Marcondes Cavalcante França Jr.
Universidade Estadual de Campinas
H-index: 38
Latin America-Brazil
Top articles of Marcondes Cavalcante França Jr.
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
Cranial Nerve Thinning Distinguishes RFC1‐Related Disorder from Other Late‐Onset Ataxias | Movement Disorders Clinical Practice | Camila C Lobo Guilherme SO Wertheimer Gabriel S Schmitt Paula CAAP Matos Thiago JR Rezende | 2024/1/1 |
Consenso da Academia Brasileira de Neurologia para diagnóstico, aconselhamento genético e uso de terapias modificadoras na atrofia muscular espinhal 5q | Arquivos de Neuro-Psiquiatria | Edmar Zanoteli Alexandra Prufer de Queiróz Campos Araujo Michele Michelin Becker Clarisse Pereira Dias Drumond Fortes Marcondes Cavalcante França Jr | 2024/2/19 |
LUMINESCE, a Phase 3 Study of Satralizumab in Generalized Myasthenia Gravis (gMG): Baseline Characteristics (P10-11.015) | Ali A Habib Chongbo Zhao Inmaculada Aban Marcondes Cavalcante França Jr Jorge Gustavo José | 2024/4/14 | |
Consensus from the Brazilian Academy of Neurology for the diagnosis, genetic counseling, and use of disease-modifying therapies in 5q spinal muscular atrophy | Arquivos de Neuro-psiquiatria | Edmar Zanoteli Alexandra Prufer de Queiróz Campos Araujo Michele Michelin Becker Clarisse Pereira Dias Drumond Fortes Marcondes Cavalcante França Jr | 2024/2/19 |
Childhood Onset Amyotrophic Lateral Sclerosis Associated with SPTLC2 Gain-of-Function Pathogenic Variants: Clinical, Genetic, and Biochemical Insights (P4-8.001) | Rotem Orbach Safoora Syeda Payam Mohassel Maike Dohrn Museer A Lone | 2024/4/14 | |
Recurrent de novo SPTLC2 variant causes childhood-onset amyotrophic lateral sclerosis (ALS) by excess sphingolipid synthesis | Journal of Neurology, Neurosurgery & Psychiatry | Safoora B Syeda Museer A Lone Payam Mohassel Sandra Donkervoort Pinki Munot | 2024/2/1 |
Prevalence and Diagnostic Journey of Friedreich’s Ataxia in the State of São Paulo, Brazil | The Cerebellum | Daiana Suelen Machado Celiana Figueiredo Viana José Luiz Pedroso Orlando Graziani Povoas Barsottini Pedro José Tomaselli | 2024/3/23 |
H-SynEx: Using synthetic images and ultra-high resolution ex vivo MRI for hypothalamus subregion segmentation | arXiv preprint arXiv:2401.17104 | Livia Rodrigues Martina Bocchetta Oula Puonti Douglas Greve Ana Carolina Londe | 2024/1/30 |
Quantitative ultrasonography reveals skeletal muscle abnormalities in carriers of DMD pathogenic variants | Muscle & Nerve | Bruna Melo Coelho Loureiro Mariana Rabelo de Brito Cristina Iwabe Sergio San Juan Dertkigil Marcondes C França Jr | 2024/3/22 |
Gene-based therapies for neuromuscular disorders | Arquivos de Neuro-psiquiatria | Edmar Zanoteli Marcondes Cavalcante França Jr Wilson Marques Jr | 2024/6 |
Optic Disc and Retinal Architecture Changes in Patients with Spinocerebellar Ataxia Type 2 | Movement Disorders | Flávio Moura Rezende Filho Neringa Jurkute João Brainer Clares de Andrade Bruna Ferraço Marianelli Fabrício Diniz de Lima | 2024/1 |
Genotype-specific spinal cord damage in spinocerebellar ataxias: an ENIGMA-Ataxia study | Journal of Neurology, Neurosurgery & Psychiatry | Thiago Junqueira Ribeiro Rezende Isaac Adanyaguh Orlando GP Barsottini Benjamin Bender Fernando Cendes | 2024/2/21 |
Clinical and Genetic Characterization of a Cohort of Brazilian Patients With Congenital Ataxia | Orphanet Journal of Rare Diseases | Corina-Marcela Rus Thomas Weissensteiner Catarina Pereira Iuliana Susnea Bright D Danquah | 2022/5/3 |
Eplontersen in hereditary ATTR-polyneuropathy: week 66 final analysis of the phase 3 NEURO-TTRansform study | American Academy of Neurology 2023 Annual Meeting. Available online at: https://www. aan. com/MSA/Public/Events/AbstractDetails/55222 (accessed 29 August, 2023) | SL Khella W Marques N Dasgupta Chi-Chao Chao Yeşim Parman | 2023/4/22 |
An exploratory survey on the care for ataxic patients in the American continents and the Caribbean | The Cerebellum | Laura Bannach Jardim Ali Hasan Sheng-han Kuo Jonathan Javier Magaña Marcondes França Jr | 2023/8 |
P128 Quantitative ultrasonography reveals skeletal muscle abnormalities in female carriers of DMD pathogenic variants | Neuromuscular Disorders | M Cavalcante França Jr B Loureiro M Brito C Iwabe S Dertkigil | 2023/10/1 |
Frequency of GAA-FGF14 Ataxia in a Large Cohort of Brazilian Patients With Unsolved Adult-Onset Cerebellar Ataxia | Neurology: Genetics | Luiz Eduardo Novis Rodrigo S Frezatti David Pellerin Pedro J Tomaselli Shahryar Alavi | 2023/10 |
O49: Newborn screening for spinal muscular atrophy using real-time PCR: A pilot study in Brazil | Genetics in Medicine Open | Alice Brinckmann Oliveira Netto Ana Carolina Brusius Facchin Julia Lemos Fernanda Bender Pasetto Paloma Wiest | 2023/1/1 |
Advanced Structural Magnetic Resonance Imaging of the Spinal Cord: Technical Aspects and Clinical Use | Lucas de MT Branco Thiago JR Rezende Fabiano Reis Marcondes C França Jr | 2023/4/5 | |
Consenso brasileiro para o diagnóstico, manejo e tratamento da polineuropatia amiloidótica familiar associada à transtirretina: segunda edição | Arquivos de Neuro-Psiquiatria | Marcus Vinicius Pinto Amilton Antunes Barreira Acary Souza Bulle Marcos Raimundo Gomes de Freitas Marcondes Cavalcante França Jr | 2018 |
