Treatment of Autosomal Dominant Hypocalcemia Type 1 with the Calcilytic NPSP795 (SHP635)

Autor: Edward F. Nemeth, Martin Schepelmann, Sarah C. Brennan, Daniela Riccardi, Mohd Ezuan Bin Khayat, Jamie Streit, Jeff Gelb, David Gash, Michael T. Collins, Beth A Brillante, Ralf Rosskamp, Eva Krusinska, Lori C. Guthrie, Donald T. Ward, Rachel I Gafni, Mary Scott Roberts

Publikováno v: Ward, D 2019, ' Treatment of Autosomal Dominant Hypocalcemia Type 1 with the Calcilytic NPSP795 (SHP635). ', Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research . https://doi.org/10.1002/jbmr.3747
J Bone Miner Res

Autosomal dominant hypocalcemia type 1 (ADH1) is a rare form of hypoparathyroidism caused by heterozygous, gain-of-function mutations of the calcium-sensing receptor gene (CAR). Individuals are hypocalcemic with inappropriately low parathyroid hormon

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc1fd563ea9b5eb45560eb4f5adf46fe
https://www.research.manchester.ac.uk/portal/en/publications/treatment-of-autosomal-dominant-hypocalcemia-type-1-with-the-calcilytic-npsp795-shp635(7c119083-254a-4840-ac56-5b5cfe3d19ab).html

Looking to the Clouds for Business Intelligence

Autor: Mark N. Frolick, Thilini Ariyachandra, David Gash

Publikováno v: Journal of Internet Commerce. 10:261-269

As cloud computing becomes more prevalent, information technology (IT) groups large and small are looking for guidance as to how they can leverage this new resource. This article specifically focuses in on the field of business intelligence (BI) and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3692cb3c9becac681b5a7f4966366225
https://doi.org/10.1080/15332861.2011.622694