Zobrazeno 1 - 10
of 17
pro vyhledávání: '"M. João Oliveira"'
Publikováno v:
Galicia Clínica, Vol 81, Iss 2, Pp 54-56 (2020)
Introduction: Insulinomas are the most frequent cause of hypoglycemia in non-diabetic patients and the most common functional endocrine pancreatic tumors. Symptoms of hypoglycemia are nonspecific so the diagnosis may be challenging. Case report: A 36
Externí odkaz:
https://doaj.org/article/7b49aa82867841ceaf68690363b77178
Autor:
Inês Ladeira, Margarida Dias, Maria Aurora Pinto Mendes, Paula Faustino, M João Oliveira, Teresa Almeida, Manuel Preto, Ivone Pascoal, Daniel Coutinho, Miguel Guimarães
Publikováno v:
Tobacco, smoking control and health education.
Introduction: There is no current evidence to recommend electronic cigarettes as a smoking cessation aid. Data regarding knowledge and use of e-cigarettes among smokers seeking to quit is scarce. Methods: Between August and December 2017, current smo
Autor:
Cátia Peixoto, B. Amaral, Jorge Luis Gavina Pereira, Luzia Lucélia Saraiva Ribeiro, M. João Oliveira, Teresa Borges, J.A. Cidade-Rodrigues, Hélia Cardoso, M. Santalha, S. Figueiredo
Publikováno v:
Anales de Pediatría, Vol 81, Iss 4, Pp 246-250 (2014)
Resumen: La pubertad precoz, a pesar de las definiciones clínicas estandarizadas y pruebas de diagnóstico disponibles, requiere, en ciertas situaciones una investigación exhaustiva y estructurada con el fin de conocer la causa.Niña de 4 años de
Autor:
Helena Cardoso, Luzia Lucélia Saraiva Ribeiro, J.A. Cidade-Rodrigues, Cátia Peixoto, B. Amaral, Jorge Luis Gavina Pereira, M. João Oliveira, Teresa Borges, M. Santalha, S. Figueiredo
Publikováno v:
Anales de Pediatría (English Edition), Vol 81, Iss 4, Pp 246-250 (2014)
Despite standard clinical definitions and availability of diagnostic tests for precocious puberty, an intensive and structured investigation is needed in order to diagnose the aetiology in particular cases.A 4-year-old, phenotypically female child wa
Autor:
M. João Oliveira, T. Silva Borges, L. Martins Ribeiro, Hélia Cardoso, Sheila Cristina Ouriques Martins
Publikováno v:
Anales de Pediatría, Vol 78, Iss 1, Pp 54-58 (2013)
Resumen: La lipodistrofia congénita generalizada es un trastorno hereditario poco común, de herencia autosómica recesiva, caracterizado por la ausencia casi total de tejido adiposo desde el nacimiento. Se asocia a la aparición precoz de anomalía
Autor:
Dária Rezende, Inês V Matos, M João Oliveira, Conceição Costa, Luciana Reis, M Guilhermina Reis, Paula Ferreira
Publikováno v:
Revista Portuguesa de Pneumologia, Vol 16, Iss 1, Pp 163-169 (2010)
O pneumomediastino espontâneo num recém-nascido (RN) de termo não submetido a ventilação mecânica ou sem patologia pulmonar subjacente é uma entidade rara. A existência de septos internos e a tendência à loculação são particularidades do
Autor:
M, Santalha, B, Amaral, J, Pereira, L, Ribeiro, M, João Oliveira, S, Figueiredo, H, Cardoso, C, Peixoto, T, Borges, J A, Cidade-Rodrigues
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 81(4)
Despite standard clinical definitions and availability of diagnostic tests for precocious puberty, an intensive and structured investigation is needed in order to diagnose the aetiology in particular cases. A 4-year-old, phenotypically female child w
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 78(1)
Congenital generalised lipodystrophy is a rare autosomal recessive disorder characterised by a marked deficiency of adipose tissue and usually recognised at birth. This disorder is associated with early development of metabolic complications such as
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Akademický článek
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