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ALI NAINI, M.D.

M.D.

Neurological Surgery Physician

NPI: 1487687620Individual

Specialties, Licenses & Credentials

Neurological Surgery PhysicianPrimary

Neurological Surgery

Code: 207T00000X

MD 00034084(WA)

Research & Publications (20)

Muscle phosphoglycerate mutase deficiency revisited.
PMID 19273759·Arch Neurol·2009
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
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
A novel tRNA(Val) mitochondrial DNA mutation causing MELAS.
PMID 18314141·J Neurol Sci·2008
8-other
Human CoQ10 deficiencies.
PMID 19096106·Biofactors·2008
8-other
Amyotrophic lateral sclerosis with ragged-red fibers.
PMID 18332255·Arch Neurol·2008
5-case
Respiratory chain dysfunction and oxidative stress correlate with severity of primary CoQ10 deficiency.
PMID 18230681·FASEB J·2008
8-other
Outcome of patients without any immunosuppressive therapy after renal allograft failure.
PMID 18087124·Saudi J Kidney Dis Transpl·2008
8-other
Oxidative stress biomarkers in sporadic ALS.
PMID 18574762·Amyotroph Lateral Scler·2008
8-other
Mitochondrial DNA depletion syndrome due to mutations in the RRM2B gene.
PMID 18504129·Neuromuscul Disord·2008
7-preclinical
Doxycycline: a pilot study to reduce diabetic proteinuria.
PMID 17429196·Am J Nephrol·2007
3-trial
Detection of mutations in mtDNA.
PMID 17445708·Methods Cell Biol·2007
6-review
Gabapentin: a promising drug for the treatment of uremic pruritus.
PMID 17679749·Saudi J Kidney Dis Transpl·2007
2-rct
The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene.
PMID 17412732·Brain·2007
8-other
Pathogenic Lrrk2 substitutions and Amyotrophic lateral sclerosis.
PMID 16865326·J Neural Transm (Vienna)·2007
8-other
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
Prevalence and clinical findings of biopsy-proven glomerulonephritidis in Iran.
PMID 17951943·Saudi J Kidney Dis Transpl·2007
4-observational
Effect of ezetimibe and/or simvastatin on coenzyme Q10 levels in plasma: a randomised trial.
PMID 16872244·Drug Saf·2006
2-rct
Exercise-induced cramp, myoglobinuria, and tubular aggregates in phosphoglycerate mutase deficiency.
PMID 16881065·Muscle Nerve·2006
5-case
Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutations.
PMID 17186472·Am J Hum Genet·2006
5-case

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

Contact & Hours

Address
13107 121ST WAY NE
KIRKLAND, WA 98034

Location

Practice Location

13107 121ST WAY NE, KIRKLAND, WA
(425) 899-6200

Quick Facts

NPI
1487687620
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
20

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