Filipa Curado
Overview
Explore the profile of Filipa Curado including associated specialties, affiliations and a list of published articles.
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Articles
14
Citations
102
Followers
0
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Recent Articles
1.
Panzavolta A, Cavallieri F, Valzania F, Radefeldt M, Lemke S, Paul J, et al.
J Neurol
. 2024 Dec;
272(1):72.
PMID: 39680152
No abstract available.
2.
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...
3.
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...
4.
Curado F, Rosner S, Zielke S, Westphal G, Grittner U, Skrahina V, et al.
Diagnostics (Basel)
. 2023 Sep;
13(17).
PMID: 37685353
Gaucher disease (GD) is a rare autosomal recessive disorder arising from bi-allelic variants in the gene, encoding glucocerebrosidase. Deficiency of this enzyme leads to progressive accumulation of the sphingolipid glucosylsphingosine...
5.
Usnich T, Olmedillas M, Schell N, Paul J, Curado F, Skobalj S, et al.
Parkinsonism Relat Disord
. 2022 Dec;
107:105248.
PMID: 36565535
No abstract available.
6.
Menkovic I, Boutin M, Alayoubi A, Curado F, Bauer P, Mercier F, et al.
Diagnostics (Basel)
. 2022 Jun;
12(6).
PMID: 35741225
Method: Urine samples were purified using solid-phase extraction. A 12 min UPLC-MS/MS method was developed. Results: Validation assays revealed high precision and accuracy for creatinine and lyso-Gb. Most lyso-Gb analogs...
7.
Menkovic I, Boutin M, Alayoubi A, Curado F, Bauer P, Mercier F, et al.
J Proteome Res
. 2022 Mar;
21(5):1321-1329.
PMID: 35349295
Gaucher disease (GD) is a lysosomal storage disorder resulting from a biallelic mutation in the gene , leading to deficiencies in the enzyme β-glucocerebrosidase (Gcase). Inabilities of the Gcase to...
8.
Kelkel M, Boutin M, Curado F, Bauer P, Beauregard-Lacroix E, Mercier F, et al.
Bioanalysis
. 2022 Feb;
14(5):289-306.
PMID: 35118880
Sphingolipidoses are caused by a defective sphingolipid catabolism, leading to an accumulation of several glycolipid species in tissues and resulting in neurotoxicity and severe systemic manifestations. Urine samples from controls...
9.
Menkovic I, Boutin M, Alayoubi A, Curado F, Bauer P, Mercier F, et al.
Bioanalysis
. 2022 Feb;
14(4):223-240.
PMID: 35118875
Gaucher disease (GD) is caused by a deficiency of the lysosomal enzyme acid β-glucocerebrosidase. Recent metabolomic studies highlighted several new metabolites increased in the plasma of GD patients. We aimed...
10.
Skrahina V, Gaber H, Vollstedt E, Forster T, Usnich T, Curado F, et al.
Mov Disord
. 2020 Dec;
36(4):1005-1010.
PMID: 33314351
Background: Genetic stratification of Parkinson's disease (PD) patients facilitates gene-tailored research studies and clinical trials. The objective of this study was to describe the design of and the initial data...