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R Schiffmann

Showing results (31-40 of 89) with videos related to

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Neurology|August 26, 1998
Mucolipidosis type IV: characteristic MRI findingsK P Frei, N J Patronas, K E Crutchfield, et al.
Journal of Child Neurology|October 1, 1993
Posterior fossa abnormalities in children with infantile spasmsR Schiffmann, G B Mannheim, C E Stafstrom, et al.
Blood|July 1, 1995
Growth factors and stromal support generate very efficient retroviral transduction of peripheral blood CD34+ cells from Gaucher patientsL C Xu, S Kluepfel-Stahl, M Blanco, et al.
Human Mutation|January 29, 2000
Five novel mutations in fourteen patients with Fabry DiseaseK M Rosenberg, R Schiffmann, C Kaneski, et al.
Blood|August 1, 1995
Transfer of the human glucocerebrosidase gene into hematopoietic stem cells of nonablated recipients: successful engraftment and long-term expression of the transgeneR Schiffmann, J A Medin, J M Ward, et al.
Journal of Inherited Metabolic Disease|January 27, 2009
Proposed high-risk screening protocol for Fabry disease in patients with renal and vascular diseaseC Auray-Blais, D S Millington, S P Young, et al.
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics|October 13, 2001
Oral and craniofacial findings in Fabry's disease: a report of 13 patientsL Baccaglini, R Schiffmann, M T Brennan, et al.
Neurology|February 15, 2001
Somatosensory evoked potentials as a marker of disease burden in type 3 Gaucher diseaseM A Garvey, C Toro, S Goldstein, et al.
Neuroscience|February 6, 2007
Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: a complex genotype-phenotype relationshipK H Kraemer, N J Patronas, R Schiffmann, et al.
Journal of Medical Genetics|December 14, 2004
Parkinsonism among Gaucher disease carriersO Goker-Alpan, R Schiffmann, M E LaMarca, et al.
Pageof 9

Showing results (31-40 of 89) with videos related to

Sort By:
Pageof 9
Neurology|August 26, 1998
Mucolipidosis type IV: characteristic MRI findingsK P Frei, N J Patronas, K E Crutchfield, et al.
Journal of Child Neurology|October 1, 1993
Posterior fossa abnormalities in children with infantile spasmsR Schiffmann, G B Mannheim, C E Stafstrom, et al.
Blood|July 1, 1995
Growth factors and stromal support generate very efficient retroviral transduction of peripheral blood CD34+ cells from Gaucher patientsL C Xu, S Kluepfel-Stahl, M Blanco, et al.
Human Mutation|January 29, 2000
Five novel mutations in fourteen patients with Fabry DiseaseK M Rosenberg, R Schiffmann, C Kaneski, et al.
Blood|August 1, 1995
Transfer of the human glucocerebrosidase gene into hematopoietic stem cells of nonablated recipients: successful engraftment and long-term expression of the transgeneR Schiffmann, J A Medin, J M Ward, et al.
Journal of Inherited Metabolic Disease|January 27, 2009
Proposed high-risk screening protocol for Fabry disease in patients with renal and vascular diseaseC Auray-Blais, D S Millington, S P Young, et al.
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics|October 13, 2001
Oral and craniofacial findings in Fabry's disease: a report of 13 patientsL Baccaglini, R Schiffmann, M T Brennan, et al.
Neurology|February 15, 2001
Somatosensory evoked potentials as a marker of disease burden in type 3 Gaucher diseaseM A Garvey, C Toro, S Goldstein, et al.
Neuroscience|February 6, 2007
Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: a complex genotype-phenotype relationshipK H Kraemer, N J Patronas, R Schiffmann, et al.
Journal of Medical Genetics|December 14, 2004
Parkinsonism among Gaucher disease carriersO Goker-Alpan, R Schiffmann, M E LaMarca, et al.
Pageof 9