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LEONARD GOLDFARB, M.D.
M.D.
Nuclear Medicine Physician
NPI: 1730117102Individual
Specialties, Licenses & Credentials
Nuclear Medicine PhysicianPrimary
Nuclear Medicine
Code: 207U00000X
2004030335(MO)
Research & Publications (20)
Mutational analysis of glycyl-tRNA synthetase (GARS) gene in Hirayama disease.
PMID 19412816·Amyotroph Lateral Scler·2010
8-other
Severe infantile-onset cardiomyopathy associated with a homozygous deletion in desmin.
PMID 19433360·Neuromuscul Disord·2009
5-case
Generalized muscle pseudo-hypertrophy and stiffness associated with the myotilin Ser55Phe mutation: a novel myotilinopathy phenotype?
PMID 19027924·J Neurol Sci·2009
5-case
Tragedy in a heartbeat: malfunctioning desmin causes skeletal and cardiac muscle disease.
PMID 19587455·J Clin Invest·2009
6-review
Viliuisk encephalomyelitis in Eastern Siberia - analysis of 390 cases.
PMID 19618339·Folia Neuropathol·2009
8-other
In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathy.
PMID 19050726·Eur J Hum Genet·2009
4-observational
Lower limb radiology of distal myopathy due to the S60F myotilin mutation.
PMID 19590214·Eur Neurol·2009
5-case
Global distribution of fatal familial insomnia: founder or recurrent mutations.
PMID 18568368·Neurogenetics·2008
8-other
Transcription-terminating mutation in telethonin causing autosomal recessive muscular dystrophy type 2G in a European patient.
PMID 18948002·Neuromuscul Disord·2008
5-case
T cell receptor profiling in muscle and blood lymphocytes in sporadic inclusion body myositis.
PMID 17954782·Neurology·2007
8-other
Family clustering of Viliuisk encephalomyelitis in traditional and new geographic regions.
PMID 18252102·Emerg Infect Dis·2007
8-other
Evidence for task conflict in the Stroop effect.
PMID 17924815·J Exp Psychol Hum Percept Perform·2007
8-other
The cause of the within-language Stroop superiority effect and its implications.
PMID 17455053·Q J Exp Psychol (Hove)·2007
8-other
Conspicuous involvement of desmin tail mutations in diverse cardiac and skeletal myopathies.
PMID 17221859·Hum Mutat·2007
5-case
Inclusion body myositis with human immunodeficiency virus infection: four cases with clonal expansion of viral-specific T cells.
PMID 17366634·Ann Neurol·2007
5-case
Phenotypic patterns of desminopathy associated with three novel mutations in the desmin gene.
PMID 17418574·Neuromuscul Disord·2007
8-other
Restrictive cardiomyopathy with atrioventricular conduction block resulting from a desmin mutation.
PMID 16890305·Int J Cardiol·2007
5-case
Functional analyses of glycyl-tRNA synthetase mutations suggest a key role for tRNA-charging enzymes in peripheral axons.
PMID 17035524·J Neurosci·2006
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 915 N GRAND BLVD
SAINT LOUIS, MO 63106 - Phone
- (314) 652-4100
Quick Facts
- NPI
- 1730117102
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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