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Anthony Vandersteen
Researcher at Dalhousie University
Publications - 30
Citations - 1835
Anthony Vandersteen is an academic researcher from Dalhousie University. The author has contributed to research in topics: Ehlers–Danlos syndrome & Osteogenesis imperfecta. The author has an hindex of 12, co-authored 30 publications receiving 1173 citations. Previous affiliations of Anthony Vandersteen include Izaak Walton Killam Health Centre & Halifax.
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The 2017 international classification of the Ehlers-Danlos syndromes
Fransiska Malfait,Clair A. Francomano,Peter H. Byers,John W. Belmont,Britta Berglund,James H. Black,Lara Bloom,Jessica M Bowen,Angela F. Brady,Nigel Burrows,Marco Castori,Helen Cohen,Marina Colombi,Serwet Demirdas,Julie De Backer,Anne De Paepe,Sylvie Fournel-Gigleux,Michael Frank,Neeti Ghali,Cecilia Giunta,Rodney Grahame,Alan Hakim,Xavier Jeunemaitre,Diana Johnson,Birgit Juul-Kristensen,Ines Kapferer-Seebacher,Hanadi Kazkaz,Tomoki Kosho,Mark E. Lavallee,Howard P. Levy,Roberto Mendoza-Londono,Melanie Pepin,F. Michael Pope,Eyal Reinstein,Leema Robert,Marianne Rohrbach,Lynn Sanders,Glenda Sobey,Tim Van Damme,Anthony Vandersteen,Caroline van Mourik,Nicol C. Voermans,Nigel Wheeldon,Johannes Zschocke,Brad T. Tinkle +44 more
TL;DR: The International EDS Consortium proposes a revised EDS classification, which recognizes 13 subtypes, and revised the clinical criteria for hypermobile EDS in order to allow for a better distinction from other joint hypermobility disorders.
Journal ArticleDOI
The Ehlers–Danlos syndromes, rare types
Angela F. Brady,Serwet Demirdas,Sylvie Fournel-Gigleux,Neeti Ghali,Cecilia Giunta,Ines Kapferer-Seebacher,Tomoki Kosho,Roberto Mendoza-Londono,Michael F. Pope,Marianne Rohrbach,Tim Van Damme,Anthony Vandersteen,Caroline van Mourik,Nicol C. Voermans,Johannes Zschocke,Fransiska Malfait +15 more
TL;DR: The aim of this literature review is to summarize the current knowledge on the rare EDS subtypes and highlight areas for future research.
Journal ArticleDOI
Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S, which Encode Subcomponents C1r and C1s of Complement.
Ines Kapferer-Seebacher,Melanie Pepin,Roland Werner,Timothy J. Aitman,Ann Nordgren,Heribert Stoiber,Nicole M. Thielens,Christine Gaboriaud,Albert Amberger,Anna Schossig,Robert Gruber,Cecilia Giunta,M. Bamshad,Erik Björck,Erik Björck,Chu Chen,David Chitayat,Michael O. Dorschner,Marcus Schmitt-Egenolf,Christopher J. Hale,David S. Hanna,Hans Christian Hennies,I. Heiss-Kisielewsky,Anna Lindstrand,Anna Lindstrand,Pernilla Lundberg,Anna L. Mitchell,Deborah A. Nickerson,Eyal Reinstein,Marianne Rohrbach,Nikolaus Romani,Matthias Schmuth,Rachel Silver,Fulya Taylan,Anthony Vandersteen,Jana Vandrovcova,Ruwan A. Weerakkody,M. Yang,F. M. Pope,Peter H. Byers,Johannes Zschocke +40 more
TL;DR: The findings open a connection between the inflammatory classical complement pathway and connective tissue homeostasis and the physiological basis of the condition.
Journal ArticleDOI
Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation
Marianne Rohrbach,Anthony Vandersteen,Uluç Yiş,Gul Serdaroglu,Esra Ataman,Maya Chopra,Sixto Garcia,Kristi J. Jones,Ariana Kariminejad,Marius E. Kraenzlin,Carlo Marcelis,Matthias R. Baumgartner,Cecilia Giunta +12 more
TL;DR: It is proposed that EDS VIA is a highly variable clinical entity, presenting with a broad clinical spectrum, which may also be associated with cognitive delay and an increased risk for vascular events.
Journal ArticleDOI
Mandibulofacial Dysostosis with Microcephaly: Mutation and Database Update
Lijia Huang,Megan R. Vanstone,Taila Hartley,Matthew Osmond,Nick Barrowman,Judith Allanson,Laura A. Baker,Tabib Dabir,Katrina M. Dipple,William B. Dobyns,Jane Estrella,Hanna Faghfoury,Francine Pinheiro Favaro,Himanshu Goel,Pernille Axel Gregersen,Karen W. Gripp,Art Grix,Maria Leine Guion-Almeida,Margaret H. Harr,Cindy Hudson,Alasdair G. W. Hunter,John C. Johnson,Shelagh Joss,Amy S. Kimball,Usha Kini,Antonie D. Kline,Julie Lauzon,Dorte L Lildballe,Vanesa López-González,Johanna Martinezmoles,Cliff J Meldrum,Ghayda M. Mirzaa,Chantal F. Morel,Jenny Morton,Louise C. Pyle,Fabiola Quintero-Rivera,Julie Richer,Angela E. Scheuerle,Bitten Schönewolf-Greulich,Deborah J. Shears,Josh Silver,Amanda C. Smith,I. Karen Temple,Jiddeke M. van de Kamp,Fleur S van Dijk,Anthony Vandersteen,Susan M. White,Elaine H. Zackai,Ruobing Zou,Dennis E. Bulman,Kym M. Boycott,Matthew A. Lines +51 more
TL;DR: The molecular basis of MFDM is reviewed in the 69 individuals described to date, and mutations in 38 new individuals are reported, bringing the total number of reported individuals to 107 individuals from 94 kindreds.