A
Alain Verloes
Researcher at University of Paris
Publications - 464
Citations - 21574
Alain Verloes is an academic researcher from University of Paris. The author has contributed to research in topics: Microcephaly & Noonan syndrome. The author has an hindex of 73, co-authored 450 publications receiving 19231 citations. Previous affiliations of Alain Verloes include Institut Universitaire de France & Max Planck Society.
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Journal ArticleDOI
Paraplegia and arthrogryposis multiplex of the lower extremities after intrauterine exposure to ergotamine.
TL;DR: The Greek letter upsilon should be translated into English only as y or u, and the condition should be named correctly either 'osteoglyphic' or 'ostEoglyphidic' dysplasia.
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Möbius sequence, Robin complex, and hypotonia: severe expression of brainstem disruption spectrum versus Carey-Fineman-Ziter syndrome.
Alain Verloes,Pierre Bitoun,Anne Heuskin,Dina Amrom,Hilde Van De Broeck,Sarah M. Nikkel,Albert E. Chudley,Asuri N. Prasad,Cristina Rusu,Mircea Covic,Annick Toutain,Claude Moraine,Melissa A. Parisi,Michael A. Patton,Jean-Jacques Martin,Marie Noelle Van Thienen +15 more
TL;DR: Based on a review of the literature on MS and CFZS, it is suggested designating as “Robin–Möbius phenotype” a distinct clinical variant of MS with extensive brainstem involvement, Robin complex, hypotonia without specific muscle disorder, clubfeet and variable acral anomalies.
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Temple–Baraitser syndrome: A rare and possibly unrecognized condition†
Adeline Jacquinet,Marion Gérard,Michael T. Gabbett,Michael T. Gabbett,Léon Rausin,Jean Paul Misson,Björn Menten,Geert Mortier,Lionel Van Maldergem,Alain Verloes,François-Guillaume Debray +10 more
TL;DR: It is confirmed that Temple–Baraitser syndrome represents a distinct syndrome, probably unrecognized, possibly caused by a de novo mutation in a not yet identified gene.
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Partial trisomy of chromosome 22 resulting from a supernumerary marker chromosome 22 in a child with features of cat eye syndrome.
Valérie Bélien,Marion Gérard-Blanluet,Stéphane Serero,Nathalie Le Dû,Clarisse Baumann,Marie-Line Jacquemont,Céline Dupont,Kada Krabchi,Séverine Drunat,Annie Elbez,Jean-Claude Janaud,Brigitte Benzacken,Alain Verloes,Anne-Claude Tabet,Azzedine Aboura +14 more
TL;DR: Cytogenetic analysis showed the presence of a supernumerary marker chromosome, identified by fluorescence in situ hybridization as part of chromosome 22, and conferring a proximal partial trisomy 22q22, not encompassing the DiGeorge critical region (RP11–154H4 + , TBX1‐).
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Dermatological manifestations in cardiofaciocutaneous syndrome: a prospective multicentric study of 45 mutation‐positive patients
Didier Bessis,Didier Bessis,F. Morice‐picard,Emmanuelle Bourrat,C. Abadie,Safa Aouinti,Cédric Baumann,M. Best,Anne-Claire Bursztejn,Yline Capri,Christine Chiaverini,Christine Coubes,F. Giuliano,Smail Hadj-Rabia,M.‐L. Jacquemont,Didier Lacombe,Stanislas Lyonnet,Stéphanie Mallet,Juliette Mazereeuw-Hautier,J. Miquel,J. Miquel,Nicolas Molinari,Béatrice Parfait,C. Pernet,Nicole Philip,Lucile Pinson,N. Pouvreau,Yoann Vial,Pierre Sarda,Sabine Sigaudy,Alain Verloes,Hélène Cavé,David Geneviève,David Geneviève +33 more
TL;DR: Data on dermatological manifestations of cardiofaciocutaneous syndrome (CFCS) remain heterogeneous and almost without expert dermatological classification.