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ANGEL BASSUK, MD
MD
Pediatric Surgery Physician
NPI: 1407089923Individual
Specialties, Licenses & Credentials
Pediatric Surgery PhysicianPrimary
Surgery — Pediatric Surgery
Code: 2086S0120X
036-051092(IL)
Research & Publications (20)
In cis autosomal dominant mutation of Senataxin associated with tremor/ataxia syndrome.
PMID 17096168·Neurogenetics·2007
5-case
T-cell lymphoma presenting with neurologic features in immunocompetent children.
PMID 17074600·Pediatr Neurol·2006
5-case
Systemic lymphoma mimicking acute disseminated encephalomyelitis.
PMID 14984907·Pediatr Neurol·2004
5-case
Alexander disease with serial MRS and a new mutation in the glial fibrillary acidic protein gene.
PMID 14557587·Neurology·2003
5-case
A child with spinal cord AVM presenting with raised intracranial pressure.
PMID 12771285·Neurology·2003
5-case
Acute necrotizing encephalopathy of childhood with radiographic progression over 10 hours.
PMID 12743257·Neurology·2003
5-case
FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation.
PMID 19668217·Nat Genet·2009
8-other
Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore, RANBP2.
PMID 19118815·Am J Hum Genet·2009
8-other
A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome.
PMID 18976727·Am J Hum Genet·2008
8-other
Neuroimaging findings in children with rare or novel de novo chromosomal anomalies.
PMID 18302267·Birth Defects Res A Clin Mol Teratol·2008
8-other
Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity.
PMID 18204864·Hum Genet·2008
5-case
NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects.
PMID 17530927·PLoS Genet·2007
7-preclinical
Differences in ATP7A gene expression underlie intrafamilial variability in Menkes disease/occipital horn syndrome.
PMID 17496194·J Med Genet·2007
5-case
Neural tube defects and folate pathway genes: family-based association tests of gene-gene and gene-environment interactions.
PMID 17035141·Environ Health Perspect·2006
8-other
Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2.
PMID 16237707·Birth Defects Res A Clin Mol Teratol·2005
7-preclinical
SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects.
PMID 15883837·Hum Genet·2005
8-other
Whole genomewide linkage screen for neural tube defects reveals regions of interest on chromosomes 7 and 10.
PMID 15831595·J Med Genet·2005
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
- 9655 WOODS DR
SKOKIE, IL 60077 - Phone
- (727) 460-4353
Quick Facts
- NPI
- 1407089923
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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