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Results: 1-19 |
Results: 19
ASSOCIATION OF RED-BLOOD METHYLFOLATE BUT NOT PLASMA FOLATE WITH C677T MTHFR POLYMORPHISM IN VENOUS THROMBOEMBOLIC DISEASE
Authors: QUERE I WUTSCHERT R ZITTOUN J BELLET H REBER G GRIS JC JANBON C SCHVED JF DEMOERLOOSE P
Citation: I. Quere et al., ASSOCIATION OF RED-BLOOD METHYLFOLATE BUT NOT PLASMA FOLATE WITH C677T MTHFR POLYMORPHISM IN VENOUS THROMBOEMBOLIC DISEASE, Thrombosis and haemostasis, 80(4), 1998, pp. 707-709
REMETHYLATION DEFECTS - GUIDELINES FOR CLINICAL-DIAGNOSIS AND TREATMENT
Authors: DEBAULNY HO GERARD M SAUDUBRAY JM ZITTOUN J
Citation: Ho. Debaulny et al., REMETHYLATION DEFECTS - GUIDELINES FOR CLINICAL-DIAGNOSIS AND TREATMENT, European journal of pediatrics, 157, 1998, pp. 77-83
RELIABILITY OF BIOCHEMICAL PARAMETERS USED IN PRENATAL-DIAGNOSIS OF COMBINED METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA
Authors: MERINERO B PEREZCERDA C GARCIA MJ CHADEFAUXVEKEMANS B KAMOUN P TONETTI C ZITTOUN J JAKOBS C UGARTE M
Citation: B. Merinero et al., RELIABILITY OF BIOCHEMICAL PARAMETERS USED IN PRENATAL-DIAGNOSIS OF COMBINED METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, Prenatal diagnosis, 18(9), 1998, pp. 947-952
PLASMA HOMOCYSTEINE LEVELS RELATED TO INTERACTIONS BETWEEN FOLATE STATUS AND METHYLENETETRAHYDROFOLATE REDUCTASE - A STUDY IN 52 HEALTHY-SUBJECTS
Authors: ZITTOUN J TONETTI C BORIES D PIGNON JM TULLIEZ M
Citation: J. Zittoun et al., PLASMA HOMOCYSTEINE LEVELS RELATED TO INTERACTIONS BETWEEN FOLATE STATUS AND METHYLENETETRAHYDROFOLATE REDUCTASE - A STUDY IN 52 HEALTHY-SUBJECTS, Metabolism, clinical and experimental, 47(11), 1998, pp. 1413-1418
INTERACTIONS BETWEEN THE PHENOTYPE AND GENOTYPE (C677-]T POLYMORPHISM), OF METHYLENETETRAHYDROFOLATE REDUCTASE (MTHFR), HOMOCYSTEINE AND METHYLFOLATES CONCENTRATIONS - A STUDY PERFORMED IN 52 HEALTHY-VOLUNTEERS
Authors: ZITTOUN J BORIES D TONETTI C PIGNON JM TULLIEZ M
Citation: J. Zittoun et al., INTERACTIONS BETWEEN THE PHENOTYPE AND GENOTYPE (C677-]T POLYMORPHISM), OF METHYLENETETRAHYDROFOLATE REDUCTASE (MTHFR), HOMOCYSTEINE AND METHYLFOLATES CONCENTRATIONS - A STUDY PERFORMED IN 52 HEALTHY-VOLUNTEERS, Blood, 90(10), 1997, pp. 2779-2779
METHYLENETETRAHYDROFOLATE REDUCTASE THERMOLABILE VARIANT AND HUMAN LONGEVITY
Authors: FAUREDELANEF L QUERE I CHASSE JF GUERASSIMENKO O LESAULNIER M BELLET H ZITTOUN J KAMOUN P COHEN D
Citation: L. Fauredelanef et al., METHYLENETETRAHYDROFOLATE REDUCTASE THERMOLABILE VARIANT AND HUMAN LONGEVITY, American journal of human genetics, 60(4), 1997, pp. 999-1001
CHARACTERIZATION OF CONGENITAL TRANSCOBALAMIN-II (TC) DEFICIENCY IN 2PATIENTS
Authors: QIAN L REGEC A MCLOUGHLIN P QUADROS EV ZITTOUN J ROTHENBERG SP
Citation: L. Qian et al., CHARACTERIZATION OF CONGENITAL TRANSCOBALAMIN-II (TC) DEFICIENCY IN 2PATIENTS, Blood, 88(10), 1996, pp. 1953-1953
CONGENITAL ERRORS OF FOLATE METABOLISM
Authors: ZITTOUN J
Citation: J. Zittoun, CONGENITAL ERRORS OF FOLATE METABOLISM, Bailliere's clinical haematology, 8(3), 1995, pp. 603-616
CLONALITY ANALYSIS OF POLYMORPHONUCLEAR CELLS (PMN) IN ESSENTIAL THROMBOCYTHEMIA
Authors: PIGNON JM IMBERT M BORIES D JOUAULT H ZITTOUN J VERNANT JP VAINCHENKER W CASADEVALL N DUMONT V TULLIEZ M
Citation: Jm. Pignon et al., CLONALITY ANALYSIS OF POLYMORPHONUCLEAR CELLS (PMN) IN ESSENTIAL THROMBOCYTHEMIA, Blood, 86(10), 1995, pp. 181-181
MATERNAL-FETAL FOLATE STATUS AND NEURAL-TUBE DEFECTS - A CASE-CONTROLSTUDY
Authors: BUNDUKI V DOMMERGUES M ZITTOUN J MARQUET J MULLER F DUMEZ Y
Citation: V. Bunduki et al., MATERNAL-FETAL FOLATE STATUS AND NEURAL-TUBE DEFECTS - A CASE-CONTROLSTUDY, Biology of the neonate, 67(3), 1995, pp. 154-159
METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY - PRENATAL-DIAGNOSIS AND FAMILY STUDIES
Authors: MARQUET J CHADEFAUX B BONNEFONT JP SAUDUBRAY JM ZITTOUN J
Citation: J. Marquet et al., METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY - PRENATAL-DIAGNOSIS AND FAMILY STUDIES, Prenatal diagnosis, 14(1), 1994, pp. 29-33
METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY REVEALED BY A NEUROPATHY IN A PSYCHOTIC ADULT
Authors: PASQUIER F LEBERT F PETIT H ZITTOUN J MARQUET J
Citation: F. Pasquier et al., METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY REVEALED BY A NEUROPATHY IN A PSYCHOTIC ADULT, Journal of Neurology, Neurosurgery and Psychiatry, 57(6), 1994, pp. 765-766
CONTROL OF ERYTHROPOIESIS IN HUMANS DURING PROLONGED EXPOSURE TO THE ALTITUDE OF 6,542-M
Authors: RICHALET JP SOUBERBIELLE JC ANTEZANA AM DECHAUX M LETRONG JL BIENVENU A DANIEL F BLANCHOT C ZITTOUN J
Citation: Jp. Richalet et al., CONTROL OF ERYTHROPOIESIS IN HUMANS DURING PROLONGED EXPOSURE TO THE ALTITUDE OF 6,542-M, The American journal of physiology, 266(3), 1994, pp. 180000756-180000764
PHARMACOKINETICS AND IN-VITRO STUDIES OF L-LEUCOVORIN - COMPARISON WITH THE D-LEUCOVORIN AND D,L-LEUCOVORIN
Authors: ZITTOUN J
Citation: J. Zittoun, PHARMACOKINETICS AND IN-VITRO STUDIES OF L-LEUCOVORIN - COMPARISON WITH THE D-LEUCOVORIN AND D,L-LEUCOVORIN, Annals of oncology, 4, 1993, pp. 190000001-190000005
5-FLUOROURACIL COMBINED WITH THE [6S]-STEREOISOMER OF FOLINIC ACID INHIGH-DOSES FOR TREATMENT OF PATIENTS WITH ADVANCED COLORECTAL-CARCINOMA - A PHASE-I-II STUDY OF 2 CONSECUTIVE REGIMENS
Authors: MACHOVER D GRISON X GOLDSCHMIDT E ZITTOUN J METZGER G RICHAUD J LOTZ JP ANDRE T HANNOUN L MARQUET J GUILLOT T BARDON M SALMON R SEZEUR A MAUBAN S IZRAEL V PARC R
Citation: D. Machover et al., 5-FLUOROURACIL COMBINED WITH THE [6S]-STEREOISOMER OF FOLINIC ACID INHIGH-DOSES FOR TREATMENT OF PATIENTS WITH ADVANCED COLORECTAL-CARCINOMA - A PHASE-I-II STUDY OF 2 CONSECUTIVE REGIMENS, Annals of oncology, 4, 1993, pp. 190000029-190000035
PHARMACOKINETIC COMPARISON OF LEUCOVORIN AND LEVOLEUCOVORIN
Authors: ZITTOUN J TONELLI AP MARQUET J DEGIALLULY E HANCOCK C YACOBI A JOHNSON JB
Citation: J. Zittoun et al., PHARMACOKINETIC COMPARISON OF LEUCOVORIN AND LEVOLEUCOVORIN, European Journal of Clinical Pharmacology, 44(6), 1993, pp. 569-573
HYPERHOMOCYSTEINEMIA MAY BE INVOLVED IN THROMBOTIC COMPLICATIONS OF MYELOPROLIFERATIVE DISORDERS
Authors: ANKRI A CHADEFAUX B CHAHINE H MARQUET J TONETTI C ZITTOUN J
Citation: A. Ankri et al., HYPERHOMOCYSTEINEMIA MAY BE INVOLVED IN THROMBOTIC COMPLICATIONS OF MYELOPROLIFERATIVE DISORDERS, Blood, 82(10), 1993, pp. 10000613-10000613
NEONATAL HEMOLYTIC-UREMIC SYNDROME, METHY LMALONIC ACIDURIA AND HOMOCYSTINURIA DUE TO A CONGENITAL DEFECT IN INTRACELLULAR COBALAMIN METABOLISM
Authors: CHENEL C WOOD C GOURRIER E ZITTOUN J CASADEVALL I OGIER H
Citation: C. Chenel et al., NEONATAL HEMOLYTIC-UREMIC SYNDROME, METHY LMALONIC ACIDURIA AND HOMOCYSTINURIA DUE TO A CONGENITAL DEFECT IN INTRACELLULAR COBALAMIN METABOLISM, Archives francaises de pediatrie, 50(9), 1993, pp. 749-754
NEONATAL HEMOLYTIC-UREMIC SYNDROME, METHY LMALONIC ACIDURIA AND HOMOCYSTINURIA DUE TO A CONGENITAL DEFECT IN INTRACELLULAR COBALAMIN METABOLISM
Authors: CHENEL C WOOD C GOURRIER E ZITTOUN J CASADEVALL I OGIER H
Citation: C. Chenel et al., NEONATAL HEMOLYTIC-UREMIC SYNDROME, METHY LMALONIC ACIDURIA AND HOMOCYSTINURIA DUE TO A CONGENITAL DEFECT IN INTRACELLULAR COBALAMIN METABOLISM, Archives francaises de pediatrie, 50(9), 1993, pp. 749-754
Risultati: 1-19 |