Muralitharan S - Search Results

1

Clinical and genetic study of spinal muscular atrophies in Oman.

Koul R, Al Futaisi A, Chacko A, Rao V, Simsek M, Muralitharan S, Ganguly SS, Bayoumi R. Koul R, et al. Among authors: muralitharan s. J Child Neurol. 2007 Oct;22(10):1227-30. doi: 10.1177/0883073807306268. J Child Neurol. 2007. PMID: 17940251

2

Trinucleotide repeat analysis of spinocerebellar ataxia patients in Oman.

Chacko JP, Muralitharan S, Al-Ansari A, Al-Kharusi K, Al-Asmi A, Pratap CR, Bayoumi R. Chacko JP, et al. Among authors: muralitharan s. Neurosciences (Riyadh). 2005 Jan;10(1):61-3. Neurosciences (Riyadh). 2005. PMID: 22473187

3

Hereditary thrombophilia in ethnic Omani patients.

Pathare A, Al Kindi S, Al Haddabi H, Dennison D, Bayoumi R, Muralitharan S. Pathare A, et al. Among authors: muralitharan s. Am J Hematol. 2006 Feb;81(2):101-6. doi: 10.1002/ajh.20525. Am J Hematol. 2006. PMID: 16432849 Free article.

4

An inframe perforin gene deletion in familial hemophagocytic lymphohistiocytosis is associated with perforin expression.

Muralitharan S, Al Lamki Z, Dennison D, Christie BS, Wali YA, Zachariah M, Romana M, Bayoumi R, Krishnamoorthy R. Muralitharan S, et al. Am J Hematol. 2005 Jan;78(1):59-63. doi: 10.1002/ajh.20256. Am J Hematol. 2005. PMID: 15609274 Free article.

5

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. Among authors: muralitharan s. Clin Lab Haematol. 2004 Apr;26(2):143-6. doi: 10.1111/j.1365-2257.2004.00585.x. Clin Lab Haematol. 2004. PMID: 15053809

6

Lafora progressive myoclonus epilepsy: disease course homogeneity in a genetic isolate.

Turnbull J, Kumar S, Ren ZP, Muralitharan S, Naranian T, Ackerley CA, Minassian BA. Turnbull J, et al. Among authors: muralitharan s. J Child Neurol. 2008 Feb;23(2):240-2. doi: 10.1177/0883073807309245. J Child Neurol. 2008. PMID: 18263761

7

Myofibrillogenesis regulator 1 gene (MR-1) mutation in an Omani family with paroxysmal nonkinesigenic dyskinesia.

Hempelmann A, Kumar S, Muralitharan S, Sander T. Hempelmann A, et al. Among authors: muralitharan s. Neurosci Lett. 2006 Jul 10;402(1-2):118-20. doi: 10.1016/j.neulet.2006.03.048. Epub 2006 Apr 24. Neurosci Lett. 2006. PMID: 16632198

8

CD45 gene C77G mutation in haemophagocytic lymphohistiocytosis.

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

9

Novel spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis in ethnic Omani patients.

Muralitharan S, Wali YA, Dennison D, Lamki ZA, Zachariah M, Nagwa el B, Pathare A, Krishnamoorthy R. Muralitharan S, et al. Am J Hematol. 2007 Dec;82(12):1099-102. doi: 10.1002/ajh.21009. Am J Hematol. 2007. PMID: 17674359 Free article.

10

Angiotensinogen gene associated polymorphisms and risk of stroke in sickle cell anemia: Additional data supporting an association.

Romana M, Diara JP, Doumbo L, Muralitharan S, Ramasawmy R, Keclard L, Tarer V, Chaar V, Elion J, Krishnamoorthy R, Clayton J. Romana M, et al. Among authors: muralitharan s. Am J Hematol. 2004 Jul;76(3):310-1. doi: 10.1002/ajh.20078. Am J Hematol. 2004. PMID: 15224377 Free article. No abstract available.

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