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.
MeSH Number(s)
C12.777.419.815
C13.351.968.419.815
C16.320.565.861
C18.452.648.861
Concept/Terms
Renal Tubular Transport, Inborn Errors- Renal Tubular Transport, Inborn Errors
- Renal Tubular Transport, Inborn Error
- Renal Tubular Transport Errors
- Kidney Tubular Transport, Inborn Error
- Kidney Tubular Transport, Inborn Errors
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 Harvard Catalyst Profiles by year, and whether "Renal Tubular Transport, Inborn Errors" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 1 | 0 | 1 |
| 2012 | 1 | 0 | 1 |
| 2013 | 0 | 1 | 1 |
| 2016 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2019 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 1 |
Below are the most recent publications written about "Renal Tubular Transport, Inborn Errors" by people in Profiles.
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Genetic epidemiological analysis of hypouricaemia from 4993 Japanese on non-functional variants of URAT1/SLC22A12 gene. Rheumatology (Oxford). 2022 03 02; 61(3):1276-1281.
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Diagnostic Dilemma in an Adolescent Girl with an Eating Disorder, Intellectual Disability, and Hypomagnesemia. Nephron. 2021; 145(6):717-720.
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Case report: extreme coronary calcifications and hypomagnesemia in a patient with a 17q12 deletion involving HNF1B. BMC Nephrol. 2019 09 09; 20(1):353.
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Hypercalciuria and nephrolithiasis: Expanding the renal phenotype of Donnai-Barrow syndrome. Clin Genet. 2018 07; 94(1):187-188.
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Claudin 19-based familial hypomagnesemia with hypercalciuria and nephrocalcinosis in a sibling pair. Clin Nephrol. 2016 Jun; 85(6):346-52.
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Out-of-hospital use of proton pump inhibitors and hypomagnesemia at hospital admission: a nested case-control study. Am J Kidney Dis. 2013 Oct; 62(4):730-7.
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Electrolyte disorders in community subjects: prevalence and risk factors. Am J Med. 2013 Mar; 126(3):256-63.
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The molecular basis of blood pressure variation. Pediatr Nephrol. 2013 Mar; 28(3):387-99.
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Clinical and molecular characterization of Turkish patients with familial hypomagnesaemia: novel mutations in TRPM6 and CLDN16 genes. Nephrol Dial Transplant. 2012 Feb; 27(2):667-73.
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Cognitive and psychosocial development in children with familial hypomagnesaemia. Magnes Res. 2011 Mar; 24(1):7-12.