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Results: 1-25 | 26-50 | 51-75 | 76-77
Results: 1-25/77
MOLECULAR ANALYSIS AND PRENATAL-DIAGNOSIS OF HUMAN FUMARASE DEFICIENCY
Authors: COUGHLIN EM CHRISTENSEN E KUNZ PL KRISHNAMOORTHY KS WALKER V DENNIS NR CHALMERS RA ELPELEG ON WHELAN D POLLITT RJ RAMESH V MANDELL R SHIH VE
Citation: Em. Coughlin et al., MOLECULAR ANALYSIS AND PRENATAL-DIAGNOSIS OF HUMAN FUMARASE DEFICIENCY, MOLECULAR GENETICS AND METABOLISM, 63(4), 1998, pp. 254-262
GLUTARYL-COA DEHYDROGENASE MUTATIONS IN GLUTARIC ACIDEMIA (TYPE-I) - REVIEW AND REPORT OF 30 NOVEL MUTATIONS
Authors: GOODMAN SI STEIN DE SCHLESINGER S CHRISTENSEN E SCHWARTZ M GREENBERG CR ELPELEG ON
Citation: Si. Goodman et al., GLUTARYL-COA DEHYDROGENASE MUTATIONS IN GLUTARIC ACIDEMIA (TYPE-I) - REVIEW AND REPORT OF 30 NOVEL MUTATIONS, Human mutation, 12(3), 1998, pp. 141-144
PROPIONYL-COA CARBOXYLASE DEFICIENCY IN GREENLAND
Authors: RAVN K CHRISTENSEN E BRANDT NJ SIMONSEN H SCHWARTZ M
Citation: K. Ravn et al., PROPIONYL-COA CARBOXYLASE DEFICIENCY IN GREENLAND, European journal of human genetics, 6, 1998, pp. 5007-5007
THE HUMAN GLUTARYL-COA DEHYDROGENASE GENE - REPORT OF INTRONIC SEQUENCES AND OF 13 NOVEL MUTATIONS CAUSING GLUTARIC ACIDURIA TYPE-I
Authors: SCHWARTZ M CHRISTENSEN E SUPERTIFURGA A BRANDT NJ
Citation: M. Schwartz et al., THE HUMAN GLUTARYL-COA DEHYDROGENASE GENE - REPORT OF INTRONIC SEQUENCES AND OF 13 NOVEL MUTATIONS CAUSING GLUTARIC ACIDURIA TYPE-I, Human genetics, 102(4), 1998, pp. 452-458
DIAGNOSIS AND MANAGEMENT OF GLUTARIC ACIDURIA TYPE-I
Authors: BARIC I ZSCHOCKE J CHRISTENSEN E DURAN M GOODMAN SI LEONARD JV MULLER E MORTON DH SUPERTIFURGA A HOFFMANN GF
Citation: I. Baric et al., DIAGNOSIS AND MANAGEMENT OF GLUTARIC ACIDURIA TYPE-I, Journal of inherited metabolic disease, 21(4), 1998, pp. 326-340
FEASIBILITY OF MOLECULAR PRENATAL-DIAGNOSIS OF GLUTARIC ACIDURIA TYPE-I IN CHORIONIC VILLI
Authors: BUSQUETS C COLL MJ CHRISTENSEN E CAMPISTOL J CLUSELLAS N VILASECA MA RIBES A
Citation: C. Busquets et al., FEASIBILITY OF MOLECULAR PRENATAL-DIAGNOSIS OF GLUTARIC ACIDURIA TYPE-I IN CHORIONIC VILLI, Journal of inherited metabolic disease, 21(3), 1998, pp. 243-246
CLINICAL VARIABILITY IN 3 DANISH PATIENTS WITH DIHYDROPYRIMIDINE DEHYDROGENASE-DEFICIENCY ALL HOMOZYGOUS FOR THE SAME MUTATION
Authors: CHRISTENSEN E CEZANNE I KJAERGAARD S HORLYK H PEDERSEN VF VREKEN P VANKUILENBURG ABP VANGENNIP AH
Citation: E. Christensen et al., CLINICAL VARIABILITY IN 3 DANISH PATIENTS WITH DIHYDROPYRIMIDINE DEHYDROGENASE-DEFICIENCY ALL HOMOZYGOUS FOR THE SAME MUTATION, Journal of inherited metabolic disease, 21(3), 1998, pp. 272-275
LESS COLLAGEN PRODUCTION IN SMOKERS
Authors: JORGENSEN LN KALLEHAVE F CHRISTENSEN E SIANA JE GOTTRUP F
Citation: Ln. Jorgensen et al., LESS COLLAGEN PRODUCTION IN SMOKERS, Surgery, 123(4), 1998, pp. 450-455
LYCOPODIUM SPORES IN TRANSRECTAL ULTRASOUND-GUIDED CORE BIOPSIES OF THE PROSTATE
Authors: ANDERSEN TC JURGENSEN GW CHRISTENSEN E
Citation: Tc. Andersen et al., LYCOPODIUM SPORES IN TRANSRECTAL ULTRASOUND-GUIDED CORE BIOPSIES OF THE PROSTATE, Scandinavian journal of urology and nephrology, 32(2), 1998, pp. 148-149
ARTERIAL HYPOXEMIA IN CIRRHOSIS - FACT OR FICTION
Authors: MOLLER S HILLINGSO J CHRISTENSEN E HENRIKSEN JH
Citation: S. Moller et al., ARTERIAL HYPOXEMIA IN CIRRHOSIS - FACT OR FICTION, Gut, 42(6), 1998, pp. 868-874
PREDICTION OF HEPATIC-ENCEPHALOPATHY IN ACETAMINOPHEN OVERDOSE
Authors: SCHIODT FV BONDESEN S TYGSTRUP N CHRISTENSEN E
Citation: Fv. Schiodt et al., PREDICTION OF HEPATIC-ENCEPHALOPATHY IN ACETAMINOPHEN OVERDOSE, Gastroenterology, 114(4), 1998, pp. 564-564
CAN A COMPUTERIZED NEURAL-NETWORK IDENTIFY RESPONDERS TO OMEPRAZOLE IN PATIENTS WITH DYSPEPSIA - ANALYSIS OF A DANISH MULTICENTER TRIAL IN GENERAL-PRACTICE
Authors: MEINECHESCHMIDT V CHRISTENSEN E
Citation: V. Meinecheschmidt et E. Christensen, CAN A COMPUTERIZED NEURAL-NETWORK IDENTIFY RESPONDERS TO OMEPRAZOLE IN PATIENTS WITH DYSPEPSIA - ANALYSIS OF A DANISH MULTICENTER TRIAL IN GENERAL-PRACTICE, Gastroenterology, 114(4), 1998, pp. 914-914
DELAYED CLEARANCE OF SERUM HBSAG IN COMPENSATED CIRRHOSIS-B - RELATION TO INTERFERON-ALPHA THERAPY AND DISEASE PROGNOSIS
Authors: FATTOVICH G GIUSTINA G SANCHEZTAPIAS J QUERO C MAS A OLIVOTTO PG SOLINAS A ALMASIO P HADZIYANNIS S DEGOS F DEMOURA MC KROGSGAARD K PANTALENA M REALDI G CORROCHER R SCHALM SW CRAXI A DELAROCQUE E SAVVAS S COSSU PA TOCCO A OLSEN JF CHRISTENSEN E ROCHA P
Citation: G. Fattovich et al., DELAYED CLEARANCE OF SERUM HBSAG IN COMPENSATED CIRRHOSIS-B - RELATION TO INTERFERON-ALPHA THERAPY AND DISEASE PROGNOSIS, The American journal of gastroenterology, 93(6), 1998, pp. 896-900
FATTY-ACID OXIDATION DISORDERS AS PRIMARY CAUSE OF SUDDEN AND UNEXPECTED DEATH IN INFANTS AND YOUNG-CHILDREN - AN INVESTIGATION PERFORMED ON CULTURED FIBROBLASTS FROM 79 CHILDREN WHO DIED AGED BETWEEN 0-4 YEARS
Authors: LUNDEMOSE JB KOLVRAA S GREGERSEN N CHRISTENSEN E GREGERSEN M
Citation: Jb. Lundemose et al., FATTY-ACID OXIDATION DISORDERS AS PRIMARY CAUSE OF SUDDEN AND UNEXPECTED DEATH IN INFANTS AND YOUNG-CHILDREN - AN INVESTIGATION PERFORMED ON CULTURED FIBROBLASTS FROM 79 CHILDREN WHO DIED AGED BETWEEN 0-4 YEARS, Journal of clinical pathology-Molecular pathology, 50(4), 1997, pp. 212-217
HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC DETERMINATION OF LICOCHALCONE-A AND ITS METABOLITES IN BIOLOGICAL-FLUIDS
Authors: NADELMANN L TJORNELUND J CHRISTENSEN E HANSEN SH
Citation: L. Nadelmann et al., HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC DETERMINATION OF LICOCHALCONE-A AND ITS METABOLITES IN BIOLOGICAL-FLUIDS, Journal of chromatography B. Biomedical sciences and applications, 695(2), 1997, pp. 389-400
ANTIGENICITY OF CHLOROMETHYL-KETONE-INACTIVATED RECOMBINANT FVIIA (CMK-RFVIIA), EVALUATED IN AN EXPERIMENTAL HUMAN FVII-IMMUNE-TOLERANT MODEL
Authors: NICOLAISEN EM KRISTENSEN H KRISTENSEN AT EZBAN M VERLAND S CHRISTENSEN E HEDNER U
Citation: Em. Nicolaisen et al., ANTIGENICITY OF CHLOROMETHYL-KETONE-INACTIVATED RECOMBINANT FVIIA (CMK-RFVIIA), EVALUATED IN AN EXPERIMENTAL HUMAN FVII-IMMUNE-TOLERANT MODEL, Thrombosis and haemostasis, 1997, pp. 2804-2804
CONTINUOUS BLOOD-PRESSURE MONITORING IN CIRRHOSIS - RELATIONS TO SPLANCHNIC AND SYSTEMIC HEMODYNAMICS
Authors: MOLLER S CHRISTENSEN E HENRIKSEN JH
Citation: S. Moller et al., CONTINUOUS BLOOD-PRESSURE MONITORING IN CIRRHOSIS - RELATIONS TO SPLANCHNIC AND SYSTEMIC HEMODYNAMICS, Journal of hepatology, 27(2), 1997, pp. 284-294
PROGNOSTIC MODELS IN CHRONIC LIVER-DISEASE - VALIDITY, USEFULNESS ANDFUTURE-ROLE
Authors: CHRISTENSEN E
Citation: E. Christensen, PROGNOSTIC MODELS IN CHRONIC LIVER-DISEASE - VALIDITY, USEFULNESS ANDFUTURE-ROLE, Journal of hepatology, 26(6), 1997, pp. 1414-1424
A NEW PEROXISOMAL BETA-OXIDATION DISORDER IN TWIN NEONATES - DEFECTIVE OXIDATION OF BOTH CEROTIC AND PRISTANIC ACIDS
Authors: CHRISTENSEN E PEDERSEN SA LETH H JAKOBS C SCHUTGENS RBH WANDERS RJA
Citation: E. Christensen et al., A NEW PEROXISOMAL BETA-OXIDATION DISORDER IN TWIN NEONATES - DEFECTIVE OXIDATION OF BOTH CEROTIC AND PRISTANIC ACIDS, Journal of inherited metabolic disease, 20(5), 1997, pp. 658-664
COMPOUND HETEROZYGOSITY IN THE GLUTARYL-COA DEHYDROGENASE GENE WITH R227P MUTATION IN ONE ALLELE IS ASSOCIATED WITH NO OR VERY-LOW FREE GLUTARATE EXCRETION
Authors: CHRISTENSEN E RIBES A BUSQUETS C PINEDA M DURAN M POLLTHE BT GREENBERG CR LEFFERS H SCHWARTZ M
Citation: E. Christensen et al., COMPOUND HETEROZYGOSITY IN THE GLUTARYL-COA DEHYDROGENASE GENE WITH R227P MUTATION IN ONE ALLELE IS ASSOCIATED WITH NO OR VERY-LOW FREE GLUTARATE EXCRETION, Journal of inherited metabolic disease, 20(3), 1997, pp. 383-386
NERVE-CELL LESIONS CAUSED BY 3-HYDROXYGLUTARIC ACID - A POSSIBLE MECHANISM FOR NEURODEGENERATION IN GLUTARIC ACIDEMIA-I
Authors: FLOTTRAHMEL B FALTER C SCHLUFF P FINGERHUT R CHRISTENSEN E JAKOBS C MUSSHOFF U FAUTEK JD DEUFEL T LUDOLPH A ULLRICH K
Citation: B. Flottrahmel et al., NERVE-CELL LESIONS CAUSED BY 3-HYDROXYGLUTARIC ACID - A POSSIBLE MECHANISM FOR NEURODEGENERATION IN GLUTARIC ACIDEMIA-I, Journal of inherited metabolic disease, 20(3), 1997, pp. 387-390
SYNTHESIS, ISOLATION AND IDENTIFICATION OF GLUCURONIDES AND MERCAPTURIC ACIDS OF A NOVEL ANTIPARASITIC AGENT, LICOCHALCONE-A
Authors: NADELMANN L TJORNELUND J HANSEN SH CORNETT C SIDELMANN UG BRAUMANN U CHRISTENSEN E CHRISTENSEN SB
Citation: L. Nadelmann et al., SYNTHESIS, ISOLATION AND IDENTIFICATION OF GLUCURONIDES AND MERCAPTURIC ACIDS OF A NOVEL ANTIPARASITIC AGENT, LICOCHALCONE-A, Xenobiotica, 27(7), 1997, pp. 667-680
SCREENING THE PERFORMANCE OF LUBRICANTS FOR THE IRONING OF STAINLESS-STEEL WITH A STRIP REDUCTION TEST
Authors: ANDREASEN JL BAY N ANDERSEN M CHRISTENSEN E BJERRUM N
Citation: Jl. Andreasen et al., SCREENING THE PERFORMANCE OF LUBRICANTS FOR THE IRONING OF STAINLESS-STEEL WITH A STRIP REDUCTION TEST, Wear, 207(1-2), 1997, pp. 1-5
THE CLINICAL PHENOTYPE OF SUCCINIC SEMIALDEHYDE DEHYDROGENASE-DEFICIENCY (4-HYDROXYBUTYRIC ACIDURIA) - CASE-REPORTS OF 23 NEW PATIENTS
Authors: GIBSON KM CHRISTENSEN E JAKOBS C FOWLER B CLARE MA HAMMERSEN G RAAB K KOBORI J MOOSA A VOLLMER B ROSSIER E IAFOLLA AK MATERN D BROUWER OF FINELSTEIN J AKSU F WEBER HP BAKKEREN JAJM GABREELS FJM BLUESTONE D BARRON TF BEAUVAIS P RABIER D SANTOS C UMANSKY R LEHNERT W
Citation: Km. Gibson et al., THE CLINICAL PHENOTYPE OF SUCCINIC SEMIALDEHYDE DEHYDROGENASE-DEFICIENCY (4-HYDROXYBUTYRIC ACIDURIA) - CASE-REPORTS OF 23 NEW PATIENTS, Pediatrics, 99(4), 1997, pp. 567-574
2 GENERALIZATIONS OF THE GLEASON-KAHANE-ZELAZKO-THEOREM
Authors: CHRISTENSEN E
Citation: E. Christensen, 2 GENERALIZATIONS OF THE GLEASON-KAHANE-ZELAZKO-THEOREM, Pacific journal of mathematics, 177(1), 1997, pp. 27-32
Risultati: 1-25 | 26-50 | 51-75 | 76-77