Transcatheter closure of persistent ductus arteriosus in 2 to 6 kg infants: Preliminary results from an international, retrospective study

Autor: P. Padovani, M. Gewillig, G. Butera, H. Lucron, B. Lefort, H. Samion, S. El Saiedi, C. Ovaert, D. Sirico, C. Grunenwald Gronier, M. Méot, N. Benbrik, D. Bonnet, S. Malekzadeh-Milani, A.E. Baruteau

Publikováno v: Archives of Cardiovascular Diseases Supplements. 14:248

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ff78339ddef1051b2254a92d5949a209
https://doi.org/10.1016/j.acvdsp.2022.07.059

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INTU -related oral-facial-digital syndrome type VI: a confirmatory report

Autor: A. Favre, Laurence Perrin, H. Lucron, Yline Capri, Yoann Vial, A. Defo, Anne-Claude Tabet, C. Thauvin-Robinet, Alain Verloes, Sandrine Passemard, N. Elenga, Laurence Faivre, Ange-Line Bruel, Jonathan I. Levy

Publikováno v: Clinical Genetics
Clinical Genetics, Wiley, In press, 〈http://onlinelibrary.wiley.com/doi/10.1111/cge.13238/abstract;jsessionid=7F706E6AD2CB61F30C261D5257E5583E.f04t02#publication-history〉. 〈10.1111/cge.13238〉
Clinical Genetics, Wiley, 2018, 93 (6), pp.1205-1209. ⟨10.1111/cge.13238⟩

Oral-facial-digital (OFD) syndromes are a subgroup of ciliopathies distinguished by the co-occurrence of hamartomas and/or multiple frenula of the oral region and digital anomalies. Several clinical forms of OFD syndromes are distinguished by their a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::009fac9d5a06443c7e50438b8847e15e
https://hal-univ-bourgogne.archives-ouvertes.fr/hal-01731277

nter-Regional Medical Cooperation in the Caribbean: Lessons from the Ongoing Cooperation between Martinique, St Lucia, and Dominica

Autor: H Mehdaoui, D Resiere, K Compton, M Spence, JR Daniel, R Valentino, D Martin, B Megarbane, F Roques, H Lucron

Publikováno v: WIMJ Open, Vol 1, Iss 1, Pp 26-28 (2014)

Recently, Martinique was accepted as an associate member by the Council of Ministers of the Organization of Eastern Caribbean States. This membership constitutes a major asset in bringing Martiniquais closer to the other Caribbean populations and sho

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abbe93d2760763d98abca4089a2fa91a
http://www.mona.uwi.edu/wimjopen/article/57

Syndrome de délétion 22q11 et maladie de Basedow. À propos de trois observations pédiatriques

Autor: H. Lucron, B. Lebon-Labich, Bruno Leheup, J. Gosselin, F. Marçon

Publikováno v: Archives de Pédiatrie. 11:1468-1471

Resume L’hypothyroidie est une complication endocrinienne « classique » chez les patients porteurs de la microdeletion 22q11.2. L’hyperthyroidie auto-immune est une manifestation plus rare. Nous rapportons trois nouvelles observations de maladi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::fe820aac1cea6f2d09e890543aacf838
https://doi.org/10.1016/j.arcped.2004.09.002