Muscle coenzyme Q10 deficiencies in ataxia with oculomotor apraxia 1
Le Ber, I, Dubourg, O, Benoist, J-F, Jardel, C, Mochel, F, Koenig, M, Brice, A, Lombès, A, Dürr, A
Published in Neurology (23.01.2007)
Published in Neurology (23.01.2007)
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Isolated hyperechoic fetal colon before 36 weeks' gestation reveals cystinuria
Amat, S., Czerkiewicz, I., Benoist, J.‐F., Eurin, D., Fontanges, M., Muller, F.
Published in Ultrasound in obstetrics & gynecology (01.11.2011)
Published in Ultrasound in obstetrics & gynecology (01.11.2011)
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Methylmalonic and propionic acidaemias: Management and outcome
De Baulny, H. Ogier, Benoist, J. F., Rigal, O., Touati, G., Rabier, D., Saudubray, J. M.
Published in Journal of inherited metabolic disease (01.05.2005)
Published in Journal of inherited metabolic disease (01.05.2005)
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Spectrum of mutations in cystinuria patients presenting with prenatal hyperechoic colon
Tostivint, I., Royer, N., Nicolas, M., Bourillon, A., Czerkiewicz, I., Becker, P.‐H., Muller, F., Benoist, J.‐F.
Published in Clinical genetics (01.12.2017)
Published in Clinical genetics (01.12.2017)
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Procalcitonin and C-reactive protein during the early posttraumatic systemic inflammatory response syndrome
MIMOZ, O, BENOIST, J. F, EDOUARD, A. R, ASSICOT, M, BOHUON, C, SAMII, K
Published in Intensive care medicine (01.02.1998)
Published in Intensive care medicine (01.02.1998)
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Early-onset hyperargininaemia: A severe disorder?
Schiff, M., Benoist, J.-F., Cardoso, M. L., Elmaleh-Bergès, M., Forey, P., Santiago, J., Ogier de Baulny, H.
Published in Journal of inherited metabolic disease (01.12.2009)
Published in Journal of inherited metabolic disease (01.12.2009)
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Pyridoxine-dependent epilepsy: A novel mutation in a Tunisian child
Ben Younes, T., Kraoua, I., Benrhouma, H., Nasrallah, F., Ben Achour, N., Klaa, H., Hassen-Rouissi, A., Drissi, C., Benoist, J.-F., Ben Youssef-Turki, I.
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.03.2017)
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.03.2017)
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Efficacy of sodium hydroxide at 2.5 %, chlorhexidine gluconate at 0.5 % and calcium hydroxide against Candida albicans
Ndiaye, D, Diongue, K, Bane, K, Seck, A, Niang, S O, Lèye Benoist, F, Ndiaye, D, Touré, B
Published in Journal de mycologie médicale (01.12.2016)
Published in Journal de mycologie médicale (01.12.2016)
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Co-translational degradation of apolipoprotein B100 by the proteasome is prevented by microsomal triglyceride transfer protein. Synchronized translation studies on HepG2 cells treated with an inhibitor of microsomal triglyceride transfer protein
Benoist, F. (University of Ottawa Heart Institute, Ontario, Canada), Grand-Perret, T
Published in The Journal of biological chemistry (15.08.1997)
Published in The Journal of biological chemistry (15.08.1997)
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Mitochondrial neurogastrointestinal encephalomyopathy in three siblings : Clinical, genetic and neuroradiological features
SCHIIPBACH, W. M. M, MADHAVI VADDAY, K, MATTLE, H. P, SCHALLER, A, BREKENFELD, C, KAPPELER, L, BENOIST, J. F, NGUYEN-THI XUAN-HUONG, C, BURGUNDER, J. M, SEIBOLD, F, GALLATI, S
Published in Journal of neurology (01.02.2007)
Published in Journal of neurology (01.02.2007)
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Circulating cardiac troponin I in trauma patients without cardiac contusion
EDOUARD, A. R, BENOIST, J.-F, COSSON, C, MIMOZ, O, LEGRAND, A, SAMII, K
Published in Intensive care medicine (01.06.1998)
Published in Intensive care medicine (01.06.1998)
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A direct-conversion CMOS transceiver for the 802.11a/b/g WLAN standard utilizing a Cartesian feedback transmitter
Perraud, L., Recouly, M., Pinatel, C., Sornin, N., Bonnot, J.-L., Benoist, F., Massei, M., Gibrat, O.
Published in IEEE journal of solid-state circuits (01.12.2004)
Published in IEEE journal of solid-state circuits (01.12.2004)
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Conference Proceeding
Multiple OXPHOS deficiency in the liver of a patient with CblA methylmalonic aciduria sensitive to vitamin B12
Valayannopoulos, V., Hubert, L., Benoist, J. F., Romano, S., Arnoux, J. B., Chrétien, D., Kaplan, J., Fakhouri, F., Rabier, D., Rötig, A., Lebre, A. S., Munnich, A., de Keyzer, Y., de Lonlay, P.
Published in Journal of inherited metabolic disease (2009)
Published in Journal of inherited metabolic disease (2009)
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Conference Proceeding
Are we missing patients with biotinidase deficiency in France?
Deschamps, R., Stankoff, B., Vignal, C., Benoist, J.F., Wolf, B., Gout, O.
Published in Revue neurologique (01.05.2018)
Published in Revue neurologique (01.05.2018)
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Pyridoxine dependent epilepsy: Is late onset a predictor for favorable outcome?
de Rooy, R.L.P., Halbertsma, F.J., Struijs, E.A., van Spronsen, F.J., Lunsing, R.J., Schippers, H.M., van Hasselt, P.M., Plecko, B., Wohlrab, G., Whalen, S., Benoist, J.F., Valence, S., Mills, P.B., Bok, L.A.
Published in European journal of paediatric neurology (01.07.2018)
Published in European journal of paediatric neurology (01.07.2018)
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Place de l’immunohématologie dans la gestion de stock et la délivrance
Madre, F., Benoist, F., Chandesris, C., Nicola, N.
Published in Transfusion clinique et biologique (Paris) (01.12.2010)
Published in Transfusion clinique et biologique (Paris) (01.12.2010)
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Conference Proceeding
Renal transplantation in 4 patients with methylmalonic aciduria: A cell therapy for metabolic disease
Brassier, A., Boyer, O., Valayannopoulos, V., Ottolenghi, C., Krug, P., Cosson, M.A., Touati, G., Arnoux, J.B., Barbier, V., Bahi-Buisson, N., Desguerre, I., Charbit, M., Benoist, J.F., Dupic, L., Aigrain, Y., Blanc, T., Salomon, R., Rabier, D., Guest, G., de Lonlay, P., Niaudet, P.
Published in Molecular genetics and metabolism (01.09.2013)
Published in Molecular genetics and metabolism (01.09.2013)
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NK/T‐CELL LYMPHOMA, THE FRENCH EXPERIENCE
Jaccard, A., Philippe, L., Couronné, L., Benoist, J.‐F., Hermine, O.
Published in Hematological oncology (01.06.2017)
Published in Hematological oncology (01.06.2017)
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