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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
Code: 390200000X
MT197453(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
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 - Phone
- (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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