Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Catherine Sembely-Taveau"'
Autor:
Dominique Sirinelli, Maxence Serru, Baptiste Morel, Jean-Philippe Cottier, Leo Ribier, Catherine Sembely Taveau, Tobias Kober, Bénédicte Maréchal
Publikováno v:
Journal of Neuroradiology. 48:259-265
It can be challenging to depict brain volume abnormalities in the pediatric population on magnetic resonance imaging (MRI). The aim of the study was to evaluate the inter-radiologist reliability in brain MRI interpretation, including brain volume ass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cf268cdc22d66ebadc4e92ba38bb7db
https://doi.org/10.1016/j.neurad.2019.06.005
https://doi.org/10.1016/j.neurad.2019.06.005
Autor:
Maïa Proisy, Pierre-Hugue Vivier, Baptiste Morel, Bertrand Bruneau, Catherine Sembely-Taveau, Solène Vacheresse, Anne Devillers, Joseph Lecloirec, Caroline Bodet-Milin, Stéphanie Hamonic, Emma Bajeux, Anne Ganivet, Catherine Adamsbaum, Catherine Treguier, PEDIMA Study Research Group
Publikováno v:
SSRN Electronic Journal.
Background: A skeletal survey (SS) of high technical quality is the standard method of investigation for identifying bone injuries in suspected physical child abuse worldwide. We aimed to assess the contribution of Whole-Body Magnetic Resonance Imagi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79cca3e421513a587d91fcc8cf075050
https://doi.org/10.2139/ssrn.3736180
https://doi.org/10.2139/ssrn.3736180
Systematic ultrasound examinations in neonates admitted to NICU: evolution of portal vein thrombosis
Autor:
Mathieu Cabannes, Géraldine Favrais, Luciano Morales, Dominique Sirinelli, Philippe Bertrand, Catherine Sembely-Taveau, Antoine Bouissou, Amélie Favreau, Elie Saliba, Baptiste Morel
Publikováno v:
Journal of perinatology : official journal of the California Perinatal Association. 38(10)
The aim of the study was to better describe incidence, risk factors, and the natural evolution of neonatal portal vein thrombosis (PVT). One hundred and twenty-three premature newborns or with birth weight
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9bb4981dc5b3bb716058fb0e2207d2f
https://pubmed.ncbi.nlm.nih.gov/30082773
https://pubmed.ncbi.nlm.nih.gov/30082773
Autor:
Dominique Sirinelli, Catherine Sembely-Taveau, Baptiste Morel, Bénédicte Maréchal, Kathleen Gaillot, Jean-Philippe Cottier, Bruno-Bernard Rochetams
Background The aim of this preliminary study is to evaluate the results of T1-weighted dynamic contrast-enhanced (DCE) magnetic resonance imaging (MRI) in pediatric patients at 1.5T, with a low peripheral intravenous gadoteric acid injection rate of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d181fdaafa6e1245691b45a9eb2b67e
https://europepmc.org/articles/PMC5602334/
https://europepmc.org/articles/PMC5602334/
Autor:
Pauline Merenda, Joseph Fournier, Thierry Odent, Dominique Sirinelli, Baptiste Morel, Thibaut Lemoine, Catherine Sembely-Taveau
Publikováno v:
European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society. 27(5)
Although lumbar spondylolysis is encountered in general population with an incidence estimated to be 3–10%, limited information is available for children. The aim of the study is to determine the prevalence of spondylolysis according to associated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d79cb1f2518aec6c4dcd5148680010d
https://pubmed.ncbi.nlm.nih.gov/29030702
https://pubmed.ncbi.nlm.nih.gov/29030702
Autor:
Christelle Denis, Annie-Laure Suc, Antoine Listrat, Annick Toutain, Corinne Collet, Nathalie Soulé, Damien Haye, Georges Haddad, Catherine Sembely-Taveau
Publikováno v:
American Journal of Medical Genetics Part A. 164:2926-2930
Carpenter syndrome is caused by mutations of the RAB23 gene. To date, 12 distinct mutations have been identified among 34 patients from 26 unrelated families. We report on the prenatal findings in a fetus with Carpenter syndrome with a novel RAB23 mu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d41df3b68adad13ae2766a93502989ff
https://doi.org/10.1002/ajmg.a.36726
https://doi.org/10.1002/ajmg.a.36726
Autor:
Jacques Lansac, Gilles Body, Franck Perrotin, Corine Lyonnais, Georges Haddad, Catherine Sembely-Taveau
Publikováno v:
European Journal of Obstetrics & Gynecology and Reproductive Biology. 94:309-314
We present a case of a fetal dyshormonogenetic goiter diagnosed by ultrasound examination at 24 weeks of gestation, in a woman with no past history of thyroid disease or goitrogen treatment and with normal thyroid tests, including absence of auto-ant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e70cc351e95e7f97046993df08f678e5
https://doi.org/10.1016/s0301-2115(00)00346-8
https://doi.org/10.1016/s0301-2115(00)00346-8