Biblio

33557 resultats trouvés
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Rocca-Smith JR, Whyte O, Brachais C-H, Champion D, Piasente F, Marcuzzo E, Sensidoni A, Debeaufort F, Karbowiak T.  2017.  Beyond Biodegradability of Poly(lactic acid): Physical and Chemical Stability in Humid Environments. ACS SUSTAINABLE CHEMISTRY & ENGINEERING. 5:2751-2762.
Cuche A, Viarbitskaya S, Kumar U, Sharma J, Arbouet A, Girard C, Dujardin E.  2017.  Beyond dipolar regime in high-order plasmon mode bowtie antennas. OPTICS COMMUNICATIONS. 387:48-54.
Ayouba K, Le Gallo J, Vallone A.  2020.  Beyond GDP: an analysis of the socio-economic diversity of European regions. APPLIED ECONOMICS. 52:1010-1029.
Ayouba K, Le Gallo J, Vallone A.  2020.  Beyond GDP: an analysis of the socio-economic diversity of European regions. APPLIED ECONOMICS. 52:1010-1029.
Buhler T, Comby E, Vaudor L, von Pape T.  2021.  Beyond `good' and `bad' cyclists. On compensation effects between risk taking, safety equipment and secondary tasks. JOURNAL OF TRANSPORT & HEALTH. 22:101131.
Putot A, Putot S, Hacquin A, Manckoundia P.  2021.  Beyond longevity: healthy longevity. LANCET HEALTHY LONGEVITY. 2:E393-E394.
Dettmar B, Peltier C, Schlich P.  2020.  Beyond principal component analysis (PCA) of product means: Toward a psychometric view on sensory profiling data. JOURNAL OF SENSORY STUDIES. 35:e12555.
Dettmar B, Peltier C, Schlich P.  2020.  Beyond principal component analysis (PCA) of product means: Toward a psychometric view on sensory profiling data. JOURNAL OF SENSORY STUDIES. 35:e12555.
Schiele F, Bassand J-P.  2017.  Beyond Reperfusion Networks in ST-segment Elevation Myocardial Infarction: Assessment of Quality of Care. REVISTA ESPANOLA DE CARDIOLOGIA. 70:140-141.
Mazher M, Qayyum A, Ahmad I, Alassafi MO.  Submitted.  Beyond traditional approaches: a partial directed coherence with graph theory-based mental load assessment using EEG modality. NEURAL COMPUTING & APPLICATIONS.
Mazher M, Qayyum A, Ahmad I, Alassafi MO.  Submitted.  Beyond traditional approaches: a partial directed coherence with graph theory-based mental load assessment using EEG modality. NEURAL COMPUTING & APPLICATIONS.
Galmarini S, Hanusch U, Giraud M, Cayla N, Chiappe D, von Moos N, Hofmann H, Maurizi L.  2018.  Beyond Unpredictability: The Importance of Reproducibility in Understanding the Protein Corona of Nanoparticles. BIOCONJUGATE CHEMISTRY. 29:3385-3393.
Pohl B, Lorrey A, Sturman A, Quenol H, Renwick J, Fauchereau N, Pergaud J.  2021.  ``Beyond Weather Regimes'': Descriptors Monitoring Atmospheric Centers of Action-A Case Study for Aotearoa New Zealanda. JOURNAL OF CLIMATE. 34:8341-8360.
Ray-Coquard I.L, Bompas E., Cropet C., Donnat M., Bertucci F., Chaigneau L., Metzger S., Dufresne A., Guillemet C., C. Vassal P et al..  2021.  BFR ESS: A randomized phase II trial from the GSF/GETO French group evaluating the impact of interruption versus maintenance of aromatase inhibitors in patients with advanced or metastatic low grade endometrial stromal sarcoma after at least 3 years of th. ANNALS OF ONCOLOGY. 32:S772.
Mor R., Robin A.C, Figueras F., Antoja T..  2018.  BGM FASt: Besancon Galaxy Model for big data Simultaneous inference of the IMF, SFH, and density in the solar neighbourhood. ASTRONOMY & ASTROPHYSICS. 620:A79.
Dereeper E., Briois P., Vannier R.-N, Billard A..  2015.  Bi4V2O11 and BITAVOX.20 coatings deposited by reactive magnetron sputtering. MATERIALS CHEMISTRY AND PHYSICS. 153:9-16.
Lahrouchi N, Postma AV, Salazar CM, De Laughter DM, Tjong F, Piherova L, Bowling FZ, Zimmerman D, Lodder EM, Ta-Shma A et al..  2021.  Biallelic loss-of-function variants in PLD1 cause congenital right-sided cardiac valve defects and neonatal cardiomyopathy. JOURNAL OF CLINICAL INVESTIGATION. 131:e142148.
Besnard T., Sloboda N., Goldenberg A., Kury S., Cogne B., Breheret F., Trochu E., Conrad S., Vincent M., Deb W. et al..  2019.  Bi-allelic pathogenic variants in the lanosterol synthase gene LSS involved in the cholesterol biosynthesis cause alopecia with intellectual disability, a rare recessive neuroectodermal syndrome. EUROPEAN JOURNAL OF HUMAN GENETICS. 27:1376-1377.
Besnard T, Sloboda N, Goldenberg A, Kury S, Cogne B, Breheret F, Trochu E, Conrad S, Vincent M, Deb W et al..  2019.  Biallelic pathogenic variants in the lanosterol synthase gene LSS involved in the cholesterol biosynthesis cause alopecia with intellectual disability, a rare recessive neuroectodermal syndrome. GENETICS IN MEDICINE. 21:2025-2035.
Kambouris M, Thevenon J, Soldatos A, Cox A, Stephen J, Ben-Omran T, Al-Sarraj Y, Boulos H, Bone W, Mullikin JC et al..  2017.  Biallelic SCN10A mutations in neuromuscular disease and epileptic encephalopathy. ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY. 4:26-35.
Ziegler A, Duclaux-Loras R, Revenu C, Charbit-Henrion F, Begue B, Duroure K, Grimaud L, Guihot ALaure, Desquiret-Dumas V, Zarhrate M et al..  2021.  Bi-allelic variants in IPO8 cause a connective tissue disorder associated with cardiovascular defects, skeletal abnormalities, and immune dysregulation. AMERICAN JOURNAL OF HUMAN GENETICS. 108:1126-1137.
van der Knaap MS, Bugiani M, Mendes MI, Riley LG, Smith DEC, Rudinger-Thirion J, Frugier M, Breur M, Crawford J, van Gaalen J et al..  2019.  Biallelic variants in LARS2 and KARS cause deafness and ovario leukodystrophy. NEUROLOGY. 92:E1225-E1237.
Nguyen TTuyet Mai, Murakami Y, Mobilio S, Niceta M, Zampino G, Philippe C, Moutton S, Zaki MS, James KN, Musaev D et al..  2020.  Bi-allelic Variants in the GPI Transamidase Subunit PIGK Cause a Neurodevelopmental Syndrome with Hypotonia, Cerebellar Atrophy, and Epilepsy. AMERICAN JOURNAL OF HUMAN GENETICS. 106:484-495.
Lunati A., Heide S., Vuillaumier S., Leverger G., Desguerre I., Moutard M., Spentchian M., Hadouiri N., Darmency V., Thomas Q. et al..  2019.  Biallelic variants in TRAPPC11 cause syndromic intellectual disability. EUROPEAN JOURNAL OF HUMAN GENETICS. 27:1528.
Lunati A., Heide S., Vuillaumier S., Leverger G., Desguerre I., Moutard M., Spentchian M., Hadouiri N., Darmency V., Thomas Q. et al..  2019.  Biallelic variants in TRAPPC11 cause syndromic intellectual disability. EUROPEAN JOURNAL OF HUMAN GENETICS. 27:1528.

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