Literature DB >> 16203897

Familial osteofibrous dysplasia. A case series.

Lori A Karol1, David S Brown, Carol A Wise, Michael Waldron.   

Abstract

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Year:  2005        PMID： 16203897     DOI： 10.2106/JBJS.D.02575

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


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  3 in total

1.  Bilateral Symmetric Sporadic Osteofibrous Dysplasia: an Unusual Case.

Authors:  Asit Ranjan Mridha; Anubhav Narwal; Adarsh Barwad; Venkatesan Sampat Kumar; Shivanand Gamanagatti; Prashant Ramteke
Journal:  Indian J Surg Oncol       Date:  2020-10-08

2.  Mutations Preventing Regulated Exon Skipping in MET Cause Osteofibrous Dysplasia.

Authors:  Mary J Gray; Peter Kannu; Swarkar Sharma; Christine Neyt; Dongping Zhang; Nandina Paria; Philip B Daniel; Heather Whetstone; Hans-Georg Sprenger; Philipp Hammerschmidt; Angela Weng; Lucie Dupuis; Rebekah Jobling; Roberto Mendoza-Londono; Michael Dray; Peiqiang Su; Megan J Wilson; Raj P Kapur; Edward F McCarthy; Benjamin A Alman; Andrew Howard; Gino R Somers; Christian R Marshall; Simon Manners; Adrienne M Flanagan; Karl E Rathjen; Lori A Karol; Haemish Crawford; David M Markie; Jonathan J Rios; Carol A Wise; Stephen P Robertson
Journal:  Am J Hum Genet       Date:  2015-12-03       Impact factor: 11.025

3.  Autosomal dominant mesomandibular fibro-osseous dysplasia: a self-resolving inherited fibro-osseous lesion of the jaws.

Authors:  Ioannis G Koutlas; Cynthia L Forsman; Stephanos Kyrkanides; William S Oetting; Anna Petryk
Journal:  Front Physiol       Date:  2012-12-06       Impact factor: 4.566
  3 in total

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