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Journal Abstract Search

128 related items for PubMed ID: 38062639

  • 1. Recurrent transient severe hypocalcaemia in two siblings with type 1 Bartter syndrome.
    Kanda J, Kanda S, Hayashi Y, Nozu K, Ariji S, Shimoda M, Ono M, Kanda S, Yokoyama S, Takahashi K.
    Nephrology (Carlton); 2024 Mar; 29(3):164-167. PubMed ID: 38062639
    [Abstract] [Full Text] [Related]

  • 2. 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; 511():248-254. PubMed ID: 33058840
    [Abstract] [Full Text] [Related]

  • 3. Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional study.
    Verploegen MFA, Vargas-Poussou R, Walsh SB, Alpay H, Amouzegar A, Ariceta G, Atmis B, Bacchetta J, Bárány P, Baron S, Bayrakci US, Belge H, Besouw M, Blanchard A, Bökenkamp A, Boyer O, Burgmaier K, Calò LA, Decramer S, Devuyst O, van Dyck M, Ferraro PM, Fila M, Francisco T, Ghiggeri GM, Gondra L, Guarino S, Hooman N, Hoorn EJ, Houillier P, Kamperis K, Kari JA, Konrad M, Levtchenko E, Lucchetti L, Lugani F, Marzuillo P, Mohidin B, Neuhaus TJ, Osman A, Papizh S, Perelló M, Rookmaaker MB, Conti VS, Santos F, Sawaf G, Serdaroglu E, Szczepanska M, Taroni F, Topaloglu R, Trepiccione F, Vidal E, Wan ER, Weber L, Yildirim ZY, Yüksel S, Zlatanova G, Bockenhauer D, Emma F, Nijenhuis T.
    Nephrol Dial Transplant; 2022 Nov 23; 37(12):2474-2486. PubMed ID: 35137195
    [Abstract] [Full Text] [Related]

  • 4. Type-5 Bartter syndrome presenting with metabolic seizure in adulthood.
    Hussain A, Atlani M, Goyal A, Khurana AK.
    BMJ Case Rep; 2021 Feb 17; 14(2):. PubMed ID: 33597159
    [Abstract] [Full Text] [Related]

  • 5. A novel variant in the SLC12A1 gene in two families with antenatal Bartter syndrome.
    Breinbjerg A, Siggaard Rittig C, Gregersen N, Rittig S, Hvarregaard Christensen J.
    Acta Paediatr; 2017 Jan 17; 106(1):161-167. PubMed ID: 27748541
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  • 7. Severe Bartter syndrome type 1: Prompt postnatal management thanks to antenatal identification of SLC12A1 pathogenic variants.
    D'Angelantonio D, Majore S, Di Netta T, Zotta F, Parise G, Savino E, Rosignoli S, Bizzarri B, Signore F, Grammatico P, Bottillo I.
    Arch Pediatr; 2022 Oct 17; 29(7):530-533. PubMed ID: 36058813
    [Abstract] [Full Text] [Related]

  • 8. [A case of pseudohypoparathyroidism (PHP) type II associated with Bartter's syndrome--restoration of phosphaturic response to parathyroid hormone (PTH) by treatment for hypopotassemia].
    Bando Y, Miyakoshi H, Nagaoka T, Ohsawa K, Kobayashi K.
    Nihon Naibunpi Gakkai Zasshi; 1992 Jul 20; 68(7):676-87. PubMed ID: 1516722
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  • 10. 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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  • 11. Bartter Syndrome Type 1 Due to Novel SLC12A1 Mutations Associated With Pseudohypoparathyroidism Type II.
    Kiuchi Z, Nozu K, Yan K, Jüppner H.
    JCEM Case Rep; 2023 Mar 26; 1(2):luad019. PubMed ID: 37908481
    [Abstract] [Full Text] [Related]

  • 12. Australian Endocrine Surgeons Guidelines AES06/01. Postoperative parathyroid hormone measurement and early discharge after total thyroidectomy: analysis of Australian data and management recommendations.
    AES Guidelines 06/01 Group.
    ANZ J Surg; 2007 Apr 26; 77(4):199-202. PubMed ID: 17388819
    [Abstract] [Full Text] [Related]

  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14. Phosphate homeostasis in Bartter syndrome: a case-control study.
    Bettinelli A, Viganò C, Provero MC, Barretta F, Albisetti A, Tedeschi S, Scicchitano B, Bianchetti MG.
    Pediatr Nephrol; 2014 Nov 26; 29(11):2133-8. PubMed ID: 24902942
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  • 16. Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosis.
    Najafi M, Kordi-Tamandani DM, Behjati F, Sadeghi-Bojd S, Bakey Z, Karimiani EG, Schüle I, Azarfar A, Schmidts M.
    Orphanet J Rare Dis; 2019 Feb 13; 14(1):41. PubMed ID: 30760291
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  • 17. Gitelman's Syndrome Presenting with Hypocalcaemia - A Case Report.
    Cader FA, Kabir A, Mayedah R, Masud MS, Quadir F, Hossen MN.
    Mymensingh Med J; 2015 Apr 13; 24(2):411-5. PubMed ID: 26007276
    [Abstract] [Full Text] [Related]

  • 18. Osteomalacia in a Case of Adult-Onset Bartter Syndrome.
    Khan RN, Saba F.
    Eur J Case Rep Intern Med; 2018 Apr 13; 5(3):000764. PubMed ID: 30756015
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  • 19. Autosomal dominant hypocalcemia with mild type 5 Bartter syndrome.
    Vezzoli G, Arcidiacono T, Paloschi V, Terranegra A, Biasion R, Weber G, Mora S, Syren ML, Coviello D, Cusi D, Bianchi G, Soldati L.
    J Nephrol; 2006 Apr 13; 19(4):525-8. PubMed ID: 17048213
    [Abstract] [Full Text] [Related]

  • 20. Colistin-induced acquired Bartter-like syndrome: an unusual cause of meltdown.
    Tabish M, Mahendran M, Ray A, Vikram NK.
    BMJ Case Rep; 2020 Feb 05; 13(2):. PubMed ID: 32029515
    [Abstract] [Full Text] [Related]

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