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Journal of Pediatric Orthopedics. Part B
|
December 1, 2001
Mobile thoracolumbar gibbus in Morquio type A: the cause of paraparesis and its management
S Dalvie, J Skinner, A Vellodi, et al.
American Journal of Medical Genetics
|
June 5, 1995
Bone marrow transplantation in Batten disease (neuronal ceroid-lipofuscinosis). Will it work? Preliminary studies on coculture experiments and on bone marrow transplant in late infantile Batten disease
B D Lake, D C Henderson, A Oakhill, et al.
JIMD Reports
|
April 17, 2013
A Clinically Severe Variant of β-Mannosidosis, Presenting with Neonatal Onset Epilepsy with Subsequent Evolution of Hydrocephalus
A Broomfield, R Gunny, I Ali, et al.
International Journal of Pediatric Otorhinolaryngology
|
March 30, 2001
Disordered breathing during sleep in patients with mucopolysaccharidoses
S E Leighton, B Papsin, A Vellodi, et al.
Clinical and Experimental Immunology
|
June 1, 1992
Class- and subclass-specific pneumococcal antibody levels and response to immunization after bone marrow transplantation
J E Lortan, A Vellodi, E S Jurges, et al.
Journal of Inherited Metabolic Disease
|
May 19, 1998
Niemann-Pick disease type C and defective peroxisomal beta-oxidation of branched-chain substrates
J S Sequeira, A Vellodi, M T Vanier, et al.
Experimental Eye Research
|
April 1, 1996
Ultrastructural study of the cornea in a bone marrow-transplanted Hurler syndrome patient
Y Huang, A J Bron, K M Meek, et al.
Ultrastructural Pathology
|
April 25, 2007
Electron microscopy of chorionic villus samples for prenatal diagnosis of lysosomal storage disorders
D J Fowler, G Anderson, A Vellodi, et al.
Journal of Medical Genetics
|
December 1, 1998
Identification of 12 novel mutations in the alpha-N-acetylglucosaminidase gene in 14 patients with Sanfilippo syndrome type B (mucopolysaccharidosis type IIIB)
C E Beesley, E P Young, A Vellodi, et al.
Journal of Inherited Metabolic Disease
|
September 19, 2007
A severity scoring tool to assess the neurological features of neuronopathic Gaucher disease
E H Davies, R Surtees, C DeVile, et al.
Page
of 6
Search research articles
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Showing results (11-20 of 57) with videos related to
Sort By:
Page
of 6
Journal of Pediatric Orthopedics. Part B
|
December 1, 2001
Mobile thoracolumbar gibbus in Morquio type A: the cause of paraparesis and its management
S Dalvie, J Skinner, A Vellodi, et al.
American Journal of Medical Genetics
|
June 5, 1995
Bone marrow transplantation in Batten disease (neuronal ceroid-lipofuscinosis). Will it work? Preliminary studies on coculture experiments and on bone marrow transplant in late infantile Batten disease
B D Lake, D C Henderson, A Oakhill, et al.
JIMD Reports
|
April 17, 2013
A Clinically Severe Variant of β-Mannosidosis, Presenting with Neonatal Onset Epilepsy with Subsequent Evolution of Hydrocephalus
A Broomfield, R Gunny, I Ali, et al.
International Journal of Pediatric Otorhinolaryngology
|
March 30, 2001
Disordered breathing during sleep in patients with mucopolysaccharidoses
S E Leighton, B Papsin, A Vellodi, et al.
Clinical and Experimental Immunology
|
June 1, 1992
Class- and subclass-specific pneumococcal antibody levels and response to immunization after bone marrow transplantation
J E Lortan, A Vellodi, E S Jurges, et al.
Journal of Inherited Metabolic Disease
|
May 19, 1998
Niemann-Pick disease type C and defective peroxisomal beta-oxidation of branched-chain substrates
J S Sequeira, A Vellodi, M T Vanier, et al.
Experimental Eye Research
|
April 1, 1996
Ultrastructural study of the cornea in a bone marrow-transplanted Hurler syndrome patient
Y Huang, A J Bron, K M Meek, et al.
Ultrastructural Pathology
|
April 25, 2007
Electron microscopy of chorionic villus samples for prenatal diagnosis of lysosomal storage disorders
D J Fowler, G Anderson, A Vellodi, et al.
Journal of Medical Genetics
|
December 1, 1998
Identification of 12 novel mutations in the alpha-N-acetylglucosaminidase gene in 14 patients with Sanfilippo syndrome type B (mucopolysaccharidosis type IIIB)
C E Beesley, E P Young, A Vellodi, et al.
Journal of Inherited Metabolic Disease
|
September 19, 2007
A severity scoring tool to assess the neurological features of neuronopathic Gaucher disease
E H Davies, R Surtees, C DeVile, et al.
Page
of 6