Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 41

1.

Sequence and analysis of a whole genome from Kuwaiti population subgroup of Persian ancestry.

Thareja G, John S, Hebbar P, Behbehani K, Thanaraj T, Alsmadi O.

BMC Genomics. 2015 Feb 18;16(1):92. [Epub ahead of print]

PMID:
25765185
Free PMC Article
2.

Salivary glucose concentration exhibits threshold kinetics in normal-weight, overweight, and obese children.

Hartman ML, Goodson JM, Barake R, Alsmadi O, Al-Mutawa S, Ariga J, Soparkar P, Behbehani J, Behbehani K, Welty F.

Diabetes Metab Syndr Obes. 2014 Dec 17;8:9-15. doi: 10.2147/DMSO.S72744. eCollection 2015.

3.

Sudden cardiac death diagnosed with dilated cardiomyopathy in a Kuwaiti family: a case report.

Bulbanat B, Antony D, Behbehani K, Alsmadi O, Thomas D, Kamkar MM.

BMC Res Notes. 2014 Dec 16;7:914. doi: 10.1186/1756-0500-7-914.

4.

Vitamin D insufficiency in Arabs and South Asians positively associates with polymorphisms in GC and CYP2R1 genes.

Elkum N, Alkayal F, Noronha F, Ali MM, Melhem M, Al-Arouj M, Bennakhi A, Behbehani K, Alsmadi O, Abubaker J.

PLoS One. 2014 Nov 18;9(11):e113102. doi: 10.1371/journal.pone.0113102. eCollection 2014.

5.

Response to leptin and nitric oxide in blood pressure regulation in humans.

Alsmadi O, Melhem M, Hebbar P, Channanath A, Thareja G, John SE, Alkayal F, Behbehani K, Thanaraj TA.

Am J Hypertens. 2014 Nov;27(11):1429-30. doi: 10.1093/ajh/hpu178. Epub 2014 Oct 1. No abstract available.

PMID:
25273037
6.

Insight into the impact of diabetes mellitus on the increased risk of hepatocellular carcinoma: mini-review.

Ali Kamkar MM, Ahmad R, Alsmadi O, Behbehani K.

J Diabetes Metab Disord. 2014 May 22;13:57. doi: 10.1186/2251-6581-13-57. eCollection 2014. Review.

7.

Metabolic disease risk in children by salivary biomarker analysis.

Goodson JM, Kantarci A, Hartman ML, Denis GV, Stephens D, Hasturk H, Yaskell T, Vargas J, Wang X, Cugini M, Barake R, Alsmadi O, Al-Mutawa S, Ariga J, Soparkar P, Behbehani J, Behbehani K, Welty F.

PLoS One. 2014 Jun 10;9(6):e98799. doi: 10.1371/journal.pone.0098799. eCollection 2014.

8.

Genome at juncture of early human migration: a systematic analysis of two whole genomes and thirteen exomes from Kuwaiti population subgroup of inferred Saudi Arabian tribe ancestry.

Alsmadi O, John SE, Thareja G, Hebbar P, Antony D, Behbehani K, Thanaraj TA.

PLoS One. 2014 Jun 4;9(6):e99069. doi: 10.1371/journal.pone.0099069. eCollection 2014.

9.

ND4L gene concurrent 10609T>C and 10663T>C mutations are associated with Leber's hereditary optic neuropathy in a large pedigree from Kuwait.

Behbehani R, Melhem M, Alghanim G, Behbehani K, Alsmadi O.

Br J Ophthalmol. 2014 Jun;98(6):826-31. doi: 10.1136/bjophthalmol-2013-304140. Epub 2014 Feb 25.

10.

Leptin in association with common variants of MC3R mediates hypertension.

Alsmadi O, Melhem M, Hebbar P, Thareja G, John SE, Alkayal F, Behbehani K, Thanaraj TA.

Am J Hypertens. 2014 Jul;27(7):973-81. doi: 10.1093/ajh/hpt285. Epub 2014 Feb 2.

PMID:
24487982
11.

A review of adult obesity prevalence, trends, risk factors, and epidemiologic methods in Kuwait.

Karageorgi S, Alsmadi O, Behbehani K.

J Obes. 2013;2013:378650. doi: 10.1155/2013/378650. Epub 2013 Dec 17. Review.

12.

Obesity and dental decay: inference on the role of dietary sugar.

Goodson JM, Tavares M, Wang X, Niederman R, Cugini M, Hasturk H, Barake R, Alsmadi O, Al-Mutawa S, Ariga J, Soparkar P, Behbehani J, Behbehani K.

PLoS One. 2013 Oct 10;8(10):e74461. doi: 10.1371/journal.pone.0074461. eCollection 2013.

13.

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.

J Clin Immunol. 2013 Nov;33(8):1325-35. Review.

PMID:
24122029
14.

Genetic substructure of Kuwaiti population reveals migration history.

Alsmadi O, Thareja G, Alkayal F, Rajagopalan R, John SE, Hebbar P, Behbehani K, Thanaraj TA.

PLoS One. 2013 Sep 16;8(9):e74913. doi: 10.1371/journal.pone.0074913. eCollection 2013.

15.

The nexus between VEGF and NFκB orchestrates a hypoxia-independent neovasculogenesis.

DeNiro M, Al-Mohanna FH, Alsmadi O, Al-Mohanna FA.

PLoS One. 2013;8(3):e59021. doi: 10.1371/journal.pone.0059021. Epub 2013 Mar 22.

16.

Major histocompatibility complex class II deficiency in Kuwait: clinical manifestations, immunological findings and molecular profile.

Al-Herz W, Alsmadi O, Melhem M, Recher M, Frugoni F, Notarangelo LD.

J Clin Immunol. 2013 Apr;33(3):513-9. doi: 10.1007/s10875-012-9831-8. Epub 2012 Nov 10.

PMID:
23143406
17.

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.

J Clin Immunol. 2013 Jan;33(1):55-67. doi: 10.1007/s10875-012-9769-x. Epub 2012 Sep 12.

PMID:
22968740
18.

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.

Pediatr Infect Dis J. 2012 Feb;31(2):204-6. doi: 10.1097/INF.0b013e318239c3b3.

PMID:
22138680
19.

Novel mutations underlying argininosuccinic aciduria in Saudi Arabia.

Imtiaz F, Al-Sayed M, Trabzuni D, Al-Mubarak BR, Alsmadi O, Rashed MS, Meyer BF.

BMC Res Notes. 2010 Mar 18;3:79. doi: 10.1186/1756-0500-3-79.

20.

Predicting recurrent aphthous ulceration using genetic algorithms-optimized neural networks.

Dar-Odeh NS, Alsmadi OM, Bakri F, Abu-Hammour Z, Shehabi AA, Al-Omiri MK, Abu-Hammad SM, Al-Mashni H, Saeed MB, Muqbil W, Abu-Hammad OA.

Adv Appl Bioinform Chem. 2010;3:7-13. Epub 2010 May 14.

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Loading ...
Write to the Help Desk