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2,280 results

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Page 1
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.
Bartter and Gitelman syndromes are conditions characterized by renal salt-wasting. ...Hypokalemic hypochloremic metabolic alkalosis is the common feature. Bartter variants may be associated with polyuria and weakness. Gitelman syndrome is often subtle, and ty …
Bartter and Gitelman syndromes are conditions characterized by renal salt-wasting. ...Hypokalemic hypochloremic metabolic alkalosis i …
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.
BACKGOUND: Bartter's syndrome (BS) is a rare group of salt losing tubulopathies due to the impairment of transport mechanisms at the thick ascending limb of the Henle's loop. ...
BACKGOUND: Bartter's syndrome (BS) is a rare group of salt losing tubulopathies due to the impairment of transport mechanisms …
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. ...
Bartter syndrome is a rare inherited salt-losing renal tubular disorder characterized by secondary hyperaldosteronism with hyp …
Bartter's and Gitelman's syndrome.
Seyberth HW, Weber S, Kömhoff M. Seyberth HW, et al. Curr Opin Pediatr. 2017 Apr;29(2):179-186. doi: 10.1097/MOP.0000000000000447. Curr Opin Pediatr. 2017. PMID: 27906863 Review.
PURPOSE OF REVIEW: The clinical presentations of Bartter's syndrome and Gitelman's syndrome will be reviewed including two most recently described hypokalemic salt-losing tubulopathies. ...On the basis of pharmacologic tests (pharmacotyping), it appears that …
PURPOSE OF REVIEW: The clinical presentations of Bartter's syndrome and Gitelman's syndrome will be reviewed including …
Bartter syndrome.
Hebert SC. Hebert SC. Curr Opin Nephrol Hypertens. 2003 Sep;12(5):527-32. doi: 10.1097/00041552-200309000-00008. Curr Opin Nephrol Hypertens. 2003. PMID: 12920401 Review.
Consequently, individuals with Bartter syndrome exhibit renal salt wasting and lowered blood pressure, hypokalemic metabolic alkalosis and hypercalciuria with a variable risk of renal stones. ...SUMMARY: Five genes have been identified as causing Bartter s …
Consequently, individuals with Bartter syndrome exhibit renal salt wasting and lowered blood pressure, hypokalemic metabolic a …
Bartter's syndrome.
Bartter FC. Bartter FC. Urol Clin North Am. 1977 Jun;4(2):253-61. Urol Clin North Am. 1977. PMID: 331616 Review.
The syndrome of juxtaglomerular hyperplasia with hypokalemic, hypochloremic alkalosis, aldosteronism, hyperreninemia, and normal blood pressure may be familial, and is probably inherited as a recessive trait. ...These and other results suggest a partial control of renin se …
The syndrome of juxtaglomerular hyperplasia with hypokalemic, hypochloremic alkalosis, aldosteronism, hyperreninemia, and normal bloo …
Bartter syndrome: An infrequent tubulopathy of prenatal onset.
Gómez de la F CL, Novoa P JM, Caviedes R N. Gómez de la F CL, et al. Rev Chil Pediatr. 2019 Aug;90(4):437-442. doi: 10.32641/rchped.v90i4.932. Rev Chil Pediatr. 2019. PMID: 31859717 Free article. Review. English, Spanish.
INTRODUCTION: Bartter syndrome (BS) is a rare inherited tubulopathy that has two presentation forms, the first one is a severe form of antenatal onset (neonatal Bartter) and the second one is a later on set form during the first years of life (classic Bart …
INTRODUCTION: Bartter syndrome (BS) is a rare inherited tubulopathy that has two presentation forms, the first one is a severe …
Bartter's syndrome.
Chan JC. Chan JC. Nephron. 1980;26(4):155-62. doi: 10.1159/000181973. Nephron. 1980. PMID: 7001260 Review. No abstract available.
Bartter's syndrome.
Gill JR Jr. Gill JR Jr. Annu Rev Med. 1980;31:405-19. doi: 10.1146/annurev.me.31.020180.002201. Annu Rev Med. 1980. PMID: 6994620 Review. No abstract available.
Cystic Fibrosis Presenting as Pseudo-Bartter Syndrome: An Important Diagnosis that is Missed!
Mantoo MR, Kabra M, Kabra SK. Mantoo MR, et al. Indian J Pediatr. 2020 Sep;87(9):726-732. doi: 10.1007/s12098-020-03342-8. Epub 2020 Jun 5. Indian J Pediatr. 2020. PMID: 32504456 Review.
There may be a significant clinical overlap between the Classic Bartter syndrome, Gitelman syndrome and CF presenting as Pseudo-Bartter syndrome, especially in early childhood. This review focuses on Pseudo-Bartter syndrome in CF, …
There may be a significant clinical overlap between the Classic Bartter syndrome, Gitelman syndrome and CF presenting a …
2,280 results