Célia Márcia Azevedo Soares


AuthID: R-000-Z1J

Confirmed Publications: 22



11
TITLE: EYS-ASSOCIATED RETINAL DEGENERATION: NATURAL HISTORY, GENETIC LANDSCAPE AND PHENOTYPIC SPECTRUM
AUTHORS: Soares, Ricardo; Carvalho, Ana; Simao, Silvia; Soares, Celia ; Raimundo, Miguel; Alves, Henrique; Ambrosio, Antonio; Murta, Joaquim; Saraiva, Jorge; Silva, Rufino; Marques, Joao;
PUBLISHED: 2023, SOURCE: Annual Meeting of the Association-for-Research-in-Vision-and-Ophthalmology (ARVO) in INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, VOLUME: 64, ISSUE: 8
INDEXED IN: WOS
12
TITLE: Follow-up of family members of children with mtDNA-associated Leigh syndrome  Full Text
AUTHORS: Soares, Celia Azevedo ; Coelho, Margarida Paiva; Bandeira, Anabela; Martins, Rute; Ribeiro, Rosa; Tkachenko, Natalia; Fortuna, Ana Maria; Martins, Esmeralda;
PUBLISHED: 2023, SOURCE: 55th European-Society-of-Human-Genetics (ESHG) Conference in EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 31
INDEXED IN: WOS
13
TITLE: Genetic counseling and carrier screening in candidates for gamete donation at a Portuguese center
AUTHORS: Soares, Celia Azevedo ; Tkachenko, Natalia; Vale Fernandes, Emidio ; Barreiro, Marcia; Abreu, Maria; Reis, Claudia Falcao; Soares, Gabriela; Fortuna, Ana Maria; Soares, Ana Rita;
PUBLISHED: 2023, SOURCE: JORNAL BRASILEIRO DE REPRODUCAO ASSISTIDA, VOLUME: 27, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 1
IN MY: ORCID
14
TITLE: PARADIGM SHIFT IN PHENYLKETONURIA NEURODEVELOPMENTAL OUTCOMES - RETROSPECTIVE COHORT ANALYSIS  Full Text
AUTHORS: Soares, Celia Azevedo ; Almeida, Manuela Ferreira ; Fortuna, Ana Maria; Carmona, Carla ;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
INDEXED IN: WOS
15
TITLE: Predicting factors of neurodevelopmental performance in children with phenylketonuria
AUTHORS: Soares, Celia Azevedo ; Almeida, Manuela Ferreira ; Soares, Gabriela; Tkachenko, Natalia; Fortuna, Ana Maria; Carmona, Carla ;
PUBLISHED: 2023, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 191, ISSUE: 6
INDEXED IN: Scopus WOS CrossRef: 1
IN MY: ORCID
16
TITLE: THE IMPORTANCE OF CLINICAL GENETICS IN THE ASSESSMENT OF CRANIOSYNOSTOSIS - FINDINGS FROM A CASE SERIES  Full Text
AUTHORS: Capela, Ana Miguel; Marques, Isabel; Costa, Tiago Ribeiro; Menezes, Catarina; Mota, Ceu; Soares, Ana Rita; Soares, Celia Azevedo ; Tkachenko, Nataliya; Fortuna, Ana Maria; Santos, Rosario; Reis, Claudia Falcao;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
INDEXED IN: WOS
17
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
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
18
TITLE: The Young Geneticists Network and the ESHG-Young committee, a forward-looking international community
AUTHORS: Riccardi, F; Marcinkute, R; Soares, CA ; Calapod, PS; Cerqueira, JM; Avram, E; Ding, C;
PUBLISHED: 2022, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 30, ISSUE: 3
INDEXED IN: WOS CrossRef: 2
IN MY: ORCID
19
TITLE: Phenotypic characteristics of two patients with mandibulofacial dysostosis - Guion Almeida type  Full Text
AUTHORS: Celia Azevedo Soares ; Ana Maria Fortuna; Gabriela Soares;
PUBLISHED: 2020, SOURCE: 23rd Annual Meeting of the Portuguese-Society-of-Human-Genetics in MEDICINE, VOLUME: 99, ISSUE: 9
INDEXED IN: WOS
20
TITLE: Why Should SARS-CoV-2 Post-Pandemic Recovery Funding Be Used to Foster a Physician-Scientist Program?  Full Text
AUTHORS: Barbosa Breda, J ; Leal, I; Sousa, DC; Soares, CA ;
PUBLISHED: 2020, SOURCE: ACTA MEDICA PORTUGUESA, VOLUME: 33, ISSUE: 9
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
Page 2 of 3. Total results: 22.

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