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Volumn 36, Issue 4, 2007, Pages 256-261

Familial Arthropathy in Saudi Arabian Children: Demographic, Clinical, and Biochemical Features

Author keywords

camptodactyly; familial arthritis; hyalinosis; nodulosis; osteolysis; Saudi Arabia

Indexed keywords

CORTICOSTEROID; DISEASE MODIFYING ANTIRHEUMATIC DRUG; ETANERCEPT; METHOTREXATE; NONSTEROID ANTIINFLAMMATORY AGENT; PAMIDRONIC ACID; PENICILLAMINE;

EID: 33846662945     PISSN: 00490172     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.semarthrit.2006.08.008     Document Type: Article
Times cited : (12)

References (17)
  • 3
    • 0006387161 scopus 로고    scopus 로고
    • Juvenile arthritis-who gets it, where and when? A review of current data on incidence and prevalence
    • Gare A. Juvenile arthritis-who gets it, where and when? A review of current data on incidence and prevalence. Clin Exp Rheumatol 17 (1999) 367-374
    • (1999) Clin Exp Rheumatol , vol.17 , pp. 367-374
    • Gare, A.1
  • 4
    • 4344675699 scopus 로고    scopus 로고
    • A genome-wide scan for juvenile rheumatoid arthritis in affected sibpair families provides evidence of linkage
    • Thompson S., Moroldo M., Guyer L., Ryan M., Tombragel E., Shear E., et al. A genome-wide scan for juvenile rheumatoid arthritis in affected sibpair families provides evidence of linkage. Arthritis Rheum 50 (2004) 2920-2930
    • (2004) Arthritis Rheum , vol.50 , pp. 2920-2930
    • Thompson, S.1    Moroldo, M.2    Guyer, L.3    Ryan, M.4    Tombragel, E.5    Shear, E.6
  • 5
    • 0031720762 scopus 로고    scopus 로고
    • Revision of the proposed classification criteria for juvenile idiopathic arthritis: Durban 1997
    • Petty R., Southwood T., Baum J., Bhettay E., Glass D., Manners P., et al. Revision of the proposed classification criteria for juvenile idiopathic arthritis: Durban 1997. J Rheumatol 25 (1998) 1991-1994
    • (1998) J Rheumatol , vol.25 , pp. 1991-1994
    • Petty, R.1    Southwood, T.2    Baum, J.3    Bhettay, E.4    Glass, D.5    Manners, P.6
  • 6
    • 1342332097 scopus 로고    scopus 로고
    • The Arabic version of childhood health assessment questionnaire modified for Arabic children
    • Madi S., Al-Mayouf S.M., Gainger C., and Bahabri S. The Arabic version of childhood health assessment questionnaire modified for Arabic children. Saudi Med J 25 (2004) 83-87
    • (2004) Saudi Med J , vol.25 , pp. 83-87
    • Madi, S.1    Al-Mayouf, S.M.2    Gainger, C.3    Bahabri, S.4
  • 7
    • 0034946637 scopus 로고    scopus 로고
    • Mutation of the matrix metalloproteinase 2 gene (MMP2) causes a multicenteric osteolysis and arthritis syndrome
    • Martignetti J., Al Aqeel A., Al Sewairi W., Boumah C., et al. Mutation of the matrix metalloproteinase 2 gene (MMP2) causes a multicenteric osteolysis and arthritis syndrome. Nat Genet 28 (2001) 261-265
    • (2001) Nat Genet , vol.28 , pp. 261-265
    • Martignetti, J.1    Al Aqeel, A.2    Al Sewairi, W.3    Boumah, C.4
  • 8
    • 0031947369 scopus 로고    scopus 로고
    • The camptodactyly-arthropathy-coxa vara-pericarditis syndrome: clinical features and genetic mapping to human chromosome 1
    • Bahabri S., Suwairi W., Laxer R., Polinkovsky A., Dalaan A., and Warman M. The camptodactyly-arthropathy-coxa vara-pericarditis syndrome: clinical features and genetic mapping to human chromosome 1. Arthritis Rheum 41 (1998) 730-735
    • (1998) Arthritis Rheum , vol.41 , pp. 730-735
    • Bahabri, S.1    Suwairi, W.2    Laxer, R.3    Polinkovsky, A.4    Dalaan, A.5    Warman, M.6
  • 9
    • 33745939347 scopus 로고    scopus 로고
    • Novel PRG4 mutations underlie CACP in Saudi families
    • Alazami A., Al-Mayouf S.M., Wyngaard C., and Meyer B. Novel PRG4 mutations underlie CACP in Saudi families. Hum Mutat 27 (2006) 213
    • (2006) Hum Mutat , vol.27 , pp. 213
    • Alazami, A.1    Al-Mayouf, S.M.2    Wyngaard, C.3    Meyer, B.4
  • 10
    • 0018221090 scopus 로고    scopus 로고
    • Pathologic features of a familial arthropathy associated with congenital flexion contractures of fingers
    • Athreya B., and Schumacher R. Pathologic features of a familial arthropathy associated with congenital flexion contractures of fingers. Arthritis Rheum 21 (1998) 429-437
    • (1998) Arthritis Rheum , vol.21 , pp. 429-437
    • Athreya, B.1    Schumacher, R.2
  • 12
    • 33644691715 scopus 로고    scopus 로고
    • Comparison of clinical and laboratory variables in familial versus sporadic systemic onset juvenile idiopathic arthritis
    • Al-Mayouf S.M., Madi S., Almane K., and aljumaah S. Comparison of clinical and laboratory variables in familial versus sporadic systemic onset juvenile idiopathic arthritis. J Rheumatol 33 (2006) 597-600
    • (2006) J Rheumatol , vol.33 , pp. 597-600
    • Al-Mayouf, S.M.1    Madi, S.2    Almane, K.3    aljumaah, S.4
  • 13
    • 0028576438 scopus 로고
    • Radiological features in congenital camptodactyly, familial arthropathy and coax vara syndrome
    • Hugosson C., Bahabri S., McDonald P., AlDalaan A., and AlMazyed A. Radiological features in congenital camptodactyly, familial arthropathy and coax vara syndrome. Pediatr Radiol 24 (1994) 523-526
    • (1994) Pediatr Radiol , vol.24 , pp. 523-526
    • Hugosson, C.1    Bahabri, S.2    McDonald, P.3    AlDalaan, A.4    AlMazyed, A.5
  • 14
    • 25644449686 scopus 로고    scopus 로고
    • Camptodactyly-arthropathy-coxa vara-pericarditis syndrome versus juvenile idiopathic arthropathy
    • Offiah A., Woo P., Prieur A., Hansson N., and Hall C. Camptodactyly-arthropathy-coxa vara-pericarditis syndrome versus juvenile idiopathic arthropathy. Am J Roentgenol 185 (2005) 522-529
    • (2005) Am J Roentgenol , vol.185 , pp. 522-529
    • Offiah, A.1    Woo, P.2    Prieur, A.3    Hansson, N.4    Hall, C.5
  • 16
    • 0142122899 scopus 로고    scopus 로고
    • Mutations in capillary morphogenesis gene-2 result in the allelic disorders juvenile hyaline fibromatosis and infantile systemic hyalinosis
    • Dowling O., Difeo A., Ramirez M., Tukel T., Narla G., Bonfe L., et al. Mutations in capillary morphogenesis gene-2 result in the allelic disorders juvenile hyaline fibromatosis and infantile systemic hyalinosis. Am J Hum Genet 73 (2003) 957-966
    • (2003) Am J Hum Genet , vol.73 , pp. 957-966
    • Dowling, O.1    Difeo, A.2    Ramirez, M.3    Tukel, T.4    Narla, G.5    Bonfe, L.6
  • 17
    • 24744467785 scopus 로고    scopus 로고
    • Consequences of disease-causing mutations on lubricin protein synthesis, secretion, and post-translational processing
    • Rhee D., Marcelino J., Al-Mayouf S., Schelling D., Bartels C., Cui Y., Laxer R., et al. Consequences of disease-causing mutations on lubricin protein synthesis, secretion, and post-translational processing. J Biol Chem 280 (2005) 31325-31332
    • (2005) J Biol Chem , vol.280 , pp. 31325-31332
    • Rhee, D.1    Marcelino, J.2    Al-Mayouf, S.3    Schelling, D.4    Bartels, C.5    Cui, Y.6    Laxer, R.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.