Norbert Bruggemann
Overview
Explore the profile of Norbert Bruggemann including associated specialties, affiliations and a list of published articles.
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Articles
227
Citations
2742
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Recent Articles
1.
Hamami F, Prasuhn J, Well L, Lohmann K, Klein C, Bruggemann N, et al.
Parkinsonism Relat Disord
. 2025 Jan;
132:107292.
PMID: 39848138
Background: Functional neurological movement disorders are common and disabling. Little is known about their coexistence with other non-functional movement disorders and their impact on the general disease burden. Objectives: Investigating...
2.
Pauly M, Thomsen M, Tadic V, Busch H, Depienne C, Lohmann K, et al.
Parkinsonism Relat Disord
. 2025 Jan;
131():107260.
PMID: 39788039
No abstract available.
3.
Thomsen M, Ott F, Loens S, Kilic-Berkmen G, Tan A, Lim S, et al.
medRxiv
. 2024 Dec;
PMID: 39677454
Dystonia is one of the most prevalent movement disorders, characterized by significant clinical and etiological heterogeneity. Despite considerable heritability (~25%) and the identification of several disease-linked genes, the etiology in...
4.
Kiesel A, Laugwitz L, Buchert R, Grimmel M, Baumann S, Sturm M, et al.
Brain
. 2024 Dec;
PMID: 39667038
No abstract available.
5.
Andujar B, Pereira S, Busi S, Usnich T, Borsche M, Ertan S, et al.
Environ Int
. 2024 Nov;
194:109151.
PMID: 39571299
Pathogenic variants in the Leucine-rich repeat kinase 2 (LRRK2) gene are a primary monogenic cause of Parkinson's disease (PD). However, the likelihood of developing PD with inherited LRRK2 pathogenic variants...
6.
Wallings R, McFarland K, Staley H, Neighbarger N, Schaake S, Bruggemann N, et al.
Sci Transl Med
. 2024 Nov;
16(772):eadl1535.
PMID: 39504353
Age is the greatest risk factor for many neurodegenerative diseases, yet immune system aging, a contributor to neurodegeneration, is understudied. Genetic variation in the gene affects risk for both familial...
7.
von der Gablentz J, Overbeeke N, Timmann D, Ganos C, Synofzik M, Bruggemann N, et al.
Eur J Neurol
. 2024 Oct;
32(1):e16520.
PMID: 39463030
Background And Purpose: Patients with episodic ataxia type 2 (EA2) suffer from recurrent paroxysmal episodes of vertigo and oscillopsia. Pathophysiologically, altered neuronal excitability has been suspected. Vestibular excitability in 22...
8.
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...
9.
Cirkel A, Gobel H, Gobel C, Alkatout I, Khalil A, Baum S, et al.
Womens Health Rep (New Rochelle)
. 2024 Oct;
5(1):671-679.
PMID: 39391784
Background: Women are more at risk for developing long-term symptoms after a COVID-19 infection. Only limited data are available for patients with coexisting endometriosis and/or menstrual pain symptoms. Study Design:...
10.
Tschigg K, Consoli L, Bruggemann N, Hicks A, Staunton C, Mascalzoni D, et al.
J Community Genet
. 2024 Sep;
15(6):615-630.
PMID: 39325315
Recall-by-genotype (RbG) is a bottom-up approach using existing genetic data to design follow-up stratified studies. Genetic information may be partially disclosed at invitation, thus raising ethical issues which call for...