Publications
Publications 3901 - 3925 de 33557
| Titre | DOI |
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Autonomy Estimation for EV based on Road Planning Software D. Chrenko; A. Ravey; R. Roche; D. Bouquain 2014 |
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Autonomy in the Dock: Oscar Wilde's First Trial B. Coste 2014 |
10.4000/cve.1114 |
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Autonomy-Supportive and Controlling Styles of Teaching Opposite or Distinct Teaching Styles? C. Amoura; S. Berjot; N. Gillet; S. Caruana; J. Cohen; L. Finez 2015 |
10.1024/1421-0185/a000156 |
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Autopsy findings of ectodermal dysplasia and sex development disorder in a fetus with 19q12q13 microdeletion N. Mottet; C. Cabrol; J.P. Metz; C. Toubin; F. Arbez-Gindre; M. Valduga; K. McElreavey; D. Riethmuller; L. Van Maldergem; J. Piard 2019 |
10.1016/j.ejmg.2018.09.006 |
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Autoregressive functions estimation in nonlinear bifurcating autoregressive models V.Bitseki Penda; A. Olivier 2017 |
10.1007/s11203-016-9140-6 |
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Autoregulation of Pulsatile Bioprosthetic Total Artificial Heart is Involved in Endothelial Homeostasis Preservation D.M. Smadja; R. Chocron; E. Rossi; B. Poitier; Y. Pya; M. Bekbossynova; C. Peronino; J. Rancic; J.Christian Roussel; M. Kindo; N. Gendron; L. Migliozzi; A. Capel; J.Christophe Perles; P. Gaussem; P. Ivak; P. Jansen; C. Girard; A. Carpentier; C. Latremouille; C. Guerin; I. Netuka 2020 |
10.1055/s-0040-1713751 |
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Autosetting Mode-Locked Laser Using an Evolutionary Algorithm and Time-Stretch Spectral Characterization J. Girardot; F. Billard; A. Coillet; E. Hertz; P. Grelu 2020 |
10.1109/JSTQE.2020.2985297 |
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Autosetting Mode-locked Laser with Genetic Algorithm Optimization and Advanced Intracavity Controls J. Girardot; F. Billard; A. Coillet; M. Nafa; E. Hertz; P. Grelu 2021 |
10.1109/CLEO/Europe-EQEC52157.2021.9541881 |
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Autosomal dominant recurrent parotitis: an under-reported entity M.G. Serey-Gaut; C. Cabrol; J. Vallat; L. Tatu; B. Loeys; L. Van Maldergem 2019 |
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Autosomal dominant recurrent parotitis: an under-reported entity M.G. Serey-Gaut; C. Cabrol; J. Vallat; L. Tatu; B. Loeys; L. Van Maldergem 2019 |
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Autosomal dominant recurrent parotitis: an under-reported entity M.G. Serey-Gaut; C. Cabrol; J. Vallat; L. Tatu; B. Loeys; L. Van Maldergem 2019 |
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Autosomal Recessive Cutis Laxa Type 2A ( ARCL2A) Mimicking Ehlers- Danlos Syndrome by Its Dermatological Manifestations: Report of Three Affected Patients M.T. Greally; N.N. Kalis; W. Agab; K. Ardati; S. Giurgea; U. Kornak; L. Van Maldergem 2014 |
10.1002/ajmg.a.36411 |
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Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral-facial-digital syndrome with short stature and brachymesophalangia J. Thevenon; L. Duplomb; S. Phadke; T. Eguether; A. Saunier; M. Avila; V. Carmignac; A.L. Bruel; J. St-Onge; Y. Duffourd; G.J. Pazour; B. Franco; T. Attie-Bitach; A. Masurel-Paulet; J.B. Riviere; V. Cormier-Daire; C. Philippe; L. Faivre; C. Thauvin-Robinet 2016 |
10.1111/cge.12785 |
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Autosomal recessive mutations in THOC6 cause intellectual disability: syndrome delineation requiring forward and reverse phenotyping J.S. Amos; L. Huang; J. Thevenon; A. Kariminedjad; C.L. Beaulieu; A. Masurel-Paulet; H. Najmabadi; Z. Fattahi; M. Beheshtian; S.H. Tonekaboni; S. Tang; K.L. Helbig; W. Alcaraz; J.B. Riviere; L. Faivre; A.M. Innes; R.R. Lebel; K.M. Boycott; C.4R.Canada Consortium 2017 |
10.1111/cge.12793 |
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Autosomal recessive POLR1D mutation with decrease of TCOF1 mRNA is responsible for Treacher Collins syndrome E. Schaefer; C. Collet; D. Genevieve; M. Vincent; D.R. Lohmann; E. Sanchez; C. Bolender; M.M. Eliot; G. Nuernberg; M.R. Passos-Bueno; D. Wieczorek; L. Van Maldergem; B. Doray 2014 |
10.1038/gim.2014.12 |
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Autosomal recessive primary microcephaly due to ASPM mutations: An update P. Letard; S. Drunat; Y. Vial; S. Duerinckx; A. Ernault; D. Amram; S. Arpin; M. Bertoli; T. Busa; B. Ceulemans; J. Desir; M. Doco-Fenzy; S.Chafai Elalaoui; K. Devriendt; L. Faivre; C. Francannet; D. Genevieve; M. Gerard; C. Gitiaux; S. Julia; S. Lebon; T. Lubala; M. Mathieu-Dramard; H. Maurey; J. Metreau; S. Nasserereddine; M. Nizon; G. Pierquin; N. Pouvreau; C. Rivier-Ringenbach; M. Rossi; E. Schaefer; A. Sefiani; S. Sigaudy; Y. Sznajer; Y. Tunca; S.Guilmin Crepon; C. Alberti; M. Elmaleh-Berges; B. Benzacken; B. Wollnick; G. Woods; A. Rauch; M. Abramowicz; V.El Ghouzzi; P. Gressens; A. Verloes; S. Passemard 2018 |
10.1002/humu.23381 |
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Autosomal recessive truncating MAB21L1 mutation associated with a syndromic scrotal agenesis A.L. Bruel; A. Masurel-Paulet; J.B. Riviere; Y. Duffourd; D. Lehalle; C. Bensignor; F. Huet; J. Borgnon; F. Roucher; P. Kuentz; J.F. Deleuze; C. Thauvin-Robinet; L. Faivre; J. Thevenon 2017 |
10.1111/cge.12794 |
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Autosomal recessive variations of TBX6, from congenital scoliosis to spondylocostal dysostosis M. Lefebvre; Y. Duffourd; T. Jouan; C. Poe; N. Jean-Marcais; A. Verloes; J. St-Onge; J.B. Riviere; F. Petit; G. Pierquin; B. Demeer; P. Callier; C. Thauvin-Robinet; L. Faivre; J. Thevenon 2017 |
10.1111/cge.12918 |
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Autosomal-dominant early-onset spastic paraparesis with brain calcification due to IFIH1 gain-of-function L. Ruaud; G.I. Rice; C. Cabrol; J. Piard; M. Rodero; L. van Eyk; E. Boucher-Brischoux; A.Maertens de Noordhout; R. Mare; E. Scalais; F. Pauly; F.G. Debray; W. Dobyns; C. Uggenti; J.Woo Park; S. Hur; J.H. Livingston; Y.J. Crow; L. Van Maldergem 2018 |
10.1002/humu.23554 |
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Autosomal-Recessive Mutations in AP3B2, Adaptor-Related Protein Complex 3 Beta 2 Subunit, Cause an Early-Onset Epileptic Encephalopathy with Optic Atrophy M. Assoum; C. Philippe; B. Isidor; L. Perrin; P. Makrythanasis; N. Sondheimer; C. Paris; J. Douglas; G. Lesca; S. Antonarakis; H. Hamamy; T. Jouan; Y. Duffourd; S. Auvin; A. Saunier; A. Begtrup; C. Nowak; N. Chatron; D. Ville; K. Mireskandari; P. Milani; P. Jonveaux; G. Lemeur; M. Milh; M. Amamoto; M. Kato; M. Nakashima; N. Miyake; N. Matsumoto; A. Masri; C. Thauvin-Robinet; J.B. Riviere; L. Faivre; J. Thevenon 2016 |
10.1016/j.ajhg.2016.10.009 |
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Autosomal-recessive SASH1 variants associated with a new genodermatosis with pigmentation defects, palmoplantar keratoderma and skin carcinoma J.B. Courcet; S.Chafai Elalaoui; L. Duplomb; M. Tajir; J.B. Riviere; J. Thevenon; N. Gigot; N. Marle; B. Aral; Y. Duffourd; A. Sarasin; V. Naim; E. Courcet-Degrolard; M.H. Aubriot-Lorton; L. Martin; J.Eddin Abrid; C. Thauvin; A. Sefiani; P. Vabres; L. Faivre 2015 |
10.1038/ejhg.2014.213 |
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Auxin treatment of wetland and non-wetland plant species to enhance their phytoremediation efficiency to treat municipal wastewater S.A. Tandon; R. Kumar; S. Parsana 2015 |
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AV nodal reentrant tachycardia or AV reentrant tachycardia using a concealed bypass tract-related adverse events B. Brembilla-Perrot; M. Benichou; A. Brembilla; E. Bozec; S. Dorlet; J.Marc Sellal; A. Olivier; V. Manenti; T. Villemin; D. Beurrier; A. Moulin-Zinsch; C. De Chillou; N. Girerd 2015 |
10.1016/j.ijcard.2015.07.048 |
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Availability of attention affects time-to-contact estimation R. Baures; F. Maquestiaux; P.R. DeLucia; A. Defer; E. Prigent 2018 |
10.1007/s00221-018-5273-8 |
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Availability of secondary prevention services after stroke in Europe: An ESO/SAFE survey of national scientific societies and stroke experts A. Webb; M.R. Heldner; A. de Sousa; E.C. Sandset; G. Randall; Y. Bejot; B. van der Worp; V. Caso; U. Fischer; E.S.O.S.A.F.E.Secondary Sur 2019 |
10.1177/2396987318816136 |