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C B Whitley

Showing results (31-40 of 58) with videos related to

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Clinical Chemistry|March 1, 1989
Diagnostic test for mucopolysaccharidosis. I. Direct method for quantifying excessive urinary glycosaminoglycan excretionC B Whitley, M D Ridnour, K A Draper, et al.
American Journal of Medical Genetics. Supplement|January 1, 1987
Direct hyperbilirubinemia and hepatic fibrosis: a new presentation of Jeune syndrome (asphyxiating thoracic dystrophy)C B Whitley, S J Schwarzenberg, B A Burke, et al.
JAMA|April 22, 1983
Amiodarone phenocopy of Fabry's keratopathyC B Whitley, M Y Tsai, J J Heger, et al.
Journal of Chromatographic Science|May 1, 1984
Determination of urinary succinylacetone by capillary gas chromatographyM Tuchman, C B Whitley, M L Ramnaraine, et al.
Archives of Pediatrics & Adolescent Medicine|August 2, 2000
Radiological case of the month. Coarctation of the aorta in Hurler syndromeE A Braunlin, W Krivit, B A Burke, et al.
American Journal of Medical Genetics|December 18, 1996
Clinical and biochemical heterogeneity in females of a large pedigree with ornithine transcarbamylase deficiency due to the R141Q mutationM J Ahrens, S A Berry, C B Whitley, et al.
Human Gene Therapy|February 10, 1996
Preclinical studies of lymphocyte gene therapy for mild Hunter syndrome (mucopolysaccharidosis type II)S E Braun, D Pan, E L Aronovich, et al.
JIMD Reports|February 23, 2013
Cardiac Ultrasound Findings in Infants with Severe (Hurler Phenotype) Untreated Mucopolysaccharidosis (MPS) Type IL Schroeder, P Orchard, C B Whitley, et al.
Human Mutation|January 1, 1994
A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with maternally inherited cardiomyopathyG Silvestri, F M Santorelli, S Shanske, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 15, 1993
Metabolic correction and cross-correction of mucopolysaccharidosis type II (Hunter syndrome) by retroviral-mediated gene transfer and expression of human iduronate-2-sulfataseS E Braun, E L Aronovich, R A Anderson, et al.
Pageof 6

Showing results (31-40 of 58) with videos related to

Sort By:
Pageof 6
Clinical Chemistry|March 1, 1989
Diagnostic test for mucopolysaccharidosis. I. Direct method for quantifying excessive urinary glycosaminoglycan excretionC B Whitley, M D Ridnour, K A Draper, et al.
American Journal of Medical Genetics. Supplement|January 1, 1987
Direct hyperbilirubinemia and hepatic fibrosis: a new presentation of Jeune syndrome (asphyxiating thoracic dystrophy)C B Whitley, S J Schwarzenberg, B A Burke, et al.
JAMA|April 22, 1983
Amiodarone phenocopy of Fabry's keratopathyC B Whitley, M Y Tsai, J J Heger, et al.
Journal of Chromatographic Science|May 1, 1984
Determination of urinary succinylacetone by capillary gas chromatographyM Tuchman, C B Whitley, M L Ramnaraine, et al.
Archives of Pediatrics & Adolescent Medicine|August 2, 2000
Radiological case of the month. Coarctation of the aorta in Hurler syndromeE A Braunlin, W Krivit, B A Burke, et al.
American Journal of Medical Genetics|December 18, 1996
Clinical and biochemical heterogeneity in females of a large pedigree with ornithine transcarbamylase deficiency due to the R141Q mutationM J Ahrens, S A Berry, C B Whitley, et al.
Human Gene Therapy|February 10, 1996
Preclinical studies of lymphocyte gene therapy for mild Hunter syndrome (mucopolysaccharidosis type II)S E Braun, D Pan, E L Aronovich, et al.
JIMD Reports|February 23, 2013
Cardiac Ultrasound Findings in Infants with Severe (Hurler Phenotype) Untreated Mucopolysaccharidosis (MPS) Type IL Schroeder, P Orchard, C B Whitley, et al.
Human Mutation|January 1, 1994
A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with maternally inherited cardiomyopathyG Silvestri, F M Santorelli, S Shanske, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 15, 1993
Metabolic correction and cross-correction of mucopolysaccharidosis type II (Hunter syndrome) by retroviral-mediated gene transfer and expression of human iduronate-2-sulfataseS E Braun, E L Aronovich, R A Anderson, et al.
Pageof 6