Lupus Nephritis
What's New
Last Posted: Mar 23, 2023
- Genetics of longitudinal kidney function in children and adults with systemic lupus erythematosus.
Thai-Son Tang et al. Rheumatology (Oxford, England) 2023 - Natural Language Processing in Electronic Health Records in relation to healthcare decision-making: A systematic review.
Elias Hossain et al. Computers in biology and medicine 2023 155106649 - Prediction Models of Treatment Response in Lupus Nephritis.
Ayoub Isabelle et al. Kidney international 2021 - Deep Learning-Based Artificial Intelligence System for Automatic Assessment of Glomerular Pathological Findings in Lupus Nephritis.
Zheng Zhaohui et al. Diagnostics (Basel, Switzerland) 2021 11(11) - Glomerular Disease Classification and Lesion Identification by Machine Learning.
Yang Cheng-Kun et al. Biomedical journal 2021 - Influence of glutathione S transferase A1 gene polymorphism (-69C > T, rs3957356) on intravenous cyclophosphamide efficacy and side effects: a case-control study in Egyptian patients with lupus nephritis.
Attia Doaa H S et al. Clinical rheumatology 2020 Jul - An Exosomal Urinary miRNA Signature for Early Diagnosis of Renal Fibrosis in Lupus Nephritis.
Solé Cristina et al. Cells 2019 8(8) - Genome-wide assessment of genetic risk for systemic lupus erythematosus and disease severity
L Chen, BioRXIV, December 13, 2019 - Precision medicine in lupus nephritis: can biomarkers get us there?
Caster Dawn J et al. Translational research : the journal of laboratory and clinical medicine 2018 Aug - Genetics and pathogenesis of systemic lupus erythematosus and lupus nephritis.
Mohan Chandra et al. Nat Rev Nephrol 2015 Jun (6) 329-341
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About Rare Diseases PHGKB
Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
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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