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LOUISE CASTIGLIA, M.D.
M.D.
Pediatrics Physician
NPI: 1023191673Individual
Specialties, Licenses & Credentials
Research & Publications (20)
Association between the polymorphisms of TLR4 and CD14 genes and Alzheimer's disease.
PMID 19006850·Curr Pharm Des·2008
8-other
12q12 deletion: a new patient contributing to genotype-phenotype correlation.
PMID 18412123·Am J Med Genet A·2008
5-case
Evaluation of occupational exposure to antiblastic drugs in an Italian hospital oncological department.
PMID 18285644·J Occup Health·2008
8-other
A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures.
PMID 18278044·Nat Genet·2008
5-case
Partial monosomy Xq(Xq23 --> qter) and trisomy 4p(4p15.33 --> pter) in a woman with intractable focal epilepsy, borderline intellectual functioning, and dysmorphic features.
PMID 18166284·Brain Dev·2008
5-case
Analytical method validation for the evaluation of cutaneous occupational exposure to different chemical classes of pesticides.
PMID 17980681·J Chromatogr B Analyt Technol Biomed Life Sci·2007
4-observational
Schizophrenia in a patient with subtelomeric duplication of chromosome 22q.
PMID 17539913·Clin Genet·2007
5-case
6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases.
PMID 16686647·Epilepsia·2006
5-case
Narrowing the candidate region for congenital diaphragmatic hernia in chromosome 15q26: contradictory results.
PMID 16252246·Am J Hum Genet·2005
8-other
Determination of rapamycin: quantification of the sodiated species by an ion trap mass spectrometer as an alternative to the ammoniated complex analysis by triple quadrupole.
PMID 16196022·Rapid Commun Mass Spectrom·2005
4-observational
A t(4;9)(q34;p22) translocation associated with partial epilepsy, mental retardation, and dysmorphism.
PMID 16060948·Epilepsia·2005
5-case
A case study: surface contamination of cyclophosphamide due to working practices and cleaning procedures in two Italian hospitals.
PMID 15964876·Ann Occup Hyg·2005
4-observational
Mono- and diiodocyclophosphamide as possible internal standards for cyclophosphamide quantification: characterization by ion trap multi-stage mass spectrometry and effects of iodine-chlorine substitution on the fragmentation pattern.
PMID 15945034·Rapid Commun Mass Spectrom·2005
8-other
Skewed X-inactivation in a family with mental retardation and PQBP1 gene mutation.
PMID 15811016·Clin Genet·2005
5-case
Asymptomatic and mild beta-thalassemia in homozygotes and compound heterozygotes for the IVS2+1G-->A mutation: role of the beta-globin gene haplotype.
PMID 14555304·Haematologica·2003
8-other
The effect of an environmental enrichment device on individually caged rabbits in a safety assessment facility.
PMID 14510521·Contemp Top Lab Anim Sci·2003
7-preclinical
Mutational analysis of the ATRX gene by DGGE: a powerful diagnostic approach for the ATRX syndrome.
PMID 12673795·Hum Mutat·2003
8-other
Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformations.
PMID 11424927·J Med Genet·2001
5-case
How microsatellite analysis can be exploited for subtelomeric chromosomal rearrangement analysis in mental retardation.
PMID 11134240·J Med Genet·2001
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
- 156 FIRST STREET
MINEOLA, NY 11501 - Phone
- (516) 741-4082
Quick Facts
- NPI
- 1023191673
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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