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wafaa suwairi
wafaa suwairi
KSAU-HS
Verified email at ksau-hs.edu.sa
Title
Cited by
Cited by
Year
LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development
Y Gong, RB Slee, N Fukai, G Rawadi, S Roman-Roman, AM Reginato, ...
Cell 107 (4), 513-523, 2001
26682001
2016 classification criteria for macrophage activation syndrome complicating systemic juvenile idiopathic arthritis: a European League Against Rheumatism/American College of …
A Ravelli, F Minoia, S Davì, AC Horne, F Bovis, A Pistorio, M Aricò, ...
Arthritis & rheumatology 68 (3), 566-576, 2016
8502016
Loss-of-function variant in DNASE1L3 causes a familial form of systemic lupus erythematosus
SM Al-Mayouf, A Sunker, R Abdwani, SA Abrawi, F Almurshedi, ...
Nature genetics 43 (12), 1186-1188, 2011
4282011
CACP, encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndrome
J Marcelino, JD Carpten, WM Suwairi, OM Gutierrez, S Schwartz, ...
Nature genetics 23 (3), 319-322, 1999
3761999
Mutation of the matrix metalloproteinase 2 gene (MMP2) causes a multicentric osteolysis and arthritis syndrome
JA Martignetti, AA Aqeel, WA Sewairi, CE Boumah, M Kambouris, ...
Nature genetics 28 (3), 261-265, 2001
3672001
Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia
JR Hurvitz, WM Suwairi, W Van Hul, H El-Shanti, A Superti-Furga, ...
Nature genetics 23 (1), 94-98, 1999
3201999
The camptodactyly‐arthropathy‐coxa vara‐pericarditis syndrome: Clinical features and genetic mapping to human chromosome 1
SA Bahabri, WM Suwairi, RM Laxer, A Polinkovsky, AA Dalaan, ...
Arthritis & Rheumatism: Official Journal of the American College of …, 1998
1131998
Dissecting the heterogeneity of macrophage activation syndrome complicating systemic juvenile idiopathic arthritis
F Minoia, S Davì, AC Horne, F Bovis, E Demirkaya, J Akikusa, NA Ayaz, ...
The Journal of rheumatology 42 (6), 994-1001, 2015
772015
Inherited multicentric osteolysis with arthritis: a variant resembling Torg syndrome in a Saudi family
A Al Aqeel, W Al Sewairi, B Edress, RJ Gorlin, RJ Desnick, JA Martignetti
American journal of medical genetics 93 (1), 11-18, 2000
672000
Development and initial validation of the macrophage activation syndrome/primary hemophagocytic lymphohistiocytosis score, a diagnostic tool that differentiates primary …
F Minoia, F Bovis, S Davi, A Insalaco, K Lehmberg, S Shenoi, S Weitzman, ...
The Journal of pediatrics 189, 72-78. e3, 2017
652017
The combined use of intravenous and oral calcium for the treatment of vitamin D dependent rickets type II (VDDRII)
A Al‐Aqeel, P Ozand, S Sobki, W Sewairi, S Marx
Clinical endocrinology 39 (2), 229-237, 1993
561993
Shock: an unusual presentation of Kawasaki disease
F Thabet, H Bafaqih, S Al-Mohaimeed, M Al-Hilali, W Al-Sewairi, ...
European journal of pediatrics 170, 941-943, 2011
472011
Progressive pseudorheumatoid dysplasia
WM Suwairi, ML Warman
Connective Tissue and Its Heritable Disorders: Molecular, Genetic, and …, 2002
422002
Juvenile rheumatoid arthritis: the Saudi experience
S Bahabri, W Al-Sewairi, A Al-Mazyad, A Karrar, S Al-Ballaa, ...
Annals of Saudi Medicine 17 (4), 413-418, 1997
281997
Common genetics and metabolic diseases in Saudi Arabia
MD Aida Al Aqeel, CP Metabolist
Middle East Journal of Family Medicine 6 (6), 2004
212004
Al-Aqeel Sewairi syndrome, a new autosomal recessive disorder with multicentric osteolysis, nodulosis and arthropathy. The first genetic defect of matrix metalloproteinase 2 gene.
AI Al-Aqeel
Saudi medical journal 26 (1), 24-30, 2005
172005
Dysfunctional and antigenically abnormal C1q resulting from a point mutation in codon 6 of the C chain.
W Suwairi, S Bahabri, D Beving, J Wisnieski, M Warman
ARTHRITIS AND RHEUMATISM 40 (9), 1662-1662, 1997
101997
Distal acroosteolysis, poikiloderma and joint stiffness: a novel laminopathy?
W Sewairi, A Assiri, N Patel, A Alhashem, FS Alkuraya
European Journal of Human Genetics 24 (8), 1220-1222, 2016
82016
Al Aqeel-Sewairi Syndrome: An autosomal recessive syndrome with nodular arthropathy and acrolysis.
AI Al-Aqeel, W Al-Sewairy
American Journal of Human Genetics 65 (4), A140-A140, 1999
41999
Al Aqeel Sewairi Syndrome, A new autosomal recessive disorder with multicentric oesteolysis and arthritis with a novel mutation of matrix metalloproteinase 2 gene (MMP2)
A Al-Aqeel
Am J Hum Genet 69 (592), 18, 2001
32001
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