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Neurology
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August 1, 1995
Proton magnetic resonance spectroscopic imaging in childhood ataxia with diffuse central nervous system hypomyelination
G 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 data
A Mehta, M Beck, P Elliott, et al.
The Journal of Pediatrics
|
April 1, 1995
Outcome of partial splenectomy for type I Gaucher disease
A Zimran, D Elstein, R Schiffmann, et al.
Brain : a Journal of Neurology
|
November 16, 2006
Neuropathic and cerebrovascular correlates of hearing loss in Fabry disease
M 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 therapy
D F Moore, L T Scott, M T Gladwin, et al.
Annals of Neurology
|
May 1, 1997
Leukodystrophy in patients with ovarian dysgenesis
R Schiffmann, G Tedeschi, R P Kinkel, et al.
Neurology
|
June 4, 2008
Sensitivity and specificity of decreased CSF asialotransferrin for eIF2B-related disorder
A 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 sources
G A Grabowski, N W Barton, G Pastores, et al.
Annals of Neurology
|
March 1, 1994
Childhood ataxia with diffuse central nervous system hypomyelination
R 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 C
M C Patterson, A M Di Bisceglie, J J Higgins, et al.
Page
of 9
Search research articles
Search
Showing results (61-70 of 89) with videos related to
Sort By:
Page
of 9
Neurology
|
August 1, 1995
Proton magnetic resonance spectroscopic imaging in childhood ataxia with diffuse central nervous system hypomyelination
G 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 data
A Mehta, M Beck, P Elliott, et al.
The Journal of Pediatrics
|
April 1, 1995
Outcome of partial splenectomy for type I Gaucher disease
A Zimran, D Elstein, R Schiffmann, et al.
Brain : a Journal of Neurology
|
November 16, 2006
Neuropathic and cerebrovascular correlates of hearing loss in Fabry disease
M 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 therapy
D F Moore, L T Scott, M T Gladwin, et al.
Annals of Neurology
|
May 1, 1997
Leukodystrophy in patients with ovarian dysgenesis
R Schiffmann, G Tedeschi, R P Kinkel, et al.
Neurology
|
June 4, 2008
Sensitivity and specificity of decreased CSF asialotransferrin for eIF2B-related disorder
A 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 sources
G A Grabowski, N W Barton, G Pastores, et al.
Annals of Neurology
|
March 1, 1994
Childhood ataxia with diffuse central nervous system hypomyelination
R 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 C
M C Patterson, A M Di Bisceglie, J J Higgins, et al.
Page
of 9