Sarah Camargos
Overview
Explore the profile of Sarah Camargos including associated specialties, affiliations and a list of published articles.
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Articles
19
Citations
213
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0
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Recent Articles
1.
Ramchandra J, Inca-Martinez M, Leal T, Chaparro-Solano H, Salim A, Gatto E, et al.
Parkinsonism Relat Disord
. 2025 Mar;
134:107344.
PMID: 40058072
Background: Age and sex are known risk factors for Parkinson's Disease (PD), but it remains controversial if there are sex differences in the diagnosis latency. The objective of this study...
2.
Soares T, Vale T, Guedes L, Maciel R, Antunes A, Camargos S, et al.
Mov Disord Clin Pract
. 2024 Oct;
12(1):34-42.
PMID: 39460979
Background: The MDS-UPDRS has been available in English since 2008, showing satisfactory clinimetric results and being proposed as the new official benchmark scale for Parkinson's disease (PD), being cited as...
3.
Camargos S, Ribeiro P, Barbosa L
Neurology
. 2024 Feb;
102(5):e209139.
PMID: 38315936
No abstract available.
4.
Saffie Awad P, Teixeira-Dos-Santos D, Santos-Lobato B, Camargos S, Cornejo-Olivas M, Mello Rieder C, et al.
Mov Disord
. 2023 Nov;
39(1):6-16.
PMID: 37921246
Background: Identifying hereditary parkinsonism is valuable for diagnosis, genetic counseling, patient prioritization in trials, and studying the disease for personalized therapies. However, most studies were conducted in Europeans, and limited...
5.
Bally J, Kern D, Fearon C, Camargos S, Pereira da Silva-Junior F, Barbosa E, et al.
Mov Disord Clin Pract
. 2022 Jul;
9(5):659-675.
PMID: 35844288
Background: DYT-TUBB4A, formerly known as DYT4, has not been comprehensively described as only one large family and three individual cases have been published. We have recently described an in depth...
6.
Vaughn L, Frederick K, Burnett S, Sharma N, Bragg D, Camargos S, et al.
Biomolecules
. 2022 May;
12(5).
PMID: 35625640
DYT- (dystonia 16 or DYT-) is caused by mutations in the gene that encodes PACT, the protein activator of interferon (IFN)-induced double-stranded (ds) RNA-activated protein kinase (PKR). PACT participates in...
7.
Weissbach A, Pauly M, Herzog R, Hahn L, Halmans S, Hamami F, et al.
Mov Disord
. 2021 Dec;
37(2):237-252.
PMID: 34908184
Background: Pathogenic variants in 5 genes (GCH1, TH, PTS, SPR, and QDPR), involved in dopamine/tetrahydrobiopterin biosynthesis or recycling, have been linked to Dopa-responsive dystonia (DRD). Diagnosis and treatment are often...
8.
Lange L, Junker J, Loens S, Baumann H, Olschewski L, Schaake S, et al.
Mov Disord
. 2021 Jan;
36(5):1086-1103.
PMID: 33502045
This comprehensive MDSGene review is devoted to 7 genes - TOR1A, THAP1, GNAL, ANO3, PRKRA, KMT2B, and HPCA - mutations in which may cause isolated dystonia. It followed MDSGene's standardized...
9.
Bally J, Camargos S, Oliveira Dos Santos C, Kern D, Lee T, Pereira da Silva-Junior F, et al.
Neurology
. 2020 Sep;
96(14):e1887-e1897.
PMID: 32943487
Objective: To report 4 novel mutations leading to laryngeal and cervical dystonia with frequent generalization. Methods: We screened 4 families including a total of 11 definitely affected members with a...
10.
Maciel R, Camargos S, Cardoso F
Mov Disord Clin Pract
. 2019 Feb;
4(4):637-638.
PMID: 30713975
No abstract available.