Back to Search
KIMBERLY BORK, D.M.D.
D.M.D.
General Practice Dentistry
NPI: 1609216670Individual
Specialties, Licenses & Credentials
General Practice DentistryPrimary
Dentist — General Practice
Code: 1223G0001X
D1033(SD)
Research & Publications (20)
Hereditary angioedema caused by missense mutations in the factor XII gene: clinical features, trigger factors, and therapy.
PMID 19477491·J Allergy Clin Immunol·2009
8-other
Application of the gingival contour plaque index: six-month plaque and gingivitis study.
PMID 19476084·J Vet Dent·2009
4-observational
Energy reflectance and tympanometry in normal and otosclerotic ears.
PMID 19194289·Ear Hear·2009
3-trial
Increasing the sialylation of therapeutic glycoproteins: the potential of the sialic acid biosynthetic pathway.
PMID 19199295·J Pharm Sci·2009
6-review
Beyond glycosylation: sialic acid precursors act as signaling molecules and are involved in cellular control of differentiation of PC12 cells.
PMID 19361277·Biol Chem·2009
6-review
Kallikrein-kinin system and fibrinolysis in hereditary angioedema due to factor XII gene mutation Thr309Lys.
PMID 19474702·Blood Coagul Fibrinolysis·2009
8-other
Hereditary angioedema: increased number of attacks after frequent treatments with C1 inhibitor concentrate.
PMID 19635282·Am J Med·2009
8-other
Treatment of skin swellings with C1-inhibitor concentrate in patients with hereditary angio-oedema.
PMID 18445189·Allergy·2008
8-other
Benefits and risks of danazol in hereditary angioedema: a long-term survey of 118 patients.
PMID 18320917·Ann Allergy Asthma Immunol·2008
4-observational
Mutational spectrum of the C1INH (SERPING1) gene in patients with hereditary angioedema.
PMID 18758157·Cytogenet Genome Res·2008
8-other
Disease expression in women with hereditary angioedema.
PMID 18554570·Am J Obstet Gynecol·2008
8-other
Functional C1-inhibitor diagnostics in hereditary angioedema: assay evaluation and recommendations.
PMID 18655790·J Immunol Methods·2008
8-other
Hereditary angiodema: a current state-of-the-art review, VII: Canadian Hungarian 2007 International Consensus Algorithm for the Diagnosis, Therapy, and Management of Hereditary Angioedema.
PMID 18220150·Ann Allergy Asthma Immunol·2008
6-review
N-propanoylmannosamine interferes with O-GlcNAc modification of the tyrosine 3-monooxygenase and stimulates dopamine secretion.
PMID 17896794·J Neurosci Res·2008
7-preclinical
Helicobacter pylori infection as a triggering factor of attacks in patients with hereditary angioedema.
PMID 17493006·Helicobacter·2007
4-observational
Enhanced sialylation of EPO by overexpression of UDP-GlcNAc 2-epimerase/ManAc kinase containing a sialuria mutation in CHO cells.
PMID 17706199·FEBS Lett·2007
7-preclinical
Hereditary angioedema with normal C1 inhibitor: clinical symptoms and course.
PMID 17976427·Am J Med·2007
8-other
Experimental approaches to interfere with the polysialylation of the neural cell adhesion molecule in vitro and in vivo.
PMID 17986141·J Neurochem·2007
6-review
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 304 W. HIGHWAY 38, SUITE 138
HARTFORD, SD 57033 - Phone
- (605) 528-6750
Quick Facts
- NPI
- 1609216670
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile