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JONATHAN ELION, MD
MD
Cardiovascular Disease Physician
NPI: 1346260676Individual
Specialties, Licenses & Credentials
Cardiovascular Disease PhysicianPrimary
Internal Medicine — Cardiovascular Disease
Code: 207RC0000X
MD07520(RI)
Research & Publications (20)
Vaso-occlusion in sickle cell anemia: role of interactions between blood cells and endothelium.
PMID 15190308·Hematol J·2004
6-review
Commensal Escherichia coli isolates are phylogenetically distributed among geographically distinct human populations.
PMID 11390698·Microbiology (Reading)·2001
8-other
Effects of RANTES and MBL2 gene polymorphisms in sickle cell disease clinical outcomes: association of the g.In1.1T>C RANTES variant with protection against infections.
PMID 19425063·Am J Hematol·2009
8-other
[Effect of hydroxyurea on adhesion proteins in sickle cell anemia].
PMID 19167870·Arch Pediatr·2009
8-other
Modulation of erythroid adhesion receptor expression by hydroxyurea in children with sickle cell disease.
PMID 18322255·Haematologica·2008
4-observational
The spectrum of cardiac anomalies in Noonan syndrome as a result of mutations in the PTPN11 gene.
PMID 17515436·Pediatrics·2007
4-observational
Variants of the mannose-binding lectin gene in the Benin population: heterozygosity for the p.G57E allele may confer a selective advantage.
PMID 18494378·Hum Biol·2007
8-other
Sodium phenyl butyrate downregulates endothelin-1 expression in cultured human endothelial cells: relevance to sickle-cell disease.
PMID 17373676·Am J Hematol·2007
8-other
Sickle cell anemia in Guadeloupean children: pattern and prevalence of acute clinical events.
PMID 16451394·Eur J Haematol·2006
8-other
UGT1A1 polymorphism outweighs the modest effect of deletional (-3.7 kb) alpha-thalassemia on cholelithogenesis in sickle cell anemia.
PMID 16628735·Am J Hematol·2006
8-other
MtDNA haplogroup analysis of black Brazilian and sub-Saharan populations: implications for the Atlantic slave trade.
PMID 16900880·Hum Biol·2006
8-other
Origin of the prevalent SFTPB indel g.1549C > GAA (121ins2) mutation causing surfactant protein B (SP-B) deficiency.
PMID 16333843·Am J Med Genet A·2006
8-other
ET-1 and ecNOS gene polymorphisms andsusceptibility to acute chest syndrome and painful vaso-occlusive crises in children with sickle cell anemia.
PMID 16956834·Haematologica·2006
8-other
Decreased plasma endothelin-1 levels in children with sickle cell disease treated with hydroxyurea.
PMID 15749673·Haematologica·2005
8-other
Molecular basis of methylmalonyl-CoA mutase apoenzyme defect in 40 European patients affected by mut(o) and mut- forms of methylmalonic acidemia: identification of 29 novel mutations in the MUT gene.
PMID 15643616·Hum Mutat·2005
8-other
Association of UGT1A1 polymorphism with prevalence and age at onset of cholelithiasis in sickle cell anemia.
PMID 15710570·Haematologica·2005
8-other
The phylogeography of mitochondrial DNA haplogroup L3g in Africa and the Atlantic slave trade.
PMID 15284954·Am J Hum Genet·2004
8-other
The placental-umbilical unit in sickle cell disease pregnancy: a model for studying in vivo functional adjustments to hypoxia in humans.
PMID 15668892·Hum Pathol·2004
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
- 208 COLLYER ST, STE 100
PROVIDENCE, RI 02904 - Phone
- (401) 793-7191
Quick Facts
- NPI
- 1346260676
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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