE: IS IT A EUROPEAN HERITAGE?
Published in Alzheimer's & dementia (01-07-2018)Get full text
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The use of melatonin in Alzheimer's disease
Published in Neuro-endocrinology letters (01-04-2002)“…About 45% of Alzheimer's disease (AD) patients have disruptions in their sleep and sundowning agitation. Since melatonin secretion is greatly inhibited in AD…”
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