Alsmadi O - Search Results

1

Ocular manifestations in chronic granulomatous disease in Saudi Arabia.

Al-Muhsen S, Al-Hemidan A, Al-Shehri A, Al-Harbi A, Al-Ghonaium A, Al-Saud B, Al-Mousa H, Al-Dhekri H, Arnaout R, Al-Mohsen I, Alsmadi O. Al-Muhsen S, et al. Among authors: alsmadi o. J AAPOS. 2009 Aug;13(4):396-9. doi: 10.1016/j.jaapos.2009.05.011. J AAPOS. 2009. PMID: 19683193

2

Molecular analysis of T-B-NK+ severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia.

Alsmadi O, Al-Ghonaium A, Al-Muhsen S, Arnaout R, Al-Dhekri H, Al-Saud B, Al-Kayal F, Al-Saud H, Al-Mousa H. Alsmadi O, et al. BMC Med Genet. 2009 Nov 13;10:116. doi: 10.1186/1471-2350-10-116. BMC Med Genet. 2009. PMID: 19912631 Free PMC article.

3

A novel mutation in purine nucleoside phosphorylase in a child with normal uric acid levels.

Al-Saud B, Alsmadi O, Al-Muhsen S, Al-Ghonaium A, Al-Dhekri H, Arnaout R, Hershfield MS, Al-Mousa H. Al-Saud B, et al. Among authors: alsmadi o. Clin Biochem. 2009 Nov;42(16-17):1725-7. doi: 10.1016/j.clinbiochem.2009.08.017. Epub 2009 Sep 3. Clin Biochem. 2009. PMID: 19733163

4

Disseminated cryptococcal infection in patient with novel JAK3 mutation severe combined immunodeficiency, with resolution after stem cell transplantation.

Alsum Z, Al-Saud B, Al-Ghonaium A, Bin Hussain I, Alsmadi O, Al-Mousa H, Ayas M, Al-Dhekri H, Arnaout R, Al-Muhsen S. Alsum Z, et al. Among authors: alsmadi o. Pediatr Infect Dis J. 2012 Feb;31(2):204-6. doi: 10.1097/INF.0b013e318239c3b3. Pediatr Infect Dis J. 2012. PMID: 22138680

5

Clinical, immunological and molecular characterization of DOCK8 and DOCK8-like deficient patients: single center experience of twenty-five patients.

Alsum Z, Hawwari A, Alsmadi O, Al-Hissi S, Borrero E, Abu-Staiteh A, Khalak HG, Wakil S, Eldali AM, Arnaout R, Al-Ghonaium A, Al-Muhsen S, Al-Dhekri H, Al-Saud B, Al-Mousa H. Alsum Z, et al. Among authors: alsmadi o. J Clin Immunol. 2013 Jan;33(1):55-67. doi: 10.1007/s10875-012-9769-x. Epub 2012 Sep 12. J Clin Immunol. 2013. PMID: 22968740

6

Clinical, immunological, and molecular characterization of hyper-IgM syndrome due to CD40 deficiency in eleven patients.

Al-Saud BK, Al-Sum Z, Alassiri H, Al-Ghonaium A, Al-Muhsen S, Al-Dhekri H, Arnaout R, Alsmadi O, Borrero E, Abu-Staiteh A, Rawas F, Al-Mousa H, Hawwari A. Al-Saud BK, et al. Among authors: alsmadi o. J Clin Immunol. 2013 Nov;33(8):1325-35. doi: 10.1007/s10875-013-9951-9. J Clin Immunol. 2013. PMID: 24122029 Review.

7

Mutations underlying 3-hydroxy-3-methylglutaryl CoA lyase deficiency in the Saudi population.

Al-Sayed M, Imtiaz F, Alsmadi OA, Rashed MS, Meyer BF. Al-Sayed M, et al. BMC Med Genet. 2006 Dec 16;7:86. doi: 10.1186/1471-2350-7-86. BMC Med Genet. 2006. PMID: 17173698 Free PMC article.

8

Novel mutations underlying argininosuccinic aciduria in Saudi Arabia.

Imtiaz F, Al-Sayed M, Trabzuni D, Al-Mubarak BR, Alsmadi O, Rashed MS, Meyer BF. Imtiaz F, et al. Among authors: alsmadi o. BMC Res Notes. 2010 Mar 18;3:79. doi: 10.1186/1756-0500-3-79. BMC Res Notes. 2010. PMID: 20298553 Free PMC article.

9

Identification of a common novel mutation in Saudi patients with argininosuccinic aciduria.

Al-Sayed M, Alahmed S, Alsmadi O, Khalil H, Rashed MS, Imtiaz F, Meyer BF. Al-Sayed M, et al. Among authors: alsmadi o. J Inherit Metab Dis. 2005;28(6):877-83. doi: 10.1007/s10545-005-0081-2. J Inherit Metab Dis. 2005. PMID: 16435180

10

Genetic study of Saudi diabetes (GSSD): significant association of the KCNJ11 E23K polymorphism with type 2 diabetes.

Alsmadi O, Al-Rubeaan K, Wakil SM, Imtiaz F, Mohamed G, Al-Saud H, Al-Saud NA, Aldaghri N, Mohammad S, Meyer BF. Alsmadi O, et al. Diabetes Metab Res Rev. 2008 Feb;24(2):137-40. doi: 10.1002/dmrr.777. Diabetes Metab Res Rev. 2008. PMID: 17922473

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