Filtros de búsqueda

Lista de obras de Elisabeth Stögmann

A novel mutation in the MFSD8 gene in late infantile neuronal ceroid lipofuscinosis.

artículo científico publicado en 2008

Activities of Daily Living and Depressive Symptoms in Patients with Subjective Cognitive Decline, Mild Cognitive Impairment, and Alzheimer's Disease

artículo científico publicado en 2015

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Argyrophilic grain disease in individuals younger than 75 years: clinical variability in an underrecognized limbic tauopathy

artículo científico publicado en 2020

Association of an ABCB1 gene haplotype with pharmacoresistance in temporal lobe epilepsy

article

Central serotonin 1A receptor binding in temporal lobe epilepsy: a [carbonyl-(11)C]WAY-100635 PET study.

artículo científico publicado en 2010

Clinical seizure lateralization in frontal lobe epilepsy.

artículo científico publicado en 2007

Dementia and pain

artículo científico publicado en 2010

Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.

artículo científico publicado en 2013

Hereditary spastic paraplegia caused by compound heterozygous mutations outside the motor domain of the KIF1A gene

artículo científico publicado en 2017

Identification of odors, faces, cities and naming of objects in patients with subjective cognitive decline, mild cognitive impairment and Alzheimer´s disease: a longitudinal study

artículo científico publicado en 2018

Lack of Association Between ABCC2 Gene Variants and Treatment Response in Epilepsy

artículo científico publicado el 1 de enero de 2012

Macrophagic scavenging of Aβ

artículo científico publicado en 2019

Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes

article

Self-reported and informant-reported memory functioning and awareness in patients with mild cognitive impairment and Alzheimer´s disease

artículo científico publicado en 2016

Semantic memory and depressive symptoms in patients with subjective cognitive decline, mild cognitive impairment, and Alzheimer's disease

artículo científico

Sequence analysis of the complete SLITRK1 gene in Austrian patients with Touretteʼs disorder

article

The impact of depressive symptoms on health-related quality of life in patients with subjective cognitive decline, mild cognitive impairment, and Alzheimer's disease.

artículo científico publicado en 2016

[Sex differences in Alzheimer's disease]

scientific article published on 01 January 2008