Výsledky vyhledávání - "Abranches,Margarida"

Influenza B-Associated Atypical Hemolytic Uremic Syndrome

Autor: Mano,Lia, Francisco,Telma, Gaspar,Joana, Pereira,Gabriela, Santos,Raquel, Abranches,Margarida

Publikováno v: Portuguese Journal of Nephrology & Hypertension v.36 n.2 2022

Hemolytic uremic syndrome (HUS) triggered by influenza virus (iHUS) is rare. Influenza A infections have been described to trigger atypical HUS (aHUS) in individuals with an underlying genetic complement dysregulation. To date there are only few repo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______616::bdb0646b0ceb18a975f3908312de27c1
http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-01692022000200080

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Akademický článek

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Primary hyperoxaluria type 1 - two case reports

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

Publikováno v: Portuguese Journal of Nephrology & Hypertension v.34 n.1 2020
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Portuguese Journal of Nephrology & Hypertension, Volume: 34, Issue: 1, Pages: 55-57, Published: MAR 2020

Background: 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 diag

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4d691729d46f8e9978b8b213afce7b5e
http://www.scielo.mec.pt/scielo.php?script=sci_arttext&pid=S0872-01692020000100010

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Which Factors Influence Prognosis in Congenital Solitary Functioning Kidney? Date of submission: 09-01-2019 | Date of acceptance: 03-09-2019 | Published: 27-01-2020

Autor: Ganhão, Inês, Lacerda, Catarina M., Carvalho, Tânia, Francisco, Telma, Santos, Raquel, Neto, Gisela, Serrão, Ana P., Abranches, Margarida

Publikováno v: Portuguese Journal of Pediatrics (former Acta Pediátrica Portuguesa); Vol. 51 No. 1 (2020)
Portuguese Journal of Pediatrics; vol. 51 n.º 1 (2020)
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP

Introduction: Premature, low birthweight, and small for gestational age newborns may have low nephron endowment at birth. When associated with solitary functioning kidney, especially if other congenital anomalies of kidney and urinary tract or urinar

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::ba855dbf22f49b9587104ea894700aa3

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Nephrocalcinosis in a portuguese pediatric population

Autor: Bota, Sofia, Andrade, Joana V, Francisco, Telma, Santos, Raquel, Neto, Gisela, Abranches, Margarida

Publikováno v: Portuguese Journal of Nephrology & Hypertension v.33 n.1 2019
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Portuguese Journal of Nephrology & Hypertension, Volume: 33, Issue: 1, Pages: 14-18, Published: MAR 2019

Introduction and Aims: Nephrocalcinosis is characterized by the deposition of calcium in the kidney parenchyma and tubules. The renal prognosis depends on the underlying cause, emphasizing the importance of its identification. We aim to review the da

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::cde803b6ad5eeee162c1e333faf53984
http://www.scielo.mec.pt/scielo.php?script=sci_arttext&pid=S0872-01692019000100004

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Nephrolithiasis in a portuguese pediatric population

Autor: Andrade,Joana V, Bota,Sofia, Francisco,Telma, Santos,Raquel, Neto,Gisela, Abranches,Margarida

Publikováno v: Portuguese Journal of Nephrology & Hypertension, Volume: 32, Issue: 3, Pages: 258-267, Published: SEP 2018
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Portuguese Journal of Nephrology & Hypertension v.32 n.3 2018

Introduction and Aims: Nephrolithiasis incidence in children has increased considerably. It is associated with substantial morbidity, recurrence and increased adulthood cardiovascular risk and chronic kidney disease. A thorough investigation is essen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::5c00bc38b7ca325b01cb11660a1ccdfb
http://www.scielo.mec.pt/scielo.php?script=sci_arttext&pid=S0872-01692018000300005&lng=en&tlng=en

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Coexistence of pheochromocytoma and renal artery stenosis in a pediatric patient with hypertension

Autor: Serras,Inês, Baptista,Rute Baeta, Francisco,Telma, Casimiro,Anaxore, Lito,David, Alves,Rui, Abranches,Margarida

Publikováno v: Portuguese Journal of Nephrology & Hypertension, Volume: 32, Issue: 1, Pages: 78-82, Published: MAR 2018
Portuguese Journal of Nephrology & Hypertension v.32 n.1 2018
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP

Pheochromocytoma and renal artery stenosis are surgically treatable causes of hypertension. Although rare, the coexistence of pheochromocytoma and renal artery stenosis has been described in case reports. Common pathophysiological mechanisms other th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0f74cf2137227cdb61f5fe0509f4e5eb
http://www.scielo.mec.pt/scielo.php?script=sci_arttext&pid=S0872-01692018000100013&lng=en&tlng=en

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Akademický článek

X-linked hypophosphatemic rickets: a new mutation.

Autor: Maio, Patrícia, Mano, Lia, Rocha, Sara, Baeta Baptista, Rute, Francisco, Telma, Sousa, Helena, Parente Freixo, João, Abranches, Margarida

Publikováno v: Brazilian Journal of Nephrology / Jornal Brasileiro de Nefrologia; abr-jun2021, Vol. 43 Issue 2, p279-282, 4p

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Diagnóstico pré-natal das anomalias do tracto urinário:dez anos de experiência

Autor: Batista, Judite, Abranches, Margarida, Silva, Alzira, de Sousa, J. Ferra

Publikováno v: Portuguese Journal of Pediatrics (former Acta Pediátrica Portuguesa); Vol. 33 No. 5 (2002); Pag. 311-315
Portuguese Journal of Pediatrics; vol. 33 n.º 5 (2002); Pag. 311-315
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Portuguese Journal of Pediatrics, Vol 33, Iss 5 (2014)
Acta Pediátrica Portuguesa; v. 33, n. 5 (2002); Pag. 311-315

Introdução: As anomalias do tracto urinário são detectadas com uma frequência cada vez maior devido à sistematização da vigilância ecográfica durante a gravidez aliada à sofisticação técnica e à experiência dos ecografistas. Objectivo

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