Catarina Maria Nogueira Marques da Cruz Menezes
AuthID: R-001-JXB
1
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
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
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WOS
WOS2
TITLE: Estimating the Glomerular Filtration Rate in Pediatric Patients With Neurogenic Bladder: A Comparison Between Creatinine- and Cystatin C-Equations
AUTHORS: Menezes, Catarina; Costa, Teresa; Bras, Catarina; Sousa, Patricia; Mendes, Ana; Amorim, Rosa; Faria, Maria Sameiro; Mota, Conceicao;
PUBLISHED: 2023, SOURCE: CUREUS JOURNAL OF MEDICAL SCIENCE, VOLUME: 15, ISSUE: 7
AUTHORS: Menezes, Catarina; Costa, Teresa; Bras, Catarina; Sousa, Patricia; Mendes, Ana; Amorim, Rosa; Faria, Maria Sameiro; Mota, Conceicao;
PUBLISHED: 2023, SOURCE: CUREUS JOURNAL OF MEDICAL SCIENCE, VOLUME: 15, ISSUE: 7
INDEXED IN: WOS
WOS3
TITLE: Lissencephaly With Cerebellar Hypoplasia Due To a New RELN Mutation Full Text
AUTHORS: Igreja, Liliana; Menezes, Catarina; Pinto, Pedro S.; Freixo, Joao Parente; Chorao, Rui;
PUBLISHED: 2023, SOURCE: PEDIATRIC NEUROLOGY, VOLUME: 149
AUTHORS: Igreja, Liliana; Menezes, Catarina; Pinto, Pedro S.; Freixo, Joao Parente; Chorao, Rui;
PUBLISHED: 2023, SOURCE: PEDIATRIC NEUROLOGY, VOLUME: 149
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Scopus WOS
Scopus WOS