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SAMEEN BELAL DO
DO
Student in an Organized Health Care Education/Training Program
NPI: 1255072344Individual
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)
Tunisian hereditary spastic paraplegias: clinical variability supported by genetic heterogeneity.
PMID 19438933·Clin Genet·2009
8-other
Hereditary spastic paraplegia with mental impairment and thin corpus callosum in Tunisia: SPG11, SPG15, and further genetic heterogeneity.
PMID 18332254·Arch Neurol·2008
8-other
The independent components of auditory P300 and CNV evoked potentials derived from single-trial recordings.
PMID 17664670·Physiol Meas·2007
8-other
An intelligent ventilation and oxygenation management system in neonatal intensive care using fuzzy trend template fitting.
PMID 16127830·Physiol Meas·2005
8-other
[Lateral gaze palsy and progressive scoliosis in 4 Tunisian families].
PMID 15037843·Rev Neurol (Paris)·2004
5-case
Spectrophotometric and polarographic determination of enalapril and lisinopril using 2,4-dinitrofluorobenzene.
PMID 12644197·J Pharm Biomed Anal·2003
8-other
Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study.
PMID 12781588·Parkinsonism Relat Disord·2003
8-other
Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in Tunisia.
PMID 12873855·Arch Neurol·2003
8-other
The utilization of copper(II) phosphate for the anodic stripping voltammetric assay of alendronate sodium, desferrioxamine mesylate and lisinopril.
PMID 18968998·Talanta·2003
8-other
Automatic detection of distorted plethysmogram pulses in neonates and paediatric patients using an adaptive-network-based fuzzy inference system.
PMID 11830368·Artif Intell Med·2002
8-other
Serum vitamin E and lipid-adjusted vitamin E assessment in Friedreich ataxia phenotype patients and unaffected family members.
PMID 11861456·Clin Chem·2002
8-other
A fuzzy system for detecting distorted plethysmogram pulses in neonates and paediatric patients.
PMID 11411249·Physiol Meas·2001
3-trial
Genetic analysis of early onset cerebellar ataxia with retained tendon reflexes in four Tunisian families.
PMID 11298681·Clin Genet·2001
8-other
Effect of vitamin E supplementation in patients with ataxia with vitamin E deficiency.
PMID 11554913·Eur J Neurol·2001
3-trial
The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy.
PMID 11062483·Nat Genet·2000
4-observational
Clinical and genetic study of familial Parkinson's disease in Tunisia.
PMID 10762501·Neurology·2000
8-other
Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family.
PMID 10751248·Neurology·2000
3-trial
Quantitative determination of some thiazole cephalosporins through complexation with palladium (II) chloride.
PMID 10719922·J Pharm Biomed Anal·2000
8-other
Giant axonal neuropathy locus refinement to a < 590 kb critical interval.
PMID 10909853·Eur J Hum Genet·2000
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
- 101 NICOLLS RD RM 20
STONY BROOK, NY 11794 - Phone
- (631) 444-3005
Quick Facts
- NPI
- 1255072344
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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