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499 related items for PubMed ID: 34556169

  • 1. Concomitant familial hypocalciuric hypercalcemia and single parathyroid adenoma: a case report.
    Marstrand SD, Tofteng CL, Jarløv A, Borgwardt L, Schwarz P.
    J Med Case Rep; 2021 Sep 24; 15(1):471. PubMed ID: 34556169
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  • 2. Misleading localization by 18F-fluorocholine PET/CT in familial hypocalciuric hypercalcemia type-3: a case report.
    Mukhtar NN, Abouzied MEM, Alqahtani MH, Hammami MM.
    BMC Endocr Disord; 2021 Jan 26; 21(1):20. PubMed ID: 33499837
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  • 4. Familial Hypocalciuric Hypercalcemia as an Atypical Form of Primary Hyperparathyroidism.
    Marx SJ.
    J Bone Miner Res; 2018 Jan 26; 33(1):27-31. PubMed ID: 29115694
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  • 5. Plasma 25-hydroxyvitamin D, 1,25-dihydroxyvitamin D, and parathyroid hormone in familial hypocalciuric hypercalcemia and primary hyperparathyroidism.
    Christensen SE, Nissen PH, Vestergaard P, Heickendorff L, Rejnmark L, Brixen K, Mosekilde L.
    Eur J Endocrinol; 2008 Dec 26; 159(6):719-27. PubMed ID: 18787045
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  • 6. Familial hypocalciuric hypercalcemia in an index male: grey zones of the differential diagnosis from primary hyperparathyroidism in a 13-year clinical follow up.
    Zajíčková K, Dvořáková M, Moravcová J, Včelák J, Goltzman D.
    Physiol Res; 2020 Sep 30; 69(Suppl 2):S321-S328. PubMed ID: 33094630
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  • 7. Parathyroid hormone-dependent familial hypercalcemia with low measured PTH levels and a presumptive novel pathogenic mutation in CaSR.
    Mahajan A, Buse J, Kline G.
    Osteoporos Int; 2020 Jan 30; 31(1):203-207. PubMed ID: 31641801
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  • 8. Calcium-sensing-related gene mutations in hypercalcaemic hypocalciuric patients as differential diagnosis from primary hyperparathyroidism: detection of two novel inactivating mutations in an Italian population.
    Stratta P, Merlotti G, Musetti C, Quaglia M, Pagani A, Izzo C, Radin E, Airoldi A, Baorda F, Palladino T, Leone MP, Guarnieri V.
    Nephrol Dial Transplant; 2014 Oct 30; 29(10):1902-9. PubMed ID: 25104082
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  • 10. Think twice: a rare calcium sensing receptor mutation and a new diagnosis of familial hypocalciuric hypercalcaemia.
    Tellam JJ, Abdulrasool G, Ciin LCH.
    Endocrinol Diabetes Metab Case Rep; 2020 Jun 22; 2020():. PubMed ID: 32698162
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  • 11. Differentiating familial hypocalciuric hypercalcemia from primary hyperparathyroidism.
    Shinall MC, Dahir KM, Broome JT.
    Endocr Pract; 2013 Jun 22; 19(4):697-702. PubMed ID: 23425644
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  • 14. [Hereditary variants of primary hyperparathyroidism--MEN1, MEN2, HPT-JT, FHH, FIHPT].
    Frank-Raue K, Leidig-Bruckner G, Lorenz A, Rondot S, Haag C, Schulze E, Büchler M, Raue F.
    Dtsch Med Wochenschr; 2011 Sep 22; 136(38):1889-94. PubMed ID: 21915802
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  • 16. Genetics of hereditary forms of primary hyperparathyroidism.
    English KA, Lines KE, Thakker RV.
    Hormones (Athens); 2024 Mar 22; 23(1):3-14. PubMed ID: 38038882
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  • 17. Familial Hypocalciuric Hypercalcemia Types 1 and 3 and Primary Hyperparathyroidism: Similarities and Differences.
    Vargas-Poussou R, Mansour-Hendili L, Baron S, Bertocchio JP, Travers C, Simian C, Treard C, Baudouin V, Beltran S, Broux F, Camard O, Cloarec S, Cormier C, Debussche X, Dubosclard E, Eid C, Haymann JP, Kiando SR, Kuhn JM, Lefort G, Linglart A, Lucas-Pouliquen B, Macher MA, Maruani G, Ouzounian S, Polak M, Requeda E, Robier D, Silve C, Souberbielle JC, Tack I, Vezzosi D, Jeunemaitre X, Houillier P.
    J Clin Endocrinol Metab; 2016 May 22; 101(5):2185-95. PubMed ID: 26963950
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  • 18. Brown tumor due to primary hyperparathyroidism in a familial case: a case report.
    Diao Z, Zhang J, Zhao J, Sun W, Pu Z.
    BMC Endocr Disord; 2023 Oct 08; 23(1):214. PubMed ID: 37807045
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  • 19. Primary hyperparathyroidism and familial hypocalciuric hypercalcemia: relationships and clinical implications.
    Eldeiry LS, Ruan DT, Brown EM, Gaglia JL, Garber JR.
    Endocr Pract; 2012 Oct 08; 18(3):412-7. PubMed ID: 22232026
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