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SELVABARATH MURALITHARAN, M.D

M.D

Internal Medicine Physician

NPI: 1306158977Individual

Specialties, Licenses & Credentials

Student in an Organized Health Care Education/Training Program

Student in an Organized Health Care Education/Training Program

Code: 390200000X

MT197453(PA)
Internal Medicine PhysicianPrimary

Internal Medicine

Code: 207R00000X

MD449199(PA)

Research & Publications (13)

CD45 gene C77G mutation in haemophagocytic lymphohistiocytosis.
PMID 17890848·Acta Haematol·2007
5-case
Novel spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis in ethnic Omani patients.
PMID 17674359·Am J Hematol·2007
8-other
An inframe perforin gene deletion in familial hemophagocytic lymphohistiocytosis is associated with perforin expression.
PMID 15609274·Am J Hematol·2005
5-case
Beta-globin-like gene cluster haplotypes in hemoglobinopathies.
PMID 12669645·Methods Mol Med·2003
8-other
Lafora progressive myoclonus epilepsy: disease course homogeneity in a genetic isolate.
PMID 18263761·J Child Neurol·2008
8-other
Clinical and genetic study of spinal muscular atrophies in Oman.
PMID 17940251·J Child Neurol·2007
8-other
Trisomy 21 as a sole acquired abnormality in an adult Omani patient with CD7- and CD9-positive acute myeloid leukemia.
PMID 17845902·Arch Med Res·2007
5-case
Perforin A91V polymorphism and putative susceptibility to hematological malignancies.
PMID 17039227·Leukemia·2006
8-other
Myofibrillogenesis regulator 1 gene (MR-1) mutation in an Omani family with paroxysmal nonkinesigenic dyskinesia.
PMID 16632198·Neurosci Lett·2006
4-observational
Hereditary thrombophilia in ethnic Omani patients.
PMID 16432849·Am J Hematol·2006
8-other
Angiotensinogen gene associated polymorphisms and risk of stroke in sickle cell anemia: Additional data supporting an association.
PMID 15224377·Am J Hematol·2004
8-other
Heterozygous methylene tetrahydrofolate reductase mutation with mild hyperhomocysteinemia associated with deep vein thrombosis.
PMID 15053809·Clin Lab Haematol·2004
5-case
Thrombosis-associated gene variants in sickle cell anemia.
PMID 11858507·Thromb Haemost·2002
8-other

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Address
500 W BERKELEY ST
UNIONTOWN, PA 15401

Location

Practice Location

500 W BERKELEY ST, UNIONTOWN, PA
(724) 430-6598

Quick Facts

NPI
1306158977
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
2
Locations
1
Publications
13

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