Authors:
CORMIERDAIRE V
RUSTIN P
ROTIG A
CHRETIEN D
LEMERRER M
BELLI D
LEGOFF A
HUBERT P
RICOUR C
MUNNICH A
Citation: V. Cormierdaire et al., CRANIOFACIAL ANOMALIES AND MALFORMATIONS IN RESPIRATORY-CHAIN DEFICIENCY, American journal of medical genetics, 66(4), 1996, pp. 457-463
Authors:
MUNNICH A
ROTIG A
CHRETIEN D
CORMIER V
BOURGERON T
BONNEFONT JP
SAUDUBRAY JM
RUSTIN P
Citation: A. Munnich et al., CLINICAL PRESENTATION OF MITOCHONDRIAL DISORDERS IN CHILDHOOD, Journal of inherited metabolic disease, 19(4), 1996, pp. 521-527
Citation: M. Thomas et al., REAL-TIME BIOMONITORING OF WATER CONTAMINATION BY CYANIDE BASED ON ANALYSIS OF THE CONTINUOUS ELECTRIC SIGNAL EMITTED BY A TROPICAL FISH - APTERONOTUS ALBIFRONS, Water research, 30(12), 1996, pp. 3083-3091
Authors:
RUSTIN P
PARFAIT B
CHRETIEN D
BOURGERON T
DJOUADI F
BASTIN J
ROTIG A
MUNNICH A
Citation: P. Rustin et al., FLUXES OF NICOTINAMIDE ADENINE DINUCLEOTIDES THROUGH MITOCHONDRIAL-MEMBRANES IN HUMAN CULTURED-CELLS, The Journal of biological chemistry, 271(25), 1996, pp. 14785-14790
Authors:
BOURGERON T
RUSTIN P
CHRETIEN D
BIRCHMACHIN M
BOURGEOIS M
VIEGASPEQUIGNOT E
MUNNICH A
ROTIG A
Citation: T. Bourgeron et al., MUTATION OF A NUCLEAR SUCCINATE-DEHYDROGENASE GENE RESULTS IN MITOCHONDRIAL RESPIRATORY-CHAIN DEFICIENCY, Nature genetics, 11(2), 1995, pp. 144-149
Authors:
ROTIG A
BOURGERON T
CHRETIEN D
RUSTIN P
MUNNICH A
Citation: A. Rotig et al., SPECTRUM OF MITOCHONDRIAL-DNA REARRANGEMENTS IN THE PEARSON MARROW-PANCREAS SYNDROME, Human molecular genetics, 4(8), 1995, pp. 1327-1330
Authors:
SAUNIER P
CHRETIEN D
WOOD C
ROTIG A
BONNEFONT JP
SAUDUBRAY JM
RABIER D
MUNNICH A
RUSTIN P
Citation: P. Saunier et al., CYTOCHROME-C-OXIDASE DEFICIENCY PRESENTING AS RECURRENT NEONATAL MYOGLOBINURIA, Neuromuscular disorders, 5(4), 1995, pp. 285-289
Authors:
GONCALVES I
HERMANS D
CHRETIEN D
RUSTIN P
MUNNICH A
SAUDUBRAY JM
VANHOOF F
REDING R
DEGOYET JD
OTTE JB
BUTS JP
SOKAL EM
Citation: I. Goncalves et al., MITOCHONDRIAL RESPIRATORY-CHAIN DEFECT - A NEW ETIOLOGY FOR NEONATAL CHOLESTASIS AND EARLY LIVER INSUFFICIENCY, Journal of hepatology, 23(3), 1995, pp. 290-294
Authors:
POULTON J
SEWRY C
POTTER CG
BOUGERON T
CHRETIEN D
WIJBURG FA
MORTEN KJ
BROWN G
Citation: J. Poulton et al., VARIATION IN MITOCHONDRIAL-DNA LEVELS IN MUSCLE FROM NORMAL CONTROLS - IS DEPLETION OF MTDNA IN PATIENTS WITH MITOCHONDRIAL MYOPATHY A DISTINCT CLINICAL SYNDROME, Journal of inherited metabolic disease, 18(1), 1995, pp. 4-20
Authors:
ROTIG A
GOUTIERES F
NIAUDET P
RUSTIN P
CHRETIEN D
GUEST G
MIKOL J
GUBLER MC
MUNNICH A
Citation: A. Rotig et al., DELETION OF MITOCHONDRIAL-DNA IN PATIENT WITH CHRONIC TUBULOINTERSTITIAL NEPHRITIS, The Journal of pediatrics, 126(4), 1995, pp. 597-601
Citation: D. Chretien et al., STRUCTURE OF GROWING MICROTUBULE ENDS - 2-DIMENSIONAL SHEETS CLOSE INTO TUBES AT VARIABLE RATES, The Journal of cell biology, 129(5), 1995, pp. 1311-1328
Citation: Aa. Hyman et al., STRUCTURAL-CHANGES ACCOMPANYING GTP HYDROLYSIS IN MICROTUBULES - INFORMATION FROM A SLOWLY HYDROLYZABLE ANALOG GUANYLYL-(ALPHA,BETA)-METHYLENE-DIPHOSPHONATE, The Journal of cell biology, 128(1-2), 1995, pp. 117-125
Authors:
CHRETIEN D
POURRIER M
BOURGERON T
SENE M
ROTIG A
MUNNICH A
RUSTIN P
Citation: D. Chretien et al., AN IMPROVED SPECTROPHOTOMETRIC ASSAY OF PYRUVATE-DEHYDROGENASE IN LACTATE-DEHYDROGENASE CONTAMINATED MITOCHONDRIAL PREPARATIONS FROM HUMAN SKELETAL-MUSCLE, Clinica chimica acta, 240(2), 1995, pp. 129-136
Authors:
BOURGERON T
PARFAIT B
RUSTIN P
CHRETIEN D
BIRCHMACHIN M
ROTIG A
Citation: T. Bourgeron et al., MITOCHONDRIAL COMPLEX-II DEFICIENCY CAUSED BY A MUTATION OF A NUCLEARSUCCINATE-DEHYDROGENASE GENE, American journal of human genetics, 57(4), 1995, pp. 1007-1007
Authors:
ROTIG A
BOURGERON T
CHRETIEN D
RUSTIN P
MUNNICH A
Citation: A. Rotig et al., SPECTRUM OF MITOCHONDRIAL-DNA REARRANGEMENTS IN THE PEARSON MARROW PANCREAS SYNDROME, American journal of human genetics, 57(4), 1995, pp. 1047-1047
Authors:
EDERY P
GERARD B
CHRETIEN D
ROTIG A
CERRONE R
RABIER D
RAMBAUD C
FABRE M
SAUDUBRAY JM
MUNNICH A
RUSTIN P
Citation: P. Edery et al., LIVER CYTOCHROME-C-OXIDASE DEFICIENCY IN A CASE OF NEONATAL-ONSET HEPATIC-FAILURE, European journal of pediatrics, 153(3), 1994, pp. 190-194
Authors:
CHABROL B
MANCINI J
CHRETIEN D
RUSTIN P
MUNNICH A
PINSARD N
Citation: B. Chabrol et al., VALPROATE-INDUCED HEPATIC-FAILURE IN A CASE OF CYTOCHROME-C-OXIDASE DEFICIENCY, European journal of pediatrics, 153(2), 1994, pp. 133-135
Authors:
RUSTIN P
LEBIDOIS J
CHRETIEN D
BOURGERON T
PIECHAUD JF
ROTIG A
MUNNICH A
SIDI D
Citation: P. Rustin et al., ENDOMYOCARDIAL BIOPSIES FOR EARLY DETECTION OF MITOCHONDRIAL DISORDERS IN HYPERTROPHIC CARDIOMYOPATHIES, The Journal of pediatrics, 124(2), 1994, pp. 224-228
Authors:
BOURGERON T
CHRETIEN D
POGGIBACH J
DOONAN S
RABIER D
LETOUZE P
MUNNICH A
ROTIG A
LANDRIEU P
RUSTIN P
Citation: T. Bourgeron et al., MUTATION OF THE FUMARASE GENE IN 2 SIBLINGS WITH PROGRESSIVE ENCEPHALOPATHY AND FUMARASE DEFICIENCY, The Journal of clinical investigation, 93(6), 1994, pp. 2514-2518
Authors:
MAALOUM M
CHRETIEN D
KARSENTI E
HORBER JKH
Citation: M. Maaloum et al., APPROACHING MICROTUBULE STRUCTURE WITH THE SCANNING TUNNELING MICROSCOPE (STM), Journal of Cell Science, 107, 1994, pp. 3127-3131
Authors:
RUSTIN P
CHRETIEN D
BOURGERON T
LEBIDOIS J
SIDI D
ROTIG A
MUNNICH A
Citation: P. Rustin et al., INVESTIGATION OF RESPIRATORY-CHAIN ACTIVITY IN HUMAN HEART, Biochemical medicine and metabolic biology, 50(1), 1993, pp. 120-126