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CHRISTOPHER CRISCUOLO, MD

MD

Pain Medicine (Anesthesiology) Physician

NPI: 1518925114IndividualAccepts Medicare

Specialties, Licenses & Credentials

Anesthesiology Physician

Anesthesiology

Code: 207L00000X

18755(NE)
Pain Medicine (Anesthesiology) PhysicianPrimary

Anesthesiology — Pain Medicine

Code: 207LP2900X

18755(NE)

CMS Specialties

PrimaryPAIN MANAGEMENT

Additional

ANESTHESIOLOGY

Education

GEORGETOWN UNIVERSITY SCHOOL OF MEDICINE

Class of 1984

Research & Publications (20)

Interventional approaches to the management of myofascial pain syndrome.
PMID 11560805·Curr Pain Headache Rep·2001
6-review
Two novel CYP7B1 mutations in Italian families with SPG5: a clinical and genetic study.
PMID 19363635·J Neurol·2009
8-other
PINK1 homozygous W437X mutation in a patient with apparent dominant transmission of parkinsonism.
PMID 16700027·Mov Disord·2006
5-case
Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study.
PMID 16636238·Neurology·2006
8-other
Novel mutation of SACS gene in a Spanish family with autosomal recessive spastic ataxia.
PMID 16007637·Mov Disord·2005
5-case
Ataxia with oculomotor apraxia type 1 in Southern Italy: late onset and variable phenotype.
PMID 15596775·Neurology·2004
5-case
A novel mutation in SACS gene in a family from southern Italy.
PMID 14718706·Neurology·2004
5-case
FLT3 mutations have no prognostic impact in elderly patients with acute myeloid leukemia and normal karyotype.
PMID 19562748·Am J Hematol·2009
8-other
Continuous infusion idarubicin and intravenous busulphan as conditioning regimen to autologous stem cell transplantation for patients with acute myeloid leukaemia.
PMID 19475701·Hematol Oncol·2009
3-trial
Autologous stem cell transplantation for elderly patients with acute myeloid leukaemia conditioned with continuous infusion idarubicin and busulphan.
PMID 19206083·Hematol Oncol·2009
8-other
Screening of ARHSP-TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion.
PMID 19105190·Hum Mutat·2009
8-other
Genetic screening for LRRK2 gene G2019S mutation in Parkinson's disease patients from Southern Italy.
PMID 18621566·Parkinsonism Relat Disord·2009
8-other
Coexistence of mutations in PINK1 and mitochondrial DNA in early onset parkinsonism.
PMID 18524835·J Med Genet·2008
8-other
Attributions regarding unmet treatment goals after interdisciplinary chronic pain rehabilitation.
PMID 18496306·Clin J Pain·2008
8-other
Screening for POLG1 mutations in a Southern Italian ataxia population.
PMID 18080848·J Neurol·2008
8-other
Nigrostriatal involvement in ataxia with oculomotor apraxia type 1.
PMID 18004640·J Neurol·2008
8-other
Neurophysiological study in a Spanish family with recessive spastic ataxia of Charlevoix-Saguenay.
PMID 17683082·Muscle Nerve·2008
5-case
Senataxin, defective in ataxia oculomotor apraxia type 2, is involved in the defense against oxidative DNA damage.
PMID 17562789·J Cell Biol·2007
8-other
A novel mutation in GCH-1 gene in a case of dopa-responsive dystonia.
PMID 17410324·J Neurol·2007
5-case
Spastic paraplegia with thin corpus callosum: description of 20 new families, refinement of the SPG11 locus, candidate gene analysis and evidence of genetic heterogeneity.
PMID 16699786·Neurogenetics·2006
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
6901 N 72ND ST
OMAHA, NE 68122

Location

Practice Location

6901 N 72ND ST, OMAHA, NE
(402) 572-2187

Quick Facts

NPI
1518925114
Entity Type
Individual
Gender
Male
Medicare
Accepted
Specialties
2
Locations
1
Years in Practice
42
Publications
20

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