Aetiology, course and treatment of acute tubulointerstitial nephritis in paediatric patients : A cross-sectional web-based survey

Autor: Wente-Schulz, Sarah, Aksenova, Marina, Awan, Atif, Ambarsari, Cahyani Gita, Becherucci, Francesca, Emma, Francesco, Fila, Marc, Francisco, Telma, Gokce, Ibrahim, Gülhan, Bora, Hansen, Matthias, Jahnukainen, Timo, Kallash, Mahmoud, Kamperis, Konstantinos, Mason, Sherene, Mastrangelo, Antonio, Mencarelli, Francesca, Niwinska-Faryna, Bogna, Riordan, Michael, Rus, Rina R, Saygili, Seha, Serdaroglu, Erkin, Taner, Sevgin, Topaloglu, Rezan, Vidal, Enrico, Woroniecki, Robert, Yel, Sibel, Zieg, Jakub, Pape, Lars

Publikováno v: Wente-Schulz, S, Aksenova, M, Awan, A, Ambarsari, C G, Becherucci, F, Emma, F, Fila, M, Francisco, T, Gokce, I, Gülhan, B, Hansen, M, Jahnukainen, T, Kallash, M, Kamperis, K, Mason, S, Mastrangelo, A, Mencarelli, F, Niwinska-Faryna, B, Riordan, M, Rus, R R, Saygili, S, Serdaroglu, E, Taner, S, Topaloglu, R, Vidal, E, Woroniecki, R, Yel, S, Zieg, J, Pape, L & The international TIN study group 2021, ' Aetiology, course and treatment of acute tubulointerstitial nephritis in paediatric patients : A cross-sectional web-based survey ', BMJ Open, vol. 11, no. 5, e047059 . https://doi.org/10.1136/bmjopen-2020-047059
BMJ Open
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP

Background Acute tubulointerstitial nephritis (TIN) is a significant cause of acute renal failure in paediatric and adult patients. There are no large paediatric series focusing on the aetiology, treatment and courses of acute TIN. Patients, design a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::31913f561a653e5bcfbabffe89dea24e
https://www.ncbi.nlm.nih.gov/pubmed/34049919

Primary hyperoxaluria type 1 – two case reports

Autor: Marta Amorim, Dinorah Cardoso, Marisa Braga da Cruz, Susana Nobre, Inês Ganhão, Catarina Borges, Margarida Abranches, Telma Francisco

Publikováno v: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP

Primary hyperoxaluria type 1 is a rare autosomal recessive inherited disease, caused by mutations in AGXT gene, with an estimated incidence of 1:100.000 live births per year in Europe. Over 50% present with end stage renal disease at diagnosis. Case

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fac120a214ce0d864be96c345e3486c4
https://doi.org/10.32932/pjnh.2020.04.064

Portuguese Consensus Document Statement in Diagnostic and Management of Atypical Hemolytic Uremic Syndrome

Autor: Azevedo, A, Faria, B, Teixeira, C, Carvalho, F, Neto, G, Santos, J, Santos, MC, Oliveira, N, Fidalgo, T, Calado, J

Publikováno v: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP

Among thrombotic microangiopathies (TMA), the hemolytic uremic syndrome associated with dysregulation of the alternative complement pathway (aHUS) is one of the most challenging diseases a nephrologist can face. By the end of the XXth century, the co

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::d242c0307b9b341a6c5d6089e6ed0f53

A rare case of hematuria

Autor: Andreia Mascarenhas, Isabel Castro

Publikováno v: Einstein (São Paulo), Vol 9, Iss 1, Pp 81-83 (2011)

The infestation by Schistosoma haematobium is common in African countries and West Asia. Its chronic phase is characterized by the deposition of eggs of the parasite in various tissues of the body causing inflammatory response, formation of granuloma

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10d8bf0bee75f075a20a84daff7dc698
http://apps.einstein.br/revista/arquivos/PDF/1946-Einsteinv9n1_81-83_eng.pdf

Acidose Tubular Renal Distal e Surdez Neurossensorial com Mutação no Gene ATP6V1B1

Autor: Periquito, I, Casimiro, A, Santo, C, D’Elia, C, Abranches, M, Castro, I

Publikováno v: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP

Submitted by Dulce Barreto (mdulce.barreto@chlc.min-saude.pt) on 2013-07-23T15:11:14Z No. of bitstreams: 1 Port J Nephrol Hypert 2013_27_109.pdf: 265730 bytes, checksum: 626df653e0f068ab40a605e04540c392 (MD5) Made available in DSpace on 2013-07-23T15

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3056::0dd5dde6dab81686f796cf512ef86ce2