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JIHAD HAYEK, MD

MD

Clinical Pathology/Laboratory Medicine Physician

NPI: 1568441749IndividualAccepts Medicare

Specialties, Licenses & Credentials

Clinical Pathology/Laboratory Medicine PhysicianPrimary

Pathology — Clinical Pathology/Laboratory Medicine

Code: 207ZP0105X

75245(MA)

CMS Specialties

PrimaryPATHOLOGY

Education

OTHER

Class of 1986

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
Systemic oxidative stress in classic Rett syndrome.
PMID 19464363·Free Radic Biol Med·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
Rett syndrome and plasma leptin levels.
PMID 17188610·J Pediatr·2007
8-other
Images in cardiovascular medicine. Angiography of an aneurysmal aorto-left ventricular tunnel.
PMID 17893281·Circulation·2007
5-case
Magnesium profile in autism.
PMID 16443999·Biol Trace Elem Res·2006
4-observational
Neurocutaneous syndrome with mental delay, autism, blockage in intracellular vescicular trafficking and melanosome defects.
PMID 16879294·Eur J Neurol·2006
5-case
Myoclonic encephalopathy in the CDKL5 gene mutation.
PMID 16326141·Clin Neurophysiol·2006
8-other
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
125 PARKER HILL AVE
ROXBURY CROSSING, MA 02120

Location

Practice Location

125 PARKER HILL AVE, ROXBURY CROSSING, MA
(617) 754-5800

Quick Facts

NPI
1568441749
Entity Type
Individual
Gender
Male
Medicare
Accepted
Specialties
1
Locations
1
Years in Practice
40
Publications
18

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