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Journal Abstract Search

172 related items for PubMed ID: 35952717

  • 1. Late onset Bartter syndrome: Bartter syndrome type 2 presenting with isolated nephrocalcinosis and high parathyroid hormone levels mimicking primary hyperparathyroidism.
    Yıldız G, Torun Bayram M, Çinleti T, Koç A, Soylu A, Kavukçu S.
    J Pediatr Endocrinol Metab; 2022 Oct 26; 35(10):1298-1301. PubMed ID: 35952717
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  • 2. Isolated nephrocalcinosis due to compound heterozygous mutations in renal outer medullary potassium channel.
    Khandelwal P, Sabanadesan J, Sinha A, Hari P, Bagga A.
    CEN Case Rep; 2020 Aug 26; 9(3):232-236. PubMed ID: 32185747
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  • 3. Eight novel KCNJ1 variants and parathyroid hormone overaction or resistance in 5 probands with Bartter syndrome type 2.
    Zuo J, Guo W, Wang S, Lang Y, Wang S, Shi X, Zhang R, Zhao X, Han Y, Shao L.
    Clin Chim Acta; 2020 Dec 26; 511():248-254. PubMed ID: 33058840
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  • 4. Antenatal Bartter syndrome presenting as hyperparathyroidism with hypercalcemia and hypercalciuria: a case report and review.
    Gross I, Siedner-Weintraub Y, Simckes A, Gillis D.
    J Pediatr Endocrinol Metab; 2015 Jul 26; 28(7-8):943-6. PubMed ID: 25741940
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  • 5. Clinical exome sequencing uncovers an unsuspected diagnosis of Bartter syndrome type 2 in a child with incidentally detected nephrocalcinosis.
    Saha A, Pande P, Vala K, Kapadia S, Patel H.
    CEN Case Rep; 2022 Nov 26; 11(4):417-421. PubMed ID: 35195872
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  • 6. Nephrocalcinosis as adult presentation of Bartter syndrome type II.
    Huang L, Luiken GP, van Riemsdijk IC, Petrij F, Zandbergen AA, Dees A.
    Neth J Med; 2014 Feb 26; 72(2):91-3. PubMed ID: 24659592
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  • 7. A novel compound heterozygous ROMK mutation presenting as late onset Bartter syndrome associated with nephrocalcinosis and elevated 1,25(OH)(2) vitamin D levels.
    Sharma A, Linshaw MA.
    Clin Exp Nephrol; 2011 Aug 26; 15(4):572-6. PubMed ID: 21431899
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  • 8. A novel SLC12A1 gene mutation associated with hyperparathyroidism, hypercalcemia, nephrogenic diabetes insipidus, and nephrocalcinosis in four patients.
    Wongsaengsak S, Vidmar AP, Addala A, Kamil ES, Sequeira P, Fass B, Pitukcheewanont P.
    Bone; 2017 Apr 26; 97():121-125. PubMed ID: 28095294
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  • 9. Transient hyponatremia of prematurity caused by mild Bartter syndrome type II: a case report.
    Verma S, Chanchlani R, Siu VM, Filler G.
    BMC Pediatr; 2020 Jun 26; 20(1):311. PubMed ID: 32590952
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  • 12. Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: Bartter and Gitelman syndromes.
    Bettinelli A, Bianchetti MG, Girardin E, Caringella A, Cecconi M, Appiani AC, Pavanello L, Gastaldi R, Isimbaldi C, Lama G.
    J Pediatr; 1992 Jan 26; 120(1):38-43. PubMed ID: 1731022
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  • 13. Dent-2 disease with a Bartter-like phenotype caused by the Asp631Glu mutation in the OCRL gene.
    Drosataki E, Maragkou S, Dermitzaki K, Stavrakaki I, Lygerou D, Latsoudis H, Pleros C, Petrakis I, Zaganas I, Stylianou K.
    BMC Nephrol; 2022 May 12; 23(1):182. PubMed ID: 35549682
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  • 15. Hypocalcemia as the Initial Presentation of Type 2 Bartter Syndrome: A Family Report.
    London S, Levine MA, Li D, Spiegel R, Lebel A, Halevy R, Tenenbaum-Rakover Y.
    J Clin Endocrinol Metab; 2022 Mar 24; 107(4):e1679-e1688. PubMed ID: 34751387
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  • 18. Hypercalciuria with Bartter syndrome: evidence for an abnormality of vitamin D metabolism.
    Restrepo de Rovetto C, Welch TR, Hug G, Clark KE, Bergstrom W.
    J Pediatr; 1989 Sep 24; 115(3):397-404. PubMed ID: 2671327
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  • 20. Parathyroid Disorders.
    Sell J, Ramirez S, Partin M.
    Am Fam Physician; 2022 Mar 01; 105(3):289-298. PubMed ID: 35289573
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