Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Natália Cristina Pires Rossi"'
Autor:
Guilherme Bueno de Oliveira, Natália Cristina Pires Rossi, Doramarcia de Oliveira Cury, Maria Gabriela Gonçalves Coura, Carlos Roberto Antonio
Publikováno v:
Surgical & Cosmetic Dermatology, Vol 9, Iss 2, Pp 187-189 (2017)
Introdução: A esclerose tuberosa é genodermatose autossômica dominante, classicamente caracterizada por angiofibromas faciais, placas fibróticas, fibromas periungueais, máculas hipocrômicas em formato de folhas e placa fibrosa frontal. Rela
Externí odkaz:
https://doaj.org/article/2f3d86f15db84657af3036153f493f14
Autor:
João Roberto Antonio, Larissa Cannizza Pacheco de Lucca, Mariana Perez Borim, Natália Cristina Pires Rossi, Guilherme Bueno de Oliveira
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 89, Iss 6, Pp 1003-1004 (2014)
Graham-Little-Piccardi-Lassueur Syndrome is a rare form of Lichen Planus, characterized by the presence of the triad: non-scarring hair loss in the inguinal and axillary regions and follicular spinous or disseminated acuminate papules; typical, cutan
Externí odkaz:
https://doaj.org/article/2a71ff3e485d4c0984f40cd548727631
Autor:
João Roberto, Antonio, Larissa Cannizza Pacheco de, Lucca, Mariana Perez, Borim, Natália Cristina Pires, Rossi, Guilherme Bueno de, Oliveira
Publikováno v:
Anais Brasileiros de Dermatologia
Graham-Little-Piccardi-Lassueur Syndrome is a rare form of Lichen Planus, characterized by the presence of the triad: non-scarring hair loss in the inguinal and axillary regions and follicular spinous or disseminated acuminate papules; typical, cutan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f4c4a3cde853ffa545a009baa27cf0c2
https://pubmed.ncbi.nlm.nih.gov/25387513
https://pubmed.ncbi.nlm.nih.gov/25387513
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