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GABRIEL HAYEK, MD, DMD
MD, DMD
Oral and Maxillofacial Surgery (Dentist)
NPI: 1730533753Individual
Specialties, Licenses & Credentials
Oral and Maxillofacial Surgery (Dentist)Primary
Dentist — Oral and Maxillofacial Surgery
Code: 1223S0112X
38141(TX)
Research & Publications (20)
Early-onset seizure variant of Rett syndrome: definition of the clinical diagnostic criteria.
PMID 19362436·Brain Dev·2010
8-other
Diagnostic criteria for the Zappella variant of Rett syndrome (the preserved speech variant).
PMID 18562141·Brain Dev·2009
8-other
Combined sciatic, femoral and obturator nerve blocks for an infra-inguinal arterial bypass graft surgery.
PMID 19128327·Acta Anaesthesiol Scand·2009
8-other
Delineation of the phenotype associated with 7q36.1q36.2 deletion: long QT syndrome, renal hypoplasia and mental retardation.
PMID 18348270·Am J Med Genet A·2008
5-case
Correlation between central venous oxygen saturation and oxygen delivery changes following fluid therapy.
PMID 18823459·Acta Anaesthesiol Scand·2008
8-other
A case report: bone marrow mesenchymal stem cells from a Rett syndrome patient are prone to senescence and show a lower degree of apoptosis.
PMID 18059018·J Cell Biochem·2008
5-case
FOXG1 is responsible for the congenital variant of Rett syndrome.
PMID 18571142·Am J Hum Genet·2008
5-case
MECP2 deletions and genotype-phenotype correlation in Rett syndrome.
PMID 17968969·Am J Med Genet A·2007
8-other
Clinical and molecular characterization of a patient with a 2q31.2-32.3 deletion identified by array-CGH.
PMID 17352388·Am J Med Genet A·2007
5-case
[Abdominal compartment syndrome after cardiac surgery].
PMID 17629657·Ann Fr Anesth Reanim·2007
5-case
Staged anesthesia for combined carotid and coronary artery revascularization: a different approach.
PMID 17138084·J Cardiothorac Vasc Anesth·2006
8-other
Attention-deficit/hyperactivity disorder (ADHD) and variable clinical expression of Aarskog-Scott syndrome due to a novel FGD1 gene mutation (R408Q).
PMID 15809997·Am J Med Genet A·2005
5-case
CDKL5/STK9 is mutated in Rett syndrome variant with infantile spasms.
PMID 15689447·J Med Genet·2005
5-case
Germline mosaicism in Rett syndrome identified by prenatal diagnosis.
PMID 15691364·Clin Genet·2005
5-case
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome.
PMID 15917271·Hum Mol Genet·2005
7-preclinical
Real-time quantitative PCR as a routine method for screening large rearrangements in Rett syndrome: Report of one case of MECP2 deletion and one case of MECP2 duplication.
PMID 15241799·Hum Mutat·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
- 34 DALE RD STE 105
AVON, CT 06001 - Phone
- (860) 679-8079
Quick Facts
- NPI
- 1730533753
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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