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ARTHUR FEIGENBAUM, DMD
DMD
Dentist
NPI: 1972524296Individual
Specialties, Licenses & Credentials
DentistPrimary
Dentist
Code: 122300000X
033642(NY)
Research & Publications (20)
Pyruvate dehydrogenase phosphatase 1 (PDP1) null mutation produces a lethal infantile phenotype.
PMID 19184109·Hum Genet·2009
5-case
A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiency.
PMID 19157942·Mol Genet Metab·2009
6-review
Rolandic mitochondrial encephalomyelopathy and MT-ND3 mutations.
PMID 19520270·Pediatr Neurol·2009
5-case
Stepwise developmental regression associated with novel CACNA1A mutation.
PMID 18940563·Pediatr Neurol·2008
5-case
Proposal of a set of model polymer additives designed for confocal FRAP diffusion experiments.
PMID 18928296·J Agric Food Chem·2008
8-other
A novel mitochondrial DNA mutation in COX1 leads to strokes, seizures, and lactic acidosis.
PMID 19568996·Neuropediatrics·2008
5-case
Abnormal neurological features predict poor survival and should preclude liver transplantation in patients with deoxyguanosine kinase deficiency.
PMID 18825706·Liver Transpl·2008
1-meta
Ocular phenotype in patients with methylmalonic aciduria and homocystinuria, cobalamin C type.
PMID 18848477·J AAPOS·2008
5-case
The role of molecular testing and enzyme analysis in the management of hypomorphic citrullinemia.
PMID 18925679·Am J Med Genet A·2008
5-case
Hypomyelination with atrophy of the basal ganglia and cerebellum: follow-up and pathology.
PMID 17620549·Neurology·2007
8-other
Sorption of aroma compounds in PET and PVC during the storage of a strawberry syrup.
PMID 17852385·Food Addit Contam·2007
8-other
Efficacy of sapropterin dihydrochloride (tetrahydrobiopterin, 6R-BH4) for reduction of phenylalanine concentration in patients with phenylketonuria: a phase III randomised placebo-controlled study.
PMID 17693179·Lancet·2007
3-trial
Contamination of packaged food by substances migrating from a direct-contact plastic layer: Assessment using a generic quantitative household scale methodology.
PMID 17164219·Food Addit Contam·2007
8-other
Novel mutations in dihydrolipoamide dehydrogenase deficiency in two cousins with borderline-normal PDH complex activity.
PMID 16770810·Am J Med Genet A·2006
5-case
Novel mitochondrial DNA mutations associated with myopathy, cardiomyopathy, renal failure, and deafness.
PMID 16955414·Am J Med Genet A·2006
8-other
Modelling of migration from multi-layers and functional barriers: estimation of parameters.
PMID 16982526·Food Addit Contam·2006
8-other
Molecular bases of hearing loss in multi-systemic mitochondrial cytopathy.
PMID 17079881·Genet Med·2006
8-other
A child with an underrecognized form of developmental delay: a congenital disorder of glycosylation.
PMID 17116901·CMAJ·2006
5-case
Inner ear dysplasia is common in children with Down syndrome (trisomy 21).
PMID 17146381·Laryngoscope·2006
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
- 70-31A 108TH STREET, SUITE 2
FOREST HILLS, NY 11375 - Phone
- (718) 268-4742
Quick Facts
- NPI
- 1972524296
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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