Fernando Freua
Verified @hc.fm.usp.br
RECENT SCHOLAR PUBLICATIONS
- Metapneumovirus-associated necrotizing disseminated acute leukoencephalopathy
SC de Souza, A Haydar, JLS Santana, AM De March, GD Silva, F Freua, ...
Arquivos de Neuro-Psiquiatria 84 (4), s00461820527 , 2026
2026 - A Novel TUBB2A Variant Causing Ataxia With Preserved Ambulation Into Adulthood
JC da Costa Urbano, SRP da Silva Júnior, MAA Castro, PR Nóbrega, ...
American Journal of Medical Genetics Part A , 2026
2026 - iAXON-Brazil-HSP network: building a trial-ready national cohort for hereditary spastic paraplegias in the Global South
F dos Santos Maciel, FAC de Farias, DMC Arcila, C Silveira, ...
The Lancet Regional Health–Americas 56 , 2026
2026 - Giant aneurysm causing parkinsonism and rapid eye movement sleep behavior disorder
ACM Falcone, IV Brum, F Freua, JB Parmera
Arquivos de Neuro-Psiquiatria 83 (11), s00451812299 , 2025
2025 - Hematopoietic stem cell transplantation in an international cohort of Colony stimulating Factor‐1 receptor (CSF1R)‐related disorder
HAF Yska, M Golse, S Beerepoot, S Hayer, C Bergner, ARB de Paiva, ...
Movement disorders 40 (9), 1826-1835 , 2025
2025
Citations: 12 - PHARC ( Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa and Cataract ) – A Case Report and Clinical-Focused Literature Review
SR Pereira da Silva Jr, RMG Barbosa, PP Cruz, L da Cruz Caldeira, ...
The Cerebellum 24 (4), 120 , 2025
2025 - Isolated Vertical Gaze Palsy due to Unilateral Rostral Midbrain Stroke
JCC Urbano, SC de Souza, CCB Lopes, GD Silva, A Studart-Neto, ...
Journal of Neuro-Ophthalmology 45 (1), 113-114 , 2025
2025 - EEFSEC deficiency: A selenopathy with early-onset neurodegeneration
L Laugwitz, R Buchert, P Olguín, MA Estiar, M Atanasova, W Marques Jr, ...
The American Journal of Human Genetics 112 (1), 168-180 , 2025
2025
Citations: 6 - PHARC (Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa and Cataract)-A Case Report and Clinical-Focused Literature Review
SRP SILVA, RMG BARBOSA, PP CRUZ, LC CALDEIRA, DQ OMOTE, ...
SPRINGER , 2025
2025 - Further description of the phenotypic spectrum of neuronal ceroid lipofuscinosis type 11
PR Nobrega, ARB Paiva, ADA Junior, PLGSB Lima, KSS Cabral, ...
Genetics in Medicine 27 (1), 101291 , 2025
2025
Citations: 11 - Clinicogenetic characterization of cerebrotendinous xanthomatosis in Brazil
H Fussiger, PLGSB Lima, PVS Souza, F Freua, ASE Husny, EKEA Leão, ...
Clinical Genetics 106 (6), 721-732 , 2024
2024
Citations: 10 - Intracranial hemorrhage in a patient with Urbach-Wiethe disease
ALCC Hernández, GS de Araújo Torres, TT da Silva, G Tinone, ...
Arquivos de Neuro-psiquiatria 82 (11), 001-002 , 2024
2024 - Giant Aneurysm Causing Parkinsonism and REM Sleep Disorder
A Falcone, I Brum, F Freua, E Barbosa, R Cury, J Parmera
MOVEMENT DISORDERS 39, S92-S92 , 2024
2024 - " Ears of the lynx" sign in hereditary spastic paraplegias is not always the same!
VHR Marussi, BDRR Assis, F Freua
Arquivos de Neuro-Psiquiatria 82 (07), s00441788266 , 2024
2024
Citations: 1 - Young-Onset Alzheimer Dementia Due to a Novel Pathogenic Presenilin 1 Variant Initially Misdiagnosed as Autoimmune Encephalitis
NR Ronchi, MA Castro, AM Coutinho, LT Lucato, GD Silva, SM Brucki, ...
Neurology: Neuroimmunology & Neuroinflammation 11 (5), e200280 , 2024
2024
Citations: 2 - Myoclonus improvement after seizures in progressive myoclonic epilepsy type 7: a case report
PL GSB Lima, PR Nobrega, F Freua, P Braga-Neto, ARB Paiva, ...
BMC neurology 24 (1), 169 , 2024
2024
Citations: 4 - Identifying high-risk neurological phenotypes in adult-onset classic monogenic autoinflammatory diseases: when should neurologists consider testing?
GD Silva, JV Mahler, SRP da Silva Junior, LO Mendonça, ...
BMC neurology 24 (1), 130 , 2024
2024
Citations: 2 - Gerstmann‐Sträussler‐Scheinker Disease Presenting as Late‐Onset Slowly Progressive Spinocerebellar Ataxia, and Comparative Case Series with Neuropathology
CD Stephen, CM de Gusmao, SR Srinivasan, A Olsen, F Freua, F Kok, ...
Movement Disorders Clinical Practice 11 (4), 411-423 , 2024
2024
Citations: 10 - Myoclonus improvement after seizures in progressive myoclonic epilepsy type 7: a case report
TG Guimarães, PR Nóbrega, F Freua, PLG de Sá Barreto, P Braga-Neto, ...
2024 - Expanding the phenotypic spectrum of CLCN2 -related leucoencephalopathy and ataxia
PR Nóbrega, A RB de Paiva, KS Souza, JLB de Souza, PL GSB Lima, ...
Brain Communications 6 (1), fcad273 , 2024
2024
Citations: 9
MOST CITED SCHOLAR PUBLICATIONS
- Clinical and genetic characterization of leukoencephalopathies in adults
DS Lynch, A Rodrigues Brandão de Paiva, WJ Zhang, E Bugiardini, ...
Brain 140 (5), 1204-1211 , 2017
2017
Citations: 101 - A novel complex neurological phenotype due to a homozygous mutation in FDX2
J Gurgel-Giannetti, DS Lynch, ARB Paiva, LT Lucato, G Yamamoto, ...
Brain 141 (8), 2289-2298 , 2018
2018
Citations: 53 - PUS3 mutations are associated with intellectual disability, leukoencephalopathy, and nephropathy
ARB de Paiva, DS Lynch, US Melo, LT Lucato, F Freua, BDR de Assis, ...
Neurology: Genetics 5 (1), e306 , 2019
2019
Citations: 24 - Clinical and molecular characterization of a large cohort of childhood onset hereditary spastic paraplegias
GM Giordani, F Diniz, H Fussiger, C Gonzalez-Salazar, KC Donis, F Freua, ...
Scientific Reports 11 (1), 22248 , 2021
2021
Citations: 21 - Hematopoietic stem cell transplantation in an international cohort of Colony stimulating Factor‐1 receptor (CSF1R)‐related disorder
HAF Yska, M Golse, S Beerepoot, S Hayer, C Bergner, ARB de Paiva, ...
Movement disorders 40 (9), 1826-1835 , 2025
2025
Citations: 12 - Further description of the phenotypic spectrum of neuronal ceroid lipofuscinosis type 11
PR Nobrega, ARB Paiva, ADA Junior, PLGSB Lima, KSS Cabral, ...
Genetics in Medicine 27 (1), 101291 , 2025
2025
Citations: 11 - Supratentorial lymphocytic inflammation with parenchymal perivascular enhancement responsive to steroids (SLIPPERS)—Does it really exist?
F Freua, JV Mahler, PLGSB Lima, IS Neville, LB Portella, VHR Marussi, ...
Brain Sciences 13 (8), 1191 , 2023
2023
Citations: 11 - Clinical aspects of hereditary spastic paraplegia 76 and novel CAPN1 mutations.
US Melo, F Freua, DS Lynch, BD Ripa, RB Tenorio, JAM Saute, ...
Clinical Genetics 94 (5) , 2018
2018
Citations: 11 - Clinicogenetic characterization of cerebrotendinous xanthomatosis in Brazil
H Fussiger, PLGSB Lima, PVS Souza, F Freua, ASE Husny, EKEA Leão, ...
Clinical Genetics 106 (6), 721-732 , 2024
2024
Citations: 10 - Gerstmann‐Sträussler‐Scheinker Disease Presenting as Late‐Onset Slowly Progressive Spinocerebellar Ataxia, and Comparative Case Series with Neuropathology
CD Stephen, CM de Gusmao, SR Srinivasan, A Olsen, F Freua, F Kok, ...
Movement Disorders Clinical Practice 11 (4), 411-423 , 2024
2024
Citations: 10 - Arginase 1 deficiency presenting as complicated hereditary spastic paraplegia
F Freua, MEC Almeida, PR Nóbrega, ARB de Paiva, B Della-Ripa, ...
Molecular Case Studies 8 (6), a006232 , 2022
2022
Citations: 10 - Expanding the phenotypic spectrum of CLCN2 -related leucoencephalopathy and ataxia
PR Nóbrega, A RB de Paiva, KS Souza, JLB de Souza, PL GSB Lima, ...
Brain Communications 6 (1), fcad273 , 2024
2024
Citations: 9 - Chronic stage of Marchiafava-Bignami disease
LT Lucato, F Freua, F Kok
Arquivos de Neuro-Psiquiatria 73 (10), 890-890 , 2015
2015
Citations: 7 - EEFSEC deficiency: A selenopathy with early-onset neurodegeneration
L Laugwitz, R Buchert, P Olguín, MA Estiar, M Atanasova, W Marques Jr, ...
The American Journal of Human Genetics 112 (1), 168-180 , 2025
2025
Citations: 6 - Incidental magnetic resonance imaging findings leading to an unusual diagnosis: Adult onset Krabbe disease
ARB Paiva, RE Fonseca Neto, CL Afonso, F Freua, PR Nóbrega, F Kok
European journal of neurology 29 (6), 1859-1862 , 2022
2022
Citations: 5 - Myoclonus improvement after seizures in progressive myoclonic epilepsy type 7: a case report
PL GSB Lima, PR Nobrega, F Freua, P Braga-Neto, ARB Paiva, ...
BMC neurology 24 (1), 169 , 2024
2024
Citations: 4 - Subacute Partially Reversible Leukoencephalopathy Expands the Aicardi–Goutières Syndrome Phenotype
I Peixoto de Barcelos, C Bueno, LF S. Godoy, A Pessoa, L A. Costa, ...
Brain Sciences 13 (8), 1169 , 2023
2023
Citations: 4 - Case report: Rapid desensitization to ocrelizumab for multiple sclerosis is effective and safe
MV Aun, F Freua, VHR Marussi, P Giavina-Bianchi
Frontiers in Immunology 13, 840238 , 2022
2022
Citations: 4 - Malignant cerebral venous thrombosis in a transgender patient: intraoperative aspect of vein of Trolard thrombosis
CCB Lopes, VTG da SILVA, JEDC Lucio, RHG Yamashita, LR Comerlatti, ...
Arquivos de Neuro-Psiquiatria 79 (10), 938-939 , 2021
2021
Citations: 4 - Leukodystrophy with premature ovarian failure: think on vanishing white matter disease (VWMD)
F Freua, JB Parmera, DO Doria, ARB Paiva, LI Macedo-Souza, F Kok
Arquivos de Neuro-Psiquiatria 73 (1), 65-65 , 2015
2015
Citations: 4