Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Alexander Bragat"'
Autor:
Zhigang Yu, Andrew Shenker, Frank LaCreta, Stanford Jhee, Janice Pursley, Jessie Wang, Charles Frost, Alexander Bragat
Publikováno v:
Clinical Pharmacology : Advances and Applications
Charles Frost,1 Andrew Shenker,1 Stanford Jhee,2 Zhigang Yu,1 Jessie Wang,3 Alexander Bragat,1 Janice Pursley,4 Frank LaCreta1 1Exploratory Clinical and Translational Research, Bristol-Myers Squibb, Princeton, NJ, USA; 2PAREXEL International Early Ph
Publikováno v:
Clinical Pharmacology in Drug Development. 2:120-132
Migalastat HCl is an investigational, oral treatment for Fabry disease, an X-linked lysosomal storage disorder. Four Phase 1 studies were conducted to determine the pharmacokinetics, pharmacodynamics, safety, and tolerability of migalastat. Healthy v
Autor:
Jeff Castelli, Sheela Sitaraman, Dan Walker, J. Charles Jennette, Pol Boudes, Alexander Bragat, Laura Barisoni, Robert B. Colvin
Publikováno v:
Archives of Pathology & Laboratory Medicine. 136:816-824
Context.—Assessing the amount of globotriaosylceramide inclusions in renal peritubular capillaries by a semiquantitative approach is a standard and useful measure of therapeutic efficacy in Fabry disease, achievable by light microscopy analysis. Ob
Publikováno v:
Clinical pharmacology in drug development. 2(2)
Migalastat HCl is an investigational, oral treatment for Fabry disease, an X-linked lysosomal storage disorder. Four Phase 1 studies were conducted to determine the pharmacokinetics, pharmacodynamics, safety, and tolerability of migalastat. Healthy v
Autor:
Samuel J. Mann, Phyllis August, Thomas G. Pickering, Rosemerie Marion, Mark S. Pecker, Jon D. Blumenfeld, Julio E. Sotelo, Jean E. Sealey, John H. Laragh, Alexander Bragat
Publikováno v:
American journal of hypertension. 12(5)
Although beta-adrenergic-blocking drugs suppress the renin system (RAAS), plasma angiotensin II (Ang II) responses during beta-blockade have not been defined. This study quantifies the effects of beta-blockade on the RAAS and examines its impact on p
Autor:
Dominique P. Germain, Fatih Süheyl Ezgü, Sheela Sitaraman, Claudio Feliciani, Pol Boudes, Rosemary Schroyer, Suma P. Shankar, Alexander Bragat, Salim Janmohamed, Kathy Nicholls, Shiona M. Laing
Publikováno v:
Molecular Genetics and Metabolism. 108:S70
Autor:
Sheela Sitaraman, Pol Boudes, J. C. Jennette, Jeffrey P. Castelli, D. Walker, Laura Barisoni, Alexander Bragat, Robert B. Colvin
Publikováno v:
Archives of Pathology & Laboratory Medicine. 136:842-842
Autor:
David J. Lockhart, Derralynn Hughes, Jeff Castelli, Pol Boudes, Kathy Nicholls, Charles Jennette, Sheela Sitaraman, Roberto Giugliani, Laura Barisoni, Atul Mehta, Alexander Bragat, Dominique P. Germain
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 7, Iss 1, p 91 (2012)
Orphanet Journal of Rare Diseases, Vol 7, Iss 1, p 91 (2012)
Background Fabry disease (FD) is a genetic disorder resulting from deficiency of the lysosomal enzyme α-galactosidase A (α-Gal A), which leads to globotriaosylceramide (GL-3) accumulation in multiple tissues. We report on the safety and pharmacodyn
Autor:
Jeff Castelli, Alexander Bragat, Robert B. Colvin, Laura Barisoni, Pol Boudes, Charles Jennette, Sheela Sitaraman
Publikováno v:
Molecular Genetics and Metabolism. 102:S7
Autor:
Randall Stoltz, Sheela Sitaraman, Jane Royalty, Richard Lazauskas, George R. Lankas, Ken Valenzano, Douglas Stuart Greene, Alexander Bragat, Pol Boudes, Mathews Adera
Publikováno v:
Molecular Genetics and Metabolism. 102:S4