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JENNIFER CALVERT HARDY MD
MD
Pediatrics Physician
NPI: 1407903206Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
M9187(TX)
Research & Publications (20)
Design and organization of an equine intensive care unit.
PMID 15062456·Vet Clin North Am Equine Pract·2004
6-review
Functional characterization of three single-nucleotide polymorphisms present in the human APOE promoter sequence: Differential effects in neuronal cells and on DNA-protein interactions.
PMID 19504470·Am J Med Genet B Neuropsychiatr Genet·2010
7-preclinical
Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP.
PMID 18667258·Neurobiol Aging·2010
8-other
Clinical and pathological features of an Alzheimer's disease patient with the MAPT Delta K280 mutation.
PMID 17723255·Neurobiol Aging·2009
5-case
The T cell STAT signaling network is reprogrammed within hours of bacteremia via secondary signals.
PMID 19494279·J Immunol·2009
7-preclinical
Prioritising drugs for single patient (n-of-1) trials in palliative care.
PMID 19605605·Palliat Med·2009
8-other
Glucocerebrosidase mutations in 108 neuropathologically confirmed cases of multiple system atrophy.
PMID 19332698·Neurology·2009
5-case
The genetics of Parkinson's syndromes: a critical review.
PMID 19419854·Curr Opin Genet Dev·2009
6-review
Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Greece.
PMID 19383421·Neurosci Lett·2009
8-other
Clopidogrel induces an acute hemostatic deficit and increases intra abdominal bleeding in rabbits.
PMID 19128824·Thromb Res·2009
7-preclinical
Synergistic effects on gene delivery--co-formulation of small disulfide-linked dendritic polycations with Lipofectamine 2000.
PMID 19194595·Org Biomol Chem·2009
8-other
Rehabilitation for older people in long-term care.
PMID 19160233·Cochrane Database Syst Rev·2009
1-meta
Role of high-order aberrations in senescent changes in spatial vision.
PMID 19271934·J Vis·2009
8-other
A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease.
PMID 19375058·Am J Hum Genet·2009
8-other
Measures of autozygosity in decline: globalization, urbanization, and its implications for medical genetics.
PMID 19282984·PLoS Genet·2009
8-other
Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease.
PMID 19286695·Brain·2009
4-observational
Robust production of a peptide library using methodological synchronization.
PMID 19457455·Protein Expr Purif·2009
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
- 706 TURTLE CREEK DR
TYLER, TX 75701 - Phone
- (903) 595-3942
Quick Facts
- NPI
- 1407903206
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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