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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2010 | 3 |
2011 | 4 |
2012 | 1 |
2024 | 0 |
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7 results
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Page 1
Genetics of hypoparathyroidism and pseudohypoparathyroidism.
J Endocrinol Invest. 2011 Jul;34(7 Suppl):27-34.
J Endocrinol Invest. 2011.
PMID: 21985977
Review.
Deletion of the noncoding GNAS antisense transcript causes pseudohypoparathyroidism type Ib and biparental defects of GNAS methylation in cis.
Chillambhi S, Turan S, Hwang DY, Chen HC, Jüppner H, Bastepe M.
Chillambhi S, et al.
J Clin Endocrinol Metab. 2010 Aug;95(8):3993-4002. doi: 10.1210/jc.2009-2205. Epub 2010 May 5.
J Clin Endocrinol Metab. 2010.
PMID: 20444925
Free PMC article.
Item in Clipboard
Hypoparathyroidism in the adult: epidemiology, diagnosis, pathophysiology, target-organ involvement, treatment, and challenges for future research.
Bilezikian JP, Khan A, Potts JT Jr, Brandi ML, Clarke BL, Shoback D, Jüppner H, D'Amour P, Fox J, Rejnmark L, Mosekilde L, Rubin MR, Dempster D, Gafni R, Collins MT, Sliney J, Sanders J.
Bilezikian JP, et al.
J Bone Miner Res. 2011 Oct;26(10):2317-37. doi: 10.1002/jbmr.483.
J Bone Miner Res. 2011.
PMID: 21812031
Free PMC article.
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De novo STX16 deletions: an infrequent cause of pseudohypoparathyroidism type Ib that should be excluded in sporadic cases.
Turan S, Ignatius J, Moilanen JS, Kuismin O, Stewart H, Mann NP, Linglart A, Bastepe M, Jüppner H.
Turan S, et al.
J Clin Endocrinol Metab. 2012 Dec;97(12):E2314-9. doi: 10.1210/jc.2012-2920. Epub 2012 Oct 18.
J Clin Endocrinol Metab. 2012.
PMID: 23087324
Free PMC article.
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Parathyroid hormone signaling via Gαs is selectively inhibited by an NH(2)-terminally truncated Gαs: implications for pseudohypoparathyroidism.
Puzhko S, Goodyer CG, Kerachian MA, Canaff L, Misra M, Jüppner H, Bastepe M, Hendy GN.
Puzhko S, et al.
J Bone Miner Res. 2011 Oct;26(10):2473-85. doi: 10.1002/jbmr.461.
J Bone Miner Res. 2011.
PMID: 21713996
Free PMC article.
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Recessive versus imprinted disorder: consanguinity can impede establishing the diagnosis of autosomal dominant pseudohypoparathyroidism type Ib.
Turan S, Akin L, Akcay T, Adal E, Sarikaya S, Bastepe M, Jüppner H.
Turan S, et al.
Eur J Endocrinol. 2010 Sep;163(3):489-93. doi: 10.1530/EJE-10-0348. Epub 2010 Jun 10.
Eur J Endocrinol. 2010.
PMID: 20538864
Free PMC article.
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Paternal uniparental isodisomy of the entire chromosome 20 as a molecular cause of pseudohypoparathyroidism type Ib (PHP-Ib).
Bastepe M, Altug-Teber O, Agarwal C, Oberfield SE, Bonin M, Jüppner H.
Bastepe M, et al.
Bone. 2011 Mar 1;48(3):659-62. doi: 10.1016/j.bone.2010.10.168. Epub 2010 Oct 19.
Bone. 2011.
PMID: 20965295
Free PMC article.
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