Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Sara Cabet"'
Autor:
Julie Bernardor, Sacha Flammier, Sara Cabet, Sandrine Lemoine, Roland Chapurlat, Arnaud Molin, Aurélia Bertholet-Thomas, Justine Bacchetta
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Introduction: The use of teriparatide has been reported in children with hypoparathyroidism as an investigational physiologic replacement therapy.Methods: We aimed to retrospectively report our pediatric experience of bi-daily sub-cutaneous teriparat
Externí odkaz:
https://doaj.org/article/055447adfea24fcb82e3735c9de260a7
Publikováno v:
Pediatric Radiology. 53:695-705
The incidence of urolithiasis in children has increased over the two last decades. Urolithiasis formation results from urine oversaturation following insufficient water intake, urinary obstruction (notably in cases of congenital uropathies), excess p
Autor:
Didier Lacombe, Julien Van-Gils, Marine Lebrun, Aurélien Trimouille, Vincent Michaud, Sara Cabet, Jean-François Chateil, Jean-Michel Pedespan, Claire Bar, Gaetan Lesca
Publikováno v:
Brain and Development. 44:567-570
Autor:
Sara Cabet, Alexandru Szathmari, Carmine Mottolese, Patricia Franco, Laurent Guibaud, Massimiliano Rossi, Federico Di Rocco
Publikováno v:
Child's Nervous System. 38:1137-1145
To characterize natural history and early changes of craniovertebral junction stenosis in achondroplasia correlating with clinical and radiological outcome.Retrospective measures on craniovertebral junction were performed blindly, on sagittal T2-weig
Autor:
Mona Massoud, Maude Chollet, Sara Cabet, Marine Butin, Yahia Mekki, Geneviève Lina-Granade, Axel Fichez, Jocelyne Attia, Dorothée Ville, Laurent Guibaud
Publikováno v:
Fetal Diagnosis and Therapy.
Introduction Our objective was to evaluate the outcome of fetuses with first and second-trimester fetal cytomegalovirus infection (CMVi) according to prenatal imaging patterns, especially fetuses presenting with mild imaging features (MF), being curr
Autor:
Rabih Chaoui, Catherine Garel, J. Hartung, M. Delius, Gaetan Lesca, K. Karl, Laurent Guibaud, Sara Cabet
Publikováno v:
Ultrasound in Obstetrics & Gynecology. 57:493-497
To illustrate the prenatal imaging cerebral features associated with tubulinopathies, we report the data of five affected individuals from unrelated families with de novo heterozygous variants in tubulin genes (TUBA1A, TUBB2B, or TUBB3). We identifie
Autor:
Cécile Picard, Nicolas Macagno, Nadège Corradini, Perrine Marec-Bérard, Sara Cabet, Laurent Guibaud, Loic Viremouneix, Sébastien Raux, Franck Chotel, Nicolas Weinbreck, Alexandra Meurgey, Marie Karanian, Daniel Pissaloux, Frank Tirode, Frédérique Dijoud
Publikováno v:
Virchows Archiv
Virchows Archiv, 2022, 481 (4), pp.665-669. ⟨10.1007/s00428-022-03335-2⟩
Virchows Archiv, 2022, 481 (4), pp.665-669. ⟨10.1007/s00428-022-03335-2⟩
Ewing sarcoma (ES) is a highly malignant round cell sarcoma, characterized by gene fusion involving FET (FUS, EWSR1, TAF15) and ETS family genes, respectively. The involvement of the EWSR1 gene has been reported in approximately 90% of cases of ES, w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::567c534e8925068f9f77699b8e1d70bb
https://hal-amu.archives-ouvertes.fr/hal-04039767/file/main.pdf
https://hal-amu.archives-ouvertes.fr/hal-04039767/file/main.pdf
Publikováno v:
médecine/sciences
médecine/sciences, EDP Sciences, 2020, 36 (10), pp.866-871. ⟨10.1051/medsci/2020157⟩
médecine/sciences, EDP Sciences, 2020, 36 (10), pp.866-871. ⟨10.1051/medsci/2020157⟩
Les variants pathogènes du gène NDE1 sont responsables de microlissencéphalies chez l’homme et constituent le déficit de la neurogenèse le plus sévère décrit à ce jour. Le gène NDE1 code une phosphoprotéine essentielle à la neurogenèse
Autor:
Sara Cabet, Alexandre Vasiljevic, Audrey Putoux, Audrey Labalme, Damien Sanlaville, Nicolas Chatron, Gaetan Lesca, Laurent Guibaud
Publikováno v:
Prenatal diagnosisREFERENCES. 42(4)
Autor:
Alexandre Reymond, Annie Buenerd, E. Thia, Angeline H.M. Lai, Erica Schindewolf, Sara Cabet, Gaetan Lesca, Lucie Gueneau, Audrey Putoux, Laurent Guibaud, Damien Sanlaville
Publikováno v:
Prenatal Diagnosis. 40:276-281