Back to Search
SCOTT RASKIN, D.O.
D.O.
Pediatric Hematology & Oncology Physician
NPI: 1710220306IndividualAccepts Medicare
Specialties, Licenses & Credentials
Pediatric Hematology & Oncology PhysicianPrimary
Pediatrics — Pediatric Hematology-Oncology
Code: 2080P0207X
34.015227(OH)
CMS Specialties
PrimaryPEDIATRIC MEDICINE
Education
OTHER
Class of 2013
Research & Publications (20)
CTA/CTG expansions at the SCA 8 locus in multiple system atrophy.
PMID 18980793·Clin Neurol Neurosurg·2009
5-case
Unilateral pallidotomy in a patient with parkinsonism and G2019S LRRK2 mutation.
PMID 19012346·Mov Disord·2009
5-case
Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes.
PMID 19449411·Am J Med Genet A·2009
5-case
Randomized comparison of cold blood and cold crystalloid renal perfusion for renal protection during thoracoabdominal aortic aneurysm repair.
PMID 19028052·J Vasc Surg·2009
4-observational
Treatment of a child diagnosed with Niemann-Pick disease type C with miglustat: a case report in Brazil.
PMID 18937049·J Inherit Metab Dis·2008
5-case
Healthcare infections associated with care and treatment of humans and animals.
PMID 19046502·Emerg Infect Dis·2008
7-preclinical
Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients.
PMID 17544945·J Cyst Fibros·2008
8-other
The G2019S LRRK2 mutation in Brazilian patients with Parkinson's disease: phenotype in monozygotic twins.
PMID 17999435·Mov Disord·2008
8-other
Cerebellar ataxia, myoclonus, cervical lipomas, and MERRF syndrome. Case report.
PMID 18412280·Mov Disord·2008
5-case
Cystic fibrosis in a southern Brazilian population: characteristics of 90% of the alleles.
PMID 17718859·Clin Genet·2007
8-other
Non-choreic movement disorders as initial manifestations of Huntington's disease.
PMID 17665004·Arq Neuropsiquiatr·2007
8-other
Cystic fibrosis gene variability in two southern Brazilian Amerindian populations: analysis of the deltaF508 mutation and the KM19 and XV2C haplotypes.
PMID 17985657·Hum Biol·2007
8-other
Rett syndrome: clinical and molecular characterization of two Brazilian patients.
PMID 17420824·Arq Neuropsiquiatr·2007
5-case
[Multisensory environmental intervention (snoezelen) as a preventive alternative to seclusion and restraint in closed psychiatric wards].
PMID 17294840·Harefuah·2007
4-observational
Reduced penetrance in a Brazilian family with spinocerebellar ataxia type 10.
PMID 17420323·Arch Neurol·2007
5-case
The history of spinocerebellar ataxia type 10 in Brazil: travels of a gene.
PMID 18094855·Arq Neuropsiquiatr·2007
4-observational
Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations.
PMID 17056636·J Med Genet·2007
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
- 3333 BURNET AVE, ML 7018
CINCINNATI, OH 45229 - Phone
- (513) 636-4718
Quick Facts
- NPI
- 1710220306
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 13
- Publications
- 20
Are you this provider?
Claim Your Profile