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RICHARD TUPLER, MD

MD

Diagnostic Radiology Physician

NPI: 1487659496IndividualAccepts Medicare

Specialties, Licenses & Credentials

Diagnostic Radiology PhysicianPrimary

Radiology — Diagnostic Radiology

Code: 2085R0202X

09720R(LA)
Body Imaging Physician

Radiology — Body Imaging

Code: 2085B0100X

MD.09720R(LA)

CMS Specialties

PrimaryDIAGNOSTIC RADIOLOGY

Education

UNIVERSITY OF FLORIDA COLLEGE OF MEDICINE

Class of 1988

Research & Publications (14)

Molecular basis of facioscapulohumeral muscular dystrophy.
PMID 15004695·Cell Mol Life Sci·2004
6-review
Novel mitochondrial tRNA Leu(CUN) transition and D4Z4 partial deletion in a patient with a facioscapulohumeral phenotype.
PMID 18343111·Neuromuscul Disord·2008
5-case
Facioscapulohumeral muscular dystrophy: a multicenter study on hearing function.
PMID 17715463·Audiol Neurootol·2008
4-observational
Structural and functional alterations of muscle fibres in the novel mouse model of facioscapulohumeral muscular dystrophy.
PMID 17855756·J Physiol·2007
7-preclinical
Facioscapulohumeral muscular dystrophy and occurrence of heart arrhythmia.
PMID 16804309·Eur Neurol·2006
4-observational
Altered gene silencing and human diseases.
PMID 16451126·Clin Genet·2006
6-review
Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1.
PMID 16341202·Nature·2006
7-preclinical
Facioscapulohumeral muscular dystrophy type 1A in northwestern Tuscany: a molecular genetics-based epidemiological and genotype-phenotype study.
PMID 15857184·Genet Test·2005
8-other
When enough is enough: genetic diseases associated with transcriptional derepression.
PMID 15172674·Curr Opin Genet Dev·2004
6-review
Transcriptional derepression as a cause of genetic diseases.
PMID 12787785·Curr Opin Genet Dev·2003
6-review
An Italian family affected by Nasu-Hakola disease with a novel genetic mutation in the TREM2 gene.
PMID 12754369·J Neurol Neurosurg Psychiatry·2003
5-case
A locus for migraine without aura maps on chromosome 14q21.2-q22.3.
PMID 12474141·Am J Hum Genet·2003
8-other
Inappropriate gene activation in FSHD: a repressor complex binds a chromosomal repeat deleted in dystrophic muscle.
PMID 12176321·Cell·2002
7-preclinical
Expressing the human genome.
PMID 11237001·Nature·2001
7-preclinical

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

Contact & Hours

Address
1514 JEFFERSON HIGHWAY
NEW ORLEANS, LA 70121

Location

Practice Location

1514 JEFFERSON HIGHWAY, NEW ORLEANS, LA
(504) 842-4000

Quick Facts

NPI
1487659496
Entity Type
Individual
Gender
Male
Medicare
Accepted
Specialties
2
Locations
1
Years in Practice
38
Publications
14

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