Publications - 'M'
Publications 1801 - 1825 de 1879
| Titre | DOI |
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Musculoskeletal injuries in a resource-constrained environment: comparing diagnostic accuracy of on-the-spot ultrasonography and conventional radiography for bone fracture screening during the Paris-Dakar rally raid B. Dallaudiere; A. Larbi; M. Lefere; A. Perozziello; O. Hauger; F. Pommerie; B. Fraboulet; D. Jacob 2015 |
10.1177/2058460115577566 |
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Music as a mnemonic to learn gesture sequences in normal aging and Alzheimer's disease A. Moussard; E. Bigand; S. Belleville; I. Peretz 2014 |
10.3389/fnhum.2014.00294 |
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MUSIC KNOWLEDGE AND SCIENCE STUDIES Sounds, Sense, Silence J. Le Marec; F. Ribac 2019 |
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MUSIC KNOWLEDGE AND SCIENCE STUDIES Sounds, Sense, Silence J. Le Marec; F. Ribac 2019 |
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Music lessons improve auditory perceptual and cognitive performance in deaf children F. Rochette; A. Moussard; E. Bigand 2014 |
10.3389/fnhum.2014.00488 |
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Music, Architecture, Proportion and the Renaissance Way of Thinking V. Zara 2021 |
10.1017/S1062798720000435 |
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Musical Emotions in Congenital Amusia: Impaired Recognition, but Preserved Emotional Intensity Y. Leveque; P. Teyssier; P. Bouchet; E. Bigand; A. Caclin; B. Tillmann 2018 |
10.1037/neu0000461 |
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Musical familiarity in congenital amusia: Evidence from a gating paradigm B. Tillmann; P. Albouy; A. Caclin; E. Bigand 2014 |
10.1016/j.cortex.2014.07.012 |
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Mustard Goes Up My Nose and Onions Make Me Cry: Discovering a Third Unknown Chemical Sense G. Brand 2019 |
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Mutation in BRAF V600E: A Poor Prognostic Marker in Stage III Colon Cancers With Deficient MMR? S. Emambux; G. Mouillet; D. Tougeron 2017 |
10.1001/jamaoncol.2017.0262 |
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Mutation screening of MIR146A/B and BRCA1/2 3 `-UTRs in the GENESIS study A.I. Garcia; M. Buisson; F. Damiola; C. Tessereau; L. Barjhoux; C. Verny-Pierre; V. Sornin; M.G. Dondon; S. Eon-Marchais; O. Caron; M. Gautier-Villars; I. Coupier; B. Buecher; P. Vennin; M. Belotti; A. Lortholary; P. Gesta; C. Dugast; C. Nogues; J.P. Fricker; L. Faivre; D. Stoppa-Lyonnet; N. Andrieu; O.M. Sinilnikova; S. Mazoyer; G.E.N.E.S.I.S. Investigators 2016 |
10.1038/ejhg.2015.284 |
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Mutation update for the GPC3 gene involved in Simpson-Golabi-Behmel syndrome and review of the literature M.L. Vuillaunne; M.P. Moizard; ; E. Cottereau; S. Vonwill; J.L. Alessandri; T. Busa; E. Colin; M. Gerard; F. Giuliano; L. Lambert; M. Lefevre; U. Kotecha; S. Nannpoothiri; I. Netchine; M. Raynaud; F. Brioude; A. Toutain 2018 |
10.1002/humu.23428 |
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Mutation Update of the CLCN5 Gene Responsible for Dent Disease 1 L. Mansour-Hendili; A. Blanchard; N. Le Pottier; I. Roncelin; S. Lourdel; C. Treard; W. Gonzalez; A. Vergara-Jaque; G. Morin; E. Colin; M. Holder-Espinasse; J. Bacchetta; V. Baudouin; S. Benoit; E. Berard; G. Bourdat-Michel; K. Bouchireb; S. Burtey; M. Cailliez; G. Cardon; C. Cartery; G. Champion; D. Chauveau; P. Cochat; K. Dahan; R. De la Faille; F.G. Debray; L. Dehoux; G. Deschenes; E. Desport; O. Devuyst; S. Dieguez; F. Emma; M. Fischbach; D. Fouque; J. Fourcade; H. Francois; B. Gilbert-Dussardier; T. Hannedouche; P. Houillier; H. Izzedine; M. Janner; A. Karras; B. Knebelmann; M.P. Lavocat; S. Lemoine; V. Leroy; C. Loirat; M.A. Macher; D. Martin-Coignard; D. Morin; P. Niaudet; H. Nivet; F. Nobili; R. Novo; L. Faivre; C. Rigothier; G. Roussey-Kesler; R. Salomon; A. Schleich; A.L. Sellier-Leclerc; K. Soulami; A. Tiple; T. Ulinski; P. Vanhille; N. Van Regemorter; X. Jeunemaitre; R. Vargas-Poussou 2015 |
10.1002/humu.22804 |
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Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction Jden Hoed; E. de Boer; N. Voisin; A.J.M. Dingemans; N. Guex; L. Wiel; C. Nellaker; S.M. Amudhavalli; S. Banka; F.S. Bena; B. Ben-Zeev; V.R. Bonagura; A.L. Bruel; T. Brunet; H.G. Brunner; H.B. Chew; J. Chrast; L. Cimbalistiene; H. Coon; E.C. Delot; F. Demurger; A.S. Denomme-Pichon; C. Depienne; D. Donnai; D.A. Dyment; O. Elpeleg; L. Faivre; C. Gilissen; L. Granger; B. Haber; Y. Hachiya; Y.Hamzavi Abedi; J. Hanebeck; J.Y. Hehir-Kwa; B. Horist; T. Itai; A. Jackson; R. Jewell; K.L. Jones; S. Joss; H. Kashii; M. Kato; A.A. Kattentidt-Mouravieva; F. Kok; U. Kotzaeridou; V. Krishnamurthy; V. Kucinskas; A. Kuechler; A. Lavillaureix; P. Liu; L. Manwaring; N. Matsumoto; B. Mazel; K. McWalter; V. Meiner; M.A. Mikati; S. Miyatake; T. Mizuguchi; L.H. Moey; S. Mohammed; H. Mor-Shaked; H. Mountford; R. Newbury-Ecob; S. Odent; L. Orec; M. Osmond; T.B. Palculict; M. Parker; A.K. Petersen; R. Pfundt; E. Preiksaitiene; K. Radtke; E. Ranza; J.A. Rosenfeld; T. Santiago-Sim; C. Schwager; M. Sinnema; L.Snijders Blok; R.C. Spillmann; A.P.A. Stegmann; I. Thiffault; L. Tran; A. Vaknin-Dembinsky; J.H. Vedovato-dos-Santos; S.A.Schrier Vergano; E. Vilain; A. Vitobello; M. Wagner; A. Waheeb; M. Willing; B. Zuccarelli; U. Kini; D.F. Newbury; T. Kleefstra; A. Reymond; S.E. Fisher; L.E.L.M. Vissers; D.D.D. Study 2021 |
10.1016/j.ajhg.2021.01.007 |
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Mutation-specific pathophysiological mechanisms in a new SATB1-associated neurodevelopmental disorder den Hoed; E. de Boer; N. Voisin; N. Guex; S. Blok; J. Chrast; L. Manwaring; M. Willing; A. Waheeb; M. Osmond; K. McWalter; A. Vitobello; F. Demurger; A. Lavillaureix; S. Odent; B. Mazel; L. Faivre; I. Thiffault; C. Schwager; S.M. Amudhavalli; J.A. Rosenfeld; K. Radtke; E. Preiksaitiene; E. Ranza; C. Depienne; A. Kuechler; S. Mohammed; H. Abedi; V.R. Bonagura; B. Zuccarelli; B. Horist; V. Krishnamurthy; A.A. Kattentidt-Mouravieva; L. Granger; A. Petersen; K.L. Jones; M. Sinnema; A.P.A. Stegmann; R. Newbury-Ecob; U. Kini; D.F. Newbury; C. Gilissen; H. Brunner; T. Kleefstra; A. Reymond; L.E.L.M. Vissers; S.E. Fisher; D.D.D. Study 2020 |
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Mutation-specific pathophysiological mechanisms in a new SATB1-associated neurodevelopmental disorder den Hoed; E. de Boer; N. Voisin; N. Guex; S. Blok; J. Chrast; L. Manwaring; M. Willing; A. Waheeb; M. Osmond; K. McWalter; A. Vitobello; F. Demurger; A. Lavillaureix; S. Odent; B. Mazel; L. Faivre; I. Thiffault; C. Schwager; S.M. Amudhavalli; J.A. Rosenfeld; K. Radtke; E. Preiksaitiene; E. Ranza; C. Depienne; A. Kuechler; S. Mohammed; H. Abedi; V.R. Bonagura; B. Zuccarelli; B. Horist; V. Krishnamurthy; A.A. Kattentidt-Mouravieva; L. Granger; A. Petersen; K.L. Jones; M. Sinnema; A.P.A. Stegmann; R. Newbury-Ecob; U. Kini; D.F. Newbury; C. Gilissen; H. Brunner; T. Kleefstra; A. Reymond; L.E.L.M. Vissers; S.E. Fisher; D.D.D. Study 2020 |
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Mutational analysis of apoptotic genes in familial aggregation of hematological malignancies W.Sabri Hamadou; R. Mani; N. Bouali; S. Besbes; V. Bourdon; R.El Abed; Y. Ben Youssef; V. Mari; P. Gesta; H. Dreyfus; V. Bonadona; C. Dugast; H. Zattara; L. Faivre; T. Noguchi; A. Khelif; H. Sobol; Z. Soua 2021 |
10.1016/j.bulcan.2021.04.009 |
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Mutational analysis of JAK2, CBL, RUNX1, and NPM1 genes in familial aggregation of hematological malignancies W.S. Hamadou; V. Bourdon; P. Gaildrat; S. Besbes; A. Fabre; Y.B. Youssef; H. Regaieg; M.A. Laatiri; F. Eisinger; V. Mari; P. Gesta; H. Dreyfus; V. Bonadona; C. Dugast; H. Zattara; L. Faivre; S.Yacoub Jemni; T. Noguchi; A. Khelif; H. Sobol; Z. Soua 2016 |
10.1007/s00277-016-2678-y |
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Mutational landscape of gray zone lymphoma C. Sarkozy; S.S. Hung; E.A. Chavez; G. Duns; K. Takata; L.C. Chong; T. Aoki; A. Jiang; T. Miyata-Takata; A. Telenius; G.W. Slack; T.Jo Molina; S. Ben-Neriah; P. Farinha; P. Dartigues; D. Damotte; A. Mottok; G.A. Salles; R.O. Casasnovas; K.J. Savage; C. Laurent; D.W. Scott; A. Traverse-Glehen; C. Steidl 2021 |
10.1182/blood.2020007507 |
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Mutational profile and benefit of gemtuzumab ozogamicin in acute myeloid leukemia E. Fournier; N. Duployez; B. Ducourneau; E. Raffoux; P. Turlure; D. Caillot; X. Thomas; A. Marceau-Renaut; S. Chantepie; J.V. Malfuson; E. Lemasle; M. Cheok; K. Celli-Lebras; E. Guerin; C. Terre; J. Lambert; C. Pautas; H. Dombret; S. Castaigne; C. Preudhomme; N. Boissel; ALFA 2020 |
10.1182/blood.2019003471 |
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Mutational Profile of Metastatic Breast Cancers: A Retrospective Analysis C. Lefebvre; T. Bachelot; T. Filleron; M. Pedrero; M. Campone; J.C. Soria; C. Massard; C. Levy; M. Arnedos; M. Lacroix-Triki; J. Garrabey; Y. Boursin; M. Deloger; Y. Fu; F. Commo; V. Scott; L. Lacroix; M.Vittoria Dieci; M. Kamal; V. Dieras; A. Goncalves; J.M. Ferrerro; G. Romieu; L. Vanlemmens; M.A.Mouret Reynier; J.C. Thery; F. Le Du; S. Guiu; F. Dalenc; G. Clapisson; H. Bonnefoi; M. Jimenez; C. Le Tourneau; F. Andre 2016 |
10.1371/journal.pmed.1002201 |
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Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations T.R. Rebbeck; T.M. Friebel; E. Friedman; U. Hamann; D. Huo; A. Kwong; E. Olah; O.I. Olopade; A.R. Solano; S.H. Teo; M. Thomassen; J.N. Weitzel; T.L. Chan; F.J. Couch; D.E. Goldgar; T.A. Kruse; E.Inez Palmero; S.Kyung Park; D. Torres; E.J. van Rensburg; L. McGuffog; M.T. Parsons; G. Leslie; C.M. Aalfs; J. Abugattas; J. Adlard; S. Agata; K. Aittomaki; L. Andrews; I.L. Andrulis; A. Arason; N. Arnold; B.K. Arun; E. Asseryanis; L. Auerbach; J. Azzollini; J. Balmana; M. Barile; R.B. Barkardottir; D. Barrowdale; J. Benitez; A. Berger; R. Berger; A.M. Blanco; K.R. Blazer; M.J. Blok; V. Bonadona; B. Bonanni; A.R. Bradbury; C. Brewer; B. Buecher; S.S. Buys; T. Caldes; A. Caliebe; M.A. Caligo; I. Campbell; S.M. Caputo; J. Chiquette; W.K. Chung; K.B.M. Claes; M. Collee; J. Cook; R. Davidson; M. de la Hoya; K. De Leeneer; A. de Pauw; C. Delnatte; O. Diez; Y.Chun Ding; N. Ditsch; S.M. Domchek; C.M. Dorfling; C. Velazquez; B. Dworniczak; J. Eason; D.F. Easton; R. Eeles; H. Ehrencrona; B. Ejlertsen; C. Engel; S. Engert; G. Evans; L. Faivre; L. Feliubadalo; S.Fert Ferrer; L. Foretova; J. Fowler; D. Frost; H.C.R. Galvao; P.A. Ganz; J. Garber; M. Gauthier-Villars; A. Gehrig; A.M. Gerdes; P. Gesta; G. Giannini; S. Giraud; G. Glendon; A.K. Godwin; M.H. Greene; J. Gronwald; A. Gutierrez-Barrera; E. Hahnen; J. Hauke; A. Henderson; J. Hentschel; F.B.L. Hogervorst; E. Honisch; E.N. Imyanitov; C. Isaacs; L. Izatt; A. Izquierdo; A. Jakubowska; P. James; R. Janavicius; U.Birk Jensen; E.M. John; J. Vijai; K. Kaczmarek; B.Y. Karlan; K. Kast; S.W. Kim; I. Konstantopoulou; J. Korach; Y. Laitman; A. Lasa; C. Lasset; C. Lazaro; A. Lee; M.Hyuk Lee; J. Lester; F. Lesueur; A. Liljegren; N.M. Lindor; M. Longy; J.T. Loud; K.H. Lu; J. Lubinski; E. Machackova; S. Manoukian; V. Mari; C. Martinez-Bouzas; Z. Matrai; N. Mebirouk; H.E.J. Meijers-Heijboer; A. Meindl; A.R. Mensenkamp; U. Mickys; A. Miller; M. Montagna; K.B. Moysich; A.Marie Mulligan; J. Musinsky; S.L. Neuhausen; H. Nevanlinna; J. Ngeow; H.Phuc Nguyen; D. Niederacher; H.Roed Nielsen; F.Cilius Nielsen; R.L. Nussbaum; K. Offit; A. Ofverholm; Kren Ong; A. Osorio; L. Papi; J. Papp; B. Pasini; I.Sokilde Pedersen; A. Peixoto; N. Peruga; P. Peterlongo; E. Pohl; N. Pradhan; K. Prajzendanc; F. Prieur; P. Pujol; P. Radice; S.J. Ramus; J. Rantala; M.Usman Rashid; K. Rhiem; M. Robson; G.C. Rodriguez; M.T. Rogers; V. Rudaitis; A.Y. Schmidt; R.Katharina Schmutzler; L. Senter; P.D. Shah; P. Sharma; L.E. Side; J. Simard; C.F. Singer; A.B. Skytte; T.P. Slavin; K. Snape; H. Sobol; M. Southey; L. Steele; D. Steinemann; G. Sukiennicki; C. Sutter; C.I. Szabo; Y.Y. Tan; M.R. Teixeira; M.Beth Terry; A. Teule; A. Thomas; D.L. Thull; M. Tischkowitz; S. Tognazzo; A.Ewart Toland; S. Topka; A.H. Trainer; N. Tung; C.J. van Asperen; A.H. van der Hout; L.E. van der Kolk; R.B. van der Luijt; M. Van Heetvelde; L. Varesco; R. Varon-Mateeva; A. Vega; C. Villarreal-Garza; A. von Wachenfeldt; L. Walker; S. Wang-Gohrke; B. Wappenschmidt; B.H.F. Weber; D. Yannoukakos; S.Y. Yoon; C. Zanzottera; J. Zidan; K.K. Zorn; C.G.Hutten Selkirk; P.J. Hulick; G. Chenevix-Trench; A.B. Spurdle; A.C. Antoniou; K.L. Nathanson; EMBRACE; G.E.M.O.Study Collaborators; HEBON; K.C.F. Investigators 2018 |
10.1002/humu.23406 |
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Mutational Spectrum in Holoprosencephaly Shows That FGF is a New Major Signaling Pathway C. Dubourg; W. Carre; H. Hamdi-Roze; C. Mouden; J. Roume; B. Abdelmajid; D. Amram; C. Baumann; N. Chassaing; C. Coubes; L. Faivre-Olivier; E. Ginglinger; M. Gonzales; A. Levy-Mozziconacci; S.A. Lynch; S. Naudion; L. Pasquier; A. Poidvin; F. Prieur; P. Sarda; A. Toutain; V. Dupe; L. Akloul; S. Odent; M. de Tayrac; V. David 2016 |
10.1002/humu.23038 |
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Mutational spectrum in PIK3CA-Related Overgrowth Spectrum (PROS) and recommendations for molecular testing P. Kuentz; Y. Duffourd; J. St-Onge; T. Jouan; A. Sorlin; C. Thauvin-Robinet; J. Thevenon; J. Riviere; L. Faivre; P. Vabres 2016 |
10.1016/j.jid.2016.06.204 |
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Mutations in ACTRT1 and its enhancer RNA elements lead to aberrant activation of Hedgehog signaling in inherited and sporadic basal cell carcinomas E. Bal; H.S. Park; Z. Belaid-Choucair; H. Kayserili; M. Naville; M. Madrange; E. Chiticariu; S. Hadj-Rabia; N. Cagnard; F. Kuonen; D. Bachmann; M. Huber; C. Le Gall; F. Cote; S. Hanein; R.Ozgur Rosti; A.Dilruba Aslanger; Q. Waisfisz; C. Bodemer; O. Hermine; F. Morice-Picard; B. Labeille; F. Caux; J. Mazereeuw-Hautier; N. Philip; N. Levy; A. Taieb; M.F. Avril; D.J. Headon; G. Gyapay; T. Magnaldo; S. Fraitag; H.Roest Crollius; P. Vabres; D. Hohl; A. Munnich; A. Smahi 2017 |
10.1038/nm.4368 |