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MERCELL ENAYAT, DMD
DMD
Dentist
NPI: 1851181085Individual
Specialties, Licenses & Credentials
DentistPrimary
Dentist
Code: 122300000X
111458(CA)
Research & Publications (13)
Unique heterozygous intron 22 inversion band pattern in a haemophilic male detected by long polymerase chain reaction (PCR).
PMID 18392336·Thromb Haemost·2008
5-case
Signal-averaged P-wave ECG as a marker of atrial electrical instability in patients with right ventricular dysfunction.
PMID 18204176·J Physiol Pharmacol·2007
8-other
The R2464C missense mutation in the von Willebrand factor gene causes a novel abnormality of multimer electrophoretic mobility and falls into the subgroup of type 2 von Willebrand disease 'unclassified'.
PMID 17200787·Thromb Haemost·2007
8-other
Distinguishing between type 2B and pseudo-von Willebrand disease and its clinical importance.
PMID 16704444·Br J Haematol·2006
8-other
Mutation analysis in F9 gene of 17 families with haemophilia B from Iran.
PMID 15569175·Haemophilia·2004
8-other
Identification of intron 1 and 22 inversion mutations in the factor VIII gene of 124 Iranian families with severe haemophilia A.
PMID 15230960·Haemophilia·2004
8-other
Successful treatment of congenital thrombotic thrombocytopenic purpura using the intermediate purity factor VIII concentrate BPL 8Y.
PMID 12358923·Br J Haematol·2002
5-case
Aberrant dimerization of von Willebrand factor as the result of mutations in the carboxy-terminal region: identification of 3 mutations in members of 3 different families with type 2A (phenotype IID) von Willebrand disease.
PMID 11468166·Blood·2001
7-preclinical
Site and type of mutations in the factor VIII gene in patients and carriers of haemophilia A.
PMID 11442643·Haemophilia·2001
8-other
Homozygous gene conversion in von Willebrand factor gene as a cause of type 3 von Willebrand disease and predisposition to inhibitor development.
PMID 11439975·Blood·2001
5-case
Identification of type 2 von Willebrand disease in previously diagnosed type 1 patients: a reappraisal using phenotypes, genotypes and molecular modelling.
PMID 11154147·Thromb Haemost·2000
4-observational
A new candidate missense mutation (Leu 1657 IIe) in an apparently asymptomatic type 2A (phenotype IIA) von Willebrand disease family.
PMID 11019957·Thromb Haemost·2000
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 200 S WELLS RD STE 225
VENTURA, CA 93004 - Phone
- (805) 659-0560
Quick Facts
- NPI
- 1851181085
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 13
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