-
2
-
-
0035035203
-
Juvenile idiopathic arthritis in multicase families
-
Saila H., Savolainen A., Kotaniemi K., Kaipiainen-Seppanen O., Leirisalo-Repo M., and Aho K. Juvenile idiopathic arthritis in multicase families. Clin Exp Rheumatol 19 (2001) 218-220
-
(2001)
Clin Exp Rheumatol
, vol.19
, pp. 218-220
-
-
Saila, H.1
Savolainen, A.2
Kotaniemi, K.3
Kaipiainen-Seppanen, O.4
Leirisalo-Repo, M.5
Aho, K.6
-
3
-
-
0006387161
-
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
-
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
-
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
-
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
-
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
-
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
-
10
-
-
0018221090
-
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
-
11
-
-
24944588064
-
Infantile systemic hyalinosis: a fatal disorder commonly diagnosed among Arabs
-
Al-Mayouf S.M., AlMehaidib A., Bahabri S., Shabib S., Sakati N., and Teebi A. Infantile systemic hyalinosis: a fatal disorder commonly diagnosed among Arabs. Clin Exp Rheumatol 23 5 (2005) 717-720
-
(2005)
Clin Exp Rheumatol
, vol.23
, Issue.5
, pp. 717-720
-
-
Al-Mayouf, S.M.1
AlMehaidib, A.2
Bahabri, S.3
Shabib, S.4
Sakati, N.5
Teebi, A.6
-
12
-
-
33644691715
-
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
-
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
-
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
-
15
-
-
33846692229
-
Radiological changes in Nodulosis, Arthropathy, Osteolysis syndrome
-
Al Otaibi L., Al-Mayouf S.M., Majeed M., Al-Eid W., Bahabri S., and Hugosson C. Radiological changes in Nodulosis, Arthropathy, Osteolysis syndrome. Pediatr Radiol 23 (2002) 523-538
-
(2002)
Pediatr Radiol
, vol.23
, pp. 523-538
-
-
Al Otaibi, L.1
Al-Mayouf, S.M.2
Majeed, M.3
Al-Eid, W.4
Bahabri, S.5
Hugosson, C.6
-
16
-
-
0142122899
-
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
-
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
|