Joao Paulo Oliveira - Univ Porto | 人才画像

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个人简介

Joao Paulo Oliveira currently works at the Faculty of Medicine, Department of Pathology, Unit of Genetics, University of Porto. His main clinical and research interest is focused in the hereditary kidney diseases.

研究兴趣

论文共 142 篇作者统计合作学者相似作者

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Development of an Automated Estimation of Foot Process Width Using Deep Learning in Kidney Biopsies from Patients with Fabry, Minimal Change, and Diabetic Kidney Diseases

David Smerkous,Michael Mauer,Camilla Tondel,Einar Svarstad,Marie-Claire Gubler, Robert G. Nelson,Joao-Paulo Oliveira,Forough Sargolzaeiaval,Behzad Najafian

KIDNEY INTERNATIONAL（2024）

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#2615 Altered Peroxidasin Expression Pattern in IgA Nephropathy

Roberto Silva,Isabel Brandao, Eduardo Conde, Barbara Gomes,Hans-Peter Marti,Tony Chen,Bernardo Faria,Jorge Reis Almeida,Ines Alencastre,Joao Paulo Oliveira

NEPHROLOGY DIALYSIS TRANSPLANTATION (2024): I494-I494

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The Complexity of Decisions in Genetics: Annotation of Three Novel Variants in the PKD1 and PKD2 Genes

Rui Barata,Liliana Rocha,Isabel Tavares,Odete Pereira,Filipa Carvalho,Joao Paulo Oliveira

NEPHRONno. 7 (2024): 487-491

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Homozygosity for a Rare FASTKD2 Variant Resulting in an Adult Onset Autosomal Recessive Mitochondrial Podocytopathy

Francisco Pereira Gonçalves,Isabel Tavares,Roberto Silva,Ana Teresa Nunes, Luciano Pereira, Andreia Campos, Joel Pinto, Ana Lopes, Marta Simões,Manuela Grazina, Agnes B. Fogo,João Paulo Oliveira

American journal of kidney diseases the official journal of the National Kidney Foundationno. 1 (2024): 119-123

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DESIGUALDADE DE GÊNERO NA EDUCAÇÃO INFANTIL: REALIDADE DE SÃO PAULO DO POTENGI-RN

João Paulo Elias Oliveira

ANAIS DO I CONGRESSO BRASILEIRO DE EMPREENDEDORISMO (ON-LINE) – I COBREM – RESUMOS SIMPLES (2024)

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Kidney Failure Secondary to Hereditary Xanthinuria Due to a Homozygous Deletion of the XDH Gene in the Absence of Overt Kidney Stone Disease

Pedro Lisboa Goncalves, Hugo Diniz,Isabel Tavares,Sofia Doria, Juan Dong, McKenna Kyriss,Lynette Fairbanks,Joao Paulo Oliveira

The Nephron journals/Nephron journals（2024）

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GLA Insufficiency Should Not Be Called Fabry Disease

Gunnar Houge,Mirjam Langeveld,Joao-Paulo Oliveira

European Journal of Human Genetics (2024)

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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

Christoph Wanner,Alberto Órtiz,William R. Wilcox,Robert J. Hopkin,Jack Johnson,Elvira Ponce, Johan T. Ebels,Julie L. Batista,Manish Maski,Juan Politei,Ana María Martins,Maryam Banikazemi,Aleš Linhart,Michael Mauer,João Paulo de Oliveira,Frank Weidemann,Dominique P. Germain

Molecular genetics and metabolismno. 3 (2023): 107603-107603

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#5302 REVISITING THE PATHOGENIC ROLE OF THE SLC8A1 GENE IN A FAMILY WITH A NOVEL TERMINAL GROSS DELETION IN THE UMOD GENE

Francisco Gonçalves,Pedro Lisboa Gonçalves,Rita Quental,Susana Fernandes,Sofia Quental,Isabel Tavares,João Paulo Oliveira

Nephrology Dialysis Transplantationno. Supplement_1 (2023)

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Familial Juvenile Hyperuricemic Nephropathy: Revisiting the SLC8A1 Gene, in a Family with a Novel Terminal Gross Deletion in the UMOD Gene

Francisco Goncalves,Pedro Lisboa Goncalves,Rita Quental,Susana Fernandes,Sofia Quental,Isabel Tavares,Joao Paulo Oliveira

NEPHROLOGY DIALYSIS TRANSPLANTATION (2023): I240-I241

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