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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1976 1
1982 5
1983 1
1984 4
1985 3
1986 2
1987 1
1989 2
1991 1
1992 1
1993 4
1995 2
1998 1
1999 1
2000 4
2001 2
2002 3
2003 4
2004 2
2006 4
2007 1
2011 1
2012 1
2016 1
2018 1
2019 1
2020 1
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Similar Articles for PMID: 2909976

54 results
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Page 1
Benign familial hypocalciuric hypercalcemia.
Varghese J, Rich T, Jimenez C. Varghese J, et al. Endocr Pract. 2011 Mar-Apr;17 Suppl 1:13-7. doi: 10.4158/EP10308.RA. Endocr Pract. 2011. PMID: 21478088 Review.
Familial hypocalciuric hypercalcemia involving four members of a kindred including a girl with severe neonatal primary hyperparathyroidism.
Fujita T, Watanabe N, Fukase M, Tsutsumi M, Fukami T, Imai Y, Sakaguchi K, Okada S, Matsuo M, Takemine H. Fujita T, et al. Miner Electrolyte Metab. 1983 Jan-Feb;9(1):51-4. Miner Electrolyte Metab. 1983. PMID: 6843519
Neonatal severe hyperparathyroidism: an important clue to the aetiology.
Gabbett MT, Jones K, Cowell CT, Sillence DO, Wilson MJ. Gabbett MT, et al. J Paediatr Child Health. 2006 Dec;42(12):813-6. doi: 10.1111/j.1440-1754.2006.00983.x. J Paediatr Child Health. 2006. PMID: 17096719
[Familial hypocalciuric hypercalcemia with severe neonatal primary hyperparathyroidism (author's transl)].
Watanabe N, Yamauchi Y, Matsumoto J, Sakaguchi K, Fukase M, Tsutsumi M, Fukami T, Imai Y, Fujita T. Watanabe N, et al. Nihon Naika Gakkai Zasshi. 1982 Apr 10;71(4):479-84. Nihon Naika Gakkai Zasshi. 1982. PMID: 7108330 Japanese. No abstract available.
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. Hendy GN, et al. Hum Mutat. 2000 Oct;16(4):281-96. doi: 10.1002/1098-1004(200010)16:4<281::AID-HUMU1>3.0.CO;2-A. Hum Mutat. 2000. PMID: 11013439 Review.
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