Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Gonçalo Padeira"'
Autor:
Maria Peres, André Moreira-Rosário, Gonçalo Padeira, Patrícia Gaspar Silva, Carla Correia, Andreia Nunes, Elisabete Garcia, Ana Faria, Diana Teixeira, Conceição Calhau, Luís Pereira-da-Silva, Ana Cristina Ferreira, Júlio César Rocha
Publikováno v:
Nutrients, Vol 16, Iss 13, p 2170 (2024)
The COVID-19 pandemic lockdowns affected the lifestyles of children and adolescents, leading to an increase in childhood obesity. Paediatric patients with familial hypercholesterolemia (FH) may be more susceptible to lockdown effects due to their inc
Externí odkaz:
https://doaj.org/article/02780a7753ac4943931bcb7396f1a144
Autor:
Gonçalo Padeira, Branca M. Cavaco, Daniel Virella, Henrique Sá Couto, Maria de Lurdes Afonso-Lopes
Publikováno v:
Portuguese Journal of Pediatrics; Vol. 53 No. 1 (2022)
Portuguese Journal of Pediatrics; Vol. 53 N.º 1 (2022)
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Portuguese Journal of Pediatrics, Vol 53, Iss 1 (2022)
Portuguese Journal of Pediatrics; Vol. 53 N.º 1 (2022)
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Portuguese Journal of Pediatrics, Vol 53, Iss 1 (2022)
Heterozygous inactivating mutations of the calcium-sensing receptor encoding gene (CASR) cause autosomal dominant familial hypocalciuric hypercalcemia (FHH), whereas mutations that inactivate both alleles cause neonatal severe hyperparathyroidism (NS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4bbdddc4c679909a4a730bb430a4a5f
https://hdl.handle.net/10400.17/4281
https://hdl.handle.net/10400.17/4281
Publikováno v:
Portuguese Journal of Pediatrics, Vol 50, Iss 1 (2019)
Recém-nascido de 25 dias internado por tosse acessual, gemido, fervores crepitantes bilaterais com apneia e insuficiência respiratória aguda. A radiografia do tórax apresentava hipotransparência no hemitórax esquerdo. Analiticamente leucócitos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27122e0ed191bdf81994ac91de008277
Autor:
Ana C. M. Ferreira, Gonçalo Padeira, Ana Margarida Medeiros, Ana Catarina Alves, Mafalda Bourbon
Publikováno v:
Atherosclerosis. 263:e228
Aims: Familial Hyperpercholesterolaemia (FH) is the most common of all genetic hypercholesterolaemias. However there are other rare disorders presenting the same phenotype (phenocopies). Sitosterolaemia is one of those rare recessive disorders in whi