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FIRAS HENTATI, MD, MSCI
MD, MSCI
Student in an Organized Health Care Education/Training Program
NPI: 1326740648Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Peripheral neuropathy in inflammatory bowel disease patients: a prospective cohort study.
PMID 19681018·Scand J Gastroenterol·2009
8-other
Allelic ROBO3 heterogeneity in Tunisian patients with horizontal gaze palsy with progressive scoliosis.
PMID 19633821·J Mol Neurosci·2009
8-other
Characterization of DCTN1 genetic variability in neurodegeneration.
PMID 19506225·Neurology·2009
8-other
Man-in-the-barrel syndrome with combination of infarctions in the anterior spinal artery and posterior inferior cerebellar artery territories.
PMID 19153479·Cerebrovasc Dis·2009
5-case
LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study.
PMID 18539535·Lancet Neurol·2008
8-other
Autosomal recessive ataxia caused by three distinct gene defects in a single consanguineous family.
PMID 18569450·J Neurogenet·2008
8-other
BAFF is up-regulated in central nervous system of neuro-Behçet's disease.
PMID 18625522·J Neuroimmunol·2008
8-other
Variable cardiac involvement in Tunisian siblings harboring FKRP gene mutations.
PMID 18671187·Neuropediatrics·2008
5-case
A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease.
PMID 17433753·Parkinsonism Relat Disord·2008
8-other
The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa.
PMID 19064877·Neurology·2008
8-other
Sequence alterations within CYP7B1 implicate defective cholesterol homeostasis in motor-neuron degeneration.
PMID 18252231·Am J Hum Genet·2008
4-observational
L-2-hydroxyglutaric aciduria: clinical and molecular study in three Tunisian families. Identification of a new mutation and inter-familial phenotype variability.
PMID 18780161·J Inherit Metab Dis·2008
8-other
Wilson's disease: appreciable improvement of sub-cortical white matter abnormalities after copper chelating treatment: five years follow-up.
PMID 18991198·Neuropediatrics·2008
5-case
Osteoma of the calvaria in L-2-hydroxyglutaric aciduria.
PMID 17917788·J Inherit Metab Dis·2007
5-case
Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families.
PMID 17115391·Mov Disord·2007
8-other
[Study of dyslexia within school kids that suffer from epilepsia].
PMID 17288285·Tunis Med·2006
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 330 BROOKLINE AVE
BOSTON, MA 02215 - Phone
- (617) 667-7000
Quick Facts
- NPI
- 1326740648
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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