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R Schiffmann

Showing results (61-70 of 89) with videos related to

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Neurology|August 1, 1995
Proton magnetic resonance spectroscopic imaging in childhood ataxia with diffuse central nervous system hypomyelinationG Tedeschi, R Schiffmann, N W Barton, et al.
Lancet (London, England)|December 5, 2009
Enzyme replacement therapy with agalsidase alfa in patients with Fabry's disease: an analysis of registry dataA Mehta, M Beck, P Elliott, et al.
The Journal of Pediatrics|April 1, 1995
Outcome of partial splenectomy for type I Gaucher diseaseA Zimran, D Elstein, R Schiffmann, et al.
Brain : a Journal of Neurology|November 16, 2006
Neuropathic and cerebrovascular correlates of hearing loss in Fabry diseaseM Ries, H J Kim, C K Zalewski, et al.
Circulation|September 26, 2001
Regional cerebral hyperperfusion and nitric oxide pathway dysregulation in Fabry disease: reversal by enzyme replacement therapyD F Moore, L T Scott, M T Gladwin, et al.
Annals of Neurology|May 1, 1997
Leukodystrophy in patients with ovarian dysgenesisR Schiffmann, G Tedeschi, R P Kinkel, et al.
Neurology|June 4, 2008
Sensitivity and specificity of decreased CSF asialotransferrin for eIF2B-related disorderA Vanderver, Y Hathout, J Maletkovic, et al.
Annals of Internal Medicine|January 1, 1995
Enzyme therapy in type 1 Gaucher disease: comparative efficacy of mannose-terminated glucocerebrosidase from natural and recombinant sourcesG A Grabowski, N W Barton, G Pastores, et al.
Annals of Neurology|March 1, 1994
Childhood ataxia with diffuse central nervous system hypomyelinationR Schiffmann, J R Moller, B D Trapp, et al.
Neurology|January 1, 1993
The effect of cholesterol-lowering agents on hepatic and plasma cholesterol in Niemann-Pick disease type CM C Patterson, A M Di Bisceglie, J J Higgins, et al.
Pageof 9

Showing results (61-70 of 89) with videos related to

Sort By:
Pageof 9
Neurology|August 1, 1995
Proton magnetic resonance spectroscopic imaging in childhood ataxia with diffuse central nervous system hypomyelinationG Tedeschi, R Schiffmann, N W Barton, et al.
Lancet (London, England)|December 5, 2009
Enzyme replacement therapy with agalsidase alfa in patients with Fabry's disease: an analysis of registry dataA Mehta, M Beck, P Elliott, et al.
The Journal of Pediatrics|April 1, 1995
Outcome of partial splenectomy for type I Gaucher diseaseA Zimran, D Elstein, R Schiffmann, et al.
Brain : a Journal of Neurology|November 16, 2006
Neuropathic and cerebrovascular correlates of hearing loss in Fabry diseaseM Ries, H J Kim, C K Zalewski, et al.
Circulation|September 26, 2001
Regional cerebral hyperperfusion and nitric oxide pathway dysregulation in Fabry disease: reversal by enzyme replacement therapyD F Moore, L T Scott, M T Gladwin, et al.
Annals of Neurology|May 1, 1997
Leukodystrophy in patients with ovarian dysgenesisR Schiffmann, G Tedeschi, R P Kinkel, et al.
Neurology|June 4, 2008
Sensitivity and specificity of decreased CSF asialotransferrin for eIF2B-related disorderA Vanderver, Y Hathout, J Maletkovic, et al.
Annals of Internal Medicine|January 1, 1995
Enzyme therapy in type 1 Gaucher disease: comparative efficacy of mannose-terminated glucocerebrosidase from natural and recombinant sourcesG A Grabowski, N W Barton, G Pastores, et al.
Annals of Neurology|March 1, 1994
Childhood ataxia with diffuse central nervous system hypomyelinationR Schiffmann, J R Moller, B D Trapp, et al.
Neurology|January 1, 1993
The effect of cholesterol-lowering agents on hepatic and plasma cholesterol in Niemann-Pick disease type CM C Patterson, A M Di Bisceglie, J J Higgins, et al.
Pageof 9