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Results: 1-9 |
Results: 9
TRANSIENT 5-OXOPROLINURIA AND HIGH ANION GAP METABOLIC-ACIDOSIS - CLINICAL AND BIOCHEMICAL FINDINGS IN 11 SUBJECTS
Authors: PITT JJ HAUSER S
Citation: Jj. Pitt et S. Hauser, TRANSIENT 5-OXOPROLINURIA AND HIGH ANION GAP METABOLIC-ACIDOSIS - CLINICAL AND BIOCHEMICAL FINDINGS IN 11 SUBJECTS, Clinical chemistry, 44(7), 1998, pp. 1497-1503
SUCCINIC SEMIALDEHYDE DEHYDROGENASE-DEFICIENCY - LOW EXCRETION OF METABOLITES IN A NEONATE
Authors: PITT JJ HAWKINS R CLEARY M EGGINGTON M THORBURN DR WARWICK L
Citation: Jj. Pitt et al., SUCCINIC SEMIALDEHYDE DEHYDROGENASE-DEFICIENCY - LOW EXCRETION OF METABOLITES IN A NEONATE, Journal of inherited metabolic disease, 20(1), 1997, pp. 39-42
FASTING HYPOKETOTIC COMA IN A CHILD WITH DEFICIENCY OF MITOCHONDRIAL 3-HYDROXY-3-METHYLGLUTARYL-COA SYNTHASE
Authors: THOMPSON GN HSU BYL PITT JJ TREACY E STANLEY CA
Citation: Gn. Thompson et al., FASTING HYPOKETOTIC COMA IN A CHILD WITH DEFICIENCY OF MITOCHONDRIAL 3-HYDROXY-3-METHYLGLUTARYL-COA SYNTHASE, The New England journal of medicine, 337(17), 1997, pp. 1203-1207
OLIGOSACCHARIDE CHARACTERIZATION AND QUANTITATION USING 1-PHENYL-3-METHYL-5-PYRAZOLONE DERIVATIZATION AND MATRIX-ASSISTED LASER DESORPTION IONIZATION TIME-OF-FLIGHT MASS-SPECTROMETRY/
Authors: PITT JJ GORMAN JJ
Citation: Jj. Pitt et Jj. Gorman, OLIGOSACCHARIDE CHARACTERIZATION AND QUANTITATION USING 1-PHENYL-3-METHYL-5-PYRAZOLONE DERIVATIZATION AND MATRIX-ASSISTED LASER DESORPTION IONIZATION TIME-OF-FLIGHT MASS-SPECTROMETRY/, Analytical biochemistry, 248(1), 1997, pp. 63-75
MATRIX-ASSISTED LASER DESORPTION IONIZATION TIME-OF-FLIGHT MASS-SPECTROMETRY OF SIALYLATED GLYCOPEPTIDES AND PROTEINS USING 2,6-DIHYDROXYACETOPHENONE AS A MATRIX/
Authors: PITT JJ GORMAN JJ
Citation: Jj. Pitt et Jj. Gorman, MATRIX-ASSISTED LASER DESORPTION IONIZATION TIME-OF-FLIGHT MASS-SPECTROMETRY OF SIALYLATED GLYCOPEPTIDES AND PROTEINS USING 2,6-DIHYDROXYACETOPHENONE AS A MATRIX/, Rapid communications in mass spectrometry, 10(14), 1996, pp. 1786-1788
IN-VIVO DISPOSAL OF PHENYLALANINE IN PHENYLKETONURIA - A STUDY OF 2 SIBLINGS
Authors: TREACY E PITT JJ SELLER K THOMPSON GN RAMUS S COTTON RGH
Citation: E. Treacy et al., IN-VIVO DISPOSAL OF PHENYLALANINE IN PHENYLKETONURIA - A STUDY OF 2 SIBLINGS, Journal of inherited metabolic disease, 19(5), 1996, pp. 595-602
TRIMETHYLAMINURIA, FISH ODOR SYNDROME - A NEW METHOD OF DETECTION ANDRESPONSE TO TREATMENT WITH METRONIDAZOLE
Authors: TREACY E JOHNSON D PITT JJ DANKS DM
Citation: E. Treacy et al., TRIMETHYLAMINURIA, FISH ODOR SYNDROME - A NEW METHOD OF DETECTION ANDRESPONSE TO TREATMENT WITH METRONIDAZOLE, Journal of inherited metabolic disease, 18(3), 1995, pp. 306-312
NOVEL GLYCINE CONJUGATES IN MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY
Authors: PITT JJ
Citation: Jj. Pitt, NOVEL GLYCINE CONJUGATES IN MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY, Journal of inherited metabolic disease, 16(2), 1993, pp. 392-398
EXCRETION OF 3,6-EPOXYDICARBOXYLIC ACIDS IN PEROXISOMAL DISORDERS
Authors: PITT JJ POULOS A
Citation: Jj. Pitt et A. Poulos, EXCRETION OF 3,6-EPOXYDICARBOXYLIC ACIDS IN PEROXISOMAL DISORDERS, Clinica chimica acta, 223(1-2), 1993, pp. 23-29
Risultati: 1-9 |