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LAWRENCE GOLBE, MD

MD

Neurology Physician

NPI: 1215002795Individual

Specialties, Licenses & Credentials

Neurology PhysicianPrimary

Psychiatry & Neurology — Neurology

Code: 2084N0400X

25MA04180600(NJ)

Research & Publications (20)

The epidemiology of progressive supranuclear palsy.
PMID 18631768·Handb Clin Neurol·2008
8-other
An 81-year-old man with imbalance and memory impairment.
PMID 17404198·Neurology·2007
5-case
Glutathione S-transferase polymorphisms and onset age in alpha-synuclein A53T mutant Parkinson's disease.
PMID 17034008·Am J Med Genet B Neuropsychiatr Genet·2007
8-other
Alpha-synuclein and Parkinson's disease.
PMID 12442675·Adv Neurol·2003
6-review
Progressive Supranuclear Palsy.
PMID 11581524·Curr Treat Options Neurol·2001
8-other
The tau A0 allele in Parkinson's disease.
PMID 11391737·Mov Disord·2001
1-meta
Progressive supranuclear palsy in the molecular age.
PMID 11036887·Lancet·2000
8-other
A clinical rating scale for progressive supranuclear palsy.
PMID 17405767·Brain·2007
4-observational
Early diagnosis of progressive supranuclear palsy: bucking the odds.
PMID 19029515·Neurology·2008
8-other
The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study.
PMID 18986508·BMC Med·2008
4-observational
Huntington CAG repeat size does not modify onset age in familial Parkinson's disease: the GenePD study.
PMID 18649400·Mov Disord·2008
4-observational
Replication of association between ELAVL4 and Parkinson disease: the GenePD study.
PMID 18587682·Hum Genet·2008
4-observational
Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study.
PMID 18509094·Neurology·2008
4-observational
Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.
PMID 17357082·Am J Hum Genet·2007
8-other
Herbicide exposure modifies GSTP1 haplotype association to Parkinson onset age: the GenePD Study.
PMID 17190945·Neurology·2006
8-other
Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study.
PMID 16769863·Arch Neurol·2006
4-observational
HS1-BP3 gene variant is common in familial essential tremor.
PMID 16211613·Mov Disord·2006
8-other
Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial Parkinson's disease from the GenePD study.
PMID 15966003·Mov Disord·2005
8-other
BDNF genetic variants are associated with onset age of familial Parkinson disease: GenePD Study.
PMID 16344533·Neurology·2005
8-other
Woman with a 26-year history of parkinsonism, supranuclear ophthalmoplegia, and loss of postural reflexes.
PMID 15300663·Mov Disord·2004
5-case

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

Contact & Hours

Address
125 PATERSON ST, SUITE 6100
NEW BRUNSWICK, NJ 08901

Location

Practice Location

125 PATERSON ST, NEW BRUNSWICK, NJ
(732) 235-7733

Quick Facts

NPI
1215002795
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
20

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