Jose Luiz Pedroso
Overview
Explore the profile of Jose Luiz Pedroso including associated specialties, affiliations and a list of published articles.
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Articles
316
Citations
1520
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Recent Articles
11.
Nobrega P, Paiva A, Amorim Junior A, Lima P, Cabral K, Barcelos I, et al.
Genet Med
. 2024 Oct;
27(1):101291.
PMID: 39394881
Purpose: Ceroid lipofuscinosis type 11 (CLN11) is a very rare disease, being reported in only 13 unrelated families so far. Further reports are necessary to comprehend the clinical phenotype of...
12.
Jaques C, Gama M, de Oliveira R, Rezende T, Silva T, Franca Jr M, et al.
Mov Disord Clin Pract
. 2024 Oct;
12(1):100-104.
PMID: 39382210
No abstract available.
13.
Danzi M, Powell E, Rebelo A, Dohrn M, Beijer D, Fazal S, et al.
Exp Neurol
. 2024 Oct;
382:114978.
PMID: 39357594
In the past decade, human genetics research saw an acceleration of disease gene discovery and further dissection of the genetic architectures of many disorders. Much of this progress was enabled...
14.
Barreto M, Correia J, de Moraes M, da Silva N, Pedroso J, Barsottini O
Pract Neurol
. 2024 Oct;
25(1):82-83.
PMID: 39353731
No abstract available.
15.
Tomaz G, Barreto M, Maffei R, Rodrigues R, Araujo Neto S, de Moraes M, et al.
Arq Neuropsiquiatr
. 2024 Sep;
82(12):1-2.
PMID: 39317221
No abstract available.
16.
Sarmento F, Tamanini J, Monaco Gama S, Freitas L, Barsottini O, Pedroso J
Arq Neuropsiquiatr
. 2024 Sep;
82(12):1-3.
PMID: 39231461
No abstract available.
17.
Procaci V, Goulart L, Ferraz H, Barsottini O, Pedroso J
Parkinsonism Relat Disord
. 2024 Jul;
126:107055.
PMID: 39047351
No abstract available.
18.
Massuyama B, Gama M, Silva T, Braga-Neto P, Pedroso J, Barsottini O
Arq Neuropsiquiatr
. 2024 Jul;
82(8):1-8.
PMID: 38964341
Background: Cerebellar ataxias comprise sporadic and genetic etiologies. Ataxia may also be a presenting feature in hereditary spastic paraplegias (HSPs). Objective: To report a descriptive analysis of the frequency of...
19.
Moreira H, de Moraes M, Fraiman P, Braga V, Marussi V, Pedroso J, et al.
Parkinsonism Relat Disord
. 2024 Jun;
125:107035.
PMID: 38908053
No abstract available.
20.
Raslan I, Silva T, Kok F, Rodrigues M, Aragao M, Pinho R, et al.
Neurol Genet
. 2024 Apr;
10(3):e200153.
PMID: 38681507
Background And Objectives: Congenital ataxias are rare hereditary disorders characterized by hypotonia and developmental motor delay in the first few months of life, followed by cerebellar ataxia in early childhood....