Back to Search
ANSELMO PIZZUTI, MD
MD
Pediatrics Physician
NPI: 1699726877Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
MD07626(OR)
Research & Publications (20)
Severe neuropathy after diphtheria-tetanus-pertussis vaccination in a child carrying a novel frame-shift mutation in the small heat-shock protein 27 gene.
PMID 19435728·J Child Neurol·2010
5-case
Use of aripiprazole in tardive dyskinesia: an open label study of six cases.
PMID 19492247·World J Biol Psychiatry·2009
5-case
Clinical, neuropsychological, neurophysiologic, and genetic features of a new Italian pedigree with familial cortical myoclonic tremor with epilepsy.
PMID 19222544·Epilepsia·2009
8-other
High prevalence of epilepsy in a village in the Littoral Province of Cameroon.
PMID 18976884·Epilepsy Res·2008
8-other
Electromechanical coupling in patients with the short QT syndrome: further insights into the mechanoelectrical hypothesis of the U wave.
PMID 18242547·Heart Rhythm·2008
8-other
In vitro effect of PPAR-gamma2 Pro12Ala polymorphism on the deposition of Alzheimer's amyloid-beta peptides.
PMID 17803977·Brain Res·2007
7-preclinical
Unravelling the complexity of T cell abnormalities in common variable immunodeficiency.
PMID 17339494·J Immunol·2007
3-trial
Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer.
PMID 17545690·JAMA·2007
8-other
Functional analysis of splicing mutations in exon 7 of NF1 gene.
PMID 17295913·BMC Med Genet·2007
8-other
Clinical lumping and molecular splitting of LEOPARD and NF1/NF1-Noonan syndromes.
PMID 17366582·Am J Med Genet A·2007
8-other
Germline missense mutations affecting KRAS Isoform B are associated with a severe Noonan syndrome phenotype.
PMID 16773572·Am J Hum Genet·2006
8-other
Clinical features and outcome of familial chronic lymphocytic leukemia.
PMID 16885053·Haematologica·2006
8-other
Additive effects of genetic variation in dopamine regulating genes on working memory cortical activity in human brain.
PMID 16611807·J Neurosci·2006
8-other
Additional evidence that PTPN11 mutations play only a minor role in the pathogenesis of non-syndromic atrioventricular canal defect.
PMID 16892325·Am J Med Genet A·2006
5-case
Role of peroxisome proliferator-activated receptor gamma in amyloid precursor protein processing and amyloid beta-mediated cell death.
PMID 15946122·Biochem J·2005
8-other
Association of the matrix metalloproteinase-3 (MMP-3) promoter polymorphism with celiac disease in male subjects.
PMID 15993717·Hum Immunol·2005
8-other
CRELD1 and GATA4 gene analysis in patients with nonsyndromic atrioventricular canal defects.
PMID 16278904·Am J Med Genet A·2005
8-other
NF1 gene mutations represent the major molecular event underlying neurofibromatosis-Noonan syndrome.
PMID 16380919·Am J Hum Genet·2005
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 200 HAZEL DELL WAY, SUITE 202
CANBY, OR 97013 - Phone
- (503) 266-8500
Quick Facts
- NPI
- 1699726877
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile