Wali Y - 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: wali y. Acta Biomed. 2020 Sep 7;91(3):e2020026. doi: 10.23750/abm.v91i3.10063. Acta Biomed. 2020. PMID: 32921722 Free PMC article. Review.

2

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. Among authors: wali y. Eur J Haematol. 2008 Jan;80(1):67-70. doi: 10.1111/j.1600-0609.2007.00989.x. Eur J Haematol. 2008. PMID: 18173741

3

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. Pediatr Hematol Oncol. 2008 Jun;25(4):339-44. doi: 10.1080/08880010802016144. Pediatr Hematol Oncol. 2008. PMID: 18484479

4

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. Eur J Haematol. 2011 Jun;86(6):507-11. doi: 10.1111/j.1600-0609.2011.01606.x. Eur J Haematol. 2011. PMID: 21410534

5

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: wali y. 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

6

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

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

7

Coexistence of sickle cell disease and severe congenital neutropenia: first impressions can be deceiving.

Wali Y, Beshlawi I, Fawaz N, Alkhayat A, Zalabany M, Elshinawy M, Al-Kindi S, Al-Rawas AH, Klein C. Wali Y, et al. Eur J Haematol. 2012 Sep;89(3):245-9. doi: 10.1111/j.1600-0609.2012.01827.x. Eur J Haematol. 2012. PMID: 22758217

8

T2* MRI in regularly transfused children with thalassemia intermedia: serum ferritin does not reflect liver iron stores.

Tony S, Daar S, Elshinawy M, Al-Zadjaly S, Al-Khabori M, Wali Y. Tony S, et al. Among authors: wali y. Pediatr Hematol Oncol. 2012 Sep;29(6):579-84. doi: 10.3109/08880018.2012.708891. Epub 2012 Jul 27. Pediatr Hematol Oncol. 2012. PMID: 22839111

9

A stepwise α-thalassemia screening strategy in high-prevalence areas.

Alkindi SS, Alzadjali S, Daar S, Sindhuvi E, Wali Y, Pathare AV, Venugopal S, Lapoumeroulie C, Srivastava A, Krishnamoorthy R. Alkindi SS, et al. Among authors: wali y. Eur J Haematol. 2013 Aug;91(2):164-9. doi: 10.1111/ejh.12136. Epub 2013 Jun 15. Eur J Haematol. 2013. PMID: 23668236

10

First reported case of compound heterozygosity for HbA2-Yialousa (HBD: c.82 G>C) and HbA2-Wrens (HBD: c.295 G>A) in Oman.

Al Zadjali S, Bashir W, Gravell D, Al Riyami AZ, Wali Y, Daar S. Al Zadjali S, et al. Among authors: wali y. Int J Hematol. 2013 Aug;98(2):240-2. doi: 10.1007/s12185-013-1388-7. Int J Hematol. 2013. PMID: 23797957

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