Paula Ricci Arantes
Overview
Explore the profile of Paula Ricci Arantes 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
8
Citations
47
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Salame A, Charchar H, Dourado J, Mendonca B, Alencar G, de Araujo L, et al.
J Neurooncol
. 2024 Apr;
168(3):405-413.
PMID: 38630387
Introduction: Meningiomas are the most common primary brain and central nervous system tumors, accounting for approximately 40% of these tumors. The most important exams for the radiological study of meningiomas...
2.
de Almeida J, Castro B, Passarelli V, Chaim K, Castro-Lima H, Listik C, et al.
Epilepsia Open
. 2024 Jan;
9(2):626-634.
PMID: 38217377
Objective: To investigate the association between left epileptiform activity and language laterality indices (LI) in patients with right mesial temporal sclerosis (MTS). Methods: Twenty-two patients with right MTS and 22...
3.
Varjao Vieira E, Arantes P, Hamani C, Iglesio R, Duarte K, Teixeira M, et al.
Front Psychiatry
. 2021 Jul;
12:680484.
PMID: 34276448
Deep brain stimulation (DBS) was proposed in 1999 to treat refractory obsessive-compulsive disorder (OCD). Despite the accumulated experience over more than two decades, 30-40% of patients fail to respond to...
4.
Borlot F, Arantes P, Cardoso A, Kim C
Neurology
. 2014 Apr;
82(15):1382-3.
PMID: 24733857
Morquio A syndrome (Online Mendelian Inheritance in Man #253000) is a lysosomal storage disease caused by deficiency of N-acetylgalactosamine-6-sulfatase encoded by the GALNS gene. Key clinical features are skeletal dysplasia...
5.
Mucopolysaccharidosis type IVA: evidence of primary and secondary central nervous system involvement
Borlot F, Arantes P, Quaio C, da Silva Franco J, Lourenco C, Gomy I, et al.
Am J Med Genet A
. 2014 Jan;
164A(5):1162-9.
PMID: 24478273
Mucopolysaccharidosis type IVA is a rare lysosomal storage disease caused by a deficiency of N-acetylgalactosamine 6-sulfatase. Studies usually focus on skeletal abnormalities and their consequences. This study explores the neurological...
6.
Borlot F, Arantes P, Quaio C, da Silva Franco J, Lourenco C, Bertola D, et al.
Brain Dev
. 2013 Aug;
36(7):585-92.
PMID: 23972383
Objective: Mucopolysaccharidosis type VI is a rare autosomal recessive storage disorder, caused by deficiency of arylsulfatase B. Data on neurological involvement in mucopolysaccharidosis type VI patients under enzyme-replacement therapy are...
7.
Arantes P, Gobato H, Davoglio B, Barreiros M, Felicio A, Barsottini O, et al.
Einstein (Sao Paulo)
. 2012 Oct;
10(2):171-9.
PMID: 23052452
Objective: To identify the effect of levodopa in language areas in Parkinson's disease patients. Methods: We evaluated 50 patients with mild to moderate Parkinson's disease, age and gender paired to...
8.
Gray M, Kim C, Bertola D, Arantes P, Stewart H, Simpson M, et al.
Eur J Hum Genet
. 2011 Jun;
20(1):122-4.
PMID: 21712856
Serpentine fibula polycystic kidney syndrome (SFPKS; MIM600330) is a rare skeletal dysplasia that has polycystic kidneys and dysmorphic facies as additional defining phenotypic components. The nosological classification of this disease...