Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Kawahira, Rachel Sayuri Honjo"'
Autor:
Silva, Liliane Aparecida Fagundes, Kawahira, Rachel Sayuri Honjo, Kim, Chong Ae, Matas, Carla Gentile
Publikováno v:
In International Journal of Pediatric Otorhinolaryngology July 2021 146
Autor:
Ceroni, Jose Ricardo Magliocco *, Soares, Diogo Cordeiro de Queiroz, Testai, Larissa de Cássia, Kawahira, Rachel Sayuri Honjo, Yamamoto, Guilherme Lopes, Sugayama, Sofia Mizuho Miura, Oliveira, Luiz Antonio Nunes de, Bertola, Debora Romeo, Kim, Chong Ae
Publikováno v:
In Clinics 2018 73
Akademický článek
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Autor:
de Albuquerque Albuquerque, Edoarda Vasco, de Assis Funari, Mariana Ferreira, de Souza Quedas, Elisângela Pereira, Kawahira, Rachel Sayuri Honjo, Jallad, Raquel Soares, Homma, Thaís Kataoka, Martin, Regina Matsunaga, Brito, Vinicius Nahime, Malaquias, Alexsandra Christianne, Lerario, Antonio Marcondes, Rosenberg, Carla, Krepischi, Ana Cristina Victorino, Chong Ae Kim, Arnhold, Ivo Jorge Prado, de Lima Jorge, Alexander Augusto
Publikováno v:
European Journal of Endocrinology; Feb2020, Vol. 182 Issue 2, p139-147, 9p
Autor:
Faria, Karla Tomáz
Publikováno v:
Biblioteca Digital de Teses e Dissertações do Mackenzie
Universidade Presbiteriana Mackenzie (MACKENZIE)
instacron:MACKENZIE
Universidade Presbiteriana Mackenzie (MACKENZIE)
instacron:MACKENZIE
Williams syndrome (WS) is a rare genetic disorder caused by multiple gene microdeletion of region 11.23 of the long arm of chromosome 7 (region 7q11.23). Scientific evidences indicate that the evaluation of adaptive functioning (AF) is fundamental in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::7a67fbf8640cbcf9211b7873790141d9
http://dspace.mackenzie.br/handle/10899/27926
http://dspace.mackenzie.br/handle/10899/27926
Autor:
Capra, Siriana Mansur
Publikováno v:
Biblioteca Digital de Teses e Dissertações do Mackenzie
Universidade Presbiteriana Mackenzie (MACKENZIE)
instacron:MACKENZIE
Universidade Presbiteriana Mackenzie (MACKENZIE)
instacron:MACKENZIE
Williams-Beuren syndrome (WBS) is caused by microdeletions in the region 7q11.23. The main clinical features of the syndrome are congenital heart disease, typical facial dysmorphisms, friendly personality and intellectual disabilities. Previous studi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::c3360919b42d2515d0f08e9a875d55c0
http://dspace.mackenzie.br/handle/10899/22697
http://dspace.mackenzie.br/handle/10899/22697
Autor:
Ranzani Martins R; Department of Neurology, Universidade de Sao Paulo - Hospital das Clinicas, Sao Paulo, Brazil rebecca.rmartins@hc.fm.usp.br., da Silva Paiva ML; Department of Medical Genetics, Universidade de Sao Paulo - Hospital das Clinicas, Sao Paulo, Brazil., da Silva Teixeira WC; Department of Neurology, Universidade de Sao Paulo - Hospital das Clinicas, Sao Paulo, Brazil., Kawahira RSH; Department of Medical Genetics, Universidade de Sao Paulo - Hospital das Clinicas, Sao Paulo, Brazil., Freua F; Department of Neurology, Universidade de Sao Paulo - Hospital das Clinicas, Sao Paulo, Brazil., Castro MAA; Department of Medical Genetics, Universidade de Sao Paulo - Hospital das Clinicas, Sao Paulo, Brazil., Kim CA; Department of Medical Genetics, Universidade de Sao Paulo - Hospital das Clinicas, Sao Paulo, Brazil., Kok F; Department of Neurology, Universidade de Sao Paulo - Hospital das Clinicas, Sao Paulo, Brazil.
Publikováno v:
Practical neurology [Pract Neurol] 2023 Oct; Vol. 23 (5), pp. 436-438. Date of Electronic Publication: 2023 Jul 17.
Autor:
Silva LAF; Departamento de Fisioterapia, Fonoaudiologia e Terapia Ocupacional, Faculdade de Medicina - FM, Universidade de São Paulo - USP - São Paulo (SP), Brasil., Kawahira RSH; Unidade de Genética, Faculdade de Medicina - FM, Instituto da Criança, Hospital das Clinicas - HC, Universidade de São Paulo - USP - São Paulo (SP), Brasil., Kim CA; Unidade de Genética, Faculdade de Medicina - FM, Instituto da Criança, Hospital das Clinicas - HC, Universidade de São Paulo - USP - São Paulo (SP), Brasil., Matas CG; Departamento de Fisioterapia, Fonoaudiologia e Terapia Ocupacional, Faculdade de Medicina - FM, Universidade de São Paulo - USP - São Paulo (SP), Brasil.
Publikováno v:
CoDAS [Codas] 2022 Jan 12; Vol. 34 (3), pp. e20210041. Date of Electronic Publication: 2022 Jan 12 (Print Publication: 2022).