Publications - 'P'
Publications 726 - 750 de 2458
| Titre | DOI |
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Phenotypes of atopic dermatitis depending on the timing of onset and progression in childhood C. Roduit; R. Frei; M. Depner; A.M. Karvonen; H. Renz; C. Braun-Fahrlander; E. Schmausser-Hechfellner; J. Pekkanen; J. Riedler; J.C. Dalphin; E. Von Mutius; R. Lauener 2017 |
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Phenotypic and biochemical analysis of an international cohort of individuals with variants in NAA10 and NAA15 H. Cheng; L. Gottlieb; E. Marchi; R. Kleyner; P. Bhardwaj; A.F. Rope; S. Rosenheck; S. Moutton; C. Philippe; W. Eyaid; F.S. Alkuraya; J. Toribio; R. Mena; C.E. Prada; H. Stessman; R. Bernier; M. Wermuth; B. Kauffmann; B. Blaumeiser; F. Kooy; D. Baralle; G.M.S. Mancini; S.J. Conway; F. Xia; Z. Chen; L. Meng; L. Mihajlovic; R. Marmorstein; G.J. Lyon 2019 |
10.1093/hmg/ddz111 |
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Phenotypic and biochemical analysis of an international cohort of individuals with variants in NAA10 and NAA15 (vol 28, pg 2900, 2019) H. Cheng; L. Gottlieb; E. Marchi; R. Kleyner; P. Bhardwaj; A.F. Rope; S. Rosenheck; S. Moutton; C. Philippe; W. Eyaid; F.S. Alkuraya; J. Toribio; R. Mena; C.E. Prada; H. Stessman; R. Bernier; M. Wermuth; B. Kauffmann; B. Blaumeiser; F. Kooy; D. Baralle; G.M.S. Mancini; S.J. Conway; F. Xia; Z. Chen; L. Meng; L. Mihajlovic; R. Marmorstein; G.J. Lyon 2020 |
10.1093/hmg/ddz173 |
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Phenotypic and functional heterogeneity of tissue resident memory T-cells in colorectal cancer liver metastasis S. Abdeljaoued; M. Kroemer; M. Ben Khelil; J. Viot; A. Bouard; F. Monnien; V. Mougey; R. Loyon; A. Doussot; B. Heyd; C. Borg 2021 |
10.1016/j.annonc.2021.10.192 |
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PHENOTYPIC AND GENOTYPIC CONVERGENCES ARE INFLUENCED BY HISTORICAL CONTINGENCY AND ENVIRONMENT IN YEAST A. Spor; D.J. Kvitek; T. Nidelet; J. Martin; J. Legrand; C. Dillmann; A. Bourgais; D. De Vienne; G. Sherlock; D. Sicard 2014 |
10.1111/evo.12302 |
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Phenotypic and genotypic description of 44 patients with variants in DLG4 encoding the post-synaptic density protein PSD-95 R.P. Seuma; M. Boerrigter; G. Mandrile; A. Pelle; E. Giorgio; A. Lindstrand; M. Johansson; M. Kvarnung; D. Everman; V. Bahrambeigi; A. MacKenzie; J. Morton; C. Ruivenkamp; T. Challman; A. Hurst; J. Hoyer; F. Elmslie; T. Dye; B. Isidor; C. Haldeman-Englert; D. Gomez-Andres; A. Schluter; S. de Man; J. Shieh; C. Prada; S. Moutton; A. Denomme-Pichon; S. Motti; A. Bruel; T. Mau-Them; S. Reiter; C. van Ravenswaaij-Arts; C. Shaw-Smith; S. Parikh; K. Aldinger; A. Lovgren; A. Rauch; M. Ross; P. Gomez-Puertas; B. De Vries; A. Pujol; Z. Tumer 2020 |
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Phenotypic and genotypic description of 44 patients with variants in DLG4 encoding the post-synaptic density protein PSD-95 R.P. Seuma; M. Boerrigter; G. Mandrile; A. Pelle; E. Giorgio; A. Lindstrand; M. Johansson; M. Kvarnung; D. Everman; V. Bahrambeigi; A. MacKenzie; J. Morton; C. Ruivenkamp; T. Challman; A. Hurst; J. Hoyer; F. Elmslie; T. Dye; B. Isidor; C. Haldeman-Englert; D. Gomez-Andres; A. Schluter; S. de Man; J. Shieh; C. Prada; S. Moutton; A. Denomme-Pichon; S. Motti; A. Bruel; T. Mau-Them; S. Reiter; C. van Ravenswaaij-Arts; C. Shaw-Smith; S. Parikh; K. Aldinger; A. Lovgren; A. Rauch; M. Ross; P. Gomez-Puertas; B. De Vries; A. Pujol; Z. Tumer 2020 |
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Phenotypic and genotypic description of 44 patients with variants in DLG4 encoding the post-synaptic density protein PSD-95 R.P. Seuma; M. Boerrigter; G. Mandrile; A. Pelle; E. Giorgio; A. Lindstrand; M. Johansson; M. Kvarnung; D. Everman; V. Bahrambeigi; A. MacKenzie; J. Morton; C. Ruivenkamp; T. Challman; A. Hurst; J. Hoyer; F. Elmslie; T. Dye; B. Isidor; C. Haldeman-Englert; D. Gomez-Andres; A. Schluter; S. de Man; J. Shieh; C. Prada; S. Moutton; A. Denomme-Pichon; S. Motti; A. Bruel; T. Mau-Them; S. Reiter; C. van Ravenswaaij-Arts; C. Shaw-Smith; S. Parikh; K. Aldinger; A. Lovgren; A. Rauch; M. Ross; P. Gomez-Puertas; B. De Vries; A. Pujol; Z. Tumer 2020 |
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Phenotypic and molecular insights into CASK-related disorders in males U. Moog; T. Bierhals; K. Brand; J. Bautsch; S. Biskup; T. Brune; J. Denecke; C.E. de Die-Smulders; C. Evers; M. Hempel; M. Henneke; H. Yntema; B. Menten; J. Pietz; R. Pfundt; J. Schmidtke; D. Steinemann; C.T. Stumpel; L. Van Maldergem; K. Kutsche 2015 |
10.1186/s13023-015-0256-3 |
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Phenotypic differentiation of Ponto-Caspian gobies during a contemporary invasion of the upper Danube River A.F. Cerwenka; P. Alibert; J. Brandner; J. Geist; U.K. Schliewen 2014 |
10.1007/s10750-013-1668-5 |
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Phenotypic discordance between primary and metastatic breast cancer (MBC) in a large scale real-life multicentre French cohort S. Lefevre; A. Lusque; N. Joyon; L. Arnould; F. Penault-Llorca; G. MacGrogan; I. Treilleux; A. Vincent-Salomon; J. Haudebourg; A. Maran-Gonzalez; E. Charafe-Jauffret; C. Courtinard; C. Franchet; V. Verriele; E. Brain; P. Tas; S. Delaloge; T. Filleron; M. Lacroix-Triki 2019 |
10.1158/1538-7445.SABCS18-P5-12-05 |
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Phenotypic discordance between primary and metastatic breast cancer in the large-scale real-life multicenter French ESME cohort T. Grinda; N. Joyon; A. Lusque; S. Lefevre; L. Arnould; F. Penault-Llorca; G. MacGrogan; I. Treilleux; A. Vincent-Salomon; J. Haudebourg; A. Maran-Gonzalez; E. Charafe-Jauffret; C. Courtinard; C. Franchet; V. Verriele; E. Brain; P. Tas; C. Blanc-Fournier; A. Leroux; D. Loussouarn; A. Berghian; E. Brabencova; J.Pierre Ghnassia; J.Y. Scoazec; S. Delaloge; T. Filleron; M. Lacroix-Triki 2021 |
10.1038/s41523-021-00252-6 |
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Phenotypic expansion in DDX3X - a common cause of intellectual disability in females X. Wang; J.E. Posey; J.A. Rosenfeld; C.A. Bacino; F. Scaglia; L.D. Immken; J.M. Harris; S.E. Hickey; T.M. Mosher; A. Slavotinek; J. Zhang; J. Beuten; M.S. Leduc; W. He; F. Vetrini; M.A. Walkiewicz; W. Bi; R. Xiao; P. Liu; Y. Shao; A. Gezdirici; E.Y. Gulec; Y. Jiang; S.A. Darilek; A.W. Hansen; M.M. Khayat; D. Pehlivan; J. Piard; D.M. Muzny; N. Hanchard; J.W. Belmont; L. Van Maldergem; R.A. Gibbs; M.K. Eldomery; Z.C. Akdemir; A.M. Adesina; S. Chen; Y.C. Lee; B. Lee; J.R. Lupski; C.M. Eng; F. Xia; Y. Yang; B.H. Graham; P. Moretti; U.Dis Network 2018 |
10.1002/acn3.622 |
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Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations E.Adele Colombo; H. Mutlu-Albayrak; Y. Shafeghati; M. Balasar; J. Piard; D. Gentilini; A.Maria Di Blasio; C. Gervasini; L. Van Maldergem; L. Larizza 2019 |
10.3389/fped.2019.00210 |
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Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita A. Laquerriere; D. Jaber; E. Abiusi; J. Maluenda; D. Mejlachowicz; A. Vivanti; K. Dieterich; R. Stoeva; L. Quevarec; F. Nolent; V. Biancalana; P. Latour; D. Sternberg; Y. Capri; A. Verloes; B. Bessieres; L. Loeuillet; T. Attie-Bitach; J. Martinovic; S. Blesson; F. Petit; C. Beneteau; S. Whalen; F. Marguet; J. Bouligand; D. Heron; G. Viot; J. Amiel; D. Amram; C. Bellesme; M. Bucourt; L. Faivre; P.S. Jouk; S. Khung; S. Sigaudy; A.L. Delezoide; A. Goldenberg; M.L. Jacquemont; L. Lambert; V. Layet; S. Lyonnet; A. Munnich; L. Van Maldergem; J. Piard; F. Guimiot; P. Landrieu; P. Letard; F. Pelluard; L. Perrin; M.H. Saint-Frison; H. Topaloglu; L. Trestard; C. Vincent-Delorme; H. Amthor; C. Barnerias; A. Benachi; E. Bieth; E. Boucher; V. Cormier-Daire; A. Delahaye-Duriez; I. Desguerre; B. Eymard; C. Francannet; S. Grotto; D. Lacombe; F. Laffargue; M. Legendre; D. Martin-Coignard; A. Megarbane; S. Mercier; M. Nizon; L. Rigonnot; F. Prieur; C. Quelin; H. Ranjatoelina-Randrianaivo; N. Resta; A. Toutain; H. Verhelst; M. Vincent; E. Colin; C. Fallet-Bianco; M. Granier; R. Grigorescu; J. Saada; M. Gonzales; A. Guiochon-Mantel; J.L. Bessereau; M. Tawk; I. Gut; C. Gitiaux; J. Melki Submitted |
10.1136/jmedgenet-2020-107595 |
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Phenotypic spectrum and incidence of TRPV4 mutations in patients with inherited axonal neuropathy A. Echaniz-Laguna; O. Dubourg; P. Carlier; R.Y. Carlier; P. Sabouraud; Y. Pereon; F. Chapon; C. Thauvin-Robinet; P. Laforet; B. Eymard; P. Latour; T. Stojkovic 2014 |
10.1212/WNL.0000000000000450 |
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Phenotypic spectrum associated with SPECC1L pathogenic variants: new families and critical review of the nosology of Teebi, Opitz GBBB, and Baraitser-Winter syndromes E.J. Bhoj; D. Haye; A. Toutain; D. Bonneau; I.Kibaek Nielsen; I.Bay Lund; P. Bogaard; S. Leenskjold; K. Karaer; K.T. Wild; K.L. Grand; M.C. Astiazaran; L.A. Gonzalez-Nieto; A. Carvalho; D. Lehalle; S.M. Amudhavalli; E. Repnikova; C. Saunders; I. Thiffault; I. Saadi; D. Li; H. Hakonarson; Y. Vial; E. Zackai; P. Callier; S. Drunat; A. Verloes 2019 |
10.1016/j.ejmg.2018.11.022 |
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Phenotypic spectrum associated with SPECC1L pathogenic variants: new families and critical review of the nosology of Teebi, Opitz GBBB, and Baraitser-Winter syndromes A. Verloes; D. Haye; A. Toutain; D. Bonneau; K. Nielsen; B. Lund; P. Bogaard; S. Leenskjold; K. Karaer; K.T. Wild; K.L. Grand; M.C. Astiazaran; L.A. Gonzalez-Nieto; A. Carvalho; D. Lehalle; S.M. Amudhavalli; E. Repnikova; C. Saunders; I. Thiffault; I. Thiffault; I. Saadi; D. Li; H. Hakonarson; Y. Vial; E. Zackai; P. Callier; S. Drunat; E.E. Bhoj 2019 |
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Phenotypic spectrum of SPECC1L mutations encompasses Teebi hypertelorism syndrome but not Opitz BBBG syndrome: report of new families and critical review of the literature A. Verloes; D. Haye; A. Toutain; D. Bonneau; D. Lehalle; P. Caillier; S. Drunat; I. Lund; E. Bhoj; P. Bogaard; S. Leenskjold; E. Zackay; D. Li; H. Hakonarson; M. Petersen; I. Nielsen 2018 |
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Phenotypic spectrum of SPECC1L mutations encompasses Teebi hypertelorism syndrome but not Opitz BBBG syndrome: report of new families and critical review of the literature A. Verloes; D. Haye; A. Toutain; D. Bonneau; D. Lehalle; P. Caillier; S. Drunat; I. Lund; E. Bhoj; P. Bogaard; S. Leenskjold; E. Zackay; D. Li; H. Hakonarson; M. Petersen; I. Nielsen 2018 |
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Phenoxyamidine Zn and Al Complexes: Synthesis, Characterization, and Use in the Ring-Opening Polymerization of Lactide F. Chotard; R. Lapenta; A. Bolley; A. Trommenschlager; C. Balan; J. Bayardon; R. Malacea-Kabbara; Q. Bonnin; E. Bodio; H. Cattey; P. Richard; S. Milione; A. Grassi; S. Dagorne; P. Le Gendre 2019 |
10.1021/acs.organomet.9b00501 |
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phi-FEM: A FINITE ELEMENT METHOD ON DOMAINS DEFINED BY LEVEL-SETS M. Duprez; A. Lozinski 2020 |
10.1137/19M1248947 |
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PHILOSOPHY AND RELIGIONS J. Ferrari 2015 |
10.5840/jpr201540Supplement22 |
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Philosophy and Technology in the French Tradition. The Legacy of Francois Dagognet G. Chazal 2018 |
10.1007/978-3-319-89518-5_2 |
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PHM-oriented Degradation Indicators for Batteries and Fuel Cells D. Zhang; C. Cadet; N. Yousfi-Steiner; F. Druart; C. Berenguer 2017 |
10.1002/fuce.201600075 |