Maria Denise Fernandes Carvalho de Andrade

Universidade Estadual do Ceará · CE · 7 publicações em 2022–2026

docente de pós-graduaçãoORCID 0000-0003-1890-4721

Metabolism and Genetic DisordersGenomics and Rare DiseasesMosquito-borne diseases and controlGlycogen Storage Diseases and MyoclonusLysosomal Storage Disorders Research

Programas de pós-graduação (CAPES)

3TransplantesUECE · docente colaborador (2024)

Principais coautores no Nordeste tamanho = publicações em comum

Ellaine Dóris Fernandes Carvalho Erlane Marques Ribeiro Isabella Fernandes Carvalho André Luiz Santos Pessoa Angelina Xavier Acosta Camila Ferreira Ramos Carolina F. Amoretti Carolina Fischinger Moura de Souza Katiane Embiruçu Emilia Marcela Câmara Machado Costa Ney Boa‐Sorte Paula Frassinetti Vasconcelos de Medeiros

Publicações recentes

2026 1

Rare diseases in Brazil: a nationwide analysis of the diagnostic odyssey
Bioquímica, genética e biologia molecular · Journal of Community Genetics

2025 1

Prevalence and Risk Factors for Bruxism in Children with Congenital Zika Virus Syndrome: A Case-Control Study
Odontologia · Pesquisa Brasileira em Odontopediatria e Clínica Integrada

2024 3

Epidemiological characterization of rare diseases in Brazil: A retrospective study of the Brazilian Rare Diseases Network
Bioquímica, genética e biologia molecular · Orphanet Journal of Rare Diseases
Classic and Atypical Late Infantile Neuronal Ceroid Lipofuscinosis in Latin America: Clinical and Genetic Aspects, and Treatment Outcome with Cerliponase Alfa
Medicina · Molecular Genetics and Metabolism Reports
Corrigendum to “Classic and atypical late infantile neuronal ceroid lipofuscinosis in Latin America: Clinical and genetic aspects, and treatment outcome with cerliponase alfa.” [Molecular Genetics and Metabolism ReportsVolume 38 (2024) 101060]
Medicina · Molecular Genetics and Metabolism Reports

2023 1

Investigation of the impact of AXL , TLR3 , and STAT2 in congenital Zika syndrome through genetic polymorphisms and protein–protein interaction network analyses
Medicina · Birth Defects Research

2022 1

Contribution of miR-124 rs531564 polymorphism to the occurrence of congenital Zika syndrome
Medicina · Epigenetics

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