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Results: 1-23 |
Results: 23
SURFACE-STRUCTURE OF HUMAN MUCIN USING X-RAY PHOTOELECTRON-SPECTROSCOPY
Authors: RUSSELL BG MODDEMAN WE BIRKBECK JC WRIGHT SE MILLINGTON DS STEVENS RD DOMBROWSKI KE
Citation: Bg. Russell et al., SURFACE-STRUCTURE OF HUMAN MUCIN USING X-RAY PHOTOELECTRON-SPECTROSCOPY, Biospectroscopy, 4(4), 1998, pp. 257-266
HYPOXIA INHIBITS NITRIC-OXIDE SYNTHESIS IN ISOLATED RABBIT LUNG
Authors: KANTROW SP HUANG YCT WHORTON AR GRAYCK EN KNIGHT JM MILLINGTON DS PIANTADOSI CA
Citation: Sp. Kantrow et al., HYPOXIA INHIBITS NITRIC-OXIDE SYNTHESIS IN ISOLATED RABBIT LUNG, American journal of physiology. Lung cellular and molecular physiology, 16(6), 1997, pp. 1167-1173
VALPROATE-ASSOCIATED CARNITINE DEFICIENCY AND MALIGNANT CEREBRAL EDEMA IN THE ABSENCE OF HEPATIC-FAILURE
Authors: TRIGGS WJ GILMORE RL MILLINGTON DS CIBULA J BUNCH TS HARMAN E
Citation: Wj. Triggs et al., VALPROATE-ASSOCIATED CARNITINE DEFICIENCY AND MALIGNANT CEREBRAL EDEMA IN THE ABSENCE OF HEPATIC-FAILURE, International journal of clinical pharmacology and therapeutics, 35(9), 1997, pp. 353-356
CHRONIC SODIUM BENZOATE THERAPY IN CHILDREN WITH INBORN-ERRORS OF UREA SYNTHESIS - EFFECT ON CARNITINE METABOLISM AND AMMONIA NITROGEN REMOVAL
Authors: FEOLIFONSECA JC LAMBERT M MITCHELL G MELANCON SB DALLAIRE L MILLINGTON DS QURESHI IA
Citation: Jc. Feolifonseca et al., CHRONIC SODIUM BENZOATE THERAPY IN CHILDREN WITH INBORN-ERRORS OF UREA SYNTHESIS - EFFECT ON CARNITINE METABOLISM AND AMMONIA NITROGEN REMOVAL, Biochemical and molecular medicine, 57(1), 1996, pp. 31-36
RETROSPECTIVE DIAGNOSIS OF CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY BY ACYLCARNITINE ANALYSIS IN THE PROBAND GUTHRIE CARD AND ENZYMATIC STUDIES IN THE PARENTS
Authors: BRIVET M SLAMA A MILLINGTON DS ROE CR DEMAUGRE F LEGRAND A BOUTRON A POGGI F SAUDUBRAY JM
Citation: M. Brivet et al., RETROSPECTIVE DIAGNOSIS OF CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY BY ACYLCARNITINE ANALYSIS IN THE PROBAND GUTHRIE CARD AND ENZYMATIC STUDIES IN THE PARENTS, Journal of inherited metabolic disease, 19(2), 1996, pp. 181-184
ACETYL-L-CARNITINE DEFICIENCY AS A CAUSE OF ALTERED NERVE MYOINOSITOLCONTENT, NA,K-ATPASE ACTIVITY, AND MOTOR CONDUCTION-VELOCITY IN THE STREPTOZOTOCIN-DIABETIC RAT
Authors: STEVENS MJ LATTIMER SA FELDMAN EL HELTON ED MILLINGTON DS SIMA AAF GREENE DA
Citation: Mj. Stevens et al., ACETYL-L-CARNITINE DEFICIENCY AS A CAUSE OF ALTERED NERVE MYOINOSITOLCONTENT, NA,K-ATPASE ACTIVITY, AND MOTOR CONDUCTION-VELOCITY IN THE STREPTOZOTOCIN-DIABETIC RAT, Metabolism, clinical and experimental, 45(7), 1996, pp. 865-872
RAPID DIAGNOSIS OF HOMOCYSTINURIA AND OTHER HYPERMETHIONINEMIAS FROM NEWBORNS BLOOD SPOTS BY TANDEM MASS-SPECTROMETRY
Authors: CHACE DH HILLMAN SL MILLINGTON DS KAHLER SG ADAM BW LEVY HL
Citation: Dh. Chace et al., RAPID DIAGNOSIS OF HOMOCYSTINURIA AND OTHER HYPERMETHIONINEMIAS FROM NEWBORNS BLOOD SPOTS BY TANDEM MASS-SPECTROMETRY, Clinical chemistry, 42(3), 1996, pp. 349-355
ACUTE FATTY LIVER OF PREGNANCY, HEMOLYSIS, ELEVATED LIVER-ENZYMES, AND LOW PLATELETS SYNDROME, AND LONG-CHAIN 3-HYDROXYACYL-COENZYME-A DEHYDROGENASE-DEFICIENCY
Authors: TREEM WR SHOUP ME HALE DE BENNETT MJ RINALDO P MILLINGTON DS STANLEY CA RIELY CA HYAMS JS
Citation: Wr. Treem et al., ACUTE FATTY LIVER OF PREGNANCY, HEMOLYSIS, ELEVATED LIVER-ENZYMES, AND LOW PLATELETS SYNDROME, AND LONG-CHAIN 3-HYDROXYACYL-COENZYME-A DEHYDROGENASE-DEFICIENCY, The American journal of gastroenterology, 91(11), 1996, pp. 2293-2300
FATTY-ACID OXIDATION ABNORMALITIES IN CHILDHOOD-ONSET SPINAL MUSCULAR-ATROPHY - PRIMARY OR SECONDARY DEFECT(S)
Authors: TEIN I SLOANE AE DONNER EJ LEHOTAY DC MILLINGTON DS KELLEY RI
Citation: I. Tein et al., FATTY-ACID OXIDATION ABNORMALITIES IN CHILDHOOD-ONSET SPINAL MUSCULAR-ATROPHY - PRIMARY OR SECONDARY DEFECT(S), Pediatric neurology, 12(1), 1995, pp. 21-30
BENZOATE THERAPY AND CARNITINE DEFICIENCY IN NONKETOTIC HYPERGLYCINEMIA
Authors: VANHOVE JLK KISHNANI P MUENZER J WENSTRUP RJ SUMMAR ML BRUMMOND MR LACHIEWICZ AM MILLINGTON DS KAHLER SG
Citation: Jlk. Vanhove et al., BENZOATE THERAPY AND CARNITINE DEFICIENCY IN NONKETOTIC HYPERGLYCINEMIA, American journal of medical genetics, 59(4), 1995, pp. 444-453
3-HYDROXYISOVALERYLCARNITINE IN 3-METHYLCROTONYL-COA CARBOXYLASE DEFICIENCY
Authors: VANHOVE JLK RUTLEDGE SL NADA MA KAHLER SG MILLINGTON DS
Citation: Jlk. Vanhove et al., 3-HYDROXYISOVALERYLCARNITINE IN 3-METHYLCROTONYL-COA CARBOXYLASE DEFICIENCY, Journal of inherited metabolic disease, 18(5), 1995, pp. 592-601
CARNITINE ACYLCARNITINE TRANSLOCASE DEFICIENCY - BENIGN COURSE WITHOUT CARDIAC INVOLVEMENT
Authors: DIONSIVICI C GARAVAGLIA B BARTULI A INVERNIZZI F DIDONATO S SABETTA G KAHLER SG MILLINGTON DS
Citation: C. Dionsivici et al., CARNITINE ACYLCARNITINE TRANSLOCASE DEFICIENCY - BENIGN COURSE WITHOUT CARDIAC INVOLVEMENT, Pediatric research, 37(4), 1995, pp. 147-147
RAPID DIAGNOSIS OF MAPLE-SYRUP-URINE-DISEASE IN BLOOD SPOTS FROM NEWBORNS BY TANDEM MASS-SPECTROMETRY
Authors: CHACE DH HILLMAN SL MILLINGTON DS KAHLER SG ROE CR NAYLOR EW
Citation: Dh. Chace et al., RAPID DIAGNOSIS OF MAPLE-SYRUP-URINE-DISEASE IN BLOOD SPOTS FROM NEWBORNS BY TANDEM MASS-SPECTROMETRY, Clinical chemistry, 41(1), 1995, pp. 62-68
3-HYDROXYISOVALERYLCARNITINE IN PATIENTS WITH DEFICIENCY OF 3-METHYLCROTONYL COA CARBOXYLASE
Authors: ROSCHINGER W MILLINGTON DS GAGE DA HUANG ZH IWAMOTO T YANO S PACKMAN S JOHNSTON K BERRY SA SWEETMAN L
Citation: W. Roschinger et al., 3-HYDROXYISOVALERYLCARNITINE IN PATIENTS WITH DEFICIENCY OF 3-METHYLCROTONYL COA CARBOXYLASE, Clinica chimica acta, 240(1), 1995, pp. 35-51
ETHYLMALONIC ACIDURIA - AN ORGANIC ACIDEMIA WITH CNS INVOLVEMENT AND VASCULOPATHY
Authors: OZAND PT RASHED M MILLINGTON DS SAKATI N HAZZAA S RAHBEENI Z ALODAIB A YOUSSEF N MAZROU A GASCON GG BRISMAR J
Citation: Pt. Ozand et al., ETHYLMALONIC ACIDURIA - AN ORGANIC ACIDEMIA WITH CNS INVOLVEMENT AND VASCULOPATHY, Brain & development, 16, 1994, pp. 12-22
PATTY ACID OXIDATION ABNORMALITIES IN CHILDHOOD-ONSET SPINAL MUSCULAR-ATROPHY - PRIMARY OR SECONDARY DEFECT(S)
Authors: TEIN I SLOANE AE DONNER E LEHOTAY DC MILLINGTON DS KELLEY RI
Citation: I. Tein et al., PATTY ACID OXIDATION ABNORMALITIES IN CHILDHOOD-ONSET SPINAL MUSCULAR-ATROPHY - PRIMARY OR SECONDARY DEFECT(S), Annals of neurology, 36(3), 1994, pp. 492-493
APPLICATION OF ELECTROSPRAY-IONIZATION MASS-SPECTROMETRY FOR ANALYSISOF HEMOGLOBIN ADDUCTS WITH ACRYLONITRILE
Authors: STEVENS RD BONAVENTURA J BONAVENTURA C FENNEL TR MILLINGTON DS
Citation: Rd. Stevens et al., APPLICATION OF ELECTROSPRAY-IONIZATION MASS-SPECTROMETRY FOR ANALYSISOF HEMOGLOBIN ADDUCTS WITH ACRYLONITRILE, Biochemical Society transactions, 22(2), 1994, pp. 543-547
ACUTE FATTY LIVER OF PREGNANCY AND LONG-CHAIN 3-HYDROXYACYL COENZYME-A DEHYDROGENASE-DEFICIENCY
Authors: TREEM WR RINALDO P HALE DE STANLEY CA MILLINGTON DS HYAMS JS JACKSON S TURNBULL DM
Citation: Wr. Treem et al., ACUTE FATTY LIVER OF PREGNANCY AND LONG-CHAIN 3-HYDROXYACYL COENZYME-A DEHYDROGENASE-DEFICIENCY, Hepatology, 19(2), 1994, pp. 339-345
INTRAVENOUS L-CARNITINE AND ACETYL-L-CARNITINE IN MEDIUM-CHAIN ACYL-COENZYME-A DEHYDROGENASE-DEFICIENCY AND ISOVALERIC ACIDEMIA
Authors: VANHOVE JLK KAHLER SG MILLINGTON DS ROE DS CHACE DH HEALES SJR ROE CR
Citation: Jlk. Vanhove et al., INTRAVENOUS L-CARNITINE AND ACETYL-L-CARNITINE IN MEDIUM-CHAIN ACYL-COENZYME-A DEHYDROGENASE-DEFICIENCY AND ISOVALERIC ACIDEMIA, Pediatric research, 35(1), 1994, pp. 96-101
PERFORMANCE OF THE SERUM COBALAMIN ASSAY FOR DIAGNOSIS OF COBALAMIN DEFICIENCY
Authors: MATCHAR DB MCCRORY DC MILLINGTON DS FEUSSNER JR
Citation: Db. Matchar et al., PERFORMANCE OF THE SERUM COBALAMIN ASSAY FOR DIAGNOSIS OF COBALAMIN DEFICIENCY, The American journal of the medical sciences, 308(5), 1994, pp. 276-283
RAPID OPTIMIZATION OF ENZYME SUBSTRATES FOR MATRIX METALLOPROTEASES USING DEFINED SUBSTRATE MIXTURES
Authors: WISEMAN J GREEN M BERMAN J ANDEREGG R KASSEL D MILLINGTON DS NORWOOD D MCGEEHAN J BICKETT DM
Citation: J. Wiseman et al., RAPID OPTIMIZATION OF ENZYME SUBSTRATES FOR MATRIX METALLOPROTEASES USING DEFINED SUBSTRATE MIXTURES, Journal of cellular biochemistry, 1993, pp. 118-118
ACYLCARNITINES IN AMNIOTIC-FLUID - APPLICATION TO THE PRENATAL-DIAGNOSIS OF PROPIONIC ACIDEMIA
Authors: VANHOVE JLK CHACE DH KAHLER SG MILLINGTON DS
Citation: Jlk. Vanhove et al., ACYLCARNITINES IN AMNIOTIC-FLUID - APPLICATION TO THE PRENATAL-DIAGNOSIS OF PROPIONIC ACIDEMIA, Journal of inherited metabolic disease, 16(2), 1993, pp. 361-367
MEDIUM-CHAIN ACYL-COA DEHYDROGENASE (MCAD) DEFICIENCY - DIAGNOSIS BY ACYLCARNITINE ANALYSIS IN BLOOD
Authors: VANHOVE JLK ZHANG W KAHLER SG ROE CR CHEN YT TERADA N CHACE DH IAFOLLA AK DING JH MILLINGTON DS
Citation: Jlk. Vanhove et al., MEDIUM-CHAIN ACYL-COA DEHYDROGENASE (MCAD) DEFICIENCY - DIAGNOSIS BY ACYLCARNITINE ANALYSIS IN BLOOD, American journal of human genetics, 52(5), 1993, pp. 958-966
Risultati: 1-23 |