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	Provedor de dados BJID (2) Genet. Mol. Biol. (2) Autor Cintra,Maria Letícia (4) Marques-de-Faria,Antonia Paula (2) Steiner,Carlos Eduardo (2) Velho,Paulo Eduardo Neves Ferreira (2) Fogagnolo,Letícia (1) Mariotto,Andréia (1) Moraes,Aparecida Machado de (1) Oliveira,Gisele Viana de (1) Souza,Elemir Macedo de (1) Uthida-Tanaka,Ana Maria (1) Mais... Palavra-chave Bacillary angiomatosis (1) Bart-Pumphrey syndrome (1) Bartonella (1) Carrion's disease (1) Cat-scratch disease (1) Cutis laxa (1) De Barsy syndrome (1) Deafness (1) Erythema nodosum (1) Gerodermia osteodysplastica (1) Hyperkeratosis (1) Knuckle pads (1) Lepromatous (1) Leprosy (1) Palmoplantar keratoderma (1) Trench fever (1) Vasculitis (1) Wrinkly skin syndrome (1) Mais... Tipo do documento Info:eu-repo/semantics/article (2) Info:eu-repo/semantics/other (2) Ano 2007 (1) 2005 (1) 2003 (2) País Brazil (4) Idioma Inglês (4)		Ordenar por:  Relevância Autor Título Ano Registros recuperados: 4 Primeira ... 1 ... Última What do we (not) know about the human bartonelloses? BJID Velho,Paulo Eduardo Neves Ferreira; Cintra,Maria Letícia; Uthida-Tanaka,Ana Maria; Moraes,Aparecida Machado de; Mariotto,Andréia. The human bartonelloses are a group of diseases with a rapidly increasing clinical spectrum. Well known manifestations such as Carrion's disease, trench fever, cat-scratch disease, and bacillary angiomatosis are examples of Bartonella spp. infection. Along with these diseases, recurrent bacteremia, endocarditis, septicemia, erythema nodosum, erythema multiforme, trombocytopenic purpura and other syndromes have been reported having been caused by bacteria of this genus. The infectious process and the pathogenesis of these microorganisms are poorly understood. The bartonelloses may have a benign and self-limited evolution in a host, or a potentially fatal one. These bacteria can provoke a granulomatous or an angioproliferative histopathologic response. As... Tipo: Info:eu-repo/semantics/other Palavras-chave: Bartonella; Carrion's disease; Trench fever; Cat-scratch disease; Bacillary angiomatosis. Ano: 2003 URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1413-86702003000100001 Vasculonecrotic reactions in leprosy BJID Fogagnolo,Letícia; Souza,Elemir Macedo de; Cintra,Maria Letícia; Velho,Paulo Eduardo Neves Ferreira. Multibacillary, lepromatous or borderline leprosy patients may present two types of vasculonecrotic reactions: Lucio phenomenon and that associated with erythema nodosum leprosum. Despite they can be distinguished through clinical and histological characteristics; both are often used as synonyms. It is said that leprosy reaction should be properly classified for therapeutic reasons, since it is well known that in Lucio phenomenon there is not a good response to thalidomide. The authors reported two cases of vasculonecrotic phenomena in lepromatous leprosy sharing clinical and histopathological characteristics of both reaction subtypes. The findings may indicate the spectral nature of the reaction phenomena in leprosy and emphasize the importance of the... Tipo: Info:eu-repo/semantics/article Palavras-chave: Leprosy; Lepromatous; Erythema nodosum; Vasculitis. Ano: 2007 URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1413-86702007000300016 Cutis laxa with growth and developmental delay, wrinkly skin syndrome and gerodermia osteodysplastica: a report of two unrelated patients and a literature review Genet. Mol. Biol. Steiner,Carlos Eduardo; Cintra,Maria Letícia; Marques-de-Faria,Antonia Paula. Two unrelated patients of different sexes are described, both presenting with congenital redundant skin (cutis laxa), growth deficiency, mental retardation and bone dystrophy. Parental consanguinity in both families and a more pronounced severity of the neurological disease in the male patient were present. Both patients were diagnosed in infancy as having De Barsy syndrome, but clinical follow-up revealed that the clinical picture was compatible with the diagnosis of cutis laxa with growth and developmental delay (CLGDD), gerodermia osteodysplastica (GO) and wrinkly-skin syndrome (WWS). It has recently been suggested that cutis laxa with growth and developmental delay, gerodermia osteodysplastica and wrinkly skin syndrome are the same condition. A review... Tipo: Info:eu-repo/semantics/article Palavras-chave: Cutis laxa; De Barsy syndrome; Gerodermia osteodysplastica; Wrinkly skin syndrome. Ano: 2005 URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572005000200001 Deafness, palmoplantar hyperkeratosis, and knuckle pads with male-to-male transmission: Bart-Pumphrey syndrome Genet. Mol. Biol. Oliveira,Gisele Viana de; Steiner,Carlos Eduardo; Cintra,Maria Letícia; Marques-de-Faria,Antonia Paula. We report on a 22-year-old male patient and his father, both presenting with congenital sensorineural deafness, diffuse palmoplantar keratoderma and knuckle pads. These findings are similar to those previously described in the Bart-Pumphrey syndrome, a rare autosomal dominant disorder. Several conditions including keratoderma and deafness are briefly reviewed. Tipo: Info:eu-repo/semantics/other Palavras-chave: Deafness; Knuckle pads; Palmoplantar keratoderma; Hyperkeratosis; Bart-Pumphrey syndrome. Ano: 2003 URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572003000200004 Registros recuperados: 4 Primeira ... 1 ... Última

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