Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Laiza Gabriela Garcia Pires"'
Autor:
João Roberto Antonio, Guilherme Bueno de Oliveira, Natalia Cristina Pires Rossi, Laiza Gabriela Garcia Pires
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 89, Iss 5, Pp 819-821 (2014)
Buschke-Fisher-Brauer keratoderma is a rare hereditary autosomal dominant disease of incomplete penetrance. Important differential diagnoses include other palmoplantar keratinization disorders, acquired or hereditary, which is done based on the histo
Externí odkaz:
https://doaj.org/article/8eb89123a0f44206a54d12fafa321292
Autor:
Regina Célia Ajeje Pires de Albuquerque, Felipe Pires de Albuquerque, Kamila Motta Stradiotti, Laiza Gabriela Garcia Pires, Maria Laura Silveira de Castro
Publikováno v:
Políticas e Serviços de Saúde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::acd41721c5598e10bc257390cb41cc50
https://doi.org/10.22533/at.ed.1752105015
https://doi.org/10.22533/at.ed.1752105015
Autor:
Joe Luiz Vieira Garcia Novo, Laiza Gabriela Garcia Pires, Nádia Pesce Dias, Celeste Gomez Sardinha Oshiro, Neil Ferreira Novo, Antonio Rozas
Publikováno v:
Revista da Faculdade de Ciências Médicas de Sorocaba, Vol 14, Iss 1, Pp 8-18 (2012)
Objectives: to assess the anthropometrics assets and outcomes of birthplace newborns from patients classified how low weight through the body weight index. Methods: a retrospective study of patients in labor and newborns from Hospital Santa Lucinda s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::5cef72979948d900405da0dcb4a6fd6f
http://revistas.pucsp.br/index.php/RFCMS/article/view/5173
http://revistas.pucsp.br/index.php/RFCMS/article/view/5173
Autor:
Laiza Gabriela Garcia Pires, Guilherme Bueno de Oliveira, João Roberto Antonio, Natalia Cristina Pires Rossi
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 89, Iss 5, Pp 819-821 (2014)
Anais Brasileiros de Dermatologia
Anais Brasileiros de Dermatologia
Buschke-Fisher-Brauer keratoderma is a rare hereditary autosomal dominant disease of incomplete penetrance. Important differential diagnoses include other palmoplantar keratinization disorders, acquired or hereditary, which is done based on the histo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::698b8c537ac603cbb4a4faa5d6b19c3f
https://doi.org/10.1590/abd1806-4841.20142923
https://doi.org/10.1590/abd1806-4841.20142923