Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia von Hul, Els Van, Warman, Matthew L, Al-Alami, Jamil, Roudier, Jean, Bahabri, Sultan A, Hurvitz, Jennifer R, Pauli, Richard M, El-Shanti, Hatem, Rezai-Delui, Hossien, Van Hul, Wim, Suwairi, Wafaa M, Legius, Eric, Holderbaum, Daniel, Herd, J. Kenneth, Superti-Furga, Andrea, Le Merrer, Martine

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Mutation of the matrix metalloproteinase 2 gene ( MMP2 ) causes a multicentric osteolysis and arthritis syndrome von Martignetti, John A, Aqeel, Aida Al, Sewairi, Wafaa Al, Boumah, Christine E, Kambouris, Marios, Mayouf, S. Al, Sheth, K.V, Eid, W. Al, Dowling, Oonagh, Harris, Juliette, Glucksman, Marc J, Bahabri, Sultan, Meyer, Brian F, Desnick, Robert J

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Clinical features of Behçet's disease in children: An international collaborative study of 86 cases von Koné-Paut, Isabelle, Yurdakul, Sebahattin, Bahabri, Sultan A., Shafae, Nahid, Ozen, Seza, Özdogan, Huri, Bernard, Jean Louis

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The Buzz and the Sting von Bahabri, Sultan Abdullah

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Prevalence of systemic lupus erythematosus in central Saudi Arabia von AL-ARFAJ, Abdurhman S, AL-BALLA, Suliman R, AL-DALAAN, Abdullah N, AL-SALEH, Salman S, BAHABRI, Sultan A, MOUSA, Mohammed M, SEKEIT, Mohammed A

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How common is back pain in Al-Qaseem region von AL-ARFAJ, Abdurhman S, AL-SALEH, Salman S, ALBALLA, Suliman R, AL-DALAAN, Abdullah N, BAHABRI, Sultan A, AL-SEKEIT, Mohammed A, MOUSA, Mohammed A

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Pseudotumor cerebri and leukoencephalopathy in childhood lupus von Chaves-Carballo, E, Dabbagh, Omar, Bahabri, Sultan

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CACP , encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndrome von Trent, Jeffrey M, Warman, Matthew L, Marcelino, Jose, Carpten, John D, Suwairi, Wafaa M, Gutierrez, Orlando M, Schwartz, Stuart, Robbins, Christiane, Sood, Raman, Makalowska, Izabela, Baxevanis, Andy, Johnstone, Brian, Laxer, Ronald M, Zemel, Lawrence, Kim, Chong Ae, Herd, J. Kenneth, Ihle, Johannes, Williams, Cal, Johnson, Mark, Raman, Vidya, Alonso, Luís Garcia, Brunoni, Decio, Gerstein, Amy, Papadopoulos, Nickolas, Bahabri, Sultan A

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The Arabic version of childhood health assessment questionnaire modified for Arabic children von MADI, Sanaa M, AL-MAYOUF, Sulaiman M, GRAINGER, Carol G, BAHABRI, Sultan A

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Musculoskeletal pain in the community von AL-ARFAJ, Abdurhman S, ALBALLA, Suliman R, AL-DALAAN, Abdullah N, AL-SALEH, Salman S, AL-SEKEIT, Mohammed A, BAHABRI, Sultan A, MOUSA, Mohammed A

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Evaluation of parental knowledge of Pediatric rheumatic diseases von AL-EID, Wea'Am M, MADI, Sanaa M, BAHABRI, Sultan A, AL-MAYOUF, Sulaiman M

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Mouth and genital ulcerations in the community von AL-ARFAJ, Abdurhman S, ALBALLA, Suliman R, SEKEIT, Mohammed A, AL-SALEH, Salman S, AL-DALAAN, Abdulla N, BAHABRI, Sultan A, MOSSA, Mohammed A

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Cutaneous leukocytoclastic vasculitis associated with mycobacterial and salmonella infection von Al-Mayouf, Sulaiman M, Bahabri, Sultan, Majeed, Mahmuod

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Infantile systemic hyalinosis : A fatal disorder commonly diagnosed among Arabs von AL-MAYOUF, S. M, ALMEHAIDIB, A, BAHABRI, S, SHABIB, S, SAKATI, N, TEEBI, A. S

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HEMOPHAGOCYTOSIS COMPLICATING KAWASAKI DISEASE von Al-Eid, Wea'am, Al-Jefri, Abdullah, Bahabri, Sultan, Al-Mayouf, Sulaiman

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Hemophagocytosis complicating Kawasaki disease von al-Eid, W, al-Jefri, A, Bahabri, S, al-Mayouf, S

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Juvenile dermatomyositis : Clinical profile and disease course in 25 patients von SHEHATA, R, AL-MAYOUF, S, AL-DALAAN, A, AL-MAZAID, A, AL-BALAA, S, BAHABRI, S

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Radiological findings in NAO syndrome von AL-OTAIBI, Leftan, AL-MAYOUF, Sulalman M, MAJEED, Mahmoud, AL-EID, Wea'Am, BAHABRI, Sultan, HUGOSSON, Claes O

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The camptodactyly‐arthropathy‐coxa vara‐pericarditis syndrome: Clinical features and genetic mapping to human chromosome 1 von Bahabri, Sultan A., Suwairi, Wafaa M., Laxer, Ronald M., Polinkovsky, Alexander, Dalaan, Abdullah A., Warman, Matthew L.

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Coexistent Linear Scleroderma and Juvenile Systemic Lupus Erythematosus von Majeed, Mahmoud, Al‐Mayouf, Sulaiman M., Al‐Sabban, Essam, Bahabri, Sultan

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