Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Diana Rita Oliveira"'
Autor:
Cristiana Maximiano, Alexandra Vilas Fabião, Diana Rita Oliveira, Ângela Dias, Filipa Correia, Sofia A. Martins
Publikováno v:
Gazeta Médica, Vol 1, Iss 1 (2023)
INTRODUCTION: Type 1 diabetes is a chronic disease characterized by a selective loss of pancreatic ?-cells with a disproportionate recent increase at ages under 5-years old. Its etiology is multifactorial, to which immune factors contribute through p
Externí odkaz:
https://doaj.org/article/8bd2842a41b64520a30b387ad5387fa9
Autor:
Diana Rita Oliveira, Joana Freitas Rebelo, Cristiana Maximiano, Maria Miguel Gomes, Vânia Martins, Carla Meireles, Henedina Antunes, Sofia Martins
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 66, Iss 2, Pp 229-236 (2022)
ABSTRACT Objectives: Evaluate the celiac disease (CD) markers, within the scope of its screening, in a pediatric population with diagnosis of type 1 diabetes (T1D) at Hospital de Braga (HB) and determine the prevalence of CD in the sample. Reflect on
Externí odkaz:
https://doaj.org/article/87023df207934ff88078f5a61c6d80bb
Autor:
Vasco Carvalho, Diana Rita Oliveira, Marta Ribeiro Silva, Lídia Leite, Miguel Gonçalves Rocha, Liliana Pinheiro, Almerinda Pereira
Publikováno v:
Journal of Pediatric and Neonatal Individualized Medicine, Vol 11, Iss 1, Pp e110128-e110128 (2021)
Introduction: Stickler syndrome is a connective tissue disorder that can include midfacial underdevelopment and cleft palate, ocular findings (myopia, cataract, and retinal detachment), hearing loss that is both conductive and sensorineural and mild
Externí odkaz:
https://doaj.org/article/1b36901edbc04c2289d2a5c1de9076ff
Autor:
Diana Rita Oliveira, Cristiana Maximiano, Lídia Leite, Margarida Abreu, Filipa Tavares Almeida, Olga Ferreira, Augusta Gonçalves, Manuela Costa Alves, Ariana Afonso
Publikováno v:
Gazeta Médica, Vol 8, Iss 1 (2021)
INTRODUÇÃO: A púrpura de Henoch-Schönlein (PHS) caracteriza-se por púrpura palpável associada a dor abdominal, artralgia ou atingimento renal. A variante bolhosa é rara em pediatria, geralmente com bom prognóstico. CASO CLÍNICO: Menino de 3
Externí odkaz:
https://doaj.org/article/7c581ba983594e118d88ec35a336bfd8
Autor:
Diana Rita Oliveira, Marta Ribeiro Silva, Maria Miguel Gomes, Rui Santos, Filipa Almeida, Manuela Costa Alves, Augusta Gonçalves, Ana Paula Vieira, Ângela Pereira
Publikováno v:
Ecos do Minho, Vol 12, Iss 1, Pp 17-20 (2017)
Tinea capitis, uma infeção do couro cabeludo por dermatófitos, é a infeção fúngica mais comum em idade pediátrica. A apresentação clínica é variável, desde uma dermatose descamativa não inflamatória até à evolução para lesões tipo
Externí odkaz:
https://doaj.org/article/78395a059cbc452c9eb9fe5c29dafeee
Autor:
Rita Quental, Iva Brito, João Luís Barreira, Graça Barros Loureiro, Carla Pinto Moura, Rúben Dos-Reis-Maia, Mariana Rodrigues, Sara Ganhão, Francisca Aguiar, Diana Rita Oliveira
Publikováno v:
Clinical Rheumatology. 39:3853-3860
Deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessive disease resulting from loss-of-function pathogenic variants in ADA2 gene, which might resemble polyarteritis nodosa (PAN). The authors present two pediatric cases of ADA2 deficienc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::914fd3583d4138c96f2fa37a523c40ce
https://doi.org/10.1007/s10067-020-05210-4
https://doi.org/10.1007/s10067-020-05210-4
Autor:
Filipa Tavares Almeida, Manuela Costa Alves, Ariana Afonso, Cristiana Maximiano, Augusta Gonçalves, Margarida Abreu, Olga Ferreira, Lídia Leite, Diana Rita Oliveira
Publikováno v:
Gazeta Médica, Vol 8, Iss 1 (2021)
INTRODUCTION: Henoch-Schonlein purpura is characterized by palpable purpura associated with abdominal pain, arthralgia or kidney lesion. The bullous variant is rare in children and generally has a good prognosis.CASE REPORT: A 3-year and 8-month-old
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f185099ec22723aeb3140dcc8b7af70a
https://doi.org/10.29315/gm.v8i1.390
https://doi.org/10.29315/gm.v8i1.390
Autor:
Francisca Aguiar, Graça Barros Loureiro, Sara Ganhão, Diana Rita Oliveira, Mariana Rodrigues, Iva Brito
Publikováno v:
Abstracts Accepted for Publication.
Background Polyarteritis nodosa (PAN) is a rare form of primary systemic vasculitis with heterogeneous presentations, treatments and disease course. There have been improvements in understanding of certain causes of PAN such as the association of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed41b6c07af4720f105c623c5d5d461f
https://doi.org/10.1136/annrheumdis-2019-eular.7627
https://doi.org/10.1136/annrheumdis-2019-eular.7627
