Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Daniel Gruskin"'
Autor:
Han-Wook Yoo, Christoph Wanner, Daniel Gruskin, Roberta Lemay, Juan Politei, João Paulo Oliveira, William R. Wilcox, Dominique P. Germain, Robert J. Hopkin, Daniel G. Bichet, David G. Warnock
Publikováno v:
Molecular Genetics and Metabolism. 123:S65-S66
Autor:
Daniel Gruskin
Publikováno v:
Nature Biotechnology. 30:211-214
As parts of the developing world embrace biotech, the focus is shifting from food production to fuels, industrial chemicals and even drugs. Daniel Grushkin investigates.
Autor:
Daniel Gruskin, Joan Keutzer
Publikováno v:
Blood Cells, Molecules, and Diseases. 64:13-14
Autor:
Neal J. Weinreb, Larry Blankstein, Daniel Gruskin, Gustavo Maegawa, Michael J. Gambello, Ozlem Goker-Alpan, Khan Nedd
Publikováno v:
JIMD Reports ISBN: 9783662496671
Agalsidase alfa and agalsidase beta, recombinant enzyme preparations for treatment of Fabry disease (FD), have different approved dosing schedules: 0.2 mg/kg and 1.0 mg/kg every other week (EOW), respectively.This open-label, multicenter, exploratory
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6aa28a3a5323ceca6e32815321f494c
https://europepmc.org/articles/PMC5059194/
https://europepmc.org/articles/PMC5059194/
Autor:
Christoph Wanner, Daniel Gruskin, Dominique P. Germain, Roberta Lemay, Juan Politei, João Paulo Oliveira, David G. Warnock, Daniel G. Bichet, Han-Wook Yoo, Robert J. Hopkin, William R. Wilcox
Publikováno v:
Nephrology Dialysis Transplantation. 32:iii113-iii113
Autor:
David G. Warnock, Roberta Lemay, João Paulo Oliveira, Daniel Gruskin, Dominique P. Germain, Han-Wook Yoo, William R. Wilcox, Christoph Wanner, Daniel G. Bichet, Robert J. Hopkin, Juan Politei
Publikováno v:
Molecular Genetics and Metabolism. 120:S51
Autor:
Marta Cizmarik, Linda Massey, Hugh Findlay, Kathleen Faherty, Virginia O’Neil, Bill Hartman, Virginia McMillin, Christiane Denzel, Betsy Loisel, Cinde L. Clatterbuck, Jean Foster, Susan Sparks, Danielle Dong, Katherine Belk, Kristin A. Moy, Anja Glaetzer, Zarla Ludin, Julie L. Batista, Rafael Ioschpe, Daniel Gruskin
Publikováno v:
Molecular Genetics and Metabolism. 120:S43
Autor:
Daniel Gruskin, Heather S. Hipp, Opal Y. Ousley, Dawn Laney, Ami Mehta, Joseph F. Cubells, Paul M. Fernhoff
Publikováno v:
Journal of inherited metabolic disease. 33
Fabry disease (FD) is an X-linked lysosomal storage disorder caused by the deficiency of alpha-galactosidase A. In addition to the debilitating physical symptoms of FD, there are also under-recognized and poorly characterized psychiatric features. As
Autor:
Gilles Morin, Chen-En Tsai, R. Parini, Elisa C. Tsao, Hanna Mandel, Michael Beck, Mislen Bauer, Nancy D. Leslie, Tara O’Meara, Deya Corzo, Brian W.H. Tsai, Susan M. Richards, Mikael Jokic, Daniel Gruskin, John P. Clancy, Claire Morgan, Ans T. van der Ploeg, Priya S. Kishnani
Publikováno v:
Pediatric research. 66(3)
In a previous 52-week trial, treatment with alglucosidase alfa markedly improved cardiomyopathy, ventilatory function, and overall survival among 18 children
Autor:
Yin-Hsiu Chien, A.T. van der Ploeg, Wuh-Liang Hwu, Beth L. Thurberg, R. Parini, M Beck, James E. Wraith, G. Morin, John P. Clancy, Nancy D. Leslie, Barry J. Byrne, Susan M. Richards, Jennifer S. Li, Marie T. McDonald, M. A. Worden, D. Bartholomew, J. Dumontier, Priya S. Kishnani, M. Davison, Marc Nicolino, M. Halberthal, M. Jokic, S. Vijayaraghavan, Carolyn T. Spencer, Robert J. Hopkin, G. S. De la Gastine, Deyanira Corzo, Hanna Mandel, Yuan-Tsong Chen, Deeksha Bali, Daniel Gruskin, J. Levine
Publikováno v:
Neurology, 68(2), 99-109. Lippincott Williams & Wilkins
Background: Pompe disease is a progressive metabolic neuromuscular disorder resulting from deficiency of lysosomal acid α-glucosidase (GAA). Infantile-onset Pompe disease is characterized by cardiomyopathy, respiratory and skeletal muscle weakness,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::037e3b4ae59a4a3297c2ba548879116b
https://pure.eur.nl/en/publications/8eedab6b-f2b3-4619-999b-f0a3d3fdd5fd
https://pure.eur.nl/en/publications/8eedab6b-f2b3-4619-999b-f0a3d3fdd5fd