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KRISTIN BRADSHAW, PHARMD, BCPS
PHARMD, BCPS
Pharmacist
NPI: 1508640285Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
057205(NY)
Research & Publications (20)
On the dimensionality of the Proactive Coping Inventory: 7, 5, 3 factors?
PMID 19253071·Anxiety Stress Coping·2009
8-other
Family behavior therapy for substance abuse and other associated problems: a review of its intervention components and applicability.
PMID 19592601·Behav Modif·2009
6-review
Description of a standardized treatment center that utilizes evidence-based clinic operations to facilitate implementation of an evidence-based treatment.
PMID 19535671·Behav Modif·2009
8-other
Sequence variation at the human FOXO3 locus: a study of premature ovarian failure and primary amenorrhea.
PMID 17959613·Hum Reprod·2008
7-preclinical
Contribution of post-receptoral cells to the a-wave of the human photopic electroretinogram.
PMID 17850841·Vision Res·2007
8-other
High-field actively detuneable transverse electromagnetic (TEM) coil with low-bias voltage for high-power RF transmission.
PMID 17534919·Magn Reson Med·2007
8-other
4T split TEM volume head and knee coils for improved sensitivity and patient accessibility.
PMID 17533142·J Magn Reson·2007
8-other
The post-menopausal ovary displays a unique pattern of steroidogenic enzyme expression.
PMID 16253961·Hum Reprod·2006
8-other
Autophosphorylation of alphaCaMKII is not a general requirement for NMDA receptor-dependent LTP in the adult mouse.
PMID 16728448·J Physiol·2006
7-preclinical
Magnetic resonance imaging identifies features in clinically unaffected knees predicting extension of arthritis in children with monoarthritis.
PMID 16981289·J Rheumatol·2006
3-trial
Congenital stationary night blindness associated with mutations in GRM6 encoding glutamate receptor MGluR6.
PMID 16622103·Br J Ophthalmol·2006
5-case
Identification of novel RPGR ORF15 mutations in X-linked progressive cone-rod dystrophy (XLCORD) families.
PMID 15914600·Invest Ophthalmol Vis Sci·2005
8-other
X-linked retinoschisis: clinical phenotype and RS1 genotype in 86 UK patients.
PMID 15937075·J Med Genet·2005
8-other
Cone-rod dystrophy, intrafamilial variability, and incomplete penetrance associated with the R172W mutation in the peripherin/RDS gene.
PMID 16019073·Ophthalmology·2005
8-other
X-linked cone dysfunction syndrome with myopia and protanopia.
PMID 15953640·Ophthalmology·2005
8-other
Temperature sensitive oculocutaneous albinism associated with missense changes in the tyrosinase gene.
PMID 16170149·Br J Ophthalmol·2005
5-case
Is optic nerve fibre mis-routing a feature of congenital stationary night blindness?
PMID 16523234·Doc Ophthalmol·2005
4-observational
Blue cone monochromatism: a phenotype and genotype assessment with evidence of progressive loss of cone function in older individuals.
PMID 15094734·Eye (Lond)·2005
5-case
Autonomous activity of CaMKII is only transiently increased following the induction of long-term potentiation in the rat hippocampus.
PMID 15579161·Eur J Neurosci·2004
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 100 TECHNOLOGY CENTER DR
STOUGHTON, MA 02072 - Phone
- (781) 566-5066
Quick Facts
- NPI
- 1508640285
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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