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SCOTT MEAD, MD
MD
Hospitalist Physician
NPI: 1528034568IndividualAccepts Medicare
Specialties, Licenses & Credentials
Hospitalist PhysicianPrimary
Hospitalist
Code: 208M00000X
46707(WI)
CMS Specialties
PrimaryHOSPITALIST
Education
UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE
Class of 2002
Research & Publications (20)
No association of PGRN 3'UTR rs5848 in frontotemporal lobar degeneration.
PMID 19446372·Neurobiol Aging·2011
8-other
Progressive logopenic/phonological aphasia: erosion of the language network.
PMID 19679189·Neuroimage·2010
8-other
A small-scale randomized controlled trial of the revised new forest parenting programme for preschoolers with attention deficit hyperactivity disorder.
PMID 19404717·Eur Child Adolesc Psychiatry·2009
2-rct
Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study.
PMID 19081515·Lancet Neurol·2009
8-other
Seven-year discordance in age at onset in monozygotic twins with inherited prion disease (P102L).
PMID 19207267·Neuropathol Appl Neurobiol·2009
5-case
HECTD2 is associated with susceptibility to mouse and human prion disease.
PMID 19214206·PLoS Genet·2009
7-preclinical
Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration.
PMID 19217189·Neurobiol Aging·2009
8-other
DNA polymerase switching: effects on spontaneous mutagenesis in Escherichia coli.
PMID 19019142·Mol Microbiol·2009
8-other
Age of onset and death in inherited prion disease are heritable.
PMID 18729123·Am J Med Genet B Neuropsychiatr Genet·2009
8-other
First report of Creutzfeldt-Jakob disease occurring in 2 siblings unexplained by PRNP mutation.
PMID 18716560·J Neuropathol Exp Neurol·2008
5-case
Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series.
PMID 18757886·Brain·2008
8-other
Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type mice.
PMID 18316717·Proc Natl Acad Sci U S A·2008
7-preclinical
Association of a null allele of SPRN with variant Creutzfeldt-Jakob disease.
PMID 18805828·J Med Genet·2008
8-other
Mapping the progression of progranulin-associated frontotemporal lobar degeneration.
PMID 18648346·Nat Clin Pract Neurol·2008
5-case
Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin gene.
PMID 18413474·Arch Neurol·2008
5-case
Successful amplification of degraded DNA for use with high-throughput SNP genotyping platforms.
PMID 18551557·Hum Mutat·2008
8-other
Discovering and differentiating new and emerging clonal populations of Chlamydia trachomatis with a novel shotgun cell culture harvest assay.
PMID 18325260·Emerg Infect Dis·2008
8-other
A clinical study of kuru patients with long incubation periods at the end of the epidemic in Papua New Guinea.
PMID 18849289·Philos Trans R Soc Lond B Biol Sci·2008
8-other
Genetic susceptibility, evolution and the kuru epidemic.
PMID 18849290·Philos Trans R Soc Lond B Biol Sci·2008
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
- 600 HIGHLAND AVE
MADISON, WI 53792 - Phone
- (608) 263-2675
Quick Facts
- NPI
- 1528034568
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 24
- Publications
- 20
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