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Neurology
|
August 26, 1998
Mucolipidosis type IV: characteristic MRI findings
K P Frei, N J Patronas, K E Crutchfield, et al.
Journal of Child Neurology
|
October 1, 1993
Posterior fossa abnormalities in children with infantile spasms
R 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 patients
L C Xu, S Kluepfel-Stahl, M Blanco, et al.
Human Mutation
|
January 29, 2000
Five novel mutations in fourteen patients with Fabry Disease
K 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 transgene
R 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 disease
C 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 patients
L 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 disease
M A Garvey, C Toro, S Goldstein, et al.
Neuroscience
|
February 6, 2007
Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: a complex genotype-phenotype relationship
K H Kraemer, N J Patronas, R Schiffmann, et al.
Journal of Medical Genetics
|
December 14, 2004
Parkinsonism among Gaucher disease carriers
O Goker-Alpan, R Schiffmann, M E LaMarca, et al.
Page
of 9
Search research articles
Search
Showing results (31-40 of 89) with videos related to
Sort By:
Page
of 9
Neurology
|
August 26, 1998
Mucolipidosis type IV: characteristic MRI findings
K P Frei, N J Patronas, K E Crutchfield, et al.
Journal of Child Neurology
|
October 1, 1993
Posterior fossa abnormalities in children with infantile spasms
R 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 patients
L C Xu, S Kluepfel-Stahl, M Blanco, et al.
Human Mutation
|
January 29, 2000
Five novel mutations in fourteen patients with Fabry Disease
K 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 transgene
R 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 disease
C 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 patients
L 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 disease
M A Garvey, C Toro, S Goldstein, et al.
Neuroscience
|
February 6, 2007
Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: a complex genotype-phenotype relationship
K H Kraemer, N J Patronas, R Schiffmann, et al.
Journal of Medical Genetics
|
December 14, 2004
Parkinsonism among Gaucher disease carriers
O Goker-Alpan, R Schiffmann, M E LaMarca, et al.
Page
of 9