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Journal Abstract Search
160 related items for PubMed ID: 35723735
21. Hypochloremic metabolic alkalosis and failure to thrive: answer. Querfeld U, Lechner S, Janecke AR. Pediatr Nephrol; 2011 Jun; 26(6):895-6. PubMed ID: 20981452 [No Abstract] [Full Text] [Related]
22. Should isolated Pseudo-Bartter syndrome be considered a CFTR-related disorder of infancy? Poli P, De Rose DU, Timpano S, Savoldi G, Padoan R. Pediatr Pulmonol; 2019 Oct; 54(10):1578-1583. PubMed ID: 31328366 [Abstract] [Full Text] [Related]
23. Hypokalemic alkalosis, hyperreninemia, aldosteronism, normal blood pressure and normal juxtaglomerular apparatus--a new syndrome of renal alkalosis. Barakat AY, Francis YK, Mufarrij AA. Int J Pediatr Nephrol; 1986 Oct; 7(2):99-100. PubMed ID: 3522459 [Abstract] [Full Text] [Related]
26. Inherited primary renal tubular hypokalemic alkalosis: a review of Gitelman and Bartter syndromes. Shaer AJ. Am J Med Sci; 2001 Dec; 322(6):316-32. PubMed ID: 11780689 [Abstract] [Full Text] [Related]
27. 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. Eur J Med Genet; 2019 Oct; 62(10):103728. PubMed ID: 31325522 [Abstract] [Full Text] [Related]
30. Analyses of subjects with hypokalemic metabolic alkolosis, Gitelman's and Bartter's syndrome. Onem Y, Kucukardali Y, Sahan B, Atasoyu EM, Ipcioğlu O, Terekeci H, Solmazgul E, Top C, Oktenli C. Ren Fail; 2008 Oct; 30(7):691-4. PubMed ID: 18704817 [Abstract] [Full Text] [Related]
36. Expanding the spectrum of genetic mutations in antenatal Bartter syndrome type II. Fretzayas A, Gole E, Attilakos A, Daskalaki A, Nicolaidou P, Papadopoulou A. Pediatr Int; 2013 Jun; 55(3):371-3. PubMed ID: 23782368 [Abstract] [Full Text] [Related]
37. The Case ∣ Metabolic alkalosis in a patient with cystic fibrosis. Geara AS, Parikh A, Rekhtman Y, Rao MK. Kidney Int; 2012 Feb; 81(4):421-2. PubMed ID: 22289798 [No Abstract] [Full Text] [Related]