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Quoted phrase not found in phrase index: "Distal Renal Tubular Acidosis, Dominant"
Page 1
The pathophysiology of distal renal tubular acidosis.
Wagner CA, Unwin R, Lopez-Garcia SC, Kleta R, Bockenhauer D, Walsh S. Wagner CA, et al. Nat Rev Nephrol. 2023 Jun;19(6):384-400. doi: 10.1038/s41581-023-00699-9. Epub 2023 Apr 4. Nat Rev Nephrol. 2023. PMID: 37016093 Review.
Impaired acid excretion by the collecting duct system causes distal renal tubular acidosis (dRTA), which is characterized by the failure to acidify urine below pH 5.5. ...Inherited forms of dRTA are caused by variants in SLC4A1, ATP6V1B1, ATP6V0A4, FOX …
Impaired acid excretion by the collecting duct system causes distal renal tubular acidosis (dRTA), which is char …
Mechanism and application of metformin in kidney diseases: An update.
Song A, Zhang C, Meng X. Song A, et al. Biomed Pharmacother. 2021 Jun;138:111454. doi: 10.1016/j.biopha.2021.111454. Epub 2021 Mar 11. Biomed Pharmacother. 2021. PMID: 33714781 Free article. Review.
In various acute kidney diseases (AKI) animal models, metformin protects renal tubular cells from inflammation, apoptosis, reactive oxygen stress (ROS), endoplasmic reticulum (ER) stress, epithelial-mesenchymal transition (EMT) via AMPK activation. ...As the common …
In various acute kidney diseases (AKI) animal models, metformin protects renal tubular cells from inflammation, apoptosis, rea …
Molecular investigation of distal renal tubular acidosis in Tunisia, evidence for founder mutations.
Nagara M, Voskarides K, Nouira S, Ben Halim N, Kefi R, Aloulou H, Romdhane L, Ben Abdallah R, Ben Rhouma F, Aissa K, Boughamoura L, Kammoun T, Azzouz H, Abroug S, Ben Turkia H, Ayadi A, Mrad R, Chabchoub I, Hachicha M, Chemli J, Deltas C, Abdelhak S. Nagara M, et al. Genet Test Mol Biomarkers. 2014 Nov;18(11):741-8. doi: 10.1089/gtmb.2014.0175. Epub 2014 Oct 6. Genet Test Mol Biomarkers. 2014. PMID: 25285676 Free PMC article. Clinical Trial.
BACKGROUND: Distal renal tubular acidosis (dRTA) is a rare genetic disease caused by mutations in different genes involved in the secretion of H+ ions in the intercalated cells of the collecting duct. Both autosomal dominant and recessive forms …
BACKGROUND: Distal renal tubular acidosis (dRTA) is a rare genetic disease caused by mutations in different gene …
A distal renal tubular acidosis showing hyperammonemia and hyperlactacidemia.
Ripoli C, Pinna A, Marras S, Fenu ML, Nurchi AM. Ripoli C, et al. Pediatr Med Chir. 2012 Jul-Aug;34(4):198-201. doi: 10.4081/pmc.2012.74. Pediatr Med Chir. 2012. PMID: 23173413
INTRODUCTION: distal renal tubular acidosis (dRTA) presents itself with variable clinical manifestations and often with late expressions that impact on prognosis. CASE REPORT: A 45-day-old male infant was admitted with stopping growth, difficult …
INTRODUCTION: distal renal tubular acidosis (dRTA) presents itself with variable clinical manifestations …
Increased intrarenal post-glomerular blood flow is a key condition for the development of calcineurin inhibitor-induced renal tubular acidosis in kidney transplant recipients.
Kaneko S, Usui J, Takahashi K, Oda T, Yamagata K. Kaneko S, et al. Clin Transplant. 2022 Jun;36(6):e14648. doi: 10.1111/ctr.14648. Epub 2022 Mar 20. Clin Transplant. 2022. PMID: 35293652
BACKGROUND: Hyperchloremic metabolic acidosis (HCMA) from renal tubular acidosis (RTA) is common in kidney transplant (KT) recipients. ...We determined the potential causes of HCMA in LDKTRs at 3 months (m) and 1 year (y) post-KT. We examined renal …
BACKGROUND: Hyperchloremic metabolic acidosis (HCMA) from renal tubular acidosis (RTA) is common in kidney trans …
Combination of furosemide and fludrocortisone as a loading test for diagnosis of distal renal tubular acidosis in a pediatric case.
Kyono Y, Nozu K, Nakagawa T, Takami Y, Fujita H, Ioroi T, Kugo M, Iijima K, Kamiyoshi N. Kyono Y, et al. CEN Case Rep. 2020 Feb;9(1):81-86. doi: 10.1007/s13730-019-00432-1. Epub 2019 Nov 8. CEN Case Rep. 2020. PMID: 31705302 Free PMC article.
Renal tubular acidosis (RTA) is a rare disease caused by a defect of urinary acidification. ...Recently, a loading test with the combination of furosemide and fludrocortisone was reported to be an alternative to the ammonium chloride loading test, with 100% s …
Renal tubular acidosis (RTA) is a rare disease caused by a defect of urinary acidification. ...Recently, a loading test …
Acetaminophen-induced anion gap metabolic acidosis and 5-oxoprolinuria (pyroglutamic aciduria) acquired in hospital.
Humphreys BD, Forman JP, Zandi-Nejad K, Bazari H, Seifter J, Magee CC. Humphreys BD, et al. Am J Kidney Dis. 2005 Jul;46(1):143-6. doi: 10.1053/j.ajkd.2005.04.010. Am J Kidney Dis. 2005. PMID: 15983968
A rare cause of high anion gap acidosis is 5-oxoproline (pyroglutamic acid), an organic acid intermediate of the gamma-glutamyl cycle. ...Predisposing factors in this case included renal dysfunction and sepsis. Clinicians need to be aware of this unusual cause of an …
A rare cause of high anion gap acidosis is 5-oxoproline (pyroglutamic acid), an organic acid intermediate of the gamma-glutamyl cycle …
Type 1 renal tubular acidosis with sensorineural deafness.
Mythili A, Subrahmanyam KA, Kumar KD. Mythili A, et al. J Assoc Physicians India. 2007 Apr;55:303-5. J Assoc Physicians India. 2007. PMID: 17694794
We report a case of Type 1 Renal Tubular Acidosis (RTA) in association with sensorineural deafness. Inherited Type 1 RTA is usually autosomal dominant, though there is a rarer recessive form associated with nerve deafness. ...
We report a case of Type 1 Renal Tubular Acidosis (RTA) in association with sensorineural deafness. Inherited Type 1 RT …