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KARI HILBERT, PHARMD
PHARMD
Pharmacist
NPI: 1306379292Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
RP438509(PA)
Research & Publications (7)
Mutations in MMP9 and MMP13 determine the mode of inheritance and the clinical spectrum of metaphyseal anadysplasia.
PMID 19615667·Am J Hum Genet·2009
7-preclinical
The Faces Symbol Test, a newly developed screening instrument to assess cognitive decline related to multiple sclerosis: first results of the Berlin Multi-Centre FST Validation Study.
PMID 17439910·Mult Scler·2007
4-observational
Du Pan syndrome phenotype caused by heterozygous pathogenic mutations in CDMP1 gene.
PMID 16222676·Am J Med Genet A·2005
5-case
Dominant negative mutations in the C-propeptide of COL2A1 cause platyspondylic lethal skeletal dysplasia, torrance type, and define a novel subfamily within the type 2 collagenopathies.
PMID 15643621·Am J Med Genet A·2005
5-case
Spondyloperipheral dysplasia is caused by truncating mutations in the C-propeptide of COL2A1.
PMID 15316962·Am J Med Genet A·2004
5-case
A novel mutation in FGFR-3 disrupts a putative N-glycosylation site and results in hypochondroplasia.
PMID 11015576·Physiol Genomics·2000
5-case
Mtr1, a novel biallelically expressed gene in the center of the mouse distal chromosome 7 imprinting cluster, is a member of the Trp gene family.
PMID 10903843·Genomics·2000
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
- 100 N ACADEMY AVE
DANVILLE, PA 17822 - Phone
- (570) 271-6211
Quick Facts
- NPI
- 1306379292
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 7
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