Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Fabiana Bazanella de Oliveira"'
Autor:
Fabiana Bazanella de Oliveira, Paula Chiamenti, Roberta de Freitas Horn, Renan Rangel Bonamigo
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 96, Iss 4, Pp 508-510 (2021)
Externí odkaz:
https://doaj.org/article/b1a39ff26fcd403d922b043de0e12be1
Autor:
Bruna Ossanai Schoenardie, Fabiana Bazanella de Oliveira, Nicolle Gollo Mazzotti, Penélope Esther Palominos, Charles Lubianca Kohem, Tania Ferreira Cestari, Juliana Catucci Boza
Publikováno v:
Clinical and Biomedical Research, Vol 41, Iss 4 (2021)
Introduction: several guidelines emphasize the advantages of multidisciplinary management of patients with psoriasis (PSO) or psoriatic arthritis (PSA). Early diagnosis of PSA relates to better outcomes in 5 years. However, early diagnosis of PSA rem
Externí odkaz:
https://doaj.org/article/f5f10cb98461465b8f993ad634b1318e
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 95, Iss 5, Pp 655-657 (2020)
Abstract We present the case of an HIV-negative man with asymptomatic penile erythematoviolaceous papules associated with similar slightly verrucous papules in the interdigital space of the right foot. A biopsy of the penile lesion confirmed Kaposi's
Externí odkaz:
https://doaj.org/article/88111c9252584d51bcee175e5214d03f
Autor:
Juliana Catucci Boza, Timotio Volnei Dorn, Fabiana Bazanella de Oliveira, Renato Marchiori Bakos
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 89, Iss 6, Pp 999-1001 (2014)
The Osler-Weber-Rendu syndrome or Hereditary Hemorrhagic Telangiectasia (HHT) is a systemic fibrovascular dysplasia characterized by defects in the elastic and vascular walls of blood vessels, making them varicose and prone to disruptions. Lesions oc
Externí odkaz:
https://doaj.org/article/66868a8f575b4f62bbe97ebc8e5c5400
Autor:
Renan Rangel Bonamigo, Wagner Bertolini, Fabiana Bazanella de Oliveira, Sérgio Ivan Torres Dornelles
Publikováno v:
Dermatology in Public Health Environments ISBN: 9783031135040
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b9c30329ab7a1390e01a86f1da9548a
https://doi.org/10.1007/978-3-031-13505-7_25
https://doi.org/10.1007/978-3-031-13505-7_25
Publikováno v:
Anais Brasileiros de Dermatologia
Anais Brasileiros de Dermatologia, Vol 95, Iss 5, Pp 655-657 (2020)
Anais Brasileiros de Dermatologia, Vol 95, Iss 5, Pp 655-657 (2020)
We present the case of an HIV-negative man with asymptomatic penile erythematoviolaceous papules associated with similar slightly verrucous papules in the interdigital space of the right foot. A biopsy of the penile lesion confirmed Kaposi's sarcoma.
Publikováno v:
Current Pharmaceutical Design. 22:5603-5613
Background: Hirsutism is defined as the presence of terminal hair with male distribution in women, and polycystic ovary syndrome (PCOS) is the most common etiology of hirsutism. Methods: The aim of this study is to review aspects of hair growth that
Autor:
Renato Marchiori Bakos, Timotio Volnei Dorn, Juliana Catucci Boza, Fabiana Bazanella de Oliveira
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 89, Iss 6, Pp 999-1001 (2014)
The Osler-Weber-Rendu syndrome or Hereditary Hemorrhagic Telangiectasia (HHT) is a systemic fibrovascular dysplasia characterized by defects in the elastic and vascular walls of blood vessels, making them varicose and prone to disruptions. Lesions oc
Autor:
Mário Reis Álvares-da-Silva, Letícia Rosito Pinto Kruel, Lucas Santos Oliboni, Alexandre de Araujo, João Reinhardt Vicenzi, Fabiana Bazanella de Oliveira, Gabriel Veber Moisés da Silva, Rita Gigliola Gomes Prieb, Fernando Comunello Schacher, Luiz Nelson Teixeira Fernandes, Aline Marino Magnus
Publikováno v:
Hepatology Research. 44:956-963
AIM Evaluate efficacy/safety of oral l-ornithine-l-aspartate (LOLA) in controlling minimal hepatic encephalopathy (MHE). METHODS Consecutive cirrhotic outpatients with MHE (defined by psychometric number connection tests A/B [NCT-A/B] and digit symbo
Autor:
Juliana Catucci, Boza, Timotio Volnei, Dorn, Fabiana Bazanella de, Oliveira, Renato Marchiori, Bakos
Publikováno v:
Anais Brasileiros de Dermatologia
The Osler-Weber-Rendu syndrome or Hereditary Hemorrhagic Telangiectasia (HHT) is a systemic fibrovascular dysplasia characterized by defects in the elastic and vascular walls of blood vessels, making them varicose and prone to disruptions. Lesions oc