Ana Westenberger
Overview
Explore the profile of Ana Westenberger including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
91
Citations
1844
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Lukic M, Milovanovic A, Mazalica N, Westenberger A, Pesic A, Petrovic I, et al.
Mov Disord Clin Pract
. 2025 Feb;
PMID: 39895394
No abstract available.
2.
Milovanovic A, Westenberger A, Dragasevic-Miskovic N
Mov Disord
. 2025 Jan;
40(2):387-388.
PMID: 39775846
No abstract available.
3.
Radefeldt M, Lemke S, Chaichoompu K, Paul J, Curado F, Valzania F, et al.
Mov Disord
. 2024 Oct;
40(1):147-151.
PMID: 39460989
Background: The p.Ser71Arg RAB32 variant was recently associated with Parkinson's disease (PD). Objective: The aim was to investigate the presence of RAB32 variants in a large multiethnic group of individuals...
4.
Doquenia M, Dy Closas A, Algodon S, Suarez-Uy R, Ng A, Laabs B, et al.
Mov Disord Clin Pract
. 2024 Oct;
11(12):1604-1608.
PMID: 39400991
Background: X-linked dystonia-parkinsonism (XDP), a neurodegenerative movement disorder endemic to the Philippines, is primarily investigated in patients from Panay Island and the Greater Manila area. However, individuals residing in geographically...
5.
Unraveling Primary Familial Brain Calcification Mechanisms: Are NAA60 and SLC20A2 Partners in Crime?
Brand M, Westenberger A
Mov Disord
. 2024 Sep;
39(10):1731.
PMID: 39221593
No abstract available.
6.
Westenberger A, Bruggemann N, Klein C
Cold Spring Harb Perspect Med
. 2024 Aug;
PMID: 39134389
The genetic architecture of Parkinson's disease (PD) comprises five autosomal dominantly inherited forms with a clinical picture overall resembling idiopathic disease (PARK-, PARK-, PARK-, PARK-, and PARK-) and three recessive...
7.
Westenberger A, Skrahina V, Usnich T, Beetz C, Vollstedt E, Laabs B, et al.
Brain
. 2024 Aug;
147(8):2652-2667.
PMID: 39087914
Estimates of the spectrum and frequency of pathogenic variants in Parkinson's disease (PD) in different populations are currently limited and biased. Furthermore, although therapeutic modification of several genetic targets has...
8.
Pozojevic J, von Holt B, Westenberger A
Med Genet
. 2024 Jun;
34(2):97-102.
PMID: 38835911
X-linked dystonia-parkinsonism (XDP) is a neurodegenerative movement disorder that primarily affects adult Filipino men. It is caused by a founder retrotransposon insertion in that contains a hexanucleotide repeat, the number...
9.
Pozojevic J, Cruz J, Westenberger A
Med Genet
. 2024 Jun;
33(4):319-324.
PMID: 38835428
X-linked dystonia-parkinsonism (XDP) is an adult-onset neurodegenerative movement disorder, caused by a founder retrotransposon insertion in an intron of the gene. This insertion contains a polymorphic hexanucleotide repeat (CCCTCT), the...
10.
Lass J, Luth T, Schluter K, Schaake S, Laabs B, Much C, et al.
Mov Disord
. 2024 Apr;
39(7):1145-1153.
PMID: 38616406
Background: X-Linked dystonia-parkinsonism (XDP) is an adult-onset neurodegenerative disorder characterized by rapidly progressive dystonia and parkinsonism. Mosaic Divergent Repeat Interruptions affecting motif Length and Sequence (mDRILS) were recently found within...