Adam S - Search Results

1

iPSC modeling of severe aplastic anemia reveals impaired differentiation and telomere shortening in blood progenitors.

Melguizo-Sanchis D, Xu Y, Taheem D, Yu M, Tilgner K, Barta T, Gassner K, Anyfantis G, Wan T, Elango R, Alharthi S, El-Harouni AA, Przyborski S, Adam S, Saretzki G, Samarasinghe S, Armstrong L, Lako M. Melguizo-Sanchis D, et al. Among authors: adam s. Cell Death Dis. 2018 Jan 26;9(2):128. doi: 10.1038/s41419-017-0141-1. Cell Death Dis. 2018. PMID: 29374141 Free PMC article.

2

Concise Review: Getting to the Core of Inherited Bone Marrow Failures.

Adam S, Melguizo Sanchis D, El-Kamah G, Samarasinghe S, Alharthi S, Armstrong L, Lako M. Adam S, et al. Stem Cells. 2017 Feb;35(2):284-298. doi: 10.1002/stem.2543. Epub 2016 Dec 4. Stem Cells. 2017. PMID: 27870251 Free PMC article. Review.

3

Quality of Life Outcomes in a Pediatric Thalassemia Population in Egypt.

Adam S, Afifi H, Thomas M, Magdy P, El-Kamah G. Adam S, et al. Hemoglobin. 2017 Jan;41(1):16-20. doi: 10.1080/03630269.2017.1312434. Epub 2017 Apr 25. Hemoglobin. 2017. PMID: 28440111

4

The prevalence of APOL1 gene variants in a cohort of renal disease patients in Western Saudi Arabia.

Adam S, Badawi M, Zaher G, Alshehri B, Basaeed A, Jelani M, Kashqari A. Adam S, et al. Saudi J Kidney Dis Transpl. 2018 Jul-Aug;29(4):793-800. doi: 10.4103/1319-2442.239658. Saudi J Kidney Dis Transpl. 2018. PMID: 30152414

5

Markers of endothelial dysfunction and leucocyte activation in Saudi and non-Saudi haplotypes of sickle cell disease.

Al Najjar S, Adam S, Ahmed N, Qari M. Al Najjar S, et al. Among authors: adam s. Ann Hematol. 2017 Jan;96(1):141-146. doi: 10.1007/s00277-016-2823-7. Epub 2016 Sep 30. Ann Hematol. 2017. PMID: 27686084

6

Evaluation of a point-of-care method for screening blood donors for sickle cell status.

Badawi M, Garoot S, Tahlawi M, Hindawi S, Adam S. Badawi M, et al. Among authors: adam s. Transfusion. 2020 Feb;60 Suppl 1:S10-S14. doi: 10.1111/trf.15586. Transfusion. 2020. PMID: 32134127

7

Depression, quality of life, and medical resource utilization in sickle cell disease.

Adam SS, Flahiff CM, Kamble S, Telen MJ, Reed SD, De Castro LM. Adam SS, et al. Blood Adv. 2017 Oct 12;1(23):1983-1992. doi: 10.1182/bloodadvances.2017006940. eCollection 2017 Oct 24. Blood Adv. 2017. PMID: 29296845 Free PMC article.

8

Concomitant multiple myeloma, gastric adenocarcinoma and Evan's syndrome in a patient presenting with anaemia.

Al-Ammari M, Adam S. Al-Ammari M, et al. Among authors: adam s. BMJ Case Rep. 2016 Dec 15;2016:bcr2016217697. doi: 10.1136/bcr-2016-217697. BMJ Case Rep. 2016. PMID: 27979847 Free PMC article.

9

Successful Long Term Eradication of Factor VIII Inhibitor in Patients with Acquired Haemophilia A in Saudi Arabia.

Zaher G, Adam S. Zaher G, et al. Among authors: adam s. Mediterr J Hematol Infect Dis. 2012;4(1):e2012021. doi: 10.4084/MJHID.2012.021. Epub 2012 Apr 2. Mediterr J Hematol Infect Dis. 2012. PMID: 22536478 Free PMC article.

10

Potential role for statins in sickle cell disease.

Adam SS, Hoppe C. Adam SS, et al. Pediatr Blood Cancer. 2013 Apr;60(4):550-7. doi: 10.1002/pbc.24443. Epub 2012 Dec 31. Pediatr Blood Cancer. 2013. PMID: 23281161 Review.

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