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ALI NAINI, PHD

PHD

Clinical Molecular Genetics Physician

NPI: 1063559045Individual

Specialties, Licenses & Credentials

Clinical Molecular Genetics PhysicianPrimary

Medical Genetics — Clinical Molecular Genetics

Code: 207SG0203X

25MS00004200(NJ)

Research & Publications (20)

Muscle phosphoglycerate mutase deficiency revisited.
PMID 19273759·Arch Neurol·2009
5-case
Detection of mutations in mtDNA.
PMID 17445708·Methods Cell Biol·2007
6-review
Identification of a novel D109Y mutation in Cu/Zn superoxide dismutase (sod1) gene associated with amyotrophic lateral sclerosis.
PMID 17257622·J Neurol Sci·2007
5-case
Novel mitochondrial DNA ND5 mutation in a patient with clinical features of MELAS and MERRF.
PMID 15767514·Arch Neurol·2005
5-case
Hypocitrullinemia in patients with MELAS: an insight into the "MELAS paradox".
PMID 15760638·J Neurol Sci·2005
3-trial
Primary coenzyme Q10 deficiency and the brain.
PMID 14695930·Biofactors·2003
4-observational
Identification of a novel mutation in Cu/Zn superoxide dismutase gene associated with familial amyotrophic lateral sclerosis.
PMID 12039658·J Neurol Sci·2002
5-case
Longitudinal changes of mtDNA A3243G mutation load and level of functioning in MELAS.
PMID 19253345·Am J Med Genet A·2009
8-other
A novel tRNA(Val) mitochondrial DNA mutation causing MELAS.
PMID 18314141·J Neurol Sci·2008
8-other
The G13513A mutation in the ND5 gene of mitochondrial DNA as a common cause of MELAS or Leigh syndrome: evidence from 12 cases.
PMID 18332249·Arch Neurol·2008
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
710 W 168TH ST
NEW YORK, NY 10032

Quick Facts

NPI
1063559045
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
20

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