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LEORA HILBERT, DMD, MS
DMD, MS
General Practice Dentistry
NPI: 1649957655Individual
Specialties, Licenses & Credentials
General Practice DentistryPrimary
Dentist — General Practice
Code: 1223G0001X
04850(NH)
Research & Publications (20)
Expression of 14 von Willebrand factor mutations identified in patients with type 1 von Willebrand disease from the MCMDM-1VWD study.
PMID 19566550·J Thromb Haemost·2009
7-preclinical
Silver-palladium surfaces inhibit biofilm formation.
PMID 19151185·Appl Environ Microbiol·2009
8-other
Nickel-containing coins: a health risk for nickel-sensitive individuals?
PMID 17107412·Br J Dermatol·2006
8-other
Type 2N von Willebrand disease due to compound heterozygosity for R854Q and a novel R763G mutation at the cleavage site of von Willebrand factor propeptide.
PMID 16953269·Thromb Haemost·2006
5-case
Measurement of von Willebrand factor binding to a recombinant fragment of glycoprotein Ibalpha in an enzyme-linked immunosorbent assay-based method: performances in patients with type 2B von Willebrand disease.
PMID 16704443·Br J Haematol·2006
8-other
GJB2 mutations and additional disabilities in a pediatric cochlear implant population.
PMID 16154643·Int J Pediatr Otorhinolaryngol·2006
8-other
First identification and expression of a type 2N von Willebrand disease mutation (E1078K) located in exon 25 of von Willebrand factor gene.
PMID 15613050·J Thromb Haemost·2004
5-case
Expression of two type 2N von Willebrand disease mutations identified in exon 18 of von Willebrand factor gene.
PMID 15461624·Br J Haematol·2004
5-case
A new candidate mutation, G1629R, in a patient with type 2A von Willebrand's disease: basic mechanisms and clinical implications.
PMID 15377475·Haematologica·2004
5-case
In vitro study of a triple-secured von Willebrand factor concentrate.
PMID 15023178·Vox Sang·2004
4-observational
Biologic response to desmopressin in patients with severe type 1 and type 2 von Willebrand disease: results of a multicenter European study.
PMID 14630825·Blood·2004
3-trial
Two novel mutations, Q1053H and C1060R, located in the D3 domain of von Willebrand factor, are responsible for decreased FVIII-binding capacity.
PMID 12588349·Br J Haematol·2003
7-preclinical
Clinical and audiological features in auditory neuropathy.
PMID 12220206·Arch Otolaryngol Head Neck Surg·2002
8-other
Identification of a new type 2M von Willebrand disease mutation also at position 1324 of von Willebrand factor.
PMID 12008946·Thromb Haemost·2002
5-case
Comparison of adhesion of the food spoilage bacterium Shewanella putrefaciens to stainless steel and silver surfaces.
PMID 11972695·J Appl Microbiol·2002
4-observational
Type 2 von Willebrand disease causing defective von Willebrand factor-dependent platelet function.
PMID 11686104·Best Pract Res Clin Haematol·2001
6-review
Type 2N von Willebrand disease: clinical manifestations, pathophysiology, laboratory diagnosis and molecular biology.
PMID 11686103·Best Pract Res Clin Haematol·2001
6-review
A standard nomenclature for von Willebrand factor gene mutations and polymorphisms. On behalf of the ISTH SSC Subcommittee on von Willebrand factor.
PMID 11372690·Thromb Haemost·2001
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
- 650 COURT ST STE 4
KEENE, NH 03431 - Phone
- (603) 352-0006
Quick Facts
- NPI
- 1649957655
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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