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Results: 51-75/77
MODULE MAPPINGS INTO VON-NEUMANN-ALGEBRAS AND INJECTIVITY
Authors: CHRISTENSEN E SINCLAIR AM
Citation: E. Christensen et Am. Sinclair, MODULE MAPPINGS INTO VON-NEUMANN-ALGEBRAS AND INJECTIVITY, Proceedings of the London Mathematical Society, 71, 1995, pp. 618-640
GLUCOCORTICOIDS ARE INEFFECTIVE IN ALCOHOLIC HEPATITIS - A METAANALYSIS ADJUSTING FOR CONFOUNDING VARIABLES
Authors: CHRISTENSEN E GLUUD C
Citation: E. Christensen et C. Gluud, GLUCOCORTICOIDS ARE INEFFECTIVE IN ALCOHOLIC HEPATITIS - A METAANALYSIS ADJUSTING FOR CONFOUNDING VARIABLES, Gut, 37(1), 1995, pp. 113-118
CLINICAL PHENOTYPE ASSOCIATED WITH TERMINAL 2Q37 DELETION
Authors: CONRAD B DEWALD G CHRISTENSEN E LOPEZ M HIGGINS J PIERPONT ME
Citation: B. Conrad et al., CLINICAL PHENOTYPE ASSOCIATED WITH TERMINAL 2Q37 DELETION, Clinical genetics, 48(3), 1995, pp. 134-139
USE OF VIBRATIONAL SPECTROSCOPY TO DETERMINE OXIDE CONTENT OF ALKALI-METAL FLUORIDE-TANTALUM MELTS
Authors: BJERRUM NJ BERG RW CHRISTENSEN E KERRIDGE DH VONBARNER JH
Citation: Nj. Bjerrum et al., USE OF VIBRATIONAL SPECTROSCOPY TO DETERMINE OXIDE CONTENT OF ALKALI-METAL FLUORIDE-TANTALUM MELTS, Analytical chemistry, 67(13), 1995, pp. 2129-2135
THE MOLECULAR-BASIS OF ASPARTOACYLASE DEFICIENCY IN EUROPEAN NON-JEWISH PATIENTS
Authors: SHAAG A ANIKSTER Y CHRISTENSEN E GLUSTEIN JZ FOIS A MICHELAKAKIS H NIGRO F PRONICKA E RIBES A ZABOT MT ELPELEG ON
Citation: A. Shaag et al., THE MOLECULAR-BASIS OF ASPARTOACYLASE DEFICIENCY IN EUROPEAN NON-JEWISH PATIENTS, American journal of human genetics, 57(4), 1995, pp. 1315-1315
THE MOLECULAR-BASIS OF CANAVAN (ASPARTOACYLASE DEFICIENCY) DISEASE INEUROPEAN NON-JEWISH PATIENTS
Authors: SHAAG A ANIKSTER Y CHRISTENSEN E GLUSTEIN JZ FOIS A MICHELAKAKIS H NIGRO F PRONICKA E RIBES A ZABOT MT ELPELEG ON
Citation: A. Shaag et al., THE MOLECULAR-BASIS OF CANAVAN (ASPARTOACYLASE DEFICIENCY) DISEASE INEUROPEAN NON-JEWISH PATIENTS, American journal of human genetics, 57(3), 1995, pp. 572-580
PRENATAL-DIAGNOSIS OF GLUTARYL-COA DEHYDROGENASE-DEFICIENCY - EXPERIENCE USING 1ST-TRIMESTER CHORIONIC VILLUS SAMPLING
Authors: CHRISTENSEN E
Citation: E. Christensen, PRENATAL-DIAGNOSIS OF GLUTARYL-COA DEHYDROGENASE-DEFICIENCY - EXPERIENCE USING 1ST-TRIMESTER CHORIONIC VILLUS SAMPLING, Prenatal diagnosis, 14(5), 1994, pp. 333-336
PROGNOSTIC VARIABLES IN PATIENTS WITH CIRRHOSIS AND ESOPHAGEAL-VARICES WITHOUT PRIOR BLEEDING
Authors: MOLLER S BENDTSEN F CHRISTENSEN E HENRIKSEN JH
Citation: S. Moller et al., PROGNOSTIC VARIABLES IN PATIENTS WITH CIRRHOSIS AND ESOPHAGEAL-VARICES WITHOUT PRIOR BLEEDING, Journal of hepatology, 21(6), 1994, pp. 940-946
THE TREATMENT EFFECT OF ALPHA-INTERFERON IN CHRONIC HEPATITIS-B IS INDEPENDENT OF PRETREATMENT VARIABLES - RESULTS BASED ON INDIVIDUAL PATIENT DATA FROM 10 CLINICAL CONTROLLED TRIALS
Authors: KROGSGAARD K BINDSLEV N CHRISTENSEN E CRAXI A SCHLICHTING P SCHALM S CARRENO V TREPO C GERKEN G THOMAS HC ANDERSEN PK RINGLARSEN H
Citation: K. Krogsgaard et al., THE TREATMENT EFFECT OF ALPHA-INTERFERON IN CHRONIC HEPATITIS-B IS INDEPENDENT OF PRETREATMENT VARIABLES - RESULTS BASED ON INDIVIDUAL PATIENT DATA FROM 10 CLINICAL CONTROLLED TRIALS, Journal of hepatology, 21(4), 1994, pp. 646-655
SURVIVAL AND PROGNOSTIC FACTORS IN 366 PATIENTS WITH COMPENSATED CIRRHOSIS TYPE-B - A MULTICENTER STUDY
Authors: REALDI G FATTOVICH G HADZIYANNIS S SCHALM SW ALMASIO P SANCHEZTAPIAS J CHRISTENSEN E GIUSTINA G NOVENTA F
Citation: G. Realdi et al., SURVIVAL AND PROGNOSTIC FACTORS IN 366 PATIENTS WITH COMPENSATED CIRRHOSIS TYPE-B - A MULTICENTER STUDY, Journal of hepatology, 21(4), 1994, pp. 656-666
THE SEGREGATION OF GLYTARYL-COA DEHYDROGENASE-DEFICIENCY AND REFSUM SYNDROME IN A FAMILY
Authors: CHRISTENSEN E BRANDT NJ ROSENBERG T BOMERS K JAKOBS C
Citation: E. Christensen et al., THE SEGREGATION OF GLYTARYL-COA DEHYDROGENASE-DEFICIENCY AND REFSUM SYNDROME IN A FAMILY, Journal of inherited metabolic disease, 17(3), 1994, pp. 287-290
SEARCHING FOR MUTATIONS IN THE ARYLSULFATASE-A GENE
Authors: SALAMON MB CHRISTENSEN E SCHWARTZ M
Citation: Mb. Salamon et al., SEARCHING FOR MUTATIONS IN THE ARYLSULFATASE-A GENE, Journal of inherited metabolic disease, 17(3), 1994, pp. 311-314
MOLECULAR-GENETIC CHARACTERIZATION AND URINARY-EXCRETION PATTERN OF METABOLITES IN 2 FAMILIES WITH MCAD DEFICIENCY DUE TO COMPOUND HETEROZYGOSITY WITH A 13 BASE-PAIR INSERTION IN ONE ALLELE
Authors: GREGERSEN N WINTER V LYONNET S SAUDUBRAY JM WENDEL U JENSEN TG ANDRESEN BS KOLVRAA S BOLUND L CHRISTENSEN E BROSS P LEHNERT W
Citation: N. Gregersen et al., MOLECULAR-GENETIC CHARACTERIZATION AND URINARY-EXCRETION PATTERN OF METABOLITES IN 2 FAMILIES WITH MCAD DEFICIENCY DUE TO COMPOUND HETEROZYGOSITY WITH A 13 BASE-PAIR INSERTION IN ONE ALLELE, Journal of inherited metabolic disease, 17(2), 1994, pp. 169-184
ON VON-NEUMANN-ALGEBRAS WHICH ARE COMPLEMENTED SUBSPACES OF B(H)
Authors: CHRISTENSEN E SINCLAIR AM
Citation: E. Christensen et Am. Sinclair, ON VON-NEUMANN-ALGEBRAS WHICH ARE COMPLEMENTED SUBSPACES OF B(H), Journal of functional analysis, 122(1), 1994, pp. 91-102
THE INFLUENCE OF OXIDE ON THE ELECTRODEPOSITION OF NIOBIUM FROM ALKALI FLUORIDE MELTS
Authors: CHRISTENSEN E WANG XD VONBARNER JH OSTFOLD T BJERRUM NJ
Citation: E. Christensen et al., THE INFLUENCE OF OXIDE ON THE ELECTRODEPOSITION OF NIOBIUM FROM ALKALI FLUORIDE MELTS, Journal of the Electrochemical Society, 141(5), 1994, pp. 1212-1220
ELECTROCHEMICAL STUDY OF TANTALUM IN FLUORIDE AND OXOFLUORIDE MELTS
Authors: POLYAKOVA LP POLYAKOV EG MATTHIESEN F CHRISTENSEN E BJERRUM NJ
Citation: Lp. Polyakova et al., ELECTROCHEMICAL STUDY OF TANTALUM IN FLUORIDE AND OXOFLUORIDE MELTS, Journal of the Electrochemical Society, 141(11), 1994, pp. 2982-2988
HETEROGENEITY IN DI TRIHYDROXYCHOLESTANOIC ACIDEMIA/
Authors: TENBRINK HJ WANDERS RJA CHRISTENSEN E BRANDT NJ JAKOBS C
Citation: Hj. Tenbrink et al., HETEROGENEITY IN DI TRIHYDROXYCHOLESTANOIC ACIDEMIA/, Annals of clinical biochemistry, 31, 1994, pp. 195-197
MOLECULAR ANALYSIS OF THE MUTATIONS IN 5 UNRELATED PATIENTS WITH THE LESCH-NYHAN SYNDROME
Authors: MARCUS S CHRISTENSEN E MALM G
Citation: S. Marcus et al., MOLECULAR ANALYSIS OF THE MUTATIONS IN 5 UNRELATED PATIENTS WITH THE LESCH-NYHAN SYNDROME, Human mutation, 2(6), 1993, pp. 473-477
MAGNETIC-RESONANCE-IMAGING IN JUVENILE CANAVAN DISEASE
Authors: TOFT PB GEISSHOLTORFF R ROLLAND MO PRYDS O MULLERFORELL W CHRISTENSEN E LEHNERT W LOU HC OTT D HENNIG J HENRIKSEN O
Citation: Pb. Toft et al., MAGNETIC-RESONANCE-IMAGING IN JUVENILE CANAVAN DISEASE, European journal of pediatrics, 152(9), 1993, pp. 750-753
MOLYBDENUM COFACTOR DEFICIENCY IN 2 SIBLINGS - DIAGNOSTIC DIFFICULTIES
Authors: HANSEN LK WULFF K DORCHE C CHRISTENSEN E
Citation: Lk. Hansen et al., MOLYBDENUM COFACTOR DEFICIENCY IN 2 SIBLINGS - DIAGNOSTIC DIFFICULTIES, European journal of pediatrics, 152(8), 1993, pp. 662-664
MUSCLE CYTOCHROME-C-OXIDASE DEFICIENCY ACCOMPANIED BY A URINARY ORGANIC-ACID PATTERN MIMICKING MULTIPLE ACYL-COA DEHYDROGENASE-DEFICIENCY
Authors: CHRISTENSEN E BRANDT NJ SCHMALBRUCH H KAMIENIECKA Z HERTZ B RUITENBEEK W
Citation: E. Christensen et al., MUSCLE CYTOCHROME-C-OXIDASE DEFICIENCY ACCOMPANIED BY A URINARY ORGANIC-ACID PATTERN MIMICKING MULTIPLE ACYL-COA DEHYDROGENASE-DEFICIENCY, Journal of inherited metabolic disease, 16(3), 1993, pp. 553-556
PEROXISOMAL BETA-OXIDATION OF POLYUNSATURATED LONG-CHAIN FATTY-ACIDS IN HUMAN FIBROBLASTS - THE POLYUNSATURATED AND THE SATURATED LONG-CHAIN FATTY-ACIDS ARE RETROCONVERTED BY THE SAME ACYL-COA OXIDASE
Authors: CHRISTENSEN E WOLDSETH B HAGVE TA POLLTHE BT WANDERS RJA SPRECHER H STOKKE O CHRISTOPHERSEN BO
Citation: E. Christensen et al., PEROXISOMAL BETA-OXIDATION OF POLYUNSATURATED LONG-CHAIN FATTY-ACIDS IN HUMAN FIBROBLASTS - THE POLYUNSATURATED AND THE SATURATED LONG-CHAIN FATTY-ACIDS ARE RETROCONVERTED BY THE SAME ACYL-COA OXIDASE, Scandinavian journal of clinical & laboratory investigation, 53, 1993, pp. 61-74
RECURRENT METABOLIC DECOMPENSATION IN PROFOUND CARNITINE PALMITOYLTRANSFERASE-II DEFICIENCY
Authors: ELPELEG ON JOSEPH A BRANSKI D CHRISTENSEN E HOLME E DEMAUGRE F SAUDUBRAY JM GUTMAN A
Citation: On. Elpeleg et al., RECURRENT METABOLIC DECOMPENSATION IN PROFOUND CARNITINE PALMITOYLTRANSFERASE-II DEFICIENCY, The Journal of pediatrics, 122(6), 1993, pp. 917-919
UPDATING PROGNOSIS IN PRIMARY BILIARY-CIRRHOSIS USING A TIME-DEPENDENT COX REGRESSION-MODEL
Authors: CHRISTENSEN E ALTMAN DG NEUBERGER J DESTAVOLA BL TYGSTRUP N WILLIAMS R
Citation: E. Christensen et al., UPDATING PROGNOSIS IN PRIMARY BILIARY-CIRRHOSIS USING A TIME-DEPENDENT COX REGRESSION-MODEL, Gastroenterology, 105(6), 1993, pp. 1865-1876
DIAGNOSIS OF PEROXISOMAL DISORDERS BY ANALYSIS OF PHYTANIC AND PRISTANIC ACIDS IN STORED-BLOOD SPOTS COLLECTED AT NEONATAL SCREENING
Authors: TENBRINK HJ VANDENHEUVEL CMM CHRISTENSEN E LARGILLIERE C JAKOBS C
Citation: Hj. Tenbrink et al., DIAGNOSIS OF PEROXISOMAL DISORDERS BY ANALYSIS OF PHYTANIC AND PRISTANIC ACIDS IN STORED-BLOOD SPOTS COLLECTED AT NEONATAL SCREENING, Clinical chemistry, 39(9), 1993, pp. 1904-1906
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