Back to Search
GENEVIEVE HAYEK, MD
MD
Vascular Surgery Physician
NPI: 1679952048IndividualAccepts Medicare
Specialties, Licenses & Credentials
Surgery Physician
Surgery
Code: 208600000X
2020014578(MO)
Vascular Surgery PhysicianPrimary
Surgery — Vascular Surgery
Code: 2086S0129X
2020014578(MO)311065(LA)
CMS Specialties
PrimaryGENERAL SURGERY
Education
OTHER
Class of 2014
Research & Publications (20)
Early-onset seizure variant of Rett syndrome: definition of the clinical diagnostic criteria.
PMID 19362436·Brain Dev·2010
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
Diagnostic criteria for the Zappella variant of Rett syndrome (the preserved speech variant).
PMID 18562141·Brain Dev·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
FOXG1 is responsible for the congenital variant of Rett syndrome.
PMID 18571142·Am J Hum Genet·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
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
Via practice · 2 locations total
- Address
- 1514 JEFFERSON HWY
NEW ORLEANS, LA 70121 - Phone
- (504) 842-5293
Quick Facts
- NPI
- 1679952048
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 2
- Years in Practice
- 12
- Publications
- 20
Are you this provider?
Claim Your Profile