Helio Van Der Linden Junior - Dissemin

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All papers authored by Helio Van Der Linden Junior

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2024 Edmar Zanoteli

ORCID

, Alexandra Prufer de Queiróz Campos Araujo

ORCID

, Michele Michelin Becker

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, Clarisse Pereira Dias Drumond Fortes

ORCID

, Marcondes Cavalcante França

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, Marcela Camara Machado-Costa

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, Wilson Marques

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, Ciro Matsui Jr

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, Rodrigo Holanda Mendonça

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, Flávia Nardes

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, Acary Souza Bulle Oliveira

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, Andre Luis Santos Pessoa

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, Jonas Alex Morales Saute

ORCID

ORCID

, Hélio Van der Linden

ORCID

and 1 other authors

Consensus from the Brazilian Academy of Neurology for the diagnosis, genetic counseling, and use of disease-modifying therapies in 5q spinal muscular atrophy

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2020 Hélio van der Linden

ORCID

, Vanessa van der Linden, André Pessoa, Kette D. Valente

ORCID

Continuous epileptiform discharges during sleep as an evolutionary pattern in patients with congenital Zika virus syndrome

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Ricardo A. Maselli

ORCID

, Hélio Linden

ORCID

, Michael Ferns

Recessive congenital myasthenic syndrome caused by a homozygous mutation inSYT2altering a highly conserved C‐terminal amino acid sequence

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2019 Anne H. O’Donnell-Luria, Lynn S. Pais, Víctor Faundes, Jordan C. Wood, Abigail Sveden, Victor Luria, Rami Abou Jamra, Andrea Accogli, Kimberly Amburgey, Britt Marie Anderlid, Silvia Azzarello-Burri, Alice A. Basinger, Claudia Bianchini, Lynne M. Bird, Rebecca Buchert and 369 other authors

Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy

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Vanessa van der Linden, Natacha Calheiros de Lima Petribu, Andre Pessoa, Igor Faquini, Alex R. Paciorkowski, Hélio van der Linden

ORCID

, Laura Silveira-Moriyama, Marli Tenório Cordeiro, Adriano Nassri Hazin, A. James Barkovich, Charles Raybaud, Marilia de Brito Abath, Erlane Ribeiro, Carlos Eduardo Barros Jucá, Maria de Fátima Viana Vasco Aragão and 2 other authors

Association of Severe Hydrocephalus With Congenital Zika Syndrome

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

2018 Hélio van der Linden

ORCID

, Maria D. Carvalho, Vanessa van der Linden, Kalyne M. Lacerda, André Pessoa, Mara L. Carneiro, Marli T. Cordeiro, Kette D. Valente

ORCID

Epilepsy Profile in Infants with Congenital Zika Virus Infection

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Juliana A. Alcantara, Silvia Vincentiis, Bernardo Santos, Daniel Kerr, Vanessa de Paula

ORCID

, Ruda Alessi, Helio Linden

ORCID

, Tiffany Chaim, Maurício Serpa, Geraldo Busatto, Wagner Gattaz, Kette D. Valente

ORCID

BDNF Val66Met polymorphism is not related with temporal lobe epilepsy caused by hippocampal sclerosis in Brazilian population

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Silvia Vincentiis, Juliana Alcantara, Patricia Rzezak

ORCID

, Daniel S. Kerr, Wagner F. Gattaz, Helio van der Linden

ORCID

, Bernardo dos Santos, Sebastiao E. Melo-Souza, Francisco Arruda, Paulo Ragazzo, Tiffany Chaim-Avancini, Mauricio H. Serpa, Fernando Fernandes, Ricardo A. Moreno, Geraldo Busatto and 3 other authors

Genetic polymorphisms of the 5HT receptors are not related with depression in temporal lobe epilepsy caused by hippocampal sclerosis

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J. A. Alcantara

ORCID

, S. Vincentis, D. S. Kerr, B. dos Santos, R. Alessi, H. van der Linden Jr

ORCID

, T. Chaim, M. H. Serpa

ORCID

, G. F. Busatto, W. F. Gattaz, R. Demarque, K. D. Valente

ORCID

Association study of functional polymorphisms of dopaminergic pathway in epilepsy-related factors of temporal lobe epilepsy in Brazilian population

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Luiz Carlos Caires-Júnior, Ernesto Goulart

ORCID

, Uirá Souto Melo, Bruno Henrique Silva Araujo

ORCID

, Lucas Alvizi, Alessandra Soares-Schanoski, Danyllo Felipe de Oliveira, Gerson Shigeru Kobayashi

ORCID

, Karina Griesi-Oliveira, Camila Manso Musso, Murilo Sena Amaral, Lucas Ferreira daSilva, Renato Mancini Astray, Sandra Fernanda Suárez-Patiño, Daniella Cristina Ventini and 29 other authors

Discordant congenital Zika syndrome twins show differential in vitro viral susceptibility of neural progenitor cells

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2017 T. C. Gheno, H. van der Linden, R. M. de Castilhos, G. V. Furtado, J. A. M. Saute, K. C. Donis, A. M. V. Fontanari, V. E. Emmel, J. L. Pedroso, O. Barsottini, C. Godeiro-Junior, E. Ternes Pereira, V. P. Cintra, W. Marques, I. Alonso and 7 other authors

Spinocerebellar ataxia type 10: common haplotype and disease progression rate in Peru and Brazil

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Vanessa van der Linden, Hélio van der Linden Junior

ORCID

, Mariana de Carvalho Leal, Epitacio Leite Rolim Filho, Ana van der Linden, Maria de Fátima Viana Vasco Aragão, Alessandra Mertens Brainer-Lima, Danielle Di Cavalcanti Sousa Cruz, Liana O. Ventura, Telma Lúcia Tabosa Florêncio, Marli Tenório Cordeiro, Silvio da Silva Caudas Neto, Regina Coeli Ramos

Discordant clinical outcomes of congenital Zika virus infection in twin pregnancies

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Kette D. Valente

ORCID

, Luciano De Paola, Andre Palmini, Eduardo Faveret, Gerardo Maria de Araujo-Filho, Helio van der Linden

ORCID

, Marino M. Bianchin, Roger Walz, Rudá Alessi, Tonicarlo Velasco, Wagner A. Teixeira, W. Curt LaFrance

ORCID

The approach to patients with psychogenic nonepileptic seizures in epilepsy surgery centers regarding diagnosis, treatment, and education

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2016 Vanessa van der Linden, André Pessoa, William Dobyns, A. James Barkovich, Hélio van der Linden Júnior

ORCID

, Epitacio Leite Rolim Filho, Erlane Marques Ribeiro, Mariana de Carvalho Leal, Pablo Picasso de Araújo Coimbra, Maria de Fátima Viana Vasco Aragão, Islane Verçosa, Camila Ventura, Regina Coeli Ramos, Danielle Di Cavalcanti Sousa Cruz, Marli Tenório Cordeiro and 4 other authors

Description of 13 Infants Born During October 2015–January 2016 With Congenital Zika Virus Infection Without Microcephaly at Birth — Brazil

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2015 Fernanda S. Pereira, Fernando R. Vargas, Hélio van der Linden, Thais L. Monte, Lucas D. Locks-Coelho, Amanda S. P. Silva, Orlando Barsottini, José L. Pedroso, Mario Cornejo-Olivas, Pilar Mazzetti, Clecio Godeiro, Maria-Angélica F. D. Lima, Maria Betânia Pereira Toralles, Paula F. V. Medeiros, Erlane Ribeiro and 6 other authors

ATXN3, ATXN7, CACNA1A, and RAI1 Genes and Mitochondrial Polymorphism A10398G Did Not Modify Age at Onset in Spinocerebellar Ataxia Type 2 Patients from South America

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2013 Raphael Machado de Castilhos, Maria Angélica de Faria Domingues de Lima, Luiz Carlos Santana da-Silva, Hélio van der Linden, Fernando Regla Vargas, Paula Frassineti Vanconcelos de Medeiros, Hector Yuri Conti Wanderley, Gabriel Vasata Furtado, Tailise Conte Gheno, Paola Schaeffer, Aline Russo, Orlando Barsottini, José Luiz Pedroso, Maria Angélica de Faria Domingues d. Lima, Diego Z. Salarini and 9 other authors

Spinocerebellar ataxias in Brazil - frequencies and modulating effects of related genes

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Juliana Gurgel-Giannetti, Gisela Nogales-Gadea, Hélio van der Linden

ORCID

, Túlio Marcus Ribeiro Bellard, Geraldo Brasileiro Filho, Alexandre Varella Giannetti, Eralda Luiza de Castro Concentino, Mariz Vainzof

Clinical and Molecular Characterization of Mcardle’s Disease in Brazilian Patients

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2010 Osvaldo Artigalás, Hélio van der Linden

ORCID

, Carolina F. Moura de Souza, Valeska Lizzi Lagranha, Maria Luiza Saraiva-Pereira

ORCID

, M. L. S. Pereira

ORCID

, Maira Graeff Burin, Charles Marques Lourenço, Helio Van der Linden, C. L. Marques, Mara Lúcia Ferreira Santos, Sergio Rosemberg, Carlos Eduardo Steiner, Fernando Kok, Laura B. Jardim and 2 other authors

Clinical and biochemical study of 29 Brazilian patients with metachromatic leukodystrophy

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