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G M Pastores

Showing results (11-20 of 63) with videos related to

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The Journal of Clinical Investigation|May 15, 1997
Identification and expression of acid beta-glucosidase mutations causing severe type 1 and neurologic type 2 Gaucher disease in non-Jewish patientsM E Grace, R J Desnick, G M Pastores
Biochemistry. Biokhimiia|September 10, 2013
Animal models for lysosomal storage disordersG M Pastores, P A Torres, B-J Zeng
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|August 6, 1998
The health-related quality of life of adults with Gaucher's disease receiving enzyme replacement therapy: results from a retrospective studyA M Damiano, G M Pastores, J E Ware
American Journal of Medical Genetics|December 11, 1991
Early childhood diagnosis of acoustic neuromas in presymptomatic individuals at risk for neurofibromatosis 2G M Pastores, V V Michels, C R Jack
QJM : Monthly Journal of the Association of Physicians|November 22, 2005
Bone crisis in stable Gaucher's diseaseJ I Pérez-Calvo, M Roca-Espiaú, G M Pastores
Neurology|August 1, 1995
Antisulfatide antibody and neuropathy in a patient with Gaucher's diseaseT McAlarney, G M Pastores, A P Hays, et al.
Pediatric Radiology|January 1, 1995
Resolution of a proximal humeral defect in type-1 Gaucher disease by enzyme replacement therapyG M Pastores, G Hermann, K Norton, et al.
Clinical Genetics|May 20, 2003
Pulmonary involvement in type 1 Gaucher disease: functional and exercise findings in patients with and without clinical interstitial lung diseaseA Miller, L K Brown, G M Pastores, et al.
Skeletal Radiology|February 7, 1998
Gaucher disease: assessment of skeletal involvement and therapeutic responses to enzyme replacementG Hermann, G M Pastores, I F Abdelwahab, et al.
Journal of Inherited Metabolic Disease|January 7, 2004
A neurological symptom survey of patients with type I Gaucher diseaseG M Pastores, N L Barnett, P Bathan, et al.
Pageof 7

Showing results (11-20 of 63) with videos related to

Sort By:
Pageof 7
The Journal of Clinical Investigation|May 15, 1997
Identification and expression of acid beta-glucosidase mutations causing severe type 1 and neurologic type 2 Gaucher disease in non-Jewish patientsM E Grace, R J Desnick, G M Pastores
Biochemistry. Biokhimiia|September 10, 2013
Animal models for lysosomal storage disordersG M Pastores, P A Torres, B-J Zeng
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|August 6, 1998
The health-related quality of life of adults with Gaucher's disease receiving enzyme replacement therapy: results from a retrospective studyA M Damiano, G M Pastores, J E Ware
American Journal of Medical Genetics|December 11, 1991
Early childhood diagnosis of acoustic neuromas in presymptomatic individuals at risk for neurofibromatosis 2G M Pastores, V V Michels, C R Jack
QJM : Monthly Journal of the Association of Physicians|November 22, 2005
Bone crisis in stable Gaucher's diseaseJ I Pérez-Calvo, M Roca-Espiaú, G M Pastores
Neurology|August 1, 1995
Antisulfatide antibody and neuropathy in a patient with Gaucher's diseaseT McAlarney, G M Pastores, A P Hays, et al.
Pediatric Radiology|January 1, 1995
Resolution of a proximal humeral defect in type-1 Gaucher disease by enzyme replacement therapyG M Pastores, G Hermann, K Norton, et al.
Clinical Genetics|May 20, 2003
Pulmonary involvement in type 1 Gaucher disease: functional and exercise findings in patients with and without clinical interstitial lung diseaseA Miller, L K Brown, G M Pastores, et al.
Skeletal Radiology|February 7, 1998
Gaucher disease: assessment of skeletal involvement and therapeutic responses to enzyme replacementG Hermann, G M Pastores, I F Abdelwahab, et al.
Journal of Inherited Metabolic Disease|January 7, 2004
A neurological symptom survey of patients with type I Gaucher diseaseG M Pastores, N L Barnett, P Bathan, et al.
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