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of 3
pro vyhledávání: '"Renata Hübner Frainer"'
Autor:
Renata Elise Tonoli, Damiê De Villa, Renata Hübner Frainer, Luana Pizzarro Meneghello, Nelson Ricachnevsky, Maurício de Quadros
Publikováno v:
Case Reports in Dermatological Medicine, Vol 2012 (2012)
Olmsted syndrome is a rare congenital, sharply circumscribed transgredient palmoplantar keratoderma. It was first described by Olmsted in 1927. The diagnosis of this rare disease depends on clinical features like symmetrical involvement of keratoderm
Externí odkaz:
https://doaj.org/article/7ec97e7999ed485694b776374883af0f
Autor:
Elisângela de Quevedo Welter, Renata Hubner Frainer, Adriana Maldotti, Alexandre Losekann, Magda Blessmann Weber
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 86, Iss 1, Pp 31-36 (2011)
FUNDAMENTOS: prurido é o sintoma mais freqüente nos pacientes nefropatas em hemodiálise. Parâmetros laboratoriais anormais têm sido encontrados, com dados conflitantes. OBJETIVO: relacionar a prevalência de prurido com alterações no metabolis
Externí odkaz:
https://doaj.org/article/5d1cd655d7ae499c991bf746d7dbbe79
Autor:
Renata Hubner Frainer, Luciana Boff de Abreu, Giselle Martins Pinto, André Vicente Esteves de Carvalho, Luana Pizarro Meneghello
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 88, Iss 1, Pp 135-137 (2013)
Congenital hypotrichosis and Stargardt macular dystrophy are rare autosomal recessive disorder of unk nown etiology respectively characterized by hair loss, macular degeneration and severe progressive vision reduc tion. There are few reports in the l
Externí odkaz:
https://doaj.org/article/114d8c3bd21a40ec9c833992e3644cff