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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1975 1
1985 1
1993 1
1994 1
1996 2
1997 1
1998 1
1999 1
2004 1
2006 2
2008 1
2009 1
2010 3
2011 3
2012 2
2013 1
2015 2
2018 2
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2020 4
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2023 3
2024 0

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39 results

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Page 1
Hypertrophic Pyloric Stenosis.
Rich BS, Dolgin SE. Rich BS, et al. Pediatr Rev. 2021 Oct;42(10):539-545. doi: 10.1542/pir.2020-003277. Pediatr Rev. 2021. PMID: 34599053
Patients typically present with nonbilious projectile emesis after feeds that may result in hypokalemic, hypochloremic metabolic alkalosis. Although inability to tolerate feeds is frequently seen with self-limited conditions such as reflux, a low threshold to …
Patients typically present with nonbilious projectile emesis after feeds that may result in hypokalemic, hypochloremic metabolic
Bartter Syndrome and Gitelman Syndrome.
Fulchiero R, Seo-Mayer P. Fulchiero R, et al. Pediatr Clin North Am. 2019 Feb;66(1):121-134. doi: 10.1016/j.pcl.2018.08.010. Pediatr Clin North Am. 2019. PMID: 30454738 Review.
Clinical presentations range from severe antenatal disease to asymptomatic with incidental diagnosis. Hypokalemic hypochloremic metabolic alkalosis is the common feature. Bartter variants may be associated with polyuria and weakness. ...
Clinical presentations range from severe antenatal disease to asymptomatic with incidental diagnosis. Hypokalemic hypochloremic me
Diagnosis and management of Bartter syndrome: executive summary of the consensus and recommendations from the European Rare Kidney Disease Reference Network Working Group for Tubular Disorders.
Konrad M, Nijenhuis T, Ariceta G, Bertholet-Thomas A, Calo LA, Capasso G, Emma F, Schlingmann KP, Singh M, Trepiccione F, Walsh SB, Whitton K, Vargas-Poussou R, Bockenhauer D. Konrad M, et al. Kidney Int. 2021 Feb;99(2):324-335. doi: 10.1016/j.kint.2020.10.035. Kidney Int. 2021. PMID: 33509356 Free article.
Bartter syndrome is a rare inherited salt-losing renal tubular disorder characterized by secondary hyperaldosteronism with hypokalemic and hypochloremic metabolic alkalosis and low to normal blood pressure. The primary pathogenic mechanism is defective salt r …
Bartter syndrome is a rare inherited salt-losing renal tubular disorder characterized by secondary hyperaldosteronism with hypokalemic and …
Bartter's syndrome: clinical findings, genetic causes and therapeutic approach.
Mrad FCC, Soares SBM, de Menezes Silva LAW, Dos Anjos Menezes PV, Simões-E-Silva AC. Mrad FCC, et al. World J Pediatr. 2021 Feb;17(1):31-39. doi: 10.1007/s12519-020-00370-4. Epub 2020 Jun 1. World J Pediatr. 2021. PMID: 32488762 Review.
Main clinical and biochemical alterations in BS include polyuria, dehydration, hypokalemia, hypochloremic metabolic alkalosis, hyperreninemia, high levels of prostaglandins, normal or low blood pressure, hypercalciuria and failure to thrive. ...
Main clinical and biochemical alterations in BS include polyuria, dehydration, hypokalemia, hypochloremic metabolic alkalos
Pathophysiology of Diuretic Resistance and Its Implications for the Management of Chronic Heart Failure.
Wilcox CS, Testani JM, Pitt B. Wilcox CS, et al. Hypertension. 2020 Oct;76(4):1045-1054. doi: 10.1161/HYPERTENSIONAHA.120.15205. Epub 2020 Aug 24. Hypertension. 2020. PMID: 32829662 Free PMC article. Review.
Pathophysiological mechanisms of diuretic resistance include an inappropriately high daily salt intake that exceeds the acute diuretic-induced salt loss, hyponatremia or hypokalemic, hypochloremic metabolic alkalosis, and reflex activation of the renal nerves …
Pathophysiological mechanisms of diuretic resistance include an inappropriately high daily salt intake that exceeds the acute diuretic-induc …
The utility of next generation sequencing in the correct diagnosis of congenital hypochloremic hypokalemic metabolic alkalosis.
Ben-David Y, Halevy R, Sakran W, Zehavi Y, Spiegel R. Ben-David Y, et al. Eur J Med Genet. 2019 Oct;62(10):103728. doi: 10.1016/j.ejmg.2019.103728. Epub 2019 Jul 17. Eur J Med Genet. 2019. PMID: 31325522
Persistent hypokalemic hypochloremic metabolic alkalosis represents a heterogeneous group of genetic disorders of which the most common is Bartter syndrome (BS). BS is an inherited renal tubulopathy caused by defective salt reabsorption in the thick ascending …
Persistent hypokalemic hypochloremic metabolic alkalosis represents a heterogeneous group of genetic disorders of which …
Neonatal Bartter syndrome.
Parkash J, Muhammad Sohail Salat, Khan IA. Parkash J, et al. J Coll Physicians Surg Pak. 2006 Aug;16(8):548-50. J Coll Physicians Surg Pak. 2006. PMID: 16899189
She was initially suffering from respiratory distress consistent with idiopathic respiratory distress syndrome, and altered electrolyte imbalance with hyponatremia, hypokalemia and hypochloremic metabolic alkalosis. However, during the third week of life when …
She was initially suffering from respiratory distress consistent with idiopathic respiratory distress syndrome, and altered electrolyte imba …
Bartter's and Gitelman's syndromes: from gene to clinic.
Naesens M, Steels P, Verberckmoes R, Vanrenterghem Y, Kuypers D. Naesens M, et al. Nephron Physiol. 2004;96(3):p65-78. doi: 10.1159/000076752. Nephron Physiol. 2004. PMID: 15056980 Review.
Bartter's and Gitelman's syndromes are characterized by hypokalemia, normal to low blood pressure and hypochloremic metabolic alkalosis. Recently, investigators have been able to demonstrate mutations of six genes encoding several renal tubular transporters a …
Bartter's and Gitelman's syndromes are characterized by hypokalemia, normal to low blood pressure and hypochloremic metabolic
39 results