Aina H. Rengmark
Oslo, Norway
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 9 publications
Correction: Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia.
Journal: PloS one
Published: October 13, 2017
Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia.
Journal: PloS one
Published: December 23, 2016
Rare variants in dementia genes and Parkinson's disease.
Journal: European journal of human genetics : EJHG
Published: June 23, 2016
Low frequency of GCH1 and TH mutations in Parkinson's disease.
Journal: Parkinsonism & related disorders
Published: June 29, 2015
Fine mapping and resequencing of the PARK16 locus in Parkinson's disease.
Journal: Journal of human genetics
Published: December 11, 2014
Parkinson's disease correlates with promoter methylation in the α-synuclein gene.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: June 20, 2014
The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease.
Journal: Alzheimer's & dementia : the journal of the Alzheimer's Association
Published: June 11, 2014
Clinical and genetic studies in a family with a novel mutation in the sepiapterin reductase gene.
Journal: Acta neurologica Scandinavica. Supplementum
Published: March 05, 2014
Effective variant detection by targeted deep sequencing of DNA pools: an example from Parkinson's disease.
Journal: Annals of human genetics
Published: December 13, 2013
Showing 1-9 of 9
Last Updated: 09/26/2026