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Gregory Pastores
Gregory Pastores
University College Dublin
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Effectiveness of enzyme replacement therapy in 1028 patients with type 1 Gaucher disease after 2 to 5 years of treatment: a report from the Gaucher Registry
NJ Weinreb, J Charrow, HC Andersson, P Kaplan, EH Kolodny, P Mistry, ...
The American journal of medicine 113 (2), 112-119, 2002
7102002
Enzyme replacement therapy for mucopolysaccharidosis I: a randomized, double-blinded, placebo-controlled, multinational study of recombinant human α-L-iduronidase (laronidase)
JE Wraith, LA Clarke, M Beck, EH Kolodny, GM Pastores, J Muenzer, ...
The Journal of pediatrics 144 (5), 581-588, 2004
6972004
The Gaucher registry: demographics and disease characteristics of 1698 patients with Gaucher disease
J Charrow, HC Andersson, P Kaplan, EH Kolodny, P Mistry, G Pastores, ...
Archives of internal medicine 160 (18), 2835-2843, 2000
6492000
Enzyme therapy in type 1 Gaucher disease: comparative efficacy of mannose-terminated glucocerebrosidase from natural and recombinant sources
GA Grabowski, NW Barton, G Pastores, JM Dambrosia, TK Banerjee, ...
Annals of internal medicine 122 (1), 33-39, 1995
6001995
Females with Fabry disease frequently have major organ involvement: lessons from the Fabry Registry
WR Wilcox, JP Oliveira, RJ Hopkin, A Ortiz, M Banikazemi, ...
Molecular genetics and metabolism 93 (2), 112-128, 2008
5952008
Therapeutic goals in the treatment of Gaucher disease
GM Pastores, NJ Weinreb, H Aerts, G Andria, TM Cox, M Giralt, ...
Seminars in hematology 41, 4-14, 2004
5502004
Fabry disease: guidelines for the evaluation and management of multi-organ system involvement
CM Eng, DP Germain, M Banikazemi, DG Warnock, C Wanner, RJ Hopkin, ...
Genetics in Medicine 8 (9), 539-548, 2006
5472006
Long-term efficacy and safety of laronidase in the treatment of mucopolysaccharidosis I
LA Clarke, JE Wraith, M Beck, EH Kolodny, GM Pastores, J Muenzer, ...
Pediatrics 123 (1), 229-240, 2009
4102009
Neurology of hereditary metabolic diseases of children
RD Adams, G Lyon
(No Title), 1982
4061982
The role of the iminosugar N‐butyldeoxynojirimycin (miglustat) in the management of type I (non‐neuronopathic) Gaucher disease: A position statement
TM Cox, J Aerts, G Andria, M Beck, N Belmatoug, B Bembi, R Chertkoff, ...
Journal of inherited metabolic disease 26 (6), 513-526, 2003
2892003
Patients with Fabry disease on dialysis in the United States
R Thadhani, M Wolf, ML West, M Tonelli, R Ruthazer, GM Pastores, ...
Kidney international 61 (1), 249-255, 2002
2722002
The MPS I registry: design, methodology, and early findings of a global disease registry for monitoring patients with Mucopolysaccharidosis Type I
GM Pastores, P Arn, M Beck, JTR Clarke, N Guffon, P Kaplan, J Muenzer, ...
Molecular genetics and metabolism 91 (1), 37-47, 2007
2692007
Enzyme therapy in Gaucher disease type 1: dosage efficacy and adverse effects in 33 patients treated for 6 to 24 months
GM Pastores, AR Sibille, GA Grabowski
2541993
Gaucher disease
GM Pastores, DA Hughes
2422018
The risk of Parkinson’s disease in type 1 Gaucher disease
G Bultron, K Kacena, D Pearson, M Boxer, R Yang, S Sathe, G Pastores, ...
Journal of inherited metabolic disease 33, 167-173, 2010
2412010
Enzyme replacement therapy for Anderson‐Fabry disease
R El Dib, H Gomaa, RP Carvalho, SE Camargo, R Bazan, P Barretti, ...
Cochrane Database of Systematic Reviews, 2016
2352016
Gaucher disease: recommendations on diagnosis, evaluation, and monitoring
J Charrow, JA Esplin, TJ Gribble, P Kaplan, EH Kolodny, GM Pastores, ...
Archives of internal medicine 158 (16), 1754-1760, 1998
2291998
Enzyme-replacement therapy with agalsidase alfa in children with Fabry disease
M Ries, JTR Clarke, C Whybra, M Timmons, C Robinson, BL Schlaggar, ...
Pediatrics 118 (3), 924-932, 2006
2162006
Gaucher disease type 1: revised recommendations on evaluations and monitoring for adult patients
NJ Weinreb, MC Aggio, HC Andersson, G Andria, J Charrow, JTR Clarke, ...
Seminars in hematology 41, 15-22, 2004
2152004
Enzyme replacement therapy and monitoring for children with type 1 Gaucher disease: consensus recommendations
J Charrow, HC Andersson, P Kaplan, EH Kolodny, P Mistry, G Pastores, ...
The Journal of pediatrics 144 (1), 112-120, 2004
2072004
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Artículos 1–20