Mariz Vainzof

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 12

Top Topics

Muscular Dystrophy

Children With Cerebral Palsy

Top Venues

Journal of molecular neuroscience : MN

Developmental medicine and child neurology

Advanced biology

This page only lists publications with an associated author ORCID identifier.

Publications

Tatiana M Fontelonga, Arielle J Hall, Jaedon L Brown, Youngsook Lucy Jung, Matthew S Alexander, Janice A Dominov, Vincent Mouly, Natassia Vieira, Mayana Zatz, Mariz Vainzof, Emanuela Gussoni
Tetraspanin CD82 Associates with Trafficking Vesicle in Muscle Cells and Binds to Dysferlin and Myoferlin. Advanced biology (2023)
Pamela V Andrade, Joilson M Santos, Anne Caroline Barbosa Teixeira, Vanessa F Sogari, Michelle S Almeida, Fabiano M Callegari, Ana Cristina Victorino Krepischi, Acary S B Oliveira, Mariz Vainzof, Helga C A Silva
Rhabdomyosarcoma Associated with Core Myopathy/Malignant Hyperthermia: Combined Effect of Germline Variants in RYR1 and ASPSCR1 May Play a Role. Genes 14 (7) (2023)
Ana Cotta, Lucas Santos Souza, Elmano Carvalho, Leticia Nogueira Feitosa, Antonio Cunha, Monica Machado Navarro, Jaquelin Valicek, Miriam Melo Menezes, Simone Vilela Nunes Neves, Rafael Xavier-Neto, Antonio Pedro Vargas, Reinaldo Issao Takata, Julia Filardi Paim, Mariz Vainzof
Central Core Disease: Facial Weakness Differentiating Biallelic from Monoallelic Forms. Genes 13 (5) (2022)
Juliana Gurgel-Giannetti, Lucas Santos Souza, Guilherme L Yamamoto, Marina Belisario, Monize Lazar, Wilson Campos, Rita de Cassia M Pavanello, Mayana Zatz, Umbertina Reed, Edmar Zanoteli, Acary Bulle Oliveira, Vilma-Lotta Lehtokari, Erasmo B Casella, Marcela C Machado-Costa, Carina Wallgren-Pettersson, Nigel G Laing, Vincenzo Nigro, Mariz Vainzof
Nemaline Myopathy in Brazilian Patients: Molecular and Clinical Characterization. International journal of molecular sciences 23 (19) (2022)
Mariz Vainzof, Juliana Gurgel-Giannetti
Muscle regeneration in spastic muscles of children with cerebral palsy. Developmental medicine and child neurology 63 (10) (2021)
Lucas Santos Souza, Priscila Calyjur, Antonio Fernando Ribeiro, Juliana Gurgel-Giannetti, Rita Cassia Mingroni Pavanello, Mayana Zatz, Mariz Vainzof
Association of Three Different Mutations in the CLCN1 Gene Modulating the Phenotype in a Consanguineous Family with Myotonia Congenita. Journal of molecular neuroscience : MN 71 (11) (2021)
Camila F Almeida, Marc Bitoun, Mariz Vainzof
Satellite cells deficiency and defective regeneration in dynamin 2-related centronuclear myopathy. FASEB journal : official publication of the Federation of American Societies for Experimental Biology 35 (4) (2021)
Stephanie de Alcantara Fernandes, Camila F Almeida, Lucas S Souza, Monize Lazar, Paula Onofre-Oliveira, Guilherme Lopes Yamamoto, Letícia Nogueira, Letícia Y Tasaki, Rafaela R Cardoso, Rita C M Pavanello, Helga Cristina Almeida da Silva, Merari F R Ferrari, Anne Bigot, Vincent Mouly, Mariz Vainzof
Altered in vitro muscle differentiation in X-linked myopathy with excessive autophagy. Disease models & mechanisms 13 (2) (2020)
Ana Cotta, Julia F Paim, Elmano Carvalho, Jaquelin Valicek, Antonio L da Cunha Junior, Monica M Navarro, Antonio P Vargas, Maria I Lima, Camila F de Almeida, Reinaldo I Takata, Mariz Vainzof
LMNA-Related Muscular Dystrophy with Clinical Intrafamilial Variability. Journal of molecular neuroscience : MN 69 (4) (2019)
Renata Ishiba, André Luis F Santos, Camila F Almeida, Luiz Carlos Caires, Antonio F Ribeiro, Danielle Ayub-Guerrieri, Stephanie A Fernandes, Lucas S Souza, Mariz Vainzof
Faster regeneration associated to high expression of Fam65b and Hdac6 in dysferlin-deficient mouse. Journal of molecular histology 50 (4) (2019)
Antonio F Ribeiro, Lucas S Souza, Camila F Almeida, Renata Ishiba, Stephanie A Fernandes, Danielle A Guerrieri, André L F Santos, Paula C G Onofre-Oliveira, Mariz Vainzof
Muscle satellite cells and impaired late stage regeneration in different murine models for muscular dystrophies. Scientific reports 9 (1) (2019)
Camila F Almeida, Poliana Cm Martins, Mariz Vainzof
Comparative transcriptome analysis of muscular dystrophy models Large(myd), Dmd(mdx)/Large(myd) and Dmd(mdx): what makes them different? European journal of human genetics : EJHG 24 (9) (2016)