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Results: 1-15 |
Results: 15

Authors: BERARD C SINDOU M BERARD J CARRIER H
Citation: C. Berard et al., SELECTIVE NEUROTOMY OF THE TIBIAL NERVE IN THE SPASTIC HEMIPLEGIC CHILD - AN EXPLANATION OF THE RECURRENCE, Journal of pediatric orthopedics. Part B, 7(1), 1998, pp. 66-70

Authors: LI JD VANDERBEKEN I YE SY CARRIER H XANS P
Citation: Jd. Li et al., PREDICTION OF THE SOLUBILITY AND GAS-LIQUID EQUILIBRIA FOR GAS-WATER AND LIGHT HYDROCARBON-WATER SYSTEMS AT HIGH-TEMPERATURES AND PRESSURESWITH A GROUP-CONTRIBUTION EQUATION OF STATE, Fluid phase equilibria, 131(1-2), 1997, pp. 107-118

Authors: PETIOT P VIAL C DESAINTVICTOR JF CHARLES N CARRIER H DEPIERRE P BADY B
Citation: P. Petiot et al., DROPPED HEAD SYNDROME - DISCUSSION ABOUT 3 CASES, Revue neurologique, 153(4), 1997, pp. 251-255

Authors: DROUET A MOUSSON B CARRIER H BAVEREL G RIBOT C
Citation: A. Drouet et al., MELAS SYNDROME WITH ONLY STROKE-LIKE EPIS ODES, Revue neurologique, 153(10), 1997, pp. 591-594

Authors: NICOLINO M FERLIN T FOREST M GODINOT C CARRIER H DAVID M CHATELAIN P MOUSSON B
Citation: M. Nicolino et al., IDENTIFICATION OF A LARGE-SCALE MITOCHONDRIAL DEOXYRIBONUCLEIC-ACID DELETION IN ENDOCRINOPATHIES AND DEAFNESS - REPORT OF 2 UNRELATED CASESWITH DIABETES-MELLITUS AND ADRENAL INSUFFICIENCY, RESPECTIVELY, The Journal of clinical endocrinology and metabolism, 82(9), 1997, pp. 3063-3067

Authors: CARRIER H
Citation: H. Carrier, PAMPHLETS AND THE VULGARIZATION OF CULTUR E IN THE 17TH-CENTURY - THEMAZARINADES FOR EXAMPLE, XVIIe siecle, (195), 1997, pp. 297-303

Authors: CONJARD A MARTIN M FERRIER B DUROZARD D CARRIER H BAVEREL G
Citation: A. Conjard et al., INCREASE IN OXIDATIVE KEY ENZYMES IN A CASE OF MUSCLE UBIQUINOL-CYTOCHROME-C REDUCTASE DEFICIENCY, Acta Neuropathologica, 93(6), 1997, pp. 592-598

Authors: BOUZIDI MF CARRIER H GODINOT C
Citation: Mf. Bouzidi et al., ANTIMYCIN RESISTANCE AND UBIQUINOL CYTOCHROME-C REDUCTASE INSTABILITYASSOCIATED WITH A HUMAN CYTOCHROME-B MUTATION, Biochimica et biophysica acta. Molecular basis of disease, 1317(3), 1996, pp. 199-209

Authors: BOUZIDI MF ENJOLRAS N CARRIER H VIAL C LOPEZMEDIAVILLA C BURTPICHAT B COUTHON F GODINOT C
Citation: Mf. Bouzidi et al., VARIATIONS OF MUSCLE MITOCHONDRIAL CREATINE-KINASE ACTIVITY IN MITOCHONDRIAL DISEASES, Biochimica et biophysica acta. Molecular basis of disease, 1316(2), 1996, pp. 61-70

Authors: CARRIER H BURTPICHAT B FLOCARD F GUFFON N MOUSSON B DUMOULIN R GODINOT C
Citation: H. Carrier et al., MOLECULAR HISTOLOGY OF MITOCHONDRIAL AND NUCLEAR TRANSCRIPTS IN THE MUSCLE OF PATIENTS HARBORING A SINGLE MITOCHONDRIAL-DNA DELETION, Acta Neuropathologica, 91(1), 1996, pp. 104-111

Authors: CONJARD A FERRIER B MARTIN M CAILLETTE A CARRIER H BAVEREL G
Citation: A. Conjard et al., EFFECTS OF CHRONIC-RENAL-FAILURE ON ENZYMES OF ENERGY-METABOLISM IN INDIVIDUAL HUMAN MUSCLE-FIBERS, Journal of the American Society of Nephrology, 6(1), 1995, pp. 68-74

Authors: VILLEFERLIN T DUMOULIN R STEPIEN G MATHA V BADY B FLOCARD F CARRIER H MATHIEU M MOUSSON B
Citation: T. Villeferlin et al., FINE MAPPING OF RANDOMLY DISTRIBUTED MULTIPLE DELETIONS OF MITOCHONDRIAL-DNA IN A CASE OF CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, Molecular and cellular probes, 9(3), 1995, pp. 207-214

Authors: MOUSSON B COLLOMBET JM DUMOULIN R CARRIER H FLOCARD F BOUZIDI M GODINOT C MAIRE I MATHIEU M QUARD S
Citation: B. Mousson et al., AN ABNORMAL EXERCISE TEST RESPONSE REVEALING A RESPIRATORY-CHAIN COMPLEX-III DEFICIENCY, Acta neurologica Scandinavica, 91(6), 1995, pp. 488-493

Authors: GUFFON N LOPEZMEDIAVILLA C DUMOULIN R MOUSSON B GODINOT C CARRIER H COLLOMBET JM DIVRY P MATHIEU M GUIBAUD P
Citation: N. Guffon et al., 2-KETOGLUTARATE DEHYDROGENASE-DEFICIENCY, A RARE CAUSE OF PRIMARY HYPERLACTATEMIA - REPORT OF A NEW CASE, Journal of inherited metabolic disease, 16(5), 1993, pp. 821-830

Authors: DUMOULIN R MANDON G COLLOMBET JM BLOND JL CARRIER H GODINOT C FLOCARD F VILLARD J GUIBAUD P MATHIEU M MOUSSON B
Citation: R. Dumoulin et al., HUMAN CULTURED MYOBLASTS - A MODEL FOR THE DIAGNOSIS OF MITOCHONDRIALDISEASES, Journal of inherited metabolic disease, 16(3), 1993, pp. 545-547
Risultati: 1-15 |