João Paulo Ferreira da Silva Oliveira


AuthID: R-000-7B1

Confirmed Publications: 121



11
TITLE: Kidney Failure Secondary to Hereditary Xanthinuria due to a Homozygous Deletion of the XDH Gene in the Absence of Overt Kidney Stone Disease
AUTHORS: Goncalves, Pedro Lisboa; Diniz, Hugo; Tavares, Isabel; Doria, Sofia ; Dong, Juan; Kyriss, McKenna; Fairbanks, Lynette; Oliveira, JP ;
PUBLISHED: 2024, SOURCE: NEPHRON, VOLUME: 148, ISSUE: 8
INDEXED IN: Scopus WOS CrossRef: 1 Unpaywall
12
TITLE: The Complexity of Decisions in Genetics: Annotation of Three Novel Variants in the PKD1 and PKD2 Genes
AUTHORS: Barata, Rui; Rocha, Liliana; Tavares, Isabel ; Pereira, Odete; Carvalho, Filipa ; Oliveira, JP ;
PUBLISHED: 2024, SOURCE: NEPHRON, VOLUME: 148, ISSUE: 7
INDEXED IN: Scopus WOS CrossRef Unpaywall
IN MY: CIÊNCIAVITAE
13
TITLE: #5302 REVISITING THE PATHOGENIC ROLE OF THE SLC8A1 GENE IN A FAMILY WITH A NOVEL TERMINAL GROSS DELETION IN THE UMOD GENE
AUTHORS: Francisco Gonçalves; Pedro Lisboa Gonçalves; Rita Quental; Susana Fernandes; Sofia Quental; Isabel Tavares; Oliveira, JP ;
PUBLISHED: 2023, SOURCE: Nephrology Dialysis Transplantation, VOLUME: 38, ISSUE: Supplement_1
INDEXED IN: CrossRef
IN MY: CIÊNCIAVITAE
14
TITLE: Characterization of peroxidasin expression in histologically normal human adult and fetal kidney tissue
AUTHORS: Isabel Brandão; Roberto Silva; Eduardo Conde; Bárbara Gomes; Sampaio, P; Ana Costa Braga; Jorge Reis Almeida; Inês Soares Alencastre; Oliveira, JP ;
PUBLISHED: 2023
INDEXED IN: CrossRef
IN MY: ORCID | CIÊNCIAVITAE
15
TITLE: Global reach of over 20 years of experience in the patient-centered Fabry Registry: Advancement of Fabry disease expertise and dissemination of real-world evidence to the Fabry community  Full Text
AUTHORS: Wanner, Christoph; Ortiz, Alberto; Wilcox, William R.; Hopkin, Robert J.; Johnson, Jack; Ponce, Elvira; Ebels, Johan T.; Batista, Julie L.; Maski, Manish; Politei, Juan M.; Martins, Ana Maria; Banikazemi, Maryam; Linhart, Ales; Mauer, Michael; Oliveira, JP ; Weidemann, Frank; Germain, Dominique P.;
PUBLISHED: 2023, SOURCE: MOLECULAR GENETICS AND METABOLISM, VOLUME: 139, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 5
IN MY: ORCID | CIÊNCIAVITAE
16
TITLE: Podocytopathy and Glomerular Basement Membrane Anomalies in Two Patients With Cubilin Gene Mutations
AUTHORS: Gomes, Sara Madureira; Igreja, Ana Isabel; Silva, Roberto; Oliveira, JP ; Pinto, Helena;
PUBLISHED: 2023, SOURCE: CUREUS JOURNAL OF MEDICAL SCIENCE, VOLUME: 15, ISSUE: 2
INDEXED IN: WOS CrossRef
IN MY: ORCID | CIÊNCIAVITAE
17
TITLE: Raising Awareness Towards Underdiagnosed Renal Hypouricemia: A Case Report
AUTHORS: Pedro Gonçalves; Filipa Ferreira; Isabel Tavares ; Oliveira, JP ;
PUBLISHED: 2023, SOURCE: Portuguese Journal of Nephrology & Hypertension, VOLUME: 37
INDEXED IN: CrossRef: 1
IN MY: ORCID | CIÊNCIAVITAE
18
TITLE: Automated estimation of foot process width using deep learning in kidney biopsies from patients with Fabry disease  Full Text
AUTHORS: Smerkous, David; Mauer, Michael; Tondel, Camilla; Svarstad, Einar; Gubler, Marie Claire; Oliveira, JP ; Sargolzaeiaval, Forough; Najafian, Behzad;
PUBLISHED: 2022, SOURCE: MOLECULAR GENETICS AND METABOLISM, VOLUME: 135, ISSUE: 2
INDEXED IN: WOS CrossRef
IN MY: ORCID | CIÊNCIAVITAE
19
TITLE: Fabry disease and COVID-19: International expert recommendations for management based on real-world experience  Full Text
AUTHORS: Laney, DA; Germain, DP; Oliveira, JP ; Burlina, AP; Cabrera, GH; Hong, GR; Hopkin, RJ; Niu, DM; Thomas, M; Trimarchi, H; Wilcox, WR; Politei, JM; Ortiz, A;
PUBLISHED: 2021, SOURCE: MOLECULAR GENETICS AND METABOLISM, VOLUME: 132, ISSUE: 2
INDEXED IN: WOS CrossRef
IN MY: ORCID | CIÊNCIAVITAE
20
TITLE: Massive Pulmonary Thrombosis Following Haemoptysis in Type IV Ehlers-Danlos Syndrome
AUTHORS: Almeida, LM; Sousa, C; Vilares, P; Fernandes, P; Amado, J; Paiva, JA ; Marinho, A; Oliveira, JP ;
PUBLISHED: 2021, SOURCE: ARCHIVOS DE BRONCONEUMOLOGIA, VOLUME: 57, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 1
IN MY: ORCID | CIÊNCIAVITAE
Page 2 of 13. Total results: 121.

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