Progressive pseudorheumatoid dysplasia with new-found gene mutation of Wntl inducible signaling pathway protein 3

[1]  Geetha Wickrematilake.  Progressive Pseudorheumatoid Dysplasia or JIA? , 2017, Case reports in rheumatology.

[2]  Lan Li,et al.  Novel WISP3 mutations causing progressive pseudorheumatoid dysplasia in two Chinese families , 2016, Human Genome Variation.

[3]  V. Balaji,et al.  WISP3 mutational analysis in Indian patients diagnosed with progressive pseudorheumatoid dysplasia and report of a novel mutation at p.Y198* , 2016, Bone & joint research.

[4]  K. Thangaraj,et al.  Whole Exome Screening Identifies Novel and Recurrent WISP3 Mutations Causing Progressive Pseudorheumatoid Dysplasia in Jammu and Kashmir-India , 2016, Scientific Reports.

[5]  E. Vallespín,et al.  Early severe scoliosis in a patient with atypical progressive pseudorheumatoid dysplasia (PPD): Identification of two WISP3 mutations, one previously unreported , 2016, American journal of medical genetics. Part A.

[6]  J. Haas,et al.  Biomechanics of walking in adolescents with progressive pseudorheumatoid arthropathy of childhood leads to physical activity recommendations as therapeutic focus. , 2016, Clinical biomechanics.

[7]  Youshui Gao,et al.  Total hip arthroplasty in a 17-year-old girl with progressive pseudorheumatoid dysplasia. , 2013, Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases.

[8]  G. Mortier,et al.  The diagnostic challenge of progressive pseudorheumatoid dysplasia (PPRD): A review of clinical features, radiographic features, and WISP3 mutations in 63 affected individuals , 2012, American journal of medical genetics. Part C, Seminars in medical genetics.

[9]  E. Liao,et al.  Cellular and molecular responses in progressive pseudorheumatoid dysplasia articular cartilage associated with compound heterozygous WISP3 gene mutation , 2007, Journal of molecular medicine.

[10]  M. Lotz,et al.  WISP3-dependent regulation of type II collagen and aggrecan production in chondrocytes. , 2004, Arthritis and rheumatism.

[11]  R. Pauli,et al.  Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia , 1999, Nature Genetics.

[12]  A. Gupta,et al.  Spondylo-epiphyseal dysplasia tarda with progressive arthropathy. , 1991, Indian pediatrics.

[13]  B. Ansell,et al.  Spondylo-epiphysial dysplasia tarda with progressive arthropathy. A "new" disorder of autosomal recessive inheritance. , 1982, The Journal of bone and joint surgery. British volume.