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24. New mutation in the CASR gene in a family with familial hypocalciuric hypercalcemia (FHH) and neonatal severe hyperparathyroidism (NSHPT). Rodrigues LS; Cáu AC; Bussmann LZ; Bastida G; Brunetto OH; Corrêa PH; Martin RM Arq Bras Endocrinol Metabol; 2011 Feb; 55(1):67-71. PubMed ID: 21468522 [TBL] [Abstract][Full Text] [Related]
25. Primary hyperparathyroidism and familial hypocalciuric hypercalcemia: relationships and clinical implications. Eldeiry LS; Ruan DT; Brown EM; Gaglia JL; Garber JR Endocr Pract; 2012; 18(3):412-7. PubMed ID: 22232026 [TBL] [Abstract][Full Text] [Related]
26. A homozygous inactivating calcium-sensing receptor mutation, Pro339Thr, is associated with isolated primary hyperparathyroidism: correlation between location of mutations and severity of hypercalcaemia. Hannan FM; Nesbit MA; Christie PT; Lissens W; Van der Schueren B; Bex M; Bouillon R; Thakker RV Clin Endocrinol (Oxf); 2010 Dec; 73(6):715-22. PubMed ID: 20846291 [TBL] [Abstract][Full Text] [Related]
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28. [Progress in diagnosis and therapy: Hypercalcemia due to primary hyperparathyroidism]. Sugimoto T Nihon Naika Gakkai Zasshi; 2007 Apr; 96(4):662-8. PubMed ID: 17506301 [No Abstract] [Full Text] [Related]
31. Primary hyperparathyroidism in a patient with familial hypocalciuric hypercalcaemia due to a novel mutation in the calcium-sensing receptor gene. Egan AM; Ryan J; Aziz MA; O'Dwyer TP; Byrne MM J Bone Miner Metab; 2013 Jul; 31(4):477-80. PubMed ID: 23081733 [TBL] [Abstract][Full Text] [Related]
32. Cinacalcet therapy in an infant with an R185Q calcium-sensing receptor mutation causing hyperparathyroidism: a case report and review of the literature. Forman TE; Niemi AK; Prahalad P; Shi RZ; Nally LM J Pediatr Endocrinol Metab; 2019 Mar; 32(3):305-310. PubMed ID: 30730839 [TBL] [Abstract][Full Text] [Related]
33. [Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism caused by inactivating mutations of calcium-sensing receptor]. Watanabe S; Fukumoto S Nihon Rinsho; 2002 Feb; 60(2):325-30. PubMed ID: 11857921 [TBL] [Abstract][Full Text] [Related]
34. Hypercalcaemic and hypocalcaemic conditions due to calcium-sensing receptor mutations. Egbuna OI; Brown EM Best Pract Res Clin Rheumatol; 2008 Mar; 22(1):129-48. PubMed ID: 18328986 [TBL] [Abstract][Full Text] [Related]
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36. Familial Hypocalciuric Hypercalcemia and Neonatal Severe Hyperparathyroidism. Vannucci L; Brandi ML Front Horm Res; 2019; 51():52-62. PubMed ID: 30641521 [TBL] [Abstract][Full Text] [Related]
37. Calcium of 28mg/dL in patient of 4 days of life. Urgent treatment and follow-up. Segura González M; Carrasco Hidalgo-Barquero MC; Hidalgo-Barquero Del Rosal E Nefrologia (Engl Ed); 2019; 39(5):552-554. PubMed ID: 30857752 [No Abstract] [Full Text] [Related]
38. A Case of a Heterozygous Inactivating CASR Variant with Adult-Onset Symptomatic Hypercalcemia Requiring Extensive Surgery. Veldeman L; Robbrecht S; Breckpot J; Weynand B; Decallonne B Calcif Tissue Int; 2020 Jul; 107(1):104-108. PubMed ID: 32306059 [TBL] [Abstract][Full Text] [Related]
39. Mutations of the calcium-sensing receptor (CASR) in familial hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia. Hendy GN; D'Souza-Li L; Yang B; Canaff L; Cole DE Hum Mutat; 2000 Oct; 16(4):281-96. PubMed ID: 11013439 [TBL] [Abstract][Full Text] [Related]
40. A homozygous CaSR mutation causing a FHH phenotype completely masked by vitamin D deficiency presenting as rickets. Szczawinska D; Schnabel D; Letz S; Schöfl C J Clin Endocrinol Metab; 2014 Jun; 99(6):E1146-53. PubMed ID: 24517148 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]