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JOSEPH HAZAN, MD

MD

Obstetrics & Gynecology Physician

NPI: 1881786960IndividualAccepts Medicare

Specialties, Licenses & Credentials

Obstetrics & Gynecology PhysicianPrimary

Obstetrics & Gynecology

Code: 207V00000X

35321(MO)

CMS Specialties

PrimaryOBSTETRICS/GYNECOLOGY

Education

OTHER

Class of 1971

Research & Publications (13)

A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21.
PMID 17515546·Neurology·2007
5-case
Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description.
PMID 17503452·Am J Med Genet B Neuropsychiatr Genet·2007
8-other
The homeodomain transcription factor drg11 is expressed in primary sensory neurons and their putative CNS targets during embryonic development of the zebrafish.
PMID 17045851·Gene Expr Patterns·2007
7-preclinical
Evidence of functional redundancy between MID proteins: implications for the presentation of Opitz syndrome.
PMID 15617684·Dev Biol·2005
4-observational
Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A.
PMID 15517445·Neurogenetics·2004
8-other
Motor system abnormalities in hereditary spastic paraparesis type 4 (SPG4) depend on the type of mutation in the spastin gene.
PMID 12876245·J Neurol Neurosurg Psychiatry·2003
8-other
Mutations of SPG4 are responsible for a loss of function of spastin, an abundant neuronal protein localized in the nucleus.
PMID 12490534·Hum Mol Genet·2003
7-preclinical
Autosomal dominant (AD) pure spastic paraplegia (HSP) linked to locus SPG4 affects almost exclusively males in a large pedigree.
PMID 12471215·J Med Genet·2002
8-other
Hereditary spastic paraplegia caused by mutations in the SPG4 gene.
PMID 11039577·Eur J Hum Genet·2000
8-other
Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis.
PMID 11015453·J Med Genet·2000
8-other
Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia.
PMID 10699187·Hum Mol Genet·2000
8-other
A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24-q34.
PMID 10677329·Am J Hum Genet·2000
8-other
No evidence for long CAG/CTG repeats in families with spastic paraplegia linked to chromosome 2p21-24.
PMID 10670783·Neurosci Lett·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
4200 N CLOVERLEAF DR, STE H
ST PETERS, MO 63376

Location

Practice Location

4200 N CLOVERLEAF DR, ST PETERS, MO
(636) 928-1800

Quick Facts

NPI
1881786960
Entity Type
Individual
Gender
Male
Medicare
Accepted
Specialties
1
Locations
1
Years in Practice
55
Publications
13

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