Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Olivia Beaudoux"'
Autor:
Olivia Beaudoux, Marine Ehret, Emilie Criquet, Joséphine Franceschi, Anne Durlach, Jean-Bapstiste Oudart, Laetitia Visseaux, Florent Grange
Publikováno v:
Acta Dermato-Venereologica, Vol 101, Iss 4, p adv00426 (2021)
Externí odkaz:
https://doaj.org/article/f556323e3b1741a0a3cf34617202268d
Autor:
John Hanna, Jennifer S. Ko, Steven D. Billings, Felix Boivin, Olivia Beaudoux, Daniel Pissaloux, Franck Tirode, Alvaro Laga, Christopher D.M. Fletcher, Arnaud de la Fouchardiere
Publikováno v:
American Journal of Surgical Pathology. 46:1457-1466
Cutaneous melanocytic tumor with CRTC1::TRIM11 fusion (CMTCT) is a recently described dermally based neoplasm with melanocytic differentiation. It can easily be confused with clear cell sarcoma and metastatic melanoma. Our understanding of this lesio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7069c58b977bb39b635bcd14bcbfa507
https://doi.org/10.1097/pas.0000000000001952
https://doi.org/10.1097/pas.0000000000001952
Autor:
Olivia Beaudoux, Jean-Baptiste Oudart, Laurence Riffaud, Laetitia Visseaux, Aude Marchal, Anne-Sophie Lebre, Florent Grange
Publikováno v:
Molecular Diagnosis & Therapy. 26:189-202
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7a6dabfa309142ab58e93625f7a61f9
https://doi.org/10.1007/s40291-021-00572-0
https://doi.org/10.1007/s40291-021-00572-0
Publikováno v:
Annales de Pathologie. 42:189-191
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2204782af59f62f06f400298ac0686df
https://doi.org/10.1016/j.annpat.2022.01.002
https://doi.org/10.1016/j.annpat.2022.01.002
Autor:
Martine Doco Fenzy, Anne-Sophie Lebre, Olivia Beaudoux, Céline Poirsier, Eric Canivet, Marta Spodenkiewicz, Charlotte Colosio
Publikováno v:
American Journal of Medical Genetics Part A. 185:937-944
Townes-Brocks syndrome (TBS) is a rare autosomal dominant syndrome, resulting from heterozygous variant in SALL1 gene and initially characterized by the triad of anorectal, thumb, and ear malformations. Essentially described in children, adult case r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a173a9d47f228ca61a48c0c517dd84da
https://doi.org/10.1002/ajmg.a.62050
https://doi.org/10.1002/ajmg.a.62050
Autor:
Anne Durlach, Marine Ehret, Olivia Beaudoux, L. Visseaux, Jean-Bapstiste Oudart, Florent Grange, Emilie Criquet, Joséphine Franceschi
Publikováno v:
Acta Dermato-Venereologica Supplementum
Acta Dermato-Venereologica Supplementum, Society for Publication of Acta Dermato-Venereologica, 2020, ⟨10.2340/00015555-3715⟩
Acta Dermato-Venereologica, Vol 101, Iss 4, p adv00426 (2021)
Acta Dermato-Venereologica Supplementum, Society for Publication of Acta Dermato-Venereologica, 2020, ⟨10.2340/00015555-3715⟩
Acta Dermato-Venereologica, Vol 101, Iss 4, p adv00426 (2021)
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f44ec2fa53508bd82ba5625afcc7048
https://hal.archives-ouvertes.fr/hal-03049031
https://hal.archives-ouvertes.fr/hal-03049031
Autor:
Gautier Julien, Firouzé Bani-Sadr, Olivia Beaudoux, Ambre Hittinger-Roux, Aurélie Brunet, Amélie Servettaz, Yohan Nguyen, Amandine Cros
Publikováno v:
Annals of Medicine
Annals of Medicine, Taylor & Francis, 2020, 52 (6), pp.265-274. ⟨10.1080/07853890.2020.1778778⟩
Ann Med
Annals of Medicine, Taylor & Francis, 2020, 52 (6), pp.265-274. ⟨10.1080/07853890.2020.1778778⟩
Ann Med
We reported two cases of Staphylococcus aureus Infective Endocarditis associated with vasculitides and glomerulonephritis respectively, before conducting an online search of previously published similar cases reports. Twenty five references were sele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::897d46dab1f84b50a56c05ca303d8047
https://hal.archives-ouvertes.fr/hal-03267071
https://hal.archives-ouvertes.fr/hal-03267071
Publikováno v:
Annales de Pathologie. 40:461-462
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0e1b0b132d09c00101a8d29a7976de1
https://doi.org/10.1016/j.annpat.2020.05.006
https://doi.org/10.1016/j.annpat.2020.05.006
Publikováno v:
Annales de Pathologie. 40:337-338
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9199169614600410f6bcb322df3f7eb1
https://doi.org/10.1016/j.annpat.2019.12.007
https://doi.org/10.1016/j.annpat.2019.12.007
Autor:
Gwenaëlle Collod-Béroud, Narasimhan Nagan, Christine Toulas, Marcia Eisenberg, Crystal M. Buell, Dominique Stoppa-Lyonnet, Stanley Letovsky, Hagay Sobol, Camille R. Nery, Céline Garrec, David Salgado, Corey D. Braastad, Danièle Muller, Charles M. Strom, Ghadi Rai, Olga M. Sinilnikova, Paul Vilquin, Angela Love, Christophe Béroud, Sandrine M. Caputo, Olivia Beaudoux, Yves-Jean Bignon, Florence Coulet, Myriam Bronner, Izabela Karbassi, Sarab Lizard, Dominique Vaur, Nicolas Derive, Brigitte Bressac-de Paillerets, Françoise Révillion, Edwin Trautman, Christina DiVincenzo, Katelyn S. Weymouth, Nicolas Sevenet, Christopher Elzinga, Alecia Willis, Claude Houdayer
Publikováno v:
Human Mutation. 37:1318-1328
As next-generation sequencing increases access to human genetic variation, the challenge of determining clinical significance of variants becomes ever more acute. Germline variants in the BRCA1 and BRCA2 genes can confer substantial lifetime risk of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::404371296808ebd168499800b81852e1
https://doi.org/10.1002/humu.23113
https://doi.org/10.1002/humu.23113