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The Journal of Pediatrics
|
August 1, 1995
Magnetic resonance imaging in phenylketonuria: reversal of cerebral white matter change
M A Cleary, J H Walter, J E Wraith, et al.
Journal of Inherited Metabolic Disease
|
September 17, 2010
Dietary modifications in patients receiving miglustat
H Champion, U Ramaswami, J Imrie, et al.
Human Genetics
|
March 1, 1992
Mucopolysaccharidosis type I (Hurler syndrome): linkage disequilibrium indicates the presence of a major allele
H S Scott, P V Nelson, A Cooper, et al.
Human Molecular Genetics
|
September 1, 1997
Novel mutations in Sanfilippo A syndrome: implications for enzyme function
B Weber, X H Guo, J E Wraith, et al.
Bone Marrow Transplantation
|
May 16, 2000
Donor bone marrow from a sibling with inborn error of metabolism for treatment of acute leukaemia - clinical and biochemical consequences in the non-affected recipient
S Meyer, M Thornley, R F Wynn, et al.
Journal of Inherited Metabolic Disease
|
May 26, 2004
Juvenile Sandhoff disease--nine new cases and a review of the literature
C J Hendriksz, P C Corry, J E Wraith, et al.
Journal of Inherited Metabolic Disease
|
January 26, 2006
Mucopolysaccharidosis I under enzyme replacement therapy with laronidase--a mortality case with autopsy report
H-Y Lin, S-P Lin, C-K Chuang, et al.
Archives of Disease in Childhood
|
February 1, 1997
Bone marrow transplantation for mucopolysaccharidosis type I: experience of two British centres
A Vellodi, E P Young, A Cooper, et al.
Journal of Inherited Metabolic Disease
|
January 26, 2006
Marrow stromal cells from patients affected by MPS I differentially support haematopoietic progenitor cell development
M A Baxter, R F Wynn, L Schyma, et al.
Lancet (London, England)
|
July 9, 1994
Magnetic resonance imaging of the brain in phenylketonuria
M A Cleary, J H Walter, J E Wraith, et al.
Page
of 12
Search research articles
Search
Showing results (71-80 of 115) with videos related to
Sort By:
Page
of 12
The Journal of Pediatrics
|
August 1, 1995
Magnetic resonance imaging in phenylketonuria: reversal of cerebral white matter change
M A Cleary, J H Walter, J E Wraith, et al.
Journal of Inherited Metabolic Disease
|
September 17, 2010
Dietary modifications in patients receiving miglustat
H Champion, U Ramaswami, J Imrie, et al.
Human Genetics
|
March 1, 1992
Mucopolysaccharidosis type I (Hurler syndrome): linkage disequilibrium indicates the presence of a major allele
H S Scott, P V Nelson, A Cooper, et al.
Human Molecular Genetics
|
September 1, 1997
Novel mutations in Sanfilippo A syndrome: implications for enzyme function
B Weber, X H Guo, J E Wraith, et al.
Bone Marrow Transplantation
|
May 16, 2000
Donor bone marrow from a sibling with inborn error of metabolism for treatment of acute leukaemia - clinical and biochemical consequences in the non-affected recipient
S Meyer, M Thornley, R F Wynn, et al.
Journal of Inherited Metabolic Disease
|
May 26, 2004
Juvenile Sandhoff disease--nine new cases and a review of the literature
C J Hendriksz, P C Corry, J E Wraith, et al.
Journal of Inherited Metabolic Disease
|
January 26, 2006
Mucopolysaccharidosis I under enzyme replacement therapy with laronidase--a mortality case with autopsy report
H-Y Lin, S-P Lin, C-K Chuang, et al.
Archives of Disease in Childhood
|
February 1, 1997
Bone marrow transplantation for mucopolysaccharidosis type I: experience of two British centres
A Vellodi, E P Young, A Cooper, et al.
Journal of Inherited Metabolic Disease
|
January 26, 2006
Marrow stromal cells from patients affected by MPS I differentially support haematopoietic progenitor cell development
M A Baxter, R F Wynn, L Schyma, et al.
Lancet (London, England)
|
July 9, 1994
Magnetic resonance imaging of the brain in phenylketonuria
M A Cleary, J H Walter, J E Wraith, et al.
Page
of 12