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EDWIN KOLODNY, M.D.
M.D.
Neurology Physician
NPI: 1669469557Individual
Specialties, Licenses & Credentials
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
091581(NY)
Research & Publications (20)
Management of neuronopathic Gaucher disease: revised recommendations.
PMID 19655269·J Inherit Metab Dis·2009
6-review
CNS pathology and vascular/circulatory abnormalities in Fabry disease.
PMID 16720466·Acta Paediatr Suppl·2006
8-other
Anderson-Fabry disease: extrarenal, neurologic manifestations.
PMID 12068029·J Am Soc Nephrol·2002
6-review
Molecular genetics of the beta-hexosaminidase isoenzymes: an introduction.
PMID 11596976·Adv Genet·2001
7-preclinical
Miglustat in late-onset Tay-Sachs disease: a 12-month, randomized, controlled clinical study with 24 months of extended treatment.
PMID 19346952·Genet Med·2009
3-trial
Long-term efficacy and safety of laronidase in the treatment of mucopolysaccharidosis I.
PMID 19117887·Pediatrics·2009
4-observational
Variable expression of a novel PLP1 mutation in members of a family with Pelizaeus-Merzbacher disease.
PMID 19151366·J Child Neurol·2009
5-case
Re: Neurocognitive testing in late-onset Tay-Sachs disease: a pilot study.
PMID 19240988·J Inherit Metab Dis·2009
8-other
Newborn screening for Krabbe disease: the New York State model.
PMID 19302934·Pediatr Neurol·2009
8-other
Acute confusional migraine may be a presenting feature of CADASIL.
PMID 19245392·Headache·2009
8-other
p.[G576S; E689K]: pathogenic combination or polymorphism in Pompe disease?
PMID 18301443·Eur J Hum Genet·2008
5-case
Juvenile-onset G(M2)-gangliosidosis in an African-American child with nystagmus.
PMID 18358410·Pediatr Neurol·2008
5-case
Late-onset Tay-Sachs disease: the spectrum of peripheral neuropathy in 30 affected patients.
PMID 18642377·Muscle Nerve·2008
8-other
Very long chain acyl-CoA dehydrogenase deficiency in a pair of mildly affected monozygotic twin sister in their late fifties.
PMID 17514507·J Inherit Metab Dis·2007
5-case
T118M PMP22 mutation causes partial loss of function and HNPP-like neuropathy.
PMID 16437560·Ann Neurol·2006
4-observational
Mild-onset presentation of Canavan's disease associated with novel G212A point mutation in aspartoacylase gene.
PMID 16437572·Ann Neurol·2006
5-case
Mutation analysis of the aspartoacylase gene in non-Jewish patients with Canavan disease.
PMID 16802711·Adv Exp Med Biol·2006
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
- 403 E 34TH ST, 2ND FL
NEW YORK, NY 10016 - Phone
- (212) 263-8344
Quick Facts
- NPI
- 1669469557
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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