Membranoproliferative Glomerulonephritis
What's New
Last Posted: Jan 29, 2024
- Anti-factor B antibodies in atypical hemolytic uremic syndrome.
Priyanka Khandelwal, et al. Pediatric nephrology (Berlin, Germany) 2024 0 - Low C3 in a 4-month-old baby: is it a problem?
Gül?ah Kaya Aksoy, et al. Pediatric nephrology (Berlin, Germany) 2023 0 - Genetic investigation of Nordic patients with complement-mediated kidney diseases.
Viktor Rydberg, et al. Frontiers in immunology 2023 0 1254759 - The Association of Class I and II Human Leukocyte Antigen Serotypes With End-Stage Kidney Disease Due to Membranoproliferative Glomerulonephritis and Dense Deposit Disease.
Halimat Afolabi, et al. American journal of kidney diseases : the official journal of the National Kidney Foundation 2023 0 - Rare Variants in Complement Gene in C3 Glomerulopathy and Immunoglobulin-Mediated Membranoproliferative Glomerulonephritis.
Marie Sophie Meuleman, et al. Clinical journal of the American Society of Nephrology : CJASN 2023 0 - Outcome of membranoproliferative glomerulonephritis and C3-glomerulopathy in children and adolescents.
Holle Johannes, et al. Pediatric nephrology (Berlin, Germany) 2018 0 (12) 2289-2298 - Lack of Evidence for an Association between Previous HEV Genotype-3 Exposure and Glomerulonephritis in General.
Pischke Sven, et al. Pathogens (Basel, Switzerland) 2022 0 (1) - Prospects of genetic testing for steroid-resistant nephrotic syndrome in Nigerian children: a narrative review of challenges and opportunities.
Anigilaje Emmanuel Ademola et al. International journal of nephrology and renovascular disease 2019 12119-136 - The role of MEFV mutations in the concurrent disorders observed in patients with familial Mediterranean fever.
Güncan Sabri, et al. European journal of rheumatology 2016 9 (3) 118-121 - Complement gene variants determine the risk of immunoglobulin-associated MPGN and C3 glomerulopathy and predict long-term renal outcome.
Iatropoulos Paraskevas, et al. Molecular immunology 2016 2 131-142
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Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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