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SARAH RAINIER, D.O.

D.O.

Anesthesiology Physician

NPI: 1235455627IndividualAccepts Medicare

Specialties, Licenses & Credentials

Anesthesiology PhysicianPrimary

Anesthesiology

Code: 207L00000X

DO2447(ME)

CMS Specialties

PrimaryANESTHESIOLOGY

Education

UNIVERSITY OF NEW ENGLAND, COLLEGE OF OSTEO MEDICINE

Class of 2010

Research & Publications (15)

Neuropathy target esterase gene mutations cause motor neuron disease.
PMID 18313024·Am J Hum Genet·2008
8-other
De novo occurrence of novel SPG3A/atlastin mutation presenting as cerebral palsy.
PMID 16533974·Arch Neurol·2006
4-observational
Myofibrillogenesis regulator 1 gene mutations cause paroxysmal dystonic choreoathetosis.
PMID 15262732·Arch Neurol·2004
4-observational
NIPA1 gene mutations cause autosomal dominant hereditary spastic paraplegia (SPG6).
PMID 14508710·Am J Hum Genet·2003
8-other
Hereditary spastic paraplegia linked to chromosome 14q11-q21: reduction of the SPG3 locus interval from 5.3 to 2.7 cM.
PMID 11694553·J Med Genet·2001
8-other
Normal dopaminergic nigrostriatal innervation in SPG3A hereditary spastic paraplegia.
PMID 19085270·J Neurogenet·2008
8-other
Cerebrotendinous xanthomatosis: possible higher prevalence than previously recognized.
PMID 16157755·Arch Neurol·2005
5-case
Spinal cord magnetic resonance imaging in autosomal dominant hereditary spastic paraplegia.
PMID 16143870·Neuroradiology·2005
8-other
Presence of alanine-to-valine substitutions in myofibrillogenesis regulator 1 in paroxysmal nonkinesigenic dyskinesia: confirmation in 2 kindreds.
PMID 15824259·Arch Neurol·2005
8-other
Hereditary spastic paraplegia: spastin phenotype and function.
PMID 15210518·Arch Neurol·2004
6-review
Spastic paraplegia, ataxia, mental retardation (SPAR): a novel genetic disorder.
PMID 11839840·Neurology·2002
8-other
Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia.
PMID 11685207·Nat Genet·2001
8-other
Acid-sensing ion channel (ASIC) 4 gene: physical mapping, genomic organisation, and evaluation as a candidate for paroxysmal dystonia.
PMID 11571555·Eur J Hum Genet·2001
8-other
Prenatal diagnosis of hereditary spastic paraplegia.
PMID 11260609·Prenat Diagn·2001
8-other
GLI-2 modulates retroviral gene expression.
PMID 11160733·J Virol·2001
7-preclinical

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Address
489 STATE ST
BANGOR, ME 04401

Location

Practice Location

489 STATE ST, BANGOR, ME
(207) 973-9700

Quick Facts

NPI
1235455627
Entity Type
Individual
Gender
Female
Medicare
Accepted
Specialties
1
Locations
1
Years in Practice
16
Publications
15

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