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ARNULF KOEPPEN, M.D.

M.D.

Neurology Physician

NPI: 1598713216IndividualAccepts Medicare

Specialties, Licenses & Credentials

Neurology PhysicianPrimary

Psychiatry & Neurology — Neurology

Code: 2084N0400X

103535(NY)

CMS Specialties

PrimaryNEUROLOGY

Additional

PATHOLOGY

Education

OTHER

Class of 1963

Research & Publications (19)

The pathology of superficial siderosis of the central nervous system.
PMID 18696091·Acta Neuropathol·2008
8-other
The dentate nucleus in Friedreich's ataxia: the role of iron-responsive proteins.
PMID 17443334·Acta Neuropathol·2007
8-other
The pathogenesis of spinocerebellar ataxia.
PMID 15895563·Cerebellum·2005
6-review
A brief history of Pelizaeus-Merzbacher disease and proteolipid protein.
PMID 15694205·J Neurol Sci·2005
7-preclinical
Heme oxygenase in experimental intracerebral hemorrhage: the benefit of tin-mesoporphyrin.
PMID 15217087·J Neuropathol Exp Neurol·2004
4-observational
Wallerian degeneration: history and clinical significance.
PMID 15140616·J Neurol Sci·2004
6-review
A brief history of brain iron research.
PMID 12614937·J Neurol Sci·2003
6-review
Pelizaeus-Merzbacher disease.
PMID 12230321·J Neuropathol Exp Neurol·2002
6-review
Tin-protoporphyrin prevents experimental superficial siderosis in rabbits.
PMID 12152784·J Neuropathol Exp Neurol·2002
7-preclinical
Iron in the Hallervorden-Spatz syndrome.
PMID 11551745·Pediatr Neurol·2001
6-review
Striatal and nigral pathology in a lentiviral rat model of Machado-Joseph disease.
PMID 18385100·Hum Mol Genet·2008
7-preclinical
Iron and iron-responsive proteins in the cardiomyopathy of Friedreich's ataxia.
PMID 17134988·Cerebellum·2006
8-other
Lamin B1 duplications cause autosomal dominant leukodystrophy.
PMID 16951681·Nat Genet·2006
7-preclinical
The dominant form of vanishing white matter-like leukoencephalopathy represents autosomal dominant leukodystrophy.
PMID 16437562·Ann Neurol·2006
8-other
Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17).
PMID 12953269·Ann Neurol·2003
8-other
Familial hemiplegic migraine.
PMID 12756128·Arch Neurol·2003
6-review
Ocular apraxia in recessive ataxia.
PMID 12020276·Arch Neurol·2002
8-other
Re.: Clinical, radiological and pathological findings in an autosomal dominant leukodystrophy.
PMID 11486760·J Neurol Sci·2001
6-review
Genetic localization of an autosomal dominant leukodystrophy mimicking chronic progressive multiple sclerosis to chromosome 5q31.
PMID 10749986·Hum Mol Genet·2000
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
113 HOLLAND AVE, NEUROLOGY SERVICE
ALBANY, NY 12208

Location

Practice Location

113 HOLLAND AVE, ALBANY, NY
(518) 626-6373

Quick Facts

NPI
1598713216
Entity Type
Individual
Gender
Male
Medicare
Accepted
Specialties
1
Locations
1
Years in Practice
63
Publications
19

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