Zobrazeno 1 - 10
of 68
pro vyhledávání: '"N Dagoneau"'
Autor:
Olivier Godet, J.-L Atteia, C. Amoros, P. Roger, L. Bouchet, J.-P Dezalay, M. Yassine, B. Arcier, S. Bordon, K. Lacombe, E. Lecomte, M. Llamas, S. Maestre, W. Marty, Stéphane Papais, P. Ramon, C. Verdeil, V. Waegebaert, S. Schanne, N. Dagoneau, F. Chateau, P. Kestener, H. Le Provost, C. Tahoulan, B. Cordier, Th. Tourrette, F. Daly, H. Triou, A. Coleiro, A. Goldwurm, C. Lachaud, P. Guillemot, J-M. Mouret, M.-C. Charmeau, L. Perraud, F. Bousquet, Y. Cervantes, Ph. Gasc, H. Pasquier, L. Perrin, M. Ruellan, O. Simonella, M. Yadallee
Publikováno v:
Space Telescopes and Instrumentation 2022: Ultraviolet to Gamma Ray.
Autor:
N. Dagoneau, S. Schanne
Publikováno v:
Astronomy and Astrophysics-A&A
Astronomy and Astrophysics-A&A, 2022, 665, pp.A40. ⟨10.1051/0004-6361/202141891⟩
Astronomy and Astrophysics-A&A, 2022, 665, pp.A40. ⟨10.1051/0004-6361/202141891⟩
The SVOM mission under development will carry four instruments, and in particular the coded-mask telescope named ECLAIRs, with a large field of view of about 2 sr, operating in the 4-150 keV energy band. The trigger software on board ECLAIRs will sea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5e0ec57392181fa3b321e26e373f114
http://arxiv.org/abs/2208.12767
http://arxiv.org/abs/2208.12767
Autor:
B. Arcier, O. Godet, N. Dagoneau, Jean-Luc Atteia, Sujay Mate, J. Rodriguez, M. G. Bernardini, S. Schanne, Diego Götz, S. Guillot
Publikováno v:
Astrophys.Space Sci.
Astrophys.Space Sci., 2020, 365 (12), pp.185. ⟨10.1007/s10509-020-03898-z⟩
Astrophys.Space Sci., 2020, 365 (12), pp.185. ⟨10.1007/s10509-020-03898-z⟩
International audience; The coincidental detection of the gravitational wave event GW 170817 and the gamma-ray burst GRB 170817A marked the advent of multi-messenger astronomy and represented a milestone in the study of GRBs. Significant progress in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a26ba5eaf4a1f03528ee36e9879d4fb0
https://hal.archives-ouvertes.fr/hal-03070594
https://hal.archives-ouvertes.fr/hal-03070594
Akademický článek
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Publikováno v:
Astronomy and Astrophysics-A&A
Astronomy and Astrophysics-A&A, 2021, 645, pp.A18. ⟨10.1051/0004-6361/202038995⟩
Astronomy and Astrophysics-A&A, EDP Sciences, 2021, 645, pp.A18. ⟨10.1051/0004-6361/202038995⟩
Astronomy and Astrophysics-A&A, 2021, 645, pp.A18. ⟨10.1051/0004-6361/202038995⟩
Astronomy and Astrophysics-A&A, EDP Sciences, 2021, 645, pp.A18. ⟨10.1051/0004-6361/202038995⟩
The SVOM mission under development will carry various instruments, and in particular the coded-mask telescope ECLAIRs, with a large field of view of about 2 sr, operating in the 4--150 keV energy band, whose goal is to detect high energy transients s
Autor:
Ali, Shad1 (AUTHOR) shad.ali88@yahoo.com
Publikováno v:
European Physical Journal C -- Particles & Fields. Nov2024, Vol. 84 Issue 11, p1-12. 12p.
Autor:
Pierre Sarda, C. Le Goff, S. Bellais, Lihadh Al-Gazali, M. Di Rocco, Valérie Cormier-Daire, N. Dagoneau, A. Munnich, Patricia Blanchet, C. Huber, Fatima Djouadi
Publikováno v:
The American Journal of Human Genetics. 80:966-970
Crisponi syndrome is a rare autosomal recessive disorder characterized by congenital muscular contractions of facial muscles, with trismus in response to stimuli, dysmorphic features, bilateral camptodactyly, major feeding and respiratory difficultie
Akademický článek
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Autor:
M. Le Merrer, Sheila Unger, Valérie Cormier-Daire, Albert David, Ben C.J. Hamel, Andrea Superti-Furga, N Dagoneau, C Jung, Geneviève Baujat, André Mégarbané, Arnold Munnich, M. Di Rocco
Publikováno v:
Clinical Genetics, 77, 3, pp. 266-72
Clinical Genetics, 77, 266-72
Clinical Genetics, 77, 266-72
Stuve-Wiedemann syndrome (SWS, OMIM 601559) is a severe autosomal recessive condition caused by mutations in the leukemia inhibitory receptor (LIFR) gene. The main characteristic features are bowing of the long bones, neonatal respiratory distress, s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70430a6b2140676cc48e6bcb2988471b
https://doi.org/10.1111/j.1399-0004.2009.01314.x
https://doi.org/10.1111/j.1399-0004.2009.01314.x
Autor:
John R. Samples, M. Le Merrer, Gwenaëlle Collod-Béroud, N. Dagoneau, Maurice Godfrey, Catherine Boileau, Mary K. Wirtz, Valérie Cormier-Daire, Arnold Munnich, Robert J. Gorlin, Laurence Faivre
Publikováno v:
Journal of Medical Genetics
Journal of Medical Genetics, BMJ Publishing Group, 2003, 40 (1), pp.34-6
Journal of Medical Genetics, BMJ Publishing Group, 2003, 40 (1), pp.34-6
Weill-Marchesani syndrome (WMS) is a connective tissue disorder characterised by short stature, brachydactyly, joint stiffness, and characteristic eye anomalies including microspherophakia, ectopia of the lenses, severe myopia, and glaucoma. Both aut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc03e6c8f7a795cc981ac20c49bb415a
http://www.hal.inserm.fr/inserm-00143439/document
http://www.hal.inserm.fr/inserm-00143439/document