Minimal Change Disease
What's New
Last Posted: Sep 15, 2023
- Nephrotic syndrome with Minimal Change Disease and Atopy in NorthAfrican adults.
Asma Hadhri, et al. La Tunisie medicale 2023 0 (2) 253-258 - Implementation and Feasibility of Clinical Genome Sequencing Embedded Into the Outpatient Nephrology Care for Patients With Proteinuric Kidney Disease.
Maddalena Marasa et al. Kidney Int Rep 2023 8(8) 1638-1647 - NPHS2 gene sequencing results in children of the Azerbaijani population with different types of nephrotic syndrome caused by chronic glomerulonephritis.
Baylarov R, et al. Bratislavske lekarske listy 2019 0 (2) 102-105 - Minimal Change Disease With Nephrotic Syndrome Associated With Coronavirus Disease 2019 After Apolipoprotein L1 Risk Variant Kidney Transplant: A Case Report.
Yamada Masaaki, et al. Transplantation proceedings 2020 0 (9) 2693-2697 - APOL1 genotype-associated morphologic changes among patients with focal segmental glomerulosclerosis.
Zee Jarcy, et al. Pediatric nephrology (Berlin, Germany) 2021 0 (9) 2747-2757 - Molecular Study of Childhood Steroid-Resistant Nephrotic Syndrome: A Hospital-Based Study.
Singh Akanksha, et al. Journal of pediatric genetics 2022 0 (3) 185-191 - Association Between NPHS2 p.R229Q and Focal Segmental Glomerular Sclerosis/Steroid-Resistant Nephrotic Syndrome.
Zhou Qiongxiu, et al. Frontiers in medicine 2022 0 937122 - Homocysteine and IgA nephropathy: observational and Mendelian randomization analyses.
Zhang Yue-Miao, et al. Chinese medical journal 2020 0 (3) 277-284 - Minimal Change Disease Is Associated with Mitochondrial Injury and STING Pathway Activation.
Yu Byung Chul, et al. Journal of clinical medicine 2022 0 (3) - Development and evaluation of deep learning-based segmentation of histologic structures in the kidney cortex with multiple histologic stains.
Jayapandian Catherine P et al. Kidney international 2020 Aug
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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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