Alkindi SS - Search Results

1

The pneumatic tube system does not affect complete blood count results; a validation study at a tertiary care hospital.

Al-Riyami AZ, Al-Khabori M, Al-Hadhrami RM, Al-Azwani IS, Davis HM, Al-Farsi KS, Alkindi SS, Daar SF. Al-Riyami AZ, et al. Among authors: alkindi ss. Int J Lab Hematol. 2014 Oct;36(5):514-20. doi: 10.1111/ijlh.12180. Epub 2013 Dec 24. Int J Lab Hematol. 2014. PMID: 24373139

2

Sickle cell-haemoglobin E (HbSE) compound heterozygosity: a clinical and haematological study.

Knox-Macaulay HH, Ahmed MM, Gravell D, Al-Kindi S, Ganesh A. Knox-Macaulay HH, et al. Int J Lab Hematol. 2007 Aug;29(4):292-301. doi: 10.1111/j.1365-2257.2006.00886.x. Int J Lab Hematol. 2007. PMID: 17617080 Review.

3

Hematopoietic stem cell transplantation in Oman.

Dennison D, Al Kindi S, Pathare A, Daar S, Nusrat N, Ur Rehman J, Zia F, Khan H, Khan MI, Alghazaly A, Al Zadjali S, Tauro M, Al Lawatia A, Ganguly S. Dennison D, et al. Bone Marrow Transplant. 2008 Aug;42 Suppl 1:S109-S113. doi: 10.1038/bmt.2008.131. Bone Marrow Transplant. 2008. PMID: 18724280

4

First report of the spectrum of δ-globin gene mutations in Omani subjects - identification of novel mutations.

Alkindi S, AlZadjali S, Daar S, Ambusaidi R, Gravell D, Al Haddabi H, Krishnamoorthy R, Pathare A. Alkindi S, et al. Int J Lab Hematol. 2015 Apr;37(2):238-43. doi: 10.1111/ijlh.12272. Epub 2014 Jul 9. Int J Lab Hematol. 2015. PMID: 25043855

5

Safety of stem cell mobilization in donors with sickle cell trait.

Al-Khabori M, Al-Ghafri F, Al-Kindi S, Al-Riyami AZ, Al-Farsi K, Al-Huneini M, Dennison D, Al-Rawas A, Khan H, Daar S. Al-Khabori M, et al. Bone Marrow Transplant. 2015 Feb;50(2):310-1. doi: 10.1038/bmt.2014.252. Epub 2014 Nov 3. Bone Marrow Transplant. 2015. PMID: 25365063 No abstract available.

6

A novel p.Pro353His SERPINC1 mutation in the thrombin-binding region affecting stability of Antithrombin molecule in an extended Omani family.

Deshpande R, Pathare A, Alkindi S, Al Zadjali S, Ghosh K, Shetty S. Deshpande R, et al. Int J Lab Hematol. 2018 Jun;40(3):e49-e51. doi: 10.1111/ijlh.12808. Epub 2018 Mar 26. Int J Lab Hematol. 2018. PMID: 29579348 No abstract available.

7

Clinical and Laboratory Features of Hemoglobin La Desirade Variant in Association with Sickle Cell and Alpha Thalassemia Genes.

Alkindi S, Al Zadjali S, Al Rawahi M, Al Haddabi H, Daar S, ElSadek RA, Sherkawy BD, Pathare AV. Alkindi S, et al. Mediterr J Hematol Infect Dis. 2021 Jan 1;13(1):e2021010. doi: 10.4084/MJHID.2021.010. eCollection 2021. Mediterr J Hematol Infect Dis. 2021. PMID: 33489049 Free PMC article. No abstract available.

8

The Use of HPLC as a Tool for Neonatal Cord Blood Screening of haemoglobinopathy: A Validation Study.

Al-Madhani A, Pathare A, Al Zadjali S, Al Rawahi M, Al-Nabhani I, Alkindi S. Al-Madhani A, et al. Mediterr J Hematol Infect Dis. 2019 Jan 1;11(1):e2019005. doi: 10.4084/MJHID.2019.005. eCollection 2019. Mediterr J Hematol Infect Dis. 2019. PMID: 30671211 Free PMC article.

9

Clinical and Laboratory Features of Sickle Cell Disease S/D Punjab: Impact of HbF and Hydroxyurea.

Alkindi S, Al-Busaidi IBM, Pathare AV. Alkindi S, et al. Mediterr J Hematol Infect Dis. 2024 May 1;16(1):e2024046. doi: 10.4084/MJHID.2024.046. eCollection 2024. Mediterr J Hematol Infect Dis. 2024. PMID: 38882454 Free PMC article.

10

Heterozygous methylene tetrahydrofolate reductase mutation with mild hyperhomocysteinemia associated with deep vein thrombosis.

Pathare A, Alkindi S, Albalushi T, Bayoumi R, Dennison D, Muralitharan S. Pathare A, et al. Clin Lab Haematol. 2004 Apr;26(2):143-6. doi: 10.1111/j.1365-2257.2004.00585.x. Clin Lab Haematol. 2004. PMID: 15053809

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