Author

GM Pastores

Observed names: G M Pastores, G Pastores, G. M. Pastores, G. Pastores, G.M Pastores, G.M. Pastores

Observed institutions: St. Louis Children's Hospital, Mater Misericordiae University Hospital, NYU Langone Health, Massachusetts General Hospital, New York University, Icahn School of Medicine at Mount Sinai

OpenAlex ID: A5111858724

Enzyme therapy in Gaucher disease type 1: dosage efficacy and adverse effects in 33 patients treated for 6 to 24 months

1993 · GM Pastores, AR Sibille, et al. · Blood · 174

Improvement of bone disease by imiglucerase (Cerezyme) therapy in patients with skeletal manifestations of type 1 Gaucher disease: results of a 48‐month longitudinal cohort study

2008 · KB Sims, GM Pastores, et al. · Clinical Genetics · 133

PDF

Imiglucerase (Cerezyme®) improves quality of life in patients with skeletal manifestations of Gaucher disease

2007 · N Weinreb, J Barranger, et al. · Clinical Genetics · 106

Pulmonary involvement in Type 1 Gaucher disease: functional and exercise findings in patients with and without clinical interstitial lung disease

2003 · A Miller, LK Brown, et al. · Clinical Genetics · 63

Safety and pharmacokinetics of agalsidase alfa in patients with Fabry disease and end-stage renal disease

2007 · G. M. Pastores, E. Boyd, et al. · Nephrology Dialysis Transplantation · 45

Therapeutic effects of astrocytes expressing both tyrosine hydroxylase and brain-derived neurotrophic factor on a rat model of Parkinson’s disease

2002 · Z.H Wang, Y Ji, et al. · Neuroscience · 39

Krabbe disease: Clinical, biochemical and molecular information on six new patients and successful retrospective diagnosis using stored newborn screening cards

2011 · R.L. Puckett, J.J. Orsini, et al. · Molecular Genetics and Metabolism · 28

Undiagnosed Phenylketonuria Can Exist Everywhere: Results From an International Survey

2021 · Annemiek M.J. van Wegberg, Friedrich Trefz, et al. · The Journal of Pediatrics · 21

PDF

A questionnaire study for 128 patients with Gaucher disease

2006 · HJ Mankin, CA Trahan, et al. · Clinical Genetics · 21

Extended interval between enzyme therapy infusions for adult patients with Gaucher's disease type 1.

2003 · J Pérez-Calvo, P Giraldo, et al. · PubMed · 13

PDF

Globoid cell leukodystrophy (Krabbe disease): Normal umbilical cord blood galactocerebrosidase activity and polymorphic mutations

2005 · S. Raghavan, B. Zeng, et al. · Journal of Inherited Metabolic Disease · 10

Agalsidase alfa: enzyme therapy for Anderson-Fabry disease

2004 · G M Pastores · Therapy · 3

The clinical expression of Gaucher disease correlates with genotype: Data from 570 patients

2000 · C.R. Scott, G. Pastores, et al. · Genetics in Medicine · 3

PDF

Pharmacological Chaperone Therapy for the Treatment of Gaucher Disease: Results of Phase 1 Clinical Trials and a Clinical Ex Vivo Response Study with a Survey of Blood Markers for 53 Gaucher Patients.

2007 · Neal J. Weinreb, G.A. Grabowski, et al. · Blood · 1

A bolt from the blue; A case report of an unusual asthma exacerbation

2019 · C. Moloney, A. Long, et al. · Respiratory Medicine Case Reports

PDF

21 Cardiac investigations in adult inborn error of metabolism cohort

2019 · S James, A Sheerin, et al. · Heart

Niemann–Pick Disease

2014 · G.M. Pastores, H.A. Lau · Elsevier eBooks

482 Safety and Efficacy of Velaglucerase Alfa in Gaucher Disease Type 1 Patients Previously Treated with Imiglucerase

2010 · G Grabowski, G Pastores, et al. · Pediatric Research

1.216 Phenotypic characterization of parkinsonism in seven patients with Gaucher Disease

2007 · S. Sathe, G. Pastores, et al. · Parkinsonism & Related Disorders

Fabry disease in genetic counselling practice: recommendations of the National Society of Genetic Counsellors

2002 · RI Bennett, K Hart, et al. · Acta Paediatrica

Autonomic failure with a fatal outcome in Fabry disease

2002 · GM Pastores, GA Charria, et al. · Acta Paediatrica

Pqp9: Quality of Life of Patients With Fabry Disease

2001 · MF Botteman, GM Pastores, et al. · Value in Health

Works count: 22

Citation count: 660

H-index: 10

I10-index: 11