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Chantal Stheneur
Chantal Stheneur
Pédiatre, Fondation Santé des étudiants de France
Adresse e-mail validée de fsef.net
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Comparison of Clinical Presentations and Outcomes Between Patients With TGFBR2 and FBN1 Mutations in Marfan Syndrome and Related Disorders
D Attias, C Stheneur, C Roy, G Collod-Béroud, D Detaint, L Faivre, ...
Circulation 120 (25), 2541-2549, 2009
2772009
Clinical and molecular study of 320 children with Marfan syndrome and related type I fibrillinopathies in a series of 1009 probands with pathogenic FBN1 mutations
L Faivre, A Masurel-Paulet, G Collod-Beroud, BL Callewaert, AH Child, ...
Pediatrics 123 (1), 391-398, 2009
2072009
Cardiovascular manifestations in men and women carrying a FBN1 mutation
D Détaint, L Faivre, G Collod-Beroud, AH Child, BL Loeys, C Binquet, ...
European heart journal 31 (18), 2223-2229, 2010
2032010
Nomograms for aortic root diameters in children using two-dimensional echocardiography
M Gautier, D Detaint, C Fermanian, P Aegerter, G Delorme, F Arnoult, ...
The American journal of cardiology 105 (6), 888-894, 2010
2032010
The new Ghent criteria for Marfan syndrome: what do they change?
L Faivre, G Collod‐Beroud, L Adès, E Arbustini, A Child, BL Callewaert, ...
Clinical genetics 81 (5), 433-442, 2012
1572012
Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probands
L Faivre, G Collod-Beroud, A Child, B Callewaert, BL Loeys, C Binquet, ...
Journal of medical genetics 45 (6), 384-390, 2008
1562008
L’achondroplasie: du génotype au phénotype
P Richette, T Bardin, C Stheneur
Revue du rhumatisme 75 (5), 405-411, 2008
1332008
Identification of the minimal combination of clinical features in probands for efficient mutation detection in the FBN1 gene
C Stheneur, G Collod-Béroud, L Faivre, JF Buyck, L Gouya, JM Le Parc, ...
European Journal of Human Genetics 17 (9), 1121-1128, 2009
1152009
Identification of 23 TGFBR2 and 6 TGFBR1 gene mutations and genotype‐phenotype investigations in 457 patients with Marfan syndrome type I and II, Loeys …
C Stheneur, G Collod‐Béroud, L Faivre, L Gouya, G Sultan, JM Le Parc, ...
Human mutation 29 (11), E284-E295, 2008
1122008
Clinical and mutation-type analysis from an international series of 198 probands with a pathogenic FBN1 exons 24–32 mutation
L Faivre, G Collod-Beroud, B Callewaert, A Child, C Binquet, E Gautier, ...
European Journal of Human Genetics 17 (4), 491-501, 2009
872009
Association of modifiers and other genetic factors explain Marfan syndrome clinical variability
M Aubart, S Gazal, P Arnaud, L Benarroch, MS Gross, J Buratti, A Boland, ...
European Journal of Human Genetics 26 (12), 1759-1772, 2018
802018
Prognosis factors in probands with an FBN1 mutation diagnosed before the age of 1 year
C Stheneur, L Faivre, G Collod-Béroud, E Gautier, C Binquet, ...
Pediatric Research 69 (3), 265-270, 2011
742011
The clinical presentation of Marfan syndrome is modulated by expression of wild-type FBN1 allele
M Aubart, MS Gross, N Hanna, MT Zabot, M Sznajder, D Detaint, L Gouya, ...
Human Molecular Genetics 24 (10), 2764-2770, 2015
692015
Medication in AN: a multidisciplinary overview of meta-analyses and systematic reviews
C Blanchet, S Guillaume, F Bat-Pitault, ME Carles, J Clarke, V Dodin, ...
Journal of clinical medicine 8 (2), 278, 2019
672019
Study of phenotype evolution during childhood in Marfan syndrome to improve clinical recognition
C Stheneur, F Tubach, M Jouneaux, C Roy, G Benoist, B Chevallier, ...
Genetics in medicine 16 (3), 246-250, 2014
622014
Renal complications in anorexia nervosa
C Stheneur, S Bergeron, AL Lapeyraque
Eating and Weight Disorders-Studies on Anorexia, Bulimia and Obesity 19, 455-460, 2014
582014
Pathogenic FBN1 mutations in 146 adults not meeting clinical diagnostic criteria for Marfan syndrome: Further delineation of type 1 fibrillinopathies and focus on …
L Faivre, G Collod‐Beroud, B Callewaert, A Child, BL Loeys, C Binquet, ...
American Journal of Medical Genetics Part A 149 (5), 854-860, 2009
552009
Basic fibroblast growth factor as a selective inducer of matrix Gla protein gene expression in proliferative chondrocytes
C Stheneur, MF Dumontier, C Guedes, MC Fulchignoni-Lataud, K Tahiri, ...
Biochemical Journal 369 (1), 63-70, 2003
452003
Iron metabolism in patients with anorexia nervosa: elevated serum hepcidin concentrations in the absence of inflammation
S Papillard-Marechal, M Sznajder, M Hurtado-Nedelec, Y Alibay, ...
The American journal of clinical nutrition 95 (3), 548-554, 2012
432012
The bulle: support and prevention of psychological decompensation of health care workers during the trauma of the COVID-19 epidemic
H Lefèvre, C Stheneur, C Cardin, L Fourcade, C Fourmaux, E Tordjman, ...
Journal of pain and symptom management 61 (2), 416-422, 2021
382021
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