Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Serafim, Sílvia"'
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Rabelo-da-Ponte, Francisco Diego, Verdolini, Norma, Goularte, Jeferson Ferraz, Serafim, Silvia Dubou, Caldieraro, Marco Antonio Knob, Vieta, Eduard, Ramos-Quiroga, J. Antoni, Amoretti, Silvia, Rosa, Adriane R.
Publikováno v:
In European Neuropsychopharmacology February 2023 67:86-94
Autor:
Simão, Laurentino, Marques, Bárbara, Serafim, Sílvia, Alves, Ana, Pedro, Sónia, Brito, Filomena, Ferreira, Cristina, Peliano, Ricardo, Silva, Marisa, Baptista, Teresa, Quintal, Idolinda, Tomás, Edite, Cascais, Inês, Correia, Hildeberto
publicado em:Medicine (Baltimore). 2021 Jan 29;100(4):e23585. doi: 10.1097/MD.0000000000023585 Introduction: Congenital heart disease (CHD) is the most common form of birth defects. The incidence of CHD is about 0.8% to 1% in live-born, full-term bir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2016::da0592d2158a0a70fcba9c285fb5ac76
https://hdl.handle.net/10400.18/8204
https://hdl.handle.net/10400.18/8204
Autor:
Laurentino, Simão R., Serafim, Sílvia S., Marques, Bárbara S., Pedro, Sónia I., Ferreira, Cristina M., Tarelho, Ana R., Brito, Filomena T., Silva, Marisa D., Alves, Ana C., Peliano, Ricardo C., Viegas, Mónica I., Carrilho, Bruno M., Carvalho, Inês S., Teixeira, Ana M., Martins, Ana T., Cohen, Álvaro E., Correia, Hildeberto O.
Caso de uma grávida com 38 anos, referenciada por ecocardiograma precoce (15 semanas) sugestivo de cardiopatia complexa parecendo tratar-se de truncus arteriosus com arco truncal direito. O teste genético de rastreio pré-natal não invasivo (NIPS)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2016::ad1b0923add58f163f7e181181e32b8b
https://hdl.handle.net/10400.18/8165
https://hdl.handle.net/10400.18/8165
Autor:
Goularte, Jeferson Ferraz, Serafim, Silvia Dubou, Colombo, Rafael, Hogg, Bridget, Caldieraro, Marco Antonio, Rosa, Adriane Ribeiro
Publikováno v:
In Journal of Psychiatric Research January 2021 132:32-37
Autor:
Soares, Marta P., Rodrigues, Márcia, Dupont, Juliette, Medeira, Ana, Freixo, João, Nunes, Sofia, Cordeiro, Isabel, Travessa, André, Soares, Gabriela, Fortuna, Ana, Ramos, Fabiana, Sá, Joaquim, Rocha, Susana, Figueiredo, Cristina, Mendonça, Carla, Tapadinhas, Fernando, Silveira-Santos, Rosário, Custódio, Sónia, Barreta, Ana, Serafim, Sílvia, Correia, Hildeberto, Val, Mariana, Carreira, Isabel M., Rendeiro, Paula, Sousa, Ana, Sousa, Ana Berta
Introduction: Koolen-de Vries Syndrome (KdVS) is a rare genetic condition, caused by a 17q21.31 microdeletion, or a pathogenic variant in KANSL1 gene. The clinical picture includes developmental delay (DD)/intellectual disability (ID) with expressive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2016::26b5f9f88f017ecb7a96bb0abf687f86
https://hdl.handle.net/10400.18/6968
https://hdl.handle.net/10400.18/6968
Autor:
Simão, Laurentino, Serafim, Sílvia, Brito, Filomena, Alves, Cristina, Silva, Marisa, Peliano, Ricardo, Ferreira, Cristina, Marques, Bárbara, Pedro, Sónia, Oliveira, Juliana, Branco, Tiago, Correia, Hildeberto
Translocations involving the short arms of the X and Y in human chromosomes are uncommon. One of the primary functions of the X and Y chromosomes is gender phenotype determination. Here we report a newborn female with ambiguous genitalia and abnormal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2016::bbe6f9cfedc585c810d9b33d0c3e6ec9
https://hdl.handle.net/10400.18/6755
https://hdl.handle.net/10400.18/6755
Autor:
Simão, Laurentino, Serafim, Sílvia, Silva, Marisa, Ambrósio, Paula, Alves, Cristina, Geraldes, Maria Céu, Marques, Bárbara, Ferreira, Cristina, Pedro, Sónia, Tarelho, Ana Rita, Furtado, José, Cohen, Álvaro, Ferreira, Ângela, Mourinha, Vera, Brito, Filomena, Correia, Hildeberto
As anomalias do crescimento fetal são uma importante causa de morbilidade e mortalidade perinatais. Os fatores envolvidos na restrição de crescimento fetal (RCF) podem ser maternos, placentários e fetais. Nos fatores fetais, as cromossomopatias e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2016::14d10796d9c2385bec55a4d7e5a12472
https://hdl.handle.net/10400.18/6810
https://hdl.handle.net/10400.18/6810
O teste genético de array é a primeira linha no diagnóstico genético pós- -natal de situações como défice cognitivo, autismo e anomalias congénitas. Em pré-natal, este teste está indicado em gravidezes com anomalias ecográficas. Comparati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2016::c02e47c16d10f13e33386258759b6f92
https://hdl.handle.net/10400.18/5678
https://hdl.handle.net/10400.18/5678
Autor:
Lima, Flávia M., Cardoso, Taiane A., Serafim, Sílvia D., Martins, Dayane S., Solé, Brisa, Martínez-Arán, Anabel, Vieta, Eduard, Rosa, Adriane R.
Publikováno v:
Trends in Psychiatry and Psychotherapy, Volume: 40, Issue: 2, Pages: 170-178, Published: APR 2018
Introduction: In Brazil, there is no valid instrument to measure subjective cognitive dysfunction in bipolar disorder. The present study analyzed the psychometric properties of the Cognitive Complaints in Bipolar Disorder Rating Assessment (COBRA) in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______608::34ecac121493dfbf7ddb725b48fe9262
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2237-60892018000200170&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2237-60892018000200170&lng=en&tlng=en