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JOSEPH HAYEK, M.D.
M.D.
Ophthalmology Physician
NPI: 1720519440IndividualAccepts Medicare
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Ophthalmology PhysicianPrimary
Ophthalmology
Code: 207W00000X
89576(GA)
CMS Specialties
PrimaryOPHTHALMOLOGY
Education
OHIO STATE UNIVERSITY COLLEGE OF MEDICINE
Class of 2017
Research & Publications (18)
[(1)H] magnetic resonance spectroscopy of urine: diagnosis of a guanidinoacetate methyl transferase deficiency case.
PMID 19461121·J Child Neurol·2010
5-case
Long-term plasma levels of leptin and adiponectin in Rett syndrome.
PMID 18710461·Clin Endocrinol (Oxf)·2009
8-other
Guanidinoacetate methyltransferase (GAMT) deficiency diagnosed by proton NMR spectroscopy of body fluids.
PMID 19288536·NMR Biomed·2009
8-other
Re: CDKL5 mutations in boys with severe encephalopathy and early-onset intractable epilepsy.
PMID 19564590·Neurology·2009
8-other
Polydactyly with ectodermal defect, osteopenia, and mental delay.
PMID 18182642·J Child Neurol·2008
5-case
Drug-resistant epilepsy and epileptic phenotype-EEG association in MECP2 mutated Rett syndrome.
PMID 18842453·Clin Neurophysiol·2008
8-other
Bone ultrasonography at phalanxes in patients with Rett syndrome: a 3-year longitudinal study.
PMID 18242156·Bone·2008
8-other
New neurocutaneous syndrome with defect in cell trafficking and melanosome pathway: the future challenge.
PMID 18226865·Brain Dev·2008
5-case
Sympathetic overactivity and plasma leptin levels in Rett syndrome.
PMID 18226448·Neurosci Lett·2008
8-other
Focal cortical dysplasia type 1b as a cause of severe epilepsy with multiple independent spike foci.
PMID 17583458·Brain Dev·2008
5-case
Kabuki syndrome with trichrome vitiligo, ectodermal defect and hypogammaglobulinemia A and G.
PMID 17174051·Brain Dev·2007
5-case
Images in cardiovascular medicine. Angiography of an aneurysmal aorto-left ventricular tunnel.
PMID 17893281·Circulation·2007
5-case
Neurocutaneous syndrome with mental delay, autism, blockage in intracellular vescicular trafficking and melanosome defects.
PMID 16879294·Eur J Neurol·2006
5-case
SCN1A (2528delG) novel truncating mutation with benign outcome of severe myoclonic epilepsy of infancy.
PMID 16505326·Neurology·2006
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
- 517 GREAT OAKS DR STE 101
MONROE, GA 30655 - Phone
- (770) 267-4561
Quick Facts
- NPI
- 1720519440
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 9
- Publications
- 18
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