Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Karen Lambot"'
Autor:
Karen Lambot, Christophe Glorion, Jean-Charles Aurégan, Caroline Dana, Stéphanie Pannier, Francis Brunelle
Publikováno v:
The Journal of Hand Surgery. 38:1779-1783
An arteriovenous malformation (AVM) is a congenital lesion with high vascular flow resulting from direct connections between arteries and veins. Its treatment is often complex, and most authors recommend a multidisciplinary approach combining surgica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d60018e51c5b01e5ebdde1e5026fdfe6
https://doi.org/10.1016/j.jhsa.2013.06.015
https://doi.org/10.1016/j.jhsa.2013.06.015
Autor:
Laurence Jonard, Vincent Couloigner, Isabelle Melki, Karen Lambot, Bénédicte Neven, Pierre Quartier, Brigitte Bader-Meunier
Publikováno v:
Pediatrics. 131:e1308-e1313
Germline mutations in the SLC29A3 gene result in a range of recessive, clinically related syndromes: H syndrome, pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome, Faisalabad histiocytosis, and sinus histiocytosis with massiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f41173132ffec33ca68484da1ce5ca3
https://doi.org/10.1542/peds.2012-2255
https://doi.org/10.1542/peds.2012-2255
Autor:
Christine Bodemer, Sylvain Breton, Olivia Boccara, Francis Brunelle, Karen Lambot, Yves de Prost, Nathalie Boddaert, Marie-Paule Vazquez, Véronique Soupre, Arnaud Picard
Publikováno v:
Sang thrombose vaisseaux. 25:10-18
L’imagerie des malformations vasculaires a ete transformee par le developpent de l’imagerie non invasive. Le scanner et surtout l’IRM non irradiante permettent d’obtenir l’ensemble des renseignements necessaires s a l’etablissement d’un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8378333f295a3687671863947c07cce1
https://doi.org/10.1684/stv.2013.0749
https://doi.org/10.1684/stv.2013.0749
Autor:
Karen Lambot, A.-E. Millischer-Bellaïche, Laureline Berteloot, A. Bobbio, Francis Brunelle, Sylvain Breton
Publikováno v:
Revue des Maladies Respiratoires. 29:820-835
Congenital lung malformations include a complex range of developmental abnormalities. Currently, most are diagnosed prenatally or during early childhood. They may, however, be discovered later, incidentally or in connection with non-specific symptoms
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e88b4f8b998c9617de2eb5cdbfe6f1ea
https://doi.org/10.1016/j.rmr.2011.10.976
https://doi.org/10.1016/j.rmr.2011.10.976
Autor:
Brigitte Bader-Meunier, Isabelle Halphen, Karen Lambot-Juhan, Nathalie Costedoat-Chalumeau, Martin Chalumeau, Dominique Monnet, Romain K. Gherardi, Christine Barnerias, Christine Bodemer, Jean-Antoine Ribeil
Publikováno v:
Pediatrics. 129:e821-e824
Juvenile dermatomyositis is a rare systemic vasculopathy that may sometimes present with acute complications. We report here the case of a 7-year-old boy with severe dermatomyositis associated with thrombocytopenia and blurry vision. The presence of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69e1703b60e498a39af0e3b663d09758
https://doi.org/10.1542/peds.2011-0338
https://doi.org/10.1542/peds.2011-0338
Autor:
Caroline Elie, Sophie Emond-Gonsard, Christophe Delacourt, David Grevent, Karen Lambot, Tania Mamou-Mani, Rola Abou Taam, Laureline Berteloot, Jacques de Blic, Francis Brunelle, Muriel Le Bourgeois
Publikováno v:
Pediatric radiology. 44(7)
Pulmonary alveolar proteinosis (PAP) is characterized by an abnormal accumulation of periodic acid-schiff-positive lipoproteinaceous material in the alveoli. Early diagnosis allows setting up of therapeutic lung lavages, which reduces the need for ox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10ad4813ac84f138c37d5bc419c2170e
https://pubmed.ncbi.nlm.nih.gov/24599270
https://pubmed.ncbi.nlm.nih.gov/24599270
Autor:
Laurence Jonard, Karen Lambot, Pierre Quartier, Bénédicte Neven, Brigitte Bader-Meunier, Vincent Couloigner, Isabelle Melki
Publikováno v:
Pediatric Rheumatology
Pediatric Rheumatology, BioMed Central, 2013, 11 (Suppl 1), pp.A259
Pediatric Rheumatology, 2013, 11 (Suppl 1), pp.A259
Pediatric Rheumatology Online Journal
Pediatric Rheumatology, BioMed Central, 2013, 11 (Suppl 1), pp.A259
Pediatric Rheumatology, 2013, 11 (Suppl 1), pp.A259
Pediatric Rheumatology Online Journal
Germline mutations in SLC29A3 result in a range of clinically related, recessive syndromes: H syndrome, pigmented hypertrichosis with insulin-dependent diabetes mellitus (PHID) syndrome, Faisalabad histiocytosis (FHC), and sinus histiocytosis with ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1542b142c9ce327c889c2e141a97ddd2
https://www.hal.inserm.fr/inserm-00881688/document
https://www.hal.inserm.fr/inserm-00881688/document
Autor:
Graziella Guariso, Mamoun Elawad, Jaroslaw Kierkus, Frédéric Rieux-Laucat, Bernadette Bègue, Neil Shah, Olivier Goulet, Frank M. Ruemmele, Rosa Lima, Bénédicte Pigneur, Cécile Talbotec, Danielle Canioni, Stephan Buderus, Karen Lambot, Benedicte Neven, Johanna C. Escher, Nadine Cerf-Bensussan
Publikováno v:
Inflammatory Bowel Diseases, 19(13), 2820-2828. Oxford University Press
Early-onset inflammatory bowel disease starting within the first months of life could be due to a particular genetic defect. We set up the GENetically determined ImmUne-mediated enteropathieS (GENIUS) network and collected infants with a proven defec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d63971bb974b940f9c4c36fa80d4a74
http://hdl.handle.net/11577/2688683
http://hdl.handle.net/11577/2688683
Autor:
Karen Rosendahl, Claudia Bracaglia, Brigitte Bader-Meunier, Maria Beatrice Damasio, Laura Tanturri de Horatio, Caroline Elie, Domenico Barbuti, Francis Brunelle, Peter Boavida, Clara Malattia, Pierre Quartier, Lil Sofie Ording Müller, Marie Desgranges, Karen Lambot
Publikováno v:
Pediatric radiology. 43(7)
There is sparse knowledge about grading tenosynovitis using MRI. The purpose of this study was to assess the reliability of a tenosynovitis MRI scoring system in juvenile idiopathic arthritis. Children with juvenile idiopathic arthritis and wrist inv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45eb9cdc3113440a5926fa3c90d8d97e
https://pubmed.ncbi.nlm.nih.gov/23381299
https://pubmed.ncbi.nlm.nih.gov/23381299
Autor:
Karen Rosendahl, Paolo Tomà, Angela Pistorio, Domenico Barbuti, Alberto Martini, Gianmichele Magnano, Chiara Mattiuz, Lil Sophie Mueller Ording, Claudia Bracaglia, Maria Beatrice Damasio, Peter Boavida, Karen Lambot Juhan, Clara Malattia, Laura Tanturri de Horatio
Publikováno v:
Pediatric radiology. 42(9)
MRI is a sensitive tool for the evaluation of synovitis in juvenile idiopathic arthritis (JIA).The purpose of this study was to introduce a novel MRI-based score for synovitis in children and to examine its inter- and intraobserver variability in a m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::347e9f140bd578a769b30d6bf82d8274
https://pubmed.ncbi.nlm.nih.gov/22832863
https://pubmed.ncbi.nlm.nih.gov/22832863