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ENDALE MENGESHA, MD

MD

Hospitalist Physician

NPI: 1528556891IndividualAccepts Medicare

Specialties, Licenses & Credentials

Internal Medicine Physician

Internal Medicine

Code: 207R00000X

87816(GA)
Student in an Organized Health Care Education/Training Program

Student in an Organized Health Care Education/Training Program

Code: 390200000X

Hospitalist PhysicianPrimary

Hospitalist

Code: 208M00000X

87816(GA)

CMS Specialties

PrimaryINTERNAL MEDICINE

Additional

HOSPITALIST

Education

OTHER

Class of 2005

Research & Publications (14)

Phenotypic expression of maternally inherited deafness is affected by RNA modification and cytoplasmic ribosomal proteins.
PMID 19482502·Mol Genet Metab·2009
8-other
Genetic epistasis of IL23/IL17 pathway genes in Crohn's disease.
PMID 19235914·Inflamm Bowel Dis·2009
8-other
MAGI2 genetic variation and inflammatory bowel disease.
PMID 18720471·Inflamm Bowel Dis·2009
4-observational
IL23R haplotypes provide a large population attributable risk for Crohn's disease.
PMID 18470928·Inflamm Bowel Dis·2008
4-observational
Pleiotropic effects and compensation mechanisms determine tissue specificity in mitochondrial myopathy and sideroblastic anemia (MLASA).
PMID 17374500·Mol Genet Metab·2007
7-preclinical
IL-23 receptor (IL-23R) gene protects against pediatric Crohn's disease.
PMID 17309073·Inflamm Bowel Dis·2007
8-other
Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations.
PMID 16826519·Am J Hum Genet·2006
8-other
Human TRMU encoding the mitochondrial 5-methylaminomethyl-2-thiouridylate-methyltransferase is a putative nuclear modifier gene for the phenotypic expression of the deafness-associated 12S rRNA mutations.
PMID 16513084·Biochem Biophys Res Commun·2006
8-other
Mitochondrial myopathy and sideroblastic anemia (MLASA): missense mutation in the pseudouridine synthase 1 (PUS1) gene is associated with the loss of tRNA pseudouridylation.
PMID 15772074·J Biol Chem·2005
8-other
Phenotype of non-syndromic deafness associated with the mitochondrial A1555G mutation is modulated by mitochondrial RNA modifying enzymes MTO1 and GTPBP3.
PMID 15542390·Mol Genet Metab·2004
4-observational
Human mitochondrial transcription factor B1 as a modifier gene for hearing loss associated with the mitochondrial A1555G mutation.
PMID 15110318·Mol Genet Metab·2004
8-other
Missense mutation in pseudouridine synthase 1 (PUS1) causes mitochondrial myopathy and sideroblastic anemia (MLASA).
PMID 15108122·Am J Hum Genet·2004
8-other
Gene responsible for mitochondrial myopathy and sideroblastic anemia (MSA) maps to chromosome 12q24.33.
PMID 15103716·Am J Med Genet A·2004
5-case
Telomere shortening and decreased replicative potential, contrasted by continued proliferation of telomerase-positive CD8+CD28(lo) T cells in patients with systemic lupus erythematosus.
PMID 11318593·Clin Immunol·2001
8-other

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

Contact & Hours

Via practice · 2 locations total

Address
1968 PEACHTREE RD NW
ATLANTA, GA 30309

Locations (2)

Practice Location

1968 PEACHTREE RD NW, ATLANTA, GA
(404) 367-3014

Practice Location

303 PARKWAY DR NE, ATLANTA, GA
(770) 265-4919

Quick Facts

NPI
1528556891
Entity Type
Individual
Gender
Male
Medicare
Accepted
Specialties
3
Locations
2
Years in Practice
21
Publications
14

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