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Quoted phrase not found in phrase index: "Bartter disease type 3"
Page 1
Diagnosis of hypokalemia: a problem-solving approach to clinical cases.
Assadi F. Assadi F. Iran J Kidney Dis. 2008 Jul;2(3):115-22. Iran J Kidney Dis. 2008. PMID: 19377223 Free article.
Metabolic acidosis with K/C ratio of 1.5 higher is often due to diabetic ketoacidosis or type 1 or type 2 distal renal tubular acidosis. Metabolic alkalosis with a K/C ratio less than 1.5 and a normal blood pressure is often due to surreptitious vomiting. Metabolic …
Metabolic acidosis with K/C ratio of 1.5 higher is often due to diabetic ketoacidosis or type 1 or type 2 distal renal tubular …
Differential diagnosis of Bartter syndrome, Gitelman syndrome, and pseudo-Bartter/Gitelman syndrome based on clinical characteristics.
Matsunoshita N, Nozu K, Shono A, Nozu Y, Fu XJ, Morisada N, Kamiyoshi N, Ohtsubo H, Ninchoji T, Minamikawa S, Yamamura T, Nakanishi K, Yoshikawa N, Shima Y, Kaito H, Iijima K. Matsunoshita N, et al. Genet Med. 2016 Feb;18(2):180-8. doi: 10.1038/gim.2015.56. Epub 2015 Apr 16. Genet Med. 2016. PMID: 25880437 Free article.
PURPOSE: Phenotypic overlap exists among type III Bartter syndrome (BS), Gitelman syndrome (GS), and pseudo-BS/GS (p-BS/GS), which are clinically difficult to distinguish. ...Of patients with type III BS, GS, and p-BS/GS, 40, 12, and 63%, respec …
PURPOSE: Phenotypic overlap exists among type III Bartter syndrome (BS), Gitelman syndrome (GS), and pseudo-BS/G …
Effects of a long-term lifestyle modification programme on peripheral neuropathy in overweight or obese adults with type 2 diabetes: the Look AHEAD study.
Look AHEAD Research Group. Look AHEAD Research Group. Diabetologia. 2017 Jun;60(6):980-988. doi: 10.1007/s00125-017-4253-z. Epub 2017 Mar 27. Diabetologia. 2017. PMID: 28349174 Free PMC article.
METHODS: Beginning in 2001, a total of 5145 overweight or obese people with type 2 diabetes, aged 45-76 years, participating in the multicentre Look AHEAD (Action for Health in Diabetes) study were randomised to ILI (n = 2570) or to a diabetes support and education …
METHODS: Beginning in 2001, a total of 5145 overweight or obese people with type 2 diabetes, aged 45-76 years, participating in the m …
Effect of nonsteroidal anti-inflammatory drugs in children with Bartter syndrome.
Gasongo G, Greenbaum LA, Niel O, Kwon T, Macher MA, Maisin A, Baudouin V, Dossier C, Deschênes G, Hogan J. Gasongo G, et al. Pediatr Nephrol. 2019 Apr;34(4):679-684. doi: 10.1007/s00467-018-4135-8. Epub 2018 Nov 13. Pediatr Nephrol. 2019. PMID: 30426218
BACKGROUND: Bartter syndrome (BS) is a salt-wasting tubulopathy with induced expression of cyclooxygenase-2 in the macula densa, leading to increased prostaglandin production and hyperreninemia. ...RESULTS: Median age at diagnosis was 0.9 months [IQR 0-6.9]. Seven p …
BACKGROUND: Bartter syndrome (BS) is a salt-wasting tubulopathy with induced expression of cyclooxygenase-2 in the macula dens …
Amikacin-induced type 5 Bartter-like syndrome with severe hypocalcemia.
Chrispal A, Boorugu H, Prabhakar AT, Moses V. Chrispal A, et al. J Postgrad Med. 2009 Jul-Sep;55(3):208-10. doi: 10.4103/0022-3859.57407. J Postgrad Med. 2009. PMID: 19884751
Aminoglycoside-induced renal tubular dysfunction could result in diffuse damage or manifest as a Fanconi-like syndrome, Bartter-like syndrome, or distal renal tubular acidosis. We discuss a patient who developed severe renal tubular dysfunction secondary to s …
Aminoglycoside-induced renal tubular dysfunction could result in diffuse damage or manifest as a Fanconi-like syndrome, Bartter …
Hypokalemic paralysis in a middle-aged female with classic Bartter syndrome.
Chiang WF, Lin SH, Chan JS, Lin SH. Chiang WF, et al. Clin Nephrol. 2014 Feb;81(2):146-50. doi: 10.5414/CN107606. Clin Nephrol. 2014. PMID: 22854165
Inherited classic Bartter syndrome (cBS) is an autosomal recessive renal tubular disorder resulting from inactivating mutations in the asolateral chloride channel (C1C-Kb) and usually presents in early infancy or childhood with mild to moderate hypokalemia. ...These …
Inherited classic Bartter syndrome (cBS) is an autosomal recessive renal tubular disorder resulting from inactivating mutation …