about
A novel mutation in the MFSD8 gene in late infantile neuronal ceroid lipofuscinosis.Self-reported and informant-reported memory functioning and awareness in patients with mild cognitive impairment and Alzheimer´s disease.Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.Semantic memory and depressive symptoms in patients with subjective cognitive decline, mild cognitive impairment, and Alzheimer's disease.The impact of depressive symptoms on health-related quality of life in patients with subjective cognitive decline, mild cognitive impairment, and Alzheimer's disease.Central serotonin 1A receptor binding in temporal lobe epilepsy: a [carbonyl-(11)C]WAY-100635 PET study.Activities of Daily Living and Depressive Symptoms in Patients with Subjective Cognitive Decline, Mild Cognitive Impairment, and Alzheimer's Disease.Hereditary spastic paraplegia caused by compound heterozygous mutations outside the motor domain of the KIF1A gene.Clinical seizure lateralization in frontal lobe epilepsy.[Dementia and pain].Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromesSequence analysis of the complete SLITRK1 gene in Austrian patients with Touretteʼs disorderAssociation of an ABCB1 gene haplotype with pharmacoresistance in temporal lobe epilepsy[Sex differences in Alzheimer's disease]
P50
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P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Elisabeth Stögmann
@ast
Elisabeth Stögmann
@en
Elisabeth Stögmann
@nl
type
label
Elisabeth Stögmann
@ast
Elisabeth Stögmann
@en
Elisabeth Stögmann
@nl
prefLabel
Elisabeth Stögmann
@ast
Elisabeth Stögmann
@en
Elisabeth Stögmann
@nl
P108
P106
P31
P496
0000-0003-4688-8482