The Anatomic Pathology laboratory adjustments in the era of COVID-19 pandemic: The experience of a laboratory in a Portuguese central hospital

Autor: Lamas, Nuno Jorge, Esteves, Sara, Alves, Joana Raposo, Costa, Francisca Emanuel, Tente, David, Fonseca, Paula, Vizcaíno, José Ramón

Publikováno v: In Annals of Diagnostic Pathology October 2020 48

Mixed cryoglobulinemia; a rare presentation of Waldenström macroglobulinemia.

Autor: Isabel Ribeiro, Catarina, Santos, Clara, Almeida, Clara, Melo, Teresa, Tente, David, Carlos Fernandes, João

Publikováno v: Journal of Nephropathology; Jul2022, Vol. 11 Issue 3, p1-4, 4p

Single symptomatic colonic metastasis as first presentation of a pulmonary mucoepidermoid carcinoma.

Autor: Franco, Inês¹, Tente, David², Coutinho, Daniel¹, Linhas, Rita¹, Antunes, Ana¹, Barroso, Ana¹

Publikováno v: Clinical Respiratory Journal. Jul2016, Vol. 10 Issue 4, p524-529. 6p.

Subcutaneous metastasis of a pulmonary carcinoid tumor

Autor: Linhas, Rita, Tente, David, China, Nuno, Conde, Sara, Barroso, Ana

Publikováno v: Medicine

Rationale: Carcinoid tumors are derived from neuroendocrine cells and are most frequently found in the gastrointestinal tract and bronchopulmonary system. They are generally characterized by an indolent clinical course but may in some instances sprea

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::5c48cd8896add0ac680b3025e6f0a271
http://europepmc.org/articles/PMC5943869

A rare case of cutaneous involvement in atypical haemolytic uraemic syndrome successfully treated with eculizumab

Autor: Lopes, Daniela, Ana Marta Gomes, Cunha, Cátia, Pereira, Susana, Tente, David, Fernandes, João Carlos

Publikováno v: Portuguese Journal of Nephrology & Hypertension, Volume: 30, Issue: 2, Pages: 150-152, Published: JUN 2016
CIÊNCIAVITAE
Portuguese Journal of Nephrology & Hypertension v.30 n.2 2016
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP

Atypical haemolytic uraemic syndrome (aHUS) is a rare, life-threatening, genetic disease, due to uncontrolled alternative pathway complement activation. Although the renal microvasculature appears to be the predominantly affected target, other organ

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::766fa0135a67b3b72e1f7cfe77bbcc1e
http://www.scielo.mec.pt/scielo.php?script=sci_arttext&pid=S0872-01692016000200010&lng=en&tlng=en