Back to Search
IRIS EISENBERG, MD
MD
Pediatric Adolescent Medicine Physician
NPI: 1326046350Individual
Specialties, Licenses & Credentials
Pediatric Adolescent Medicine PhysicianPrimary
Pediatrics — Adolescent Medicine
Code: 2080A0000X
ME32409(FL)
Research & Publications (17)
Transcriptional regulation differs in affected facioscapulohumeral muscular dystrophy patients compared to asymptomatic related carriers.
PMID 19339494·Proc Natl Acad Sci U S A·2009
4-observational
Attention deficit hyperactivity disorder in obese melanocortin-4-receptor (MC4R) deficient subjects: a newly described expression of MC4R deficiency.
PMID 18777518·Am J Med Genet B Neuropsychiatr Genet·2008
8-other
Mitochondrial processes are impaired in hereditary inclusion body myopathy.
PMID 18723858·Hum Mol Genet·2008
8-other
Distinctive patterns of microRNA expression in primary muscular disorders.
PMID 17942673·Proc Natl Acad Sci U S A·2007
8-other
Multimarker RT-PCR assay for the detection of minimal residual disease in sentinel lymph nodes of breast cancer patients.
PMID 16495929·Br J Cancer·2006
8-other
No overall hyposialylation in hereditary inclusion body myopathy myoblasts carrying the homozygous M712T GNE mutation.
PMID 15670773·Biochem Biophys Res Commun·2005
4-observational
The homozygous M712T mutation of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase results in reduced enzyme activities but not in altered overall cellular sialylation in hereditary inclusion body myopathy.
PMID 15147877·FEBS Lett·2004
7-preclinical
Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy.
PMID 12847185·Neurology·2003
8-other
Hereditary inclusion body myopathy: the Middle Eastern genetic cluster.
PMID 12743242·Neurology·2003
5-case
Mutations spectrum of GNE in hereditary inclusion body myopathy sparing the quadriceps.
PMID 12497639·Hum Mutat·2003
8-other
Establishment of the genomic structure and identification of thirteen single-nucleotide polymorphisms in the human RECK gene.
PMID 12438739·Cytogenet Genome Res·2002
8-other
Cloning and characterization of a human novel gene C9orf19 encoding a conserved putative protein with an SCP-like extracellular protein domain.
PMID 12137952·Gene·2002
8-other
Cloning and characterization of a novel human gene RNF38 encoding a conserved putative protein with a RING finger domain.
PMID 12074600·Biochem Biophys Res Commun·2002
7-preclinical
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy.
PMID 11528398·Nat Genet·2001
8-other
Physical and transcriptional map of the hereditary inclusion body myopathy locus on chromosome 9p12-p13.
PMID 11464241·Eur J Hum Genet·2001
8-other
Muscular dystrophy due to dysferlin deficiency in Libyan Jews. Clinical and genetic features.
PMID 10825360·Brain·2000
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
- 11521 N MAIN ST
JACKSONVILLE, FL 32218 - Phone
- (904) 751-9491
Quick Facts
- NPI
- 1326046350
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 17
Are you this provider?
Claim Your Profile