Publications - 'E'
Publications 2176 - 2200 de 2582
| Titre | DOI |
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EXISTENCE OF LAGRANGE MULTIPLIERS UNDER GATEAUX DIFFERENTIABLE DATA WITH APPLICATIONS TO STOCHASTIC OPTIMAL CONTROL PROBLEMS A. Jourani; F.J. Silva 2020 |
10.1137/18M1223411 |
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Existence of pattern 5 on radical prostatectomy: Poor prognostic factor associated with a lower biochemical recurrence-free survival J. Pastori; L. Balssa; J. Lillaz; G. Guichard; E. Chabannes; S. Bernardini; H. Bittard; A. Thiery-Vuillemin; F. Kleinclauss 2014 |
10.1016/j.purol.2014.03.002 |
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EXIT PROBLEM FOR ORNSTEIN-UHLENBECK PROCESSES: A RANDOM WALK APPROACH S. Herrmann; N. Massin 2020 |
10.3934/dcdsb.2020058 |
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Exit, voice, loyalty to sport organization power F. Lassalle 2020 |
10.1002/jsc.2366 |
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Exloration of High Risk Medical Devices Methodologies for Optimized Evaluations T. Lihoreau; C. Vidal; T. Wang; L. Pazart 2021 |
10.5220/0010386502850289 |
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Exogenous acquisition of Pseudomonas aeruginosa in intensive care units: a prospective multi-centre study (DYNAPYO study) M. Coppry; C. Leroyer; M. Saly; A.G. Venier; C. Slekovec; X. Bertrand; S. Parer; S. Alfandari; E. Cambau; B. Megarbane; C. Lawrence; B. Clair; A. Lepape; P. Cassier; D. Trivier; A. Boyer; H. Boulestreau; J. Asselineau; V. Dubois; R. Thiebaut; A.M. Rogues 2020 |
10.1016/j.jhin.2019.08.008 |
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Exogenous adenosine activates A2A adenosine receptor to inhibit RANKL-induced osteoclastogenesis via AP-1 pathway to facilitate bone repair X. Cheng; C. Yin; Y. Deng; Z. Li 2022 |
10.1007/s11033-021-07017-1 |
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Exogenous t-PA Administration Increases Hippocampal! Mature BDNF Levels. Plasmin- or NMDA-Dependent: Mechanism? M. Rodier; A. Prigent-Tessier; Y. Bejot; A. Jacquin; C. Mossiat; C. Marie; P. Garnier 2014 |
10.1371/journal.pone.0092416 |
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Exome Analysis of Patients Treated with Afatinib Reveals Genetic Variations Discriminating Extreme Responders J. Niogret; C. Kaderbhai; S. Chevrier; C. Chapusot; C. Truntzer; H. Mananet; P. Foucher; B. Coudert; A. Lagrange; L. Favier; L. Martin; H. Almotlak; P. Jacoulet; J. Lahourcade; O. Adotevi; V. Westeel; L. Arnould; R. Boidot 2019 |
10.1016/j.jtho.2019.08.1170 |
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EXOME ANALYSIS OF VULVAR AND VAGINAL TUMORS REVEALS AN ANTIGEN PROCESSING AND PRESENTATION DEFICIENCY L. Bengrine; J.D. Fumet; L. Favier; C. Richard; L. Arnould; R. Boidot 2019 |
10.1136/ijgc-2019-ESGO.1202 |
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Exome Analysis Reveals Genomic Markers Associated with Better Efficacy of Nivolumab in Lung Cancer Patients C. Richard; J.D. Fumet; S. Chevrier; V. Derangere; F. Ledys; A. Lagrange; L. Favier; B. Coudert; L. Arnould; C. Truntzer; R. Boidot; F. Ghiringhelli 2019 |
10.1158/1078-0432.CCR-18-1940 |
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Exome analysis to reveal genomic markers associated with better efficacy of nivolumab in lung cancer patients. C. Richard; J.D. Fumet; S. Chevrier; V. Derangere; F. Ledys; A. Lagrange; L. Favier; B.P. Coudert; L. Arnould; C. Truntzer; R. Boidot; F. Ghiringhelli 2018 |
10.1200/JCO.2018.36.15_suppl.9044 |
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Exome data clouds the pathogenicity of genetic variants in Pulmonary Arterial Hypertension Y. Abbasi; J. Jabbari; R. Jabbari; C. Glinge; S.Bahador Izadyar; E. Spiekerkoetter; R.T. Zamanian; J. Carlsen; J. Tfelt-Hansen 2018 |
10.1002/mgg3.452 |
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Exome Pool-Seq Reloaded B. Popp; G. Vasileiou; M. Zweier; A.B. Ekici; S. Moortgat; D. Lederer; I. Maystadt; A. Destree; S. Drunat; A. Verloes; A. Rauch; K. Steindl; L. Van Maldergem; J. Piard; E.B. Brischoux; C. Engel; M. Serey-Gaut; A. Reis; C. Zweier 2020 |
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Exome Pool-Seq Reloaded B. Popp; G. Vasileiou; M. Zweier; A.B. Ekici; S. Moortgat; D. Lederer; I. Maystadt; A. Destree; S. Drunat; A. Verloes; A. Rauch; K. Steindl; L. Van Maldergem; J. Piard; E.B. Brischoux; C. Engel; M. Serey-Gaut; A. Reis; C. Zweier 2020 |
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Exome sequencing allows detection of relevant pharmacogenetic variants in epileptic patients S. Verdez; P. Garret; E. Tisserant; A. Vitobello; T. Mau-Them; C. Philippe; M. Bardou; M. Luu; J. Albuisson; C. Verstuyft; P. Callier; C. Thauvin-Robinet; L. Faivre; N. Picard; Y. Duffourd 2021 |
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Exome sequencing allows detection of relevant pharmacogenetics variants in epileptic patients S. Verdez; P. Garret; E. Tisserant; A. Vitobello; T. Mau-Them; C. Philippe; M. Bardou; M. Luu; A. Juliette; C. Verstuyft; P. Callier; C. Thauvin-Robinet; L. Faivre; D. Yannis 2019 |
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Exome sequencing allows detection of relevant pharmacogenetics variants in epileptic patients S. Verdez; P. Garret; E. Tisserant; A. Vitobello; T. Mau-Them; C. Philippe; M. Bardou; M. Luu; A. Juliette; C. Verstuyft; P. Callier; C. Thauvin-Robinet; L. Faivre; D. Yannis 2019 |
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Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma M. Pertesi; M. Vallee; X. Wei; M.V. Revuelta; P. Galia; D. Demangel; J. Oliver; M. Foll; S. Chen; E. Perrial; L. Garderet; J. Corre; X. Leleu; E.M. Boyle; O. Decaux; P. Rodon; B. Kolb; B. Slama; P. Mineur; E. Voog; C. Le Bris; J. Fontan; M. Maigre; M. Beaumont; I. Azais; H. Sobol; M. Vignon; B. Royer; A. Perrot; J.G. Fuzibet; V. Dorvaux; B. Anglaret; P. Cony-Makhoul; C. Berthou; F. Desquesnes; B. Pegourie; S. Leyvraz; L. Mosser; N. Frenkiel; K. Augeul-Meunier; I. Leduc; C. Leyronnas; L. Voillat; P. Casassus; C. Mathiot; N. Cheron; E. Paubelle; P. Moreau; Y.J. Bignon; B. Joly; P. Bourquard; D. Caillot; H. Naman; S. Rigaudeau; G. Marit; M. Macro; I. Lambrecht; M. Cliquennois; L. Vincent; P. Helias; H. Avet-Loiseau; V. Moreno; R.Manuel Reis; J. Varkonyi; M. Kruszewski; A.Juul Vangsted; A. Jurczyszyn; J.Maciej Zaucha; J. Sainz; M. Krawczyk-Kulis; M. Watek; M. Pelosini; E. Iskierka-Jazdzewska; N. Grzasko; J. Martinez-Lopez; A. Jerez; D. Campa; G. Buda; F. Lesueur; M. Dudzinski; R. Garcia-Sanz; A. Nagler; M. Rymko; K. Jamroziak; A. Butrym; F. Canzian; O. Obazee; B. Nilsson; R.J. Klein; S.M. Lipkin; J.D. McKay; C. Dumontet 2019 |
10.1038/s41375-019-0452-6 |
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Exome sequencing in clinical settings: preferences and experiences of parents of children with rare diseases (SEQUAPRE study) A. Chassagne; A. Pelissier; F. Houdayer; E. Cretin; E. Gautier; D. Salvi; S. Kidri; A. Godard; C. Thauvin-Robinet; A. Masurel; D. Lehalle; N. Jean-Marcais; J. Thevenon; G. Lesca; A. Putoux; M.P. Cordier; S. Dupuis-Girod; M. Till; Y. Duffourd; J.B. Riviere; L. Joly; C. Juif; O. Putois; P. Ancet; A.S. Lapointe; P. Morin; P. Edery; M. Rossi; D. Sanlaville; S. Bejean; C. Peyron; L. Faivre 2019 |
10.1038/s41431-018-0332-y |
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Exome sequencing in congenital ataxia identifies two new candidate genes and highlights a pathophysiological link between some congenital ataxias and early infantile epileptic encephalopathies S. Valence; L. Burglen; E. Cochet; C. Rougeot; C. Garel; S. Chantot-Bastaraud; E. Lainey; A. Afenjar; M.A. Barthez; N. Bednarek; D. Doummar; L. Faivre; C. Goizet; D. Haye; B. Heron; I. Kemlin; D. Lacombe; M. Milh; M.L. Moutard; F. Riant; S. Robin; A. Roubertie; P. Sarda; A. Toutain; L. Villard; D. Ville; T.Billette de Villemeur; D. Rodriguez 2019 |
10.1038/s41436-018-0089-2 |
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Exome sequencing of pooled parental DNA: a cost-efficient ``trio-like'' strategy to increase diagnostic yield in developmental disorders T. Mau-Them; A. Vitobello; Y. Duffourd; A. Bruel; S. Moutton; A. Sorlin; S. Nambot; A. Denomme-Pichon; C. Poe; T. Jouan; M. Chevarin; M. Bordessoules; E. Tisserand; A. Mosca-Boidron; P. Callier; L. Faivre; C. Philippe; C. Thauvin-Robinet 2019 |
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Exome sequencing of pooled parental DNA: a cost-efficient ``trio-like'' strategy to increase diagnostic yield in developmental disorders T. Mau-Them; A. Vitobello; Y. Duffourd; A. Bruel; S. Moutton; A. Sorlin; S. Nambot; A. Denomme-Pichon; C. Poe; T. Jouan; M. Chevarin; M. Bordessoules; E. Tisserand; A. Mosca-Boidron; P. Callier; L. Faivre; C. Philippe; C. Thauvin-Robinet 2019 |
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Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder D.R. Krupp; R.A. Barnard; Y. Duffourd; S.A. Evans; R.M. Mulqueen; R. Bernier; J.B. Riviere; E. Fombonne; B.J. O'Roak 2017 |
10.1016/j.ajhg.2017.07.016 |
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Exophiala dermatitidis Revealing Cystic Fibrosis in Adult Patients with Chronic Pulmonary Disease F. Grenouillet; B. Cimon; H. Pana-Katatali; C. Person; M. Gainet-Brun; M.C. Malinge; Y. Le Govic; B. Richaud-Thiriez; J.P. Bouchara 2018 |
10.1007/s11046-017-0218-5 |