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V G Oberholzer

Showing results (21-30 of 35) with videos related to

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Archives of Disease in Childhood|February 1, 1978
Acute neonatal and benign citrullinaemia in one sibshipE A Burgess, V G Oberholzer, J M Semmens, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 23, 1975
Increased pyroglutamic acid levels in patients on artificial dietsV G Oberholzer, C B Wood, T Palmer, et al.
American Journal of Obstetrics and Gynecology|October 15, 1974
Argininosuccinic aciduria: antenatal investigations in an affected familyE A Burgess, V G Oberholzer, T Palmer, et al.
Clinical Science (London, England : 1979)|February 1, 1987
Effect of partial ornithine carbamoyltransferase deficiency on urea synthesis and related biochemical eventsJ D Kay, V G Oberholzer, J W Seakins, et al.
Archives of Disease in Childhood|June 1, 1974
Hyperammonaemia in 20 families. Biochemical and genetical survey, including investigations in 3 new familiesT Palmer, V G Oberholzer, E A Burgess, et al.
British Medical Journal|December 25, 1971
Protein intake and plasma amino-acids of infants of low birth weightH B Valman, R J Brown, T Palmer, et al.
Gut|May 1, 1988
Lactosylceramide in inflammatory bowel disease: a biochemical studyC R Stevens, V G Oberholzer, J A Walker-Smith, et al.
Clinical Science (London, England : 1979)|February 1, 1985
Determination of the rate of urea synthesis from serial measurements of plasma urea concentration after an alanine load: theoretical and methodological aspectsD Geiseler, J D Kay, V G Oberholzer, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1983
Neurological features and computed tomography of the brain in children with ornithine carbamoyl transferase deficiencyB E Kendall, D P Kingsley, J V Leonard, et al.
Journal of the Royal Society of Medicine|August 1, 1980
Hyperornithinaemia with gyrate atrophy of the choroid and retina in two siblingsD T Hodes, V G Oberholzer, A S Mushin, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Archives of Disease in Childhood|February 1, 1978
Acute neonatal and benign citrullinaemia in one sibshipE A Burgess, V G Oberholzer, J M Semmens, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 23, 1975
Increased pyroglutamic acid levels in patients on artificial dietsV G Oberholzer, C B Wood, T Palmer, et al.
American Journal of Obstetrics and Gynecology|October 15, 1974
Argininosuccinic aciduria: antenatal investigations in an affected familyE A Burgess, V G Oberholzer, T Palmer, et al.
Clinical Science (London, England : 1979)|February 1, 1987
Effect of partial ornithine carbamoyltransferase deficiency on urea synthesis and related biochemical eventsJ D Kay, V G Oberholzer, J W Seakins, et al.
Archives of Disease in Childhood|June 1, 1974
Hyperammonaemia in 20 families. Biochemical and genetical survey, including investigations in 3 new familiesT Palmer, V G Oberholzer, E A Burgess, et al.
British Medical Journal|December 25, 1971
Protein intake and plasma amino-acids of infants of low birth weightH B Valman, R J Brown, T Palmer, et al.
Gut|May 1, 1988
Lactosylceramide in inflammatory bowel disease: a biochemical studyC R Stevens, V G Oberholzer, J A Walker-Smith, et al.
Clinical Science (London, England : 1979)|February 1, 1985
Determination of the rate of urea synthesis from serial measurements of plasma urea concentration after an alanine load: theoretical and methodological aspectsD Geiseler, J D Kay, V G Oberholzer, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1983
Neurological features and computed tomography of the brain in children with ornithine carbamoyl transferase deficiencyB E Kendall, D P Kingsley, J V Leonard, et al.
Journal of the Royal Society of Medicine|August 1, 1980
Hyperornithinaemia with gyrate atrophy of the choroid and retina in two siblingsD T Hodes, V G Oberholzer, A S Mushin, et al.
Pageof 4