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44篇 您的检索式:作者名="LeBon M"
    题名 作者 年代 出处 被引量
1Temperament and character inventory (TCI) personality profile and sub-typing in alcoholic patients: A controlled study 显示文摘BASIAUX P LEBON O DRAMAIX M 2001Alcohol Alcohol2001,36,6:1
2Buoyant-thermocapillary instabilities in medium-prandtl-number fluid layers subject to a horizontal temperature-gradient显示文摘Parmentier P M Regnier V C Lebon G 1993International Journal of Heat and Mass Transfer1993,36,9:1
3Transla- tional and orientational order in lead zinc niobate: An optical and Raman study 显示文摘A Lebon M E1 Marssi R FarM 2001J Appl Phys2001,89,7:1
4Use of a Hpa Ⅱ-polymerase chain reaction assay to assay to study DNA methylation in the Pgk-1 CpG island of mouse embryos at the time of X-chromosome inactivation显示文摘SINGER-SAM J GRANT M LEBON JM 1990Mol Cell Biol1990,10,9:1
5Twelve-year follow-up study of hepatitis B immunization of Senegalese infants 显示文摘Coursaget P Lebon Ueux D Soumare M 1994Hepatol1994,21,:1
6Use of a HpaⅡ-polymerase chain reaction assay to study DNA methylation in the Pgk-1 CpG island of mouse embryos at the time of X-chromosome inactivation显示文摘Singer-Sam J Grant M LeBon JM etc 1990Mol Cell Biol1990,10,:1
7Nonpathogenic SIV infection of African green monkeys induces a strong but rapidly controlled type I IFN response显示文摘Jacquelin Béatrice Mayau Véronique Targat Brice Liovat Anne-Sophie Kunkel Désirée Petitjean Ga?l Dillies Marie-Agnès Roques Pierre Butor Cécile Silvestri Guido Giavedoni Luis D Lebon Pierre Barré-Sinoussi Fran?oise Benecke Arndt Müller-Trutw 2009Journal of Clinical Investigation2009,,:1
8Recurrent de novo mitochondrial DNA mutations in respirator, chain deficiency 显示文摘Lebon S Chol M Benit P 2003J Med Genet2003,40,12:1
9Recurrent denovo mitochondrial DNA mutations in respiratory chain deficiency 显示文摘Lebon S Chol M Benit P et ol 2003J Med Genet2003,40,12:1
10The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency 显示文摘Chol M Lebon S Benit P 2003J Med Genet2003,40,3:1
11Effeet of motor imagery in the rehabilitation of burn patients显示文摘Guillot A Lebon F Vernay M 2009J Burn Care Res2009,30,4:1
12An ini- tial MRI picture of limbie encephalitis in subaeute selerosing panencephalitis 显示文摘LEBON S MAEDER P MAEDER-INGVAR M 2011Eur J Paediatr Neuro2011,15,6:1
13Mutations involved in Aicardi-Gouti6res syndrome implicate SAMHD1 as regulator of the innate immune response显示文摘Rice GI Bond J Asipu A Brunette R L Manfield I W Cart I M Fuller J C Jackson R M Lamb T Briggs TA Ali M Gornall H Couthard L R Aeby A Attard-Montalto S P Bertini E Bodemer C Brockmann K Brueton L A Corry P C Desguerre I Fazzi E Cazorla A G Gener B Hamel B C Heiberg A Hunter M van der Knaap M S Kumar R Lagae L Landrieu P G Lourenco C M Marom D McDer- mott M F van der Merwe W Orcesi S Prendiville J S Rasmussen M Shalev S A Soler D M Shinawi M Spiegel R Tan T Y Vanderver A Wakeling EL Wassmer E Whittaker E Lebon P Stetson D B Bonthron D T Crow Y J 2009Nature Genetics2009,41,:1
14Measurement of procalcintonin levels in children with bacterial or viral meningitis显示文摘Gendrel D Raymond J Assicot M Moulin F Iniguez JL Lebon P 1997Clin Infect Dis1997,24,6:1
15Acute myocarditis due to Chikungunya virus assessed by contrast- enhanced MRI 显示文摘Mirabel M Vignaux O Lebon P 2007Int J Cardiol2007,121,1:1
16Multicenter EValua-tion of the Amplicor enterovirus PCR test with cerebrospinal fluidfrom patients with aseptic meningitis显示文摘Van Vliet KE Glimaker M Lebon P 1998J Clin Microbiol1998,36,:1
17Multicenter evaluation of the Amplieor enterovirus PCR test with cerebrospinal fluid from patients with aseptic meningitis显示文摘Van Vliet KE Glimaker M Lebon P 1998J Clin Microbiol1998,36,:1
18Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiency显示文摘Lebon S Chol M Benit P Mugnier C Chretien D Giurgea I 2003J Med Genet2003,40,12:1
19An initial MRI picture of limbic encephalitis in subacute sclerosing panen- eephalitis 显示文摘Lebon S Maeder P Maeder-Ingvar M 2011Eur J Paediatr Neural2011,15,6:1
20The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency显示文摘Chol M Lebon S Benit P 2003J Med Genet2003,40,3:1
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