Pia Winter
Giessen, HE, Germany
Last Updated: 09/26/2026
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Found 10 publications
Neuropsychological symptoms and subclinical disease activity in multiple sclerosis patients receiving high-efficacy therapy.
Journal: Multiple sclerosis and related disorders
Published: December 18, 2025
Disease outcomes following lateral switch among different CD20-antibodies in active multiple sclerosis.
Journal: Multiple sclerosis (Houndmills, Basingstoke, England)
Published: July 30, 2025
Association of body mass index and clinical response in patients receiving ofatumumab for treatment of multiple sclerosis.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: December 16, 2024
A Severe Dementia Syndrome Caused by Intron Retention and Cryptic Splice Site Activation in STUB1 and Exacerbated by TBP Repeat Expansions.
Journal: Frontiers in molecular neuroscience
Published: February 17, 2022
Epigenome-wide DNA methylation profiling in Progressive Supranuclear Palsy reveals major changes at DLX1.
Journal: Nature communications
Published: July 13, 2017
Three novel presenilin 1 mutations marking the wide spectrum of age at onset and clinical patterns in familial Alzheimer's disease.
Journal: Journal of neural transmission (Vienna, Austria : 1996)
Published: November 20, 2014
Previously unrecognized missense mutation E126K of PSEN2 segregates with early onset Alzheimer's disease in a family.
Journal: Journal of Alzheimer's disease : JAD
Published: May 22, 2014
Previously not recognized deletion in presenilin-1 (p.Leu174del.) in a patient with early-onset familial Alzheimer's disease.
Journal: Neuroscience letters
Published: December 28, 2012
A presenilin 1 mutation in the first case of Alzheimer's disease.
Journal: The Lancet. Neurology
Published: December 19, 2012
DYT7 gene locus for cervical dystonia on chromosome 18p is questionable.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: March 26, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026