Daar S - Search Results

1

A comprehensive update of ICET-A Network on COVID-19 in thalassemias: what we know and where we stand.

De Sanctis V, Canatan D, Corrons JLV, Karimi M, Daar S, Kattamis C, Soliman AT, Wali Y, Alkindi S, Huseynov V, Nasibova A, Tiryaki TO, Sezgin Evim M, Gunes AM, Karakas Z, Christou S, Yassin MA, Galati MC, Campisi S, Zarei T, Khater D, Oymak Y, Kaleva V, Stoyanova D, Banchev A, Skafida M, Kilinc Y. De Sanctis V, et al. Among authors: daar s. Acta Biomed. 2020 Sep 7;91(3):e2020026. doi: 10.23750/abm.v91i3.10063. Acta Biomed. 2020. PMID: 32921722 Free PMC article. Review.

2

Cytokine profile of sickle cell disease in Oman.

Pathare A, Al Kindi S, Alnaqdy AA, Daar S, Knox-Macaulay H, Dennison D. Pathare A, et al. Among authors: daar s. Am J Hematol. 2004 Dec;77(4):323-8. doi: 10.1002/ajh.20196. Am J Hematol. 2004. PMID: 15551290 Free article.

3

Haematological and clinical features of beta-thalassaemia associated with Hb Dhofar.

Daar S, Gravell D, Hussein HM, Pathare AV, Wali Y, Krishnamoorthy R. Daar S, et al. Eur J Haematol. 2008 Jan;80(1):67-70. doi: 10.1111/j.1600-0609.2007.00989.x. Eur J Haematol. 2008. PMID: 18173741

4

Invasive candidal laryngitis as a manifestation of cyclic neutropenia in an Omani infant.

Al-Kindi H, Abdoon H, Alkhabori M, Daar S, Beshlawi I, Wali YA. Al-Kindi H, et al. Among authors: daar s. Pediatr Hematol Oncol. 2008 Jun;25(4):339-44. doi: 10.1080/08880010802016144. Pediatr Hematol Oncol. 2008. PMID: 18484479

5

Forecasting hemoglobinopathy burden through neonatal screening in Omani neonates.

Alkindi S, Al Zadjali S, Al Madhani A, Daar S, Al Haddabi H, Al Abri Q, Gravell D, Berbar T, Pravin S, Pathare A, Krishnamoorthy R. Alkindi S, et al. Among authors: daar s. Hemoglobin. 2010 Jan;34(2):135-44. doi: 10.3109/03630261003677213. Hemoglobin. 2010. PMID: 20353348

6

Severity ranking of non-deletional alpha thalassemic alleles: insights from an Omani family study.

Wali Y, Zadjali SA, Elshinawy M, Beshlawi I, Fawaz N, Alkindi S, Rawas A, Alsinani S, Daar S, Krishnamoorthy R. Wali Y, et al. Among authors: daar s. Eur J Haematol. 2011 Jun;86(6):507-11. doi: 10.1111/j.1600-0609.2011.01606.x. Eur J Haematol. 2011. PMID: 21410534

7

Hb Sheffield [β58(E2)Pro→His] in Oman: potential pitfall in genetic counseling.

Al Zadjali S, Daar S, AlKindi S, Gravell D, Al Haddabi H, Berbar T, Krishnamoorthy R. Al Zadjali S, et al. Among authors: daar s. Hemoglobin. 2011;35(2):111-6. doi: 10.3109/03630269.2011.558226. Hemoglobin. 2011. PMID: 21417567

8

The β-globin promoter -71 C>T mutation is a β+ thalassemic allele.

Al Zadjali S, Wali Y, Al Lawatiya F, Gravell D, Alkindi S, Al Falahi K, Krishnamoorthy R, Daar S. Al Zadjali S, et al. Among authors: daar s. Eur J Haematol. 2011 Nov;87(5):457-60. doi: 10.1111/j.1600-0609.2011.01687.x. Epub 2011 Sep 15. Eur J Haematol. 2011. PMID: 21801233

9

Risk factors for pulmonary hypertension in patients with β thalassemia intermedia.

Karimi M, Musallam KM, Cappellini MD, Daar S, El-Beshlawy A, Belhoul K, Saned MS, Temraz S, Koussa S, Taher AT. Karimi M, et al. Among authors: daar s. Eur J Intern Med. 2011 Dec;22(6):607-10. doi: 10.1016/j.ejim.2011.05.013. Epub 2011 Jun 29. Eur J Intern Med. 2011. PMID: 22075289

10

Agranulocyosis in Beta Thalassemia Major Patients treated with Oral Iron Chelating Agent (Deferiprone).

Wali Y, Shidhani AA, Daar S. Wali Y, et al. Among authors: daar s. Oman Med J. 2008 Oct;23(4):275-7. Oman Med J. 2008. PMID: 22334841 Free PMC article.

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