Literature DB >> 9799294

International nomenclature and classification of the osteochondrodysplasias (1997).

R S Lachman1.   

Abstract

Entities:  

Mesh：

Year:  1998        PMID： 9799294     DOI： 10.1007/s002470050458

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN： 0301-0449


× No keyword cloud information.
  11 in total

1.  Loss of MMP-2 disrupts skeletal and craniofacial development and results in decreased bone mineralization, joint erosion and defects in osteoblast and osteoclast growth.

Authors:  Rebecca A Mosig; Oonagh Dowling; Analisa DiFeo; Maria Celeste M Ramirez; Ian C Parker; Etsuko Abe; Janane Diouri; Aida Al Aqeel; James D Wylie; Samantha A Oblander; Joseph Madri; Paolo Bianco; Suneel S Apte; Mone Zaidi; Stephen B Doty; Robert J Majeska; Mitchell B Schaffler; John A Martignetti
Journal:  Hum Mol Genet       Date:  2007-03-30       Impact factor: 6.150

2.  Coexistence of osteopoikilosis with reactive arthritis: a case report.

Authors:  Erkan Mesci
Journal:  Rheumatol Int       Date:  2005-09-27       Impact factor: 2.631

3.  The diagnosis and management of patients with idiopathic osteolysis.

Authors:  Ali Al Kaissi; Sabine Scholl-Buergi; Rainer Biedermann; Kathrin Maurer; Jochen G Hofstaetter; Klaus Klaushofer; Franz Grill
Journal:  Pediatr Rheumatol Online J       Date:  2011-10-13       Impact factor: 3.054

4.  Clinical and radiological diagnosis of progressive pseudorheumatoid dysplasia in two sisters with severe polyarthropathy.

Authors:  Arzu Kaya; Salih Ozgocmen; Adem Kiris; Ismail Ciftci
Journal:  Clin Rheumatol       Date:  2005-05-05       Impact factor: 2.980

5.  Inherited multicentric osteolysis with carpal-tarsal localisation mimicking juvenile idiopathic arthritis.

Authors:  Marianne R Faber; René Verlaak; Theo J W Fiselier; Ben C J Hamel; Marcel J A M Franssen; G Peter J M Gerrits
Journal:  Eur J Pediatr       Date:  2004-10       Impact factor: 3.183

6.  Spondyloepiphyseal dysplasia tarda: four cases from two families.

Authors:  Serpil Bal; Hikmet Kocyigit; Yasemin Turan; Alev Gurgan; Korhan Baris Bayram; Anil Güvenc; Zehra Kocaaga; Berna Dirim
Journal:  Rheumatol Int       Date:  2008-10-19       Impact factor: 2.631

7.  Clinical, radiographic, and genetic diagnosis of progressive pseudorheumatoid dysplasia in a patient with severe polyarthropathy.

Authors:  Stephan Ehl; Markus Uhl; Reinhard Berner; Luisa Bonafé; Andrea Superti-Furga; Antje Kirchhoff
Journal:  Rheumatol Int       Date:  2003-06-18       Impact factor: 2.631

8.  A compound heterozygote of novel and recurrent DTDST mutations results in a novel intermediate phenotype of Desbuquois dysplasia, diastrophic dysplasia, and recessive form of multiple epiphyseal dysplasia.

Authors:  Atsushi Miyake; Gen Nishimura; Toru Futami; Hirofumi Ohashi; Kazuhiro Chiba; Yoshiaki Toyama; Tatsuya Furuichi; Shiro Ikegawa
Journal:  J Hum Genet       Date:  2008-06-14       Impact factor: 3.172

Review 9.  Nosology and classification of genetic skeletal disorders: 2010 revision.

Authors:  Matthew L Warman; Valerie Cormier-Daire; Christine Hall; Deborah Krakow; Ralph Lachman; Martine LeMerrer; Geert Mortier; Stefan Mundlos; Gen Nishimura; David L Rimoin; Stephen Robertson; Ravi Savarirayan; David Sillence; Juergen Spranger; Sheila Unger; Bernhard Zabel; Andrea Superti-Furga
Journal:  Am J Med Genet A       Date:  2011-03-15       Impact factor: 2.802

10.  Progressive Pseudorheumatoid Dysplasia Misdiagnosed as Seronegative Juvenile Idiopathic Arthritis.

Authors:  Ozgur Taspinar; Fatih Kelesoglu; Yasar Keskin; Murat Uludag
Journal:  Ethiop J Health Sci       Date:  2016-07
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.