Correlating familial Alzheimer's disease gene mutations with clinical phenotype.
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Dissecting Alzheimer disease in Down syndrome using mouse modelsLysosome and calcium dysregulation in Alzheimer's disease: partners in crimeNeurological manifestations of autosomal dominant familial Alzheimer's disease: a comparison of the published literature with the Dominantly Inherited Alzheimer Network observational study (DIAN-OBS).The presenilin 1 P264L mutation presenting as non-fluent/agrammatic primary progressive aphasia.The diagnosis of young-onset dementia.Functional connectivity in autosomal dominant and late-onset Alzheimer disease.A novel study and meta-analysis of the genetic variation of the serotonin transporter promoter in the italian population do not support a large effect on Alzheimer's disease risk.Defining and describing the pre-dementia stages of familial Alzheimer's disease.Clinical, imaging, and pathological heterogeneity of the Alzheimer's disease syndrome.Magnetic resonance imaging evidence for presymptomatic change in thalamus and caudate in familial Alzheimer's disease.Posterior cerebral atrophy in the absence of medial temporal lobe atrophy in pathologically-confirmed Alzheimer's disease.Genetic influences on atrophy patterns in familial Alzheimer's disease: a comparison of APP and PSEN1 mutations.Regional brain volume differences in symptomatic and presymptomatic carriers of familial Alzheimer's disease mutations.Subjects harboring presenilin familial Alzheimer's disease mutations exhibit diverse white matter biochemistry alterations.The pattern of atrophy in familial Alzheimer disease: volumetric MRI results from the DIAN study.Fus1 KO Mouse As a Model of Oxidative Stress-Mediated Sporadic Alzheimer's Disease: Circadian Disruption and Long-Term Spatial and Olfactory Memory ImpairmentsPresymptomatic cortical thinning in familial Alzheimer disease: A longitudinal MRI study.Familial Alzheimer's disease-associated presenilin-1 alters cerebellar activity and calcium homeostasis.Presenilins function in ER calcium leak and Alzheimer's disease pathogenesis.Presenilins as endoplasmic reticulum calcium leak channels and Alzheimer's disease pathogenesis.The paradox of syndromic diversity in Alzheimer disease.Biomarker modelling of early molecular changes in Alzheimer's disease.Familial Presenilin Mutations and Sporadic Alzheimer's Disease Pathology: Is the Assumption of Biochemical Equivalence Justified?Two Novel Mutations in the First Transmembrane Domain of Presenilin1 Cause Young-Onset Alzheimer's Disease.Cerebral microbleeds in familial Alzheimer's diseaseAlzheimer's disease: An alternative approach.The needs of patients with early onset dementia.Understanding the roles of mutations in the amyloid precursor protein in Alzheimer disease.PSEN1 p.Met233Val in a Complex Neurodegenerative Movement and Neuropsychiatric Disorder.Distinct α-Synuclein strains and implications for heterogeneity among α-Synucleinopathies.mRNP assembly, axonal transport, and local translation in neurodegenerative diseases.Forgetful and robotic: tap on a gene!The genes associated with early-onset Alzheimer's disease.Blepharospasm in familial AD secondary to an APP mutation (V715M).Heritability in frontotemporal dementia: more missing pieces?Reduced penetrance of the PSEN1 H163Y autosomal dominant Alzheimer mutation: a 22-year follow-up study.A pathogenic p.His169Asn mutation associated with early-onset Alzheimer's diseaseQuestions concerning the role of amyloid-β in the definition, aetiology and diagnosis of Alzheimer's diseaseGenetics of Alzheimer's disease
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P2860
Correlating familial Alzheimer's disease gene mutations with clinical phenotype.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on February 2010
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Correlating familial Alzheimer's disease gene mutations with clinical phenotype.
@en
Correlating familial Alzheimer's disease gene mutations with clinical phenotype.
@nl
type
label
Correlating familial Alzheimer's disease gene mutations with clinical phenotype.
@en
Correlating familial Alzheimer's disease gene mutations with clinical phenotype.
@nl
prefLabel
Correlating familial Alzheimer's disease gene mutations with clinical phenotype.
@en
Correlating familial Alzheimer's disease gene mutations with clinical phenotype.
@nl
P2860
P356
P1476
Correlating familial Alzheimer's disease gene mutations with clinical phenotype.
@en
P2093
Natalie S Ryan
P2860
P304
P356
10.2217/BMM.09.92
P577
2010-02-01T00:00:00Z