Literature DB >> 20516327

Chondrosarcoma in metachondromatosis: a case report.

Andreas F Mavrogenis1, Evangelia Skarpidi, Olympia Papakonstantinou, Panayiotis J Papagelopoulos.   

Abstract

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Year:  2010        PMID： 20516327     DOI： 10.2106/JBJS.I.00693

Source DB:  PubMed          Journal:  J Bone Joint Surg Am        ISSN： 0021-9355            Impact factor:   5.284


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  5 in total

1.  EXT2-positive multiple hereditary osteochondromas with some features suggestive of metachondromatosis.

Authors:  Neil C Vining; Stephen Done; Ian A Glass; Shawn E Parnell; Darci L Sternen; Kathleen A Leppig; Vincent S Mosca; Michael J Goldberg
Journal:  Skeletal Radiol       Date:  2011-09-04       Impact factor: 2.199

2.  Metachondromatosis: more than just multiple osteochondromas.

Authors:  Thomas J Fisher; Nicole Williams; Lloyd Morris; Peter J Cundy
Journal:  J Child Orthop       Date:  2013-09-21       Impact factor: 1.548

3.  Loss-of-function mutations in PTPN11 cause metachondromatosis, but not Ollier disease or Maffucci syndrome.

Authors:  Margot E Bowen; Eric D Boyden; Ingrid A Holm; Belinda Campos-Xavier; Luisa Bonafé; Andrea Superti-Furga; Shiro Ikegawa; Valerie Cormier-Daire; Judith V Bovée; Twinkal C Pansuriya; Sérgio B de Sousa; Ravi Savarirayan; Elena Andreucci; Miikka Vikkula; Livia Garavelli; Caroline Pottinger; Toshihiko Ogino; Akinori Sakai; Bianca M Regazzoni; Wim Wuyts; Luca Sangiorgi; Elena Pedrini; Mei Zhu; Harry P Kozakewich; James R Kasser; Jon G Seidman; Kyle C Kurek; Matthew L Warman
Journal:  PLoS Genet       Date:  2011-04-14       Impact factor: 5.917

Review 4.  An unusual example of hereditary multiple exostoses: a case report and review of the literature.

Authors:  Rebecca Chilvers; James A Gallagher; Nathan Jeffery; Alistair P Bond
Journal:  BMC Musculoskelet Disord       Date:  2021-01-21       Impact factor: 2.362

5.  From an orphan disease to a generalized molecular mechanism: PTPN11 loss-of-function mutations in the pathogenesis of metachondromatosis.

Authors:  Wentian Yang; Benjamin G Neel
Journal:  Rare Dis       Date:  2013-10-02
  5 in total

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