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SARAH JOINER, M.D.
M.D.
Internal Medicine Physician
NPI: 1508245622Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
T2972(MS)
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteins.
PMID 19218199·J Gen Virol·2009
7-preclinical
Central and peripheral pathology of kuru: pathological analysis of a recent case and comparison with other forms of human prion disease.
PMID 18849292·Philos Trans R Soc Lond B Biol Sci·2008
5-case
Review. The origin of the prion agent of kuru: molecular and biological strain typing.
PMID 18849291·Philos Trans R Soc Lond B Biol Sci·2008
6-review
Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series.
PMID 18757886·Brain·2008
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
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
Creutzfeldt-Jakob disease, prion protein gene codon 129VV, and a novel PrPSc type in a young British woman.
PMID 18071044·Arch Neurol·2007
5-case
Inherited prion disease with 5-OPRI: phenotype modification by repeat length and codon 129.
PMID 17709704·Neurology·2007
8-other
Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneity.
PMID 16923955·Brain·2006
8-other
Clinical presentation and pre-mortem diagnosis of variant Creutzfeldt-Jakob disease associated with blood transfusion: a case report.
PMID 17161728·Lancet·2006
5-case
Dissociation of pathological and molecular phenotype of variant Creutzfeldt-Jakob disease in transgenic human prion protein 129 heterozygous mice.
PMID 16809423·Proc Natl Acad Sci U S A·2006
7-preclinical
Phenotypic heterogeneity in inherited prion disease (P102L) is associated with differential propagation of protease-resistant wild-type and mutant prion protein.
PMID 16597650·Brain·2006
7-preclinical
Distinct glycoform ratios of protease resistant prion protein associated with PRNP point mutations.
PMID 16415305·Brain·2006
8-other
High levels of disease related prion protein in the ileum in variant Creutzfeldt-Jakob disease.
PMID 16162963·Gut·2005
8-other
Human prion protein with valine 129 prevents expression of variant CJD phenotype.
PMID 15539564·Science·2004
7-preclinical
Characterization of two distinct prion strains derived from bovine spongiform encephalopathy transmissions to inbred mice.
PMID 15269389·J Gen Virol·2004
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
- 1500 E WOODROW WILSON AVE
JACKSON, MS 39216 - Phone
- (601) 984-5601
Quick Facts
- NPI
- 1508245622
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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