Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Carla Bastos da Costa Almeida"'
Autor:
Vitória Oshiro Orro, Carlos Henrique Marques dos Santos, Fábio Kanomata, Manuella Lugo Chaves, Carla Bastos da Costa Almeida
Publikováno v:
70° Congresso Brasileiro de Coloproctologia.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce31e832f12bdeb9fd244b492b4e987c
https://doi.org/10.1055/s-0043-1764866
https://doi.org/10.1055/s-0043-1764866
Autor:
Gabriel Dotta Abech, Caio Seiti Mestre Okabayashi, Gabriela Rangel Brandão, Paulo Ricardo Gazzola Zen, Rafael Fabiano Machado Rosa, Amanda Thum Welter, Carla Bastos da Costa Almeida, Kerolainy Alves Gadelha
Publikováno v:
J Pediatr Genet
Trisomy 21 is considered the most common chromosomal aneuploidy, and congenital heart disease (CHD) is highly prevalent and relevant to the morbidity and mortality of these patients. Ebstein anomaly (EA) is a rare CHD characterized by tricuspid valve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::379b2dc8add59b0e031596ff07fed631
https://doi.org/10.1055/s-0040-1714360
https://doi.org/10.1055/s-0040-1714360
Autor:
Gabriel Dotta Abech, Birgitt Schüle, José Antônio Monteiro Flores, Uta Francke, Paulo Ricardo Gazzola Zen, Gabriela Rangel Brandão, Carla Bastos da Costa Almeida, Amanda Thum Welter, Rafael Fabiano Machado Rosa, Marilu Fiegenbaum
Publikováno v:
J Pediatr Genet
Roberts syndrome is a rare autosomal recessive genetic disease. In this report, we report a Brazilian patient with a rare ESCO2 variant. The patient manifested a broad range of clinical findings including the significant, bilateral shortening of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40622b3a28f4e1e12a43c3c567663e3d
https://doi.org/10.1055/s-0039-1696636
https://doi.org/10.1055/s-0039-1696636