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B A Gordon

Showing results (11-20 of 46) with videos related to

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Acta Paediatrica Scandinavica|November 1, 1980
Unusual clinical and ultrastructural features in a boy with biochemically typical mannosidosisB A Gordon, R Carson, M D Haust
Neuroimage|January 7, 2014
Prefrontal gray matter volume mediates age effects on memory strategiesB A Kirchhoff, B A Gordon, D Head
AJR. American Journal of Roentgenology|December 11, 1997
Whole-body positron emission tomography: normal variations, pitfalls, and technical considerationsB A Gordon, F L Flanagan, F Dehdashti
Radiology|October 1, 1995
Pyomyositis: characteristics at CT and MR imagingB A Gordon, S Martinez, A J Collins
Clinical Biochemistry|April 1, 1977
Ornithine methyl ester. An unusual metabolite encountered in the urine of patients with a urea cycle disorder characterized by hyperammonemia, hyperornithinemia and homocitrullinuriaB A Gordon, P D Gatfield, E Taller
Human Pathology|March 1, 1981
Ultrastructure of hepatic mitochondria in a child with hyperornithinemia, hyperammonemia, and homocitrullinuriaM D Haust, P D Gatfield, B A Gordon
Journal of Inherited Metabolic Disease|January 1, 1995
Medium-chain acyl-CoA dehydrogenase deficiency is not a cause of previously diagnosed Reye syndromeC A Rupar, T W Frewen, B A Gordon
Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|July 1, 1987
The hyperornithinemia, hyperammonemia, homocitrullinuria syndrome: an ornithine transport defect remediable with ornithine supplementsB A Gordon, D P Gatfield, M D Haust
Advances in Experimental Medicine and Biology|January 1, 1976
Ultrastructure and peroxidase of leucocytes in five patients with juvenile form of ceroid lipofuscinosesM D Haust, B A Gordon, G G Hinton
Clinical Biochemistry|June 1, 1975
Defective heparan sulfate metabolism in the Sanfilippo syndrome and assay of this defect in the assessment of the mucopolysaccharidoses patientB A Gordon, V Feleki, C H Budreau, et al.
Pageof 5

Showing results (11-20 of 46) with videos related to

Sort By:
Pageof 5
Acta Paediatrica Scandinavica|November 1, 1980
Unusual clinical and ultrastructural features in a boy with biochemically typical mannosidosisB A Gordon, R Carson, M D Haust
Neuroimage|January 7, 2014
Prefrontal gray matter volume mediates age effects on memory strategiesB A Kirchhoff, B A Gordon, D Head
AJR. American Journal of Roentgenology|December 11, 1997
Whole-body positron emission tomography: normal variations, pitfalls, and technical considerationsB A Gordon, F L Flanagan, F Dehdashti
Radiology|October 1, 1995
Pyomyositis: characteristics at CT and MR imagingB A Gordon, S Martinez, A J Collins
Clinical Biochemistry|April 1, 1977
Ornithine methyl ester. An unusual metabolite encountered in the urine of patients with a urea cycle disorder characterized by hyperammonemia, hyperornithinemia and homocitrullinuriaB A Gordon, P D Gatfield, E Taller
Human Pathology|March 1, 1981
Ultrastructure of hepatic mitochondria in a child with hyperornithinemia, hyperammonemia, and homocitrullinuriaM D Haust, P D Gatfield, B A Gordon
Journal of Inherited Metabolic Disease|January 1, 1995
Medium-chain acyl-CoA dehydrogenase deficiency is not a cause of previously diagnosed Reye syndromeC A Rupar, T W Frewen, B A Gordon
Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|July 1, 1987
The hyperornithinemia, hyperammonemia, homocitrullinuria syndrome: an ornithine transport defect remediable with ornithine supplementsB A Gordon, D P Gatfield, M D Haust
Advances in Experimental Medicine and Biology|January 1, 1976
Ultrastructure and peroxidase of leucocytes in five patients with juvenile form of ceroid lipofuscinosesM D Haust, B A Gordon, G G Hinton
Clinical Biochemistry|June 1, 1975
Defective heparan sulfate metabolism in the Sanfilippo syndrome and assay of this defect in the assessment of the mucopolysaccharidoses patientB A Gordon, V Feleki, C H Budreau, et al.
Pageof 5