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H K Berry

Showing results (31-40 of 65) with videos related to

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Biomedical Mass Spectrometry|December 1, 1979
Identification and quantitation of urinary dicarboxylic acids as their dicyclohexyl esters in disease states by gas chromatography mass spectrometryE J Norman, H K Berry, M D Denton
Clinical Genetics|February 1, 1978
Galactose-1-phosphate accumulation by a Duarte-transferase deficiency double heterozygoteC H Wharton, H K Berry, M K Bofinger
American Journal of Mental Deficiency|May 1, 1971
Behavioral abnormalities in rats with neonatal jaundiceR E Butcher, R M Stutz, H K Berry
Neuroscience and Biobehavioral Reviews|January 1, 1981
Progress in experimental phenylketonuria: a critical reviewC V Vorhees, R E Butcher, H K Berry
Progress in Brain Research|January 1, 1988
Anticonvulsants and brain developmentC V Vorhees, D R Minck, H K Berry
Developmental Medicine and Child Neurology|June 1, 1970
Phenylketonuria: intellectual developmental and early treatmentD J O'Grady, H K Berry, B S Sutherland
American Journal of Diseases of Children (1960)|January 1, 1971
Cognitive development in early treated phenylketonuriaD J O'Grady, H K Berry, B S Sutherland
Clinical Chemistry|January 1, 1982
Gas-chromatographic/mass spectrometric detection of 3-hydroxy-3-methylglutaryl-CoA lyase deficiency in double first cousinsE J Norman, M D Denton, H K Berry
Journal of Inherited Metabolic Disease|January 1, 1986
Phenylketonuria and sclerodermaE H Brown, H K Berry, J Olson, et al.
Biochimica Et Biophysica Acta|March 1, 1971
Development of phenylalanine hydroxylase activity in guinea pig liverH K Berry, R Cripps, K Nicholls, et al.
Pageof 7

Showing results (31-40 of 65) with videos related to

Sort By:
Pageof 7
Biomedical Mass Spectrometry|December 1, 1979
Identification and quantitation of urinary dicarboxylic acids as their dicyclohexyl esters in disease states by gas chromatography mass spectrometryE J Norman, H K Berry, M D Denton
Clinical Genetics|February 1, 1978
Galactose-1-phosphate accumulation by a Duarte-transferase deficiency double heterozygoteC H Wharton, H K Berry, M K Bofinger
American Journal of Mental Deficiency|May 1, 1971
Behavioral abnormalities in rats with neonatal jaundiceR E Butcher, R M Stutz, H K Berry
Neuroscience and Biobehavioral Reviews|January 1, 1981
Progress in experimental phenylketonuria: a critical reviewC V Vorhees, R E Butcher, H K Berry
Progress in Brain Research|January 1, 1988
Anticonvulsants and brain developmentC V Vorhees, D R Minck, H K Berry
Developmental Medicine and Child Neurology|June 1, 1970
Phenylketonuria: intellectual developmental and early treatmentD J O'Grady, H K Berry, B S Sutherland
American Journal of Diseases of Children (1960)|January 1, 1971
Cognitive development in early treated phenylketonuriaD J O'Grady, H K Berry, B S Sutherland
Clinical Chemistry|January 1, 1982
Gas-chromatographic/mass spectrometric detection of 3-hydroxy-3-methylglutaryl-CoA lyase deficiency in double first cousinsE J Norman, M D Denton, H K Berry
Journal of Inherited Metabolic Disease|January 1, 1986
Phenylketonuria and sclerodermaE H Brown, H K Berry, J Olson, et al.
Biochimica Et Biophysica Acta|March 1, 1971
Development of phenylalanine hydroxylase activity in guinea pig liverH K Berry, R Cripps, K Nicholls, et al.
Pageof 7