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Pediatrics
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July 1, 1988
Treatable dystonia presenting as spastic cerebral palsy
J K Fink, M R Filling-Katz, N W Barton, et al.
Blood Cells, Molecules & Diseases
|
October 24, 2000
Comparative efficacy of dose regimens in enzyme replacement therapy of type I Gaucher disease
G Altarescu, R Schiffmann, C C Parker, et al.
Neurology
|
January 1, 1992
Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration (HARP syndrome)
J J Higgins, M C Patterson, N M Papadopoulos, et al.
Neurology
|
October 1, 1989
Tetrahydrobiopterin administration in biopterin-deficient progressive dystonia with diurnal variation
J K Fink, P Ravin, C E Argoff, et al.
Radiology
|
August 1, 1992
Gaucher disease: abdominal MR imaging findings in 46 patients
S C Hill, B M Damaska, A Ling, et al.
Neurology
|
June 20, 1998
Quantitative analysis of cerebral vasculopathy in patients with Fabry disease
K E Crutchfield, N J Patronas, J M Dambrosia, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 17, 1998
Proton magnetic resonance spectroscopic imaging in the clinical evaluation of patients with Niemann-Pick type C disease
G Tedeschi, S Bonavita, N W Barton, et al.
The Journal of Pediatrics
|
April 11, 2001
The efficacy of enzyme replacement therapy in patients with chronic neuronopathic Gaucher's disease
G Altarescu, S Hill, E Wiggs, et al.
American Journal of Human Genetics
|
October 1, 1993
Prevalence of nine mutations among Jewish and non-Jewish Gaucher disease patients
M Horowitz, G Tzuri, N Eyal, et al.
Pediatrics
|
May 19, 1998
Management of neutralizing antibody to Ceredase in a patient with type 3 Gaucher disease
R O Brady, G J Murray, K L Oliver, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 65) with videos related to
Sort By:
Page
of 7
Pediatrics
|
July 1, 1988
Treatable dystonia presenting as spastic cerebral palsy
J K Fink, M R Filling-Katz, N W Barton, et al.
Blood Cells, Molecules & Diseases
|
October 24, 2000
Comparative efficacy of dose regimens in enzyme replacement therapy of type I Gaucher disease
G Altarescu, R Schiffmann, C C Parker, et al.
Neurology
|
January 1, 1992
Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration (HARP syndrome)
J J Higgins, M C Patterson, N M Papadopoulos, et al.
Neurology
|
October 1, 1989
Tetrahydrobiopterin administration in biopterin-deficient progressive dystonia with diurnal variation
J K Fink, P Ravin, C E Argoff, et al.
Radiology
|
August 1, 1992
Gaucher disease: abdominal MR imaging findings in 46 patients
S C Hill, B M Damaska, A Ling, et al.
Neurology
|
June 20, 1998
Quantitative analysis of cerebral vasculopathy in patients with Fabry disease
K E Crutchfield, N J Patronas, J M Dambrosia, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 17, 1998
Proton magnetic resonance spectroscopic imaging in the clinical evaluation of patients with Niemann-Pick type C disease
G Tedeschi, S Bonavita, N W Barton, et al.
The Journal of Pediatrics
|
April 11, 2001
The efficacy of enzyme replacement therapy in patients with chronic neuronopathic Gaucher's disease
G Altarescu, S Hill, E Wiggs, et al.
American Journal of Human Genetics
|
October 1, 1993
Prevalence of nine mutations among Jewish and non-Jewish Gaucher disease patients
M Horowitz, G Tzuri, N Eyal, et al.
Pediatrics
|
May 19, 1998
Management of neutralizing antibody to Ceredase in a patient with type 3 Gaucher disease
R O Brady, G J Murray, K L Oliver, et al.
Page
of 7