Pathare A - Search Results

1

A novel deletional beta-thalassemic variant in an ethnic Qatari patient.

Al-Obaidli A, Gerard N, Al Zadjali S, Fawzi Z, Pravin S, Pathare A, Krishnamoorthy R. Al-Obaidli A, et al. Among authors: pathare a. Hemoglobin. 2009;33(3):214-9. doi: 10.1080/03630260903081398. Hemoglobin. 2009. PMID: 19657835

2

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: pathare a. Hemoglobin. 2010 Jan;34(2):135-44. doi: 10.3109/03630261003677213. Hemoglobin. 2010. PMID: 20353348

3

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. Among authors: pathare a. 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

4

Novel human pathological mutations. Gene symbol: PROC. Disease: Protein C deficiency.

Pathare A, Al Zadjali S, Shah W. Pathare A, et al. Hum Genet. 2009 Aug;126(2):336-7. Hum Genet. 2009. PMID: 19694010 No abstract available.

5

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

6

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: pathare av. Eur J Haematol. 2013 Aug;91(2):164-9. doi: 10.1111/ejh.12136. Epub 2013 Jun 15. Eur J Haematol. 2013. PMID: 23668236

7

Warfarin pharmacogenetics: polymorphisms of the CYP2C9, CYP4F2, and VKORC1 loci in a genetically admixed Omani population.

Pathare AV, Al Zadjali S, Misquith R, Alkindi SS, Panjwani V, Lapoumeroulie C, Pravin S, Paldi A, Krishnamoorthy R. Pathare AV, et al. Hum Biol. 2012 Feb;84(1):67-77. doi: 10.3378/027.084.0103. Hum Biol. 2012. PMID: 22452429

8

Neonatal Screening: Mean haemoglobin and red cell indices in cord blood from Omani neonates.

Alkindi S, Pathare A, Al-Madhani A, Al-Zadjali S, Al-Haddabi H, Al-Abri Q, Gravell D, Mathew M, Krishnamoorthy R. Alkindi S, et al. Among authors: pathare a. Sultan Qaboos Univ Med J. 2011 Nov;11(4):462-9. Epub 2011 Oct 25. Sultan Qaboos Univ Med J. 2011. PMID: 22087394 Free PMC article.

9

CD45 gene C77G mutation in haemophagocytic lymphohistiocytosis.

Muralitharan S, Pathare A, Wali Y, Dennison D, Krishnamoorthy R. Muralitharan S, et al. Among authors: pathare a. Acta Haematol. 2007;118(3):160-1. doi: 10.1159/000108638. Epub 2007 Sep 20. Acta Haematol. 2007. PMID: 17890848 No abstract available.

10

dRTA and hemolytic anemia: first detailed description of SLC4A1 A858D mutation in homozygous state.

Fawaz NA, Beshlawi IO, Al Zadjali S, Al Ghaithi HK, Elnaggari MA, Elnour I, Wali YA, Al-Said BB, Rehman JU, Pathare AV, Knox-Macaulay H, Alkindi SS. Fawaz NA, et al. Among authors: pathare av. Eur J Haematol. 2012 Apr;88(4):350-5. doi: 10.1111/j.1600-0609.2011.01739.x. Epub 2012 Jan 4. Eur J Haematol. 2012. PMID: 22126643

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