Zobrazeno 1 - 10
of 194
pro vyhledávání: '"Post-infectious glomerulonephritis"'
Publikováno v:
Nigerian Journal of Paediatrics, Vol 43, Iss 2, Pp 95-98 (2024)
Background: Acute post infectious glomerulonephritis (APIGN) describes a wide range of glomerulonephritis characterized by an immunologic response of the kidney to varieties of infectious agent commonly bacteria. It is characterized by an abrupt onse
Externí odkaz:
https://doaj.org/article/1cd1f976e3294b8eb1755c7782957dc8
Publikováno v:
Journal of Nepal Medical Association, Vol 62, Iss 272 (2024)
Introduction: Post infectious glomerulonephritis remains the most common cause leading to the majority of hospital admissions in children of developing countries like ours. The aim of our study was to find the prevalence of post infectious glomerulon
Externí odkaz:
https://doaj.org/article/0d58350aec5d477b9f16c869fe19bae3
Autor:
Sumaiya Ahmed, David Massicotte-Azarniouch, Mark Canney, Clare Booth, Paula Blanco, Gregory L. Hundemer
Publikováno v:
BMC Nephrology, Vol 23, Iss 1, Pp 1-5 (2022)
Abstract Background The clinical trajectory for patients with primary membranous nephropathy ranges widely from spontaneous remission to a rapid decline in kidney function. Etiologies for rapid progression with membranous nephropathy include concurre
Externí odkaz:
https://doaj.org/article/ea20c30122104abc97eb5406ded90629
Publikováno v:
Liaquat National Journal of Primary Care, Vol 4, Iss 1, Pp 59-62 (2022)
Post-Infectious Glomerulonephritis (PIGN) is a disease of childhood. It is an important cause of acute kidney injury in childhood. It is now frequently identified in elderly people with compromised immune status and risk factors like malignancy and
Externí odkaz:
https://doaj.org/article/2dd19e3d3ce342fe96d3b8b2d244e229
Akademický článek
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Autor:
Heba R. Gouda, Iman M. Talaat, Amal Bouzid, Hoda El-Assi, Amira Nabil, Thenmozhi Venkatachalam, Poorna Manasa Bhamidimarri, Inken Wohlers, Amena Mahdami, Saba EL-Gendi, Ahmed ElKoraie, Hauke Busch, Maha Saber-Ayad, Rifat Hamoudi, Nahed Baddour
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Glomerulonephritis (GN) is a complex disease with intricate underlying pathogenic mechanisms. The possible role of underlying complement dysregulation is not fully elucidated in some GN subsets, especially in the setting of autoimmunity or infection.
Externí odkaz:
https://doaj.org/article/ab073b6271fc47a0a92f1aa18732fd6e
Autor:
Precil Diego Miranda de Menezes Neves, Bernardo Vergara Reichert, Ramaiane Aparecida Bridi, Luis Yu, Cristiane Bitencourt Dias, Rafaela Brito Bezerra Pinheiro, Leonardo de Abreu Testagrossa, Lívia Barreira Cavalcante, Denise Maria Avancini Costa Malheiros, Lectícia Barbosa Jorge, Viktoria Woronik
Publikováno v:
BMC Nephrology, Vol 21, Iss 1, Pp 1-6 (2020)
Abstract Background Sickle cell disease (SCD) is a highly prevalent genetic disease worldwide. In the natural evolution of SCD, glomerular lesions can develop, presenting histopathological patterns of segmental or focal membranoproliferative glomerul
Externí odkaz:
https://doaj.org/article/e10a17ebbc224e64929eff2d105244a3
Akademický článek
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Autor:
Hassib Chehade, Gabriella Guzzo, Francois Cachat, Samuel Rotman, Daniel Teta, Giuseppe Pantaleo, Salima Sadallah, Amita Sharma, Ivy A. Rosales, Nina Tolkoff-Rubin, Manuel Pascual
Publikováno v:
Frontiers in Medicine, Vol 8 (2021)
Acute post-infections glomerulonephritis (APIGN) is a frequent cause of glomerulonephritis and represents the most common cause of acute glomerulonephritis in children. It can evolve to severe acute renal failure and chronic kidney disease or even en
Externí odkaz:
https://doaj.org/article/88f4d7ec87f44cde87e5766a17fb0ad3
Autor:
Ghazal Ghasempoor Dabaghi, Mehrdad Rabiee Rad, Muhammed Mubarak, Romina Amir Sardari, Golnaz K Holm, Hamid Nasri
Publikováno v:
Journal of Preventive Epidemiology, Vol 6, Iss 2, Pp e30-e30 (2021)
Immunoglobulin A nephropathy (IgAN) is the most common glomerulonephritis worldwide. However, its incidence and prevalence vary depending on racial and geographical factors. IgAN is a highly heterogeneous disease with wide clinical and pathological v
Externí odkaz:
https://doaj.org/article/ada1bf736ac647e7a711e838f47e3223