Célia Márcia Azevedo Soares
AuthID: R-000-Z1J
1
TITLE: Portuguese Society of Ophthalmology and Portuguese Society of Human Genetics Joint Clinical Practice Guidelines for Genetic Testing in Inherited Retinal Dystrophies Full Text
AUTHORS: Marques, Joao Pedro; Soares, Celia Azevedo; Carvalho, Ana Luisa; Estrela Silva, Sergio; Santos, Luisa Coutinho; Ramos, Lina; Silva, Eduardo;
PUBLISHED: 2025, SOURCE: CLINICAL GENETICS
AUTHORS: Marques, Joao Pedro; Soares, Celia Azevedo; Carvalho, Ana Luisa; Estrela Silva, Sergio; Santos, Luisa Coutinho; Ramos, Lina; Silva, Eduardo;
PUBLISHED: 2025, SOURCE: CLINICAL GENETICS
2
TITLE: The Visual Impairment of Inherited Retinal Diseases in Portugal as per the National Table of Disabilities
AUTHORS: Marta, Ana; Miranda, Vasco; Lume, Miguel; Parreira, Ricardo; Soares, Celia Azevedo; Meneres, Maria Joao; Lemos, Carolina; Beirao, Joao Melo;
PUBLISHED: 2024, SOURCE: OPHTHALMOLOGY SCIENCE, VOLUME: 4, ISSUE: 3
AUTHORS: Marta, Ana; Miranda, Vasco; Lume, Miguel; Parreira, Ricardo; Soares, Celia Azevedo; Meneres, Maria Joao; Lemos, Carolina; Beirao, Joao Melo;
PUBLISHED: 2024, SOURCE: OPHTHALMOLOGY SCIENCE, VOLUME: 4, ISSUE: 3
3
TITLE: The socioeconomic epidemiology of inherited retinal diseases in Portugal Full Text
AUTHORS: Marta, Ana; Marques, Joao Pedro; Santos, Cristina; Coutinho Santos, Luisa; Vaz Pereira, Sara; Costa, Jose; Arede, Pedro; Felix, Raquel; Geada, Sara; Gouveia, Nuno; Silva, Rui; Baptista, Margarida; Lume, Miguel; Parreira, Ricardo; Azevedo Soares, Celia; Meneres, Maria Joao; Lemos, Carolina; Melo Beirao, Joao;
PUBLISHED: 2024, SOURCE: ORPHANET JOURNAL OF RARE DISEASES, VOLUME: 19, ISSUE: 1
AUTHORS: Marta, Ana; Marques, Joao Pedro; Santos, Cristina; Coutinho Santos, Luisa; Vaz Pereira, Sara; Costa, Jose; Arede, Pedro; Felix, Raquel; Geada, Sara; Gouveia, Nuno; Silva, Rui; Baptista, Margarida; Lume, Miguel; Parreira, Ricardo; Azevedo Soares, Celia; Meneres, Maria Joao; Lemos, Carolina; Melo Beirao, Joao;
PUBLISHED: 2024, SOURCE: ORPHANET JOURNAL OF RARE DISEASES, VOLUME: 19, ISSUE: 1
4
TITLE: Autism spectrum disorder and PTEN hamartoma tumor syndrome Ó? Child and adolescent psychiatric perspective
AUTHORS: Marta P. Antunes; Natália Tkachenko; Ana R Soares; Graça Fernandes; Ana M Fortuna; Célia Azevedo-Soares;
PUBLISHED: 2024, SOURCE: Portuguese Journal of Pediatrics, VOLUME: 55, ISSUE: 2
AUTHORS: Marta P. Antunes; Natália Tkachenko; Ana R Soares; Graça Fernandes; Ana M Fortuna; Célia Azevedo-Soares;
PUBLISHED: 2024, SOURCE: Portuguese Journal of Pediatrics, VOLUME: 55, ISSUE: 2
5
TITLE: Co-occurrence of neurofibromatosis type 1, caused by Alu insertion, and 16p13.11 microduplication Full Text
AUTHORS: Quental, Rita; Pinho, Diana; Tkachenko, Natalia; Gonzaga, Diana; Mota, Maria do Ceu; Garrido, Cristina; Carmona, Carla; Quental, Sofia; Fortuna, Ana Maria; Soares, Celia Azevedo;
PUBLISHED: 2024, SOURCE: EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS, VOLUME: 25, ISSUE: 1
AUTHORS: Quental, Rita; Pinho, Diana; Tkachenko, Natalia; Gonzaga, Diana; Mota, Maria do Ceu; Garrido, Cristina; Carmona, Carla; Quental, Sofia; Fortuna, Ana Maria; Soares, Celia Azevedo;
PUBLISHED: 2024, SOURCE: EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS, VOLUME: 25, ISSUE: 1
6
TITLE: Corneal Biomechanical Changes in Patients with Inherited Retinal Diseases Full Text
AUTHORS: Marta, Ana; André Ferreira; Couto, Ines; Neves, Miguel Mesquita; Gomes, Miguel; Oliveira, Luis ; Soares, Celia Azevedo; Meneres, Maria Joao; Lemos, Carolina; Beirao, Joao Melo;
PUBLISHED: 2024, SOURCE: CLINICAL OPHTHALMOLOGY, VOLUME: 18
AUTHORS: Marta, Ana; André Ferreira; Couto, Ines; Neves, Miguel Mesquita; Gomes, Miguel; Oliveira, Luis ; Soares, Celia Azevedo; Meneres, Maria Joao; Lemos, Carolina; Beirao, Joao Melo;
PUBLISHED: 2024, SOURCE: CLINICAL OPHTHALMOLOGY, VOLUME: 18
7
TITLE: On the Power of Data Visualization in Transforming Patient Decision-Making Full Text
AUTHORS: Nogueira, Diogo; Soares, Celia Azevedo;
PUBLISHED: 2024, SOURCE: ACTA MEDICA PORTUGUESA, VOLUME: 37, ISSUE: 12
AUTHORS: Nogueira, Diogo; Soares, Celia Azevedo;
PUBLISHED: 2024, SOURCE: ACTA MEDICA PORTUGUESA, VOLUME: 37, ISSUE: 12
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TITLE: Clinical and Laboratory Findings on Glycogen Storage Disease Type V: Results from a Retrospective Observational Study in a Tertiary Hospital
AUTHORS: Ângela Pereira; Jorge Diogo da Silva; Ana Rita Soares; Arlindo Guimas; Sara Rocha; Márcio Cardoso; Cristina Garrido; Célia Azevedo Soares; Isabel Nunes; Ana Maria Fortuna; Dulce Quelhas; Sónia Figueiroa; Rosa Ribeiro; Manuela Santos; Esmeralda Martins; Nataliya Tkachenko;
PUBLISHED: 2023, SOURCE: Endocrine, Metabolic & Immune Disorders - Drug Targets, VOLUME: 23
AUTHORS: Ângela Pereira; Jorge Diogo da Silva; Ana Rita Soares; Arlindo Guimas; Sara Rocha; Márcio Cardoso; Cristina Garrido; Célia Azevedo Soares; Isabel Nunes; Ana Maria Fortuna; Dulce Quelhas; Sónia Figueiroa; Rosa Ribeiro; Manuela Santos; Esmeralda Martins; Nataliya Tkachenko;
PUBLISHED: 2023, SOURCE: Endocrine, Metabolic & Immune Disorders - Drug Targets, VOLUME: 23
9
TITLE: Eyes Shut Homolog-Associated Retinal Degeneration
AUTHORS: Ricardo Machado Soares; Ana Luísa Carvalho; Sílvia Simão; Célia Azevedo Soares; Miguel Raimundo; Henrique H Alves; António Francisco Ambrósio; Joaquim Murta; Jorge Saraiva; Rufino Silva; João Pedro Marques;
PUBLISHED: 2023, SOURCE: Ophthalmology Retina, VOLUME: 7, ISSUE: 7
AUTHORS: Ricardo Machado Soares; Ana Luísa Carvalho; Sílvia Simão; Célia Azevedo Soares; Miguel Raimundo; Henrique H Alves; António Francisco Ambrósio; Joaquim Murta; Jorge Saraiva; Rufino Silva; João Pedro Marques;
PUBLISHED: 2023, SOURCE: Ophthalmology Retina, VOLUME: 7, ISSUE: 7
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TITLE: Brain MRI findings in mandibulofacial dysostosis caused by EFTUD2 haploinsufficiency: a case report with polymicrogyria and dysmorphic caudate nuclei
AUTHORS: Silva, JS; Alves, JE; Soares, CA; Tkachenko, N; Garrido, C;
PUBLISHED: 2022, SOURCE: CLINICAL DYSMORPHOLOGY, VOLUME: 31, ISSUE: 1
AUTHORS: Silva, JS; Alves, JE; Soares, CA; Tkachenko, N; Garrido, C;
PUBLISHED: 2022, SOURCE: CLINICAL DYSMORPHOLOGY, VOLUME: 31, ISSUE: 1
