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Cecília Martins

Observed names: Martins, Cecília, Martins, Cecília Freitas
ORCID: 0000-0003-0375-2841
Observed ORCID: 0000-0003-0375-2841
OpenAlex ID: A5019614583
Risk of recurrence after a first unprovoked seizure in children
2016 · Catarina Maia, Ana Raquel Moreira, et al. · Jornal de Pediatria · 23
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Síndrome De Leigh: a Propósito De Um Caso Clínico Com Mutação No Dna Mitocondrial
2018 · Tânia Lopes, Margarida Coelho, et al. · Revista Paulista de Pediatria · 13
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The Role of AKT3 Copy Number Changes in Brain Abnormalities and Neurodevelopmental Disorders: Four New Cases and Literature Review
2019 · Fátima Lopes, Fátima Torres, et al. · Frontiers in Genetics · 12
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Pediatric neuromyelitis optica spectrum disorders in Portugal: A multicentre retrospective study
2022 · Cecília Martins, João Moura, et al. · Multiple Sclerosis and Related Disorders · 6
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Genomic imbalances defining novel intellectual disability associated loci
2019 · Fátima Lopes, Fátima Torres, et al. · Orphanet Journal of Rare Diseases · 6
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Pediatric Multiple Sclerosis—Experience of a Tertiary Care Center
2023 · Cecília Martins, Raquel Samões, et al. · Neuropediatrics · 5
Leigh Syndrome: a Case Report With a Mitochondrial Dna Mutation
2018 · Lopes, Tânia, Coelho, Margarida, et al. · Figshare · 4
Leigh Syndrome: a Case Report With a Mitochondrial Dna Mutation
2018 · Lopes, Tânia, Coelho, Margarida, et al. · Figshare · 3
Recém-nascido de mãe toxicodependente
2014 · Martins, Cecília, Guedes, Raquel, et al. · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) · 3
Phenotypic Heterogeneity of 16p11.2 Microdeletion Syndrome: 5 Case Reports
2025 · Sílvia Duarte Costa, Catarina Fraga, et al. · Journal of Child Neurology · 2
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Mastoidite aguda. Experiência de 7 anos
2014 · Martins, Cecília, Lopes, Ana, et al. · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) · 2
Risk of recurrence after a first unprovoked seizure in children
2017 · Catarina Maia, Ana Raquel Moreira, et al. · Jornal de Pediatria (Versão em Português) · 1
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MYT1L mutation in a patient with severe early-onset obesity and intellectual disability
2024 · André Costa e Silva, Inês Maio, et al. · Pediatria Polska
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Referenciação dos Cuidados de Saúde Primários ao Serviço de Urgência de Pediatria de um Hospital Nível II: Que Realidade?
2021 · Filipa Vale, Filipa Pinto, et al. · Gazeta Médica
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Hypotonia and feeding problems in the newborn: a congenital myotonic dystrophy type 1 clinical case
2017 · Silva, Cláudia Teles, Madureira, Cristina, et al. · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)
Síndrome de Ehler-Danlos: Uma Criança com Pele de Veludo
2017 · Moreira, Ana Raquel Silva, Lopes, Susana, et al. · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)
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Epilepsia em idade pediátrica – casuística da consulta de pediatria de um hospital distrital
2016 · Maia, Catarina, Moreira, Ana Raquel, et al. · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)
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Forma atípica da Síndrome de Cri-du-Chat – caso clínico
2014 · Ana Raquel Moreira, Cláudia Melo, et al. · DOAJ (DOAJ: Directory of Open Access Journals)
Evaluation of the presence of microcystin-LR by HPLC-PDA in samples from water bodies in the Grande Vitória Region
2010 · Martins, Cecília Freitas · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)
Works count: 21
Citation count: 80
H-index: 5
I10-index: 3
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