Renal Tubular Transport, Inborn Errors
"Renal Tubular Transport, Inborn Errors" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Genetic defects in the selective or non-selective transport functions of the KIDNEY TUBULES.
Descriptor ID |
D015499
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MeSH Number(s) |
C12.777.419.815 C13.351.968.419.815 C16.320.565.861 C18.452.648.861
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Concept/Terms |
Renal Tubular Transport, Inborn Errors- Renal Tubular Transport, Inborn Errors
- Renal Tubular Transport Errors
- Kidney Tubular Transport, Inborn Errors
- Renal Tubular Transport, Inborn Error
- Kidney Tubular Transport, Inborn Error
|
Below are MeSH descriptors whose meaning is more general than "Renal Tubular Transport, Inborn Errors".
Below are MeSH descriptors whose meaning is more specific than "Renal Tubular Transport, Inborn Errors".
This graph shows the total number of publications written about "Renal Tubular Transport, Inborn Errors" by people in this website by year, and whether "Renal Tubular Transport, Inborn Errors" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2018 | 0 | 1 | 1 |
2019 | 1 | 0 | 1 |
2020 | 0 | 1 | 1 |
2024 | 0 | 1 | 1 |
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Below are the most recent publications written about "Renal Tubular Transport, Inborn Errors" by people in Profiles.
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RRAGD-Associated Autosomal Dominant Kidney Hypomagnesemia with Cardiomyopathy: A Review on the Clinical Manifestations and Therapeutic Options. Kidney Blood Press Res. 2024; 49(1):637-645.
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Urinary Magnesium in the Evaluation of Hypomagnesemia. JAMA. 2020 Dec 08; 324(22):2320-2321.
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Hypomagnesemia and Survival in Patients with Ovarian Cancer Who Received Chemotherapy with Carboplatin. Oncologist. 2019 06; 24(6):e312-e317.
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Megalin mediates plasma membrane to mitochondria cross-talk and regulates mitochondrial metabolism. Cell Mol Life Sci. 2018 Nov; 75(21):4021-4040.
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A retrospective evaluation of furosemide and mannitol for prevention of cisplatin-induced nephrotoxicity. J Clin Pharm Ther. 2017 Jun; 42(3):286-291.
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Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndrome. Clin Genet. 2014 Sep; 86(3):282-6.