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NATALIA WOLF, PHARMD
PHARMD
Pharmacist
NPI: 1497191670Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
057803(NY)
Research & Publications (20)
Status epilepticus in children with Alpers' disease caused by POLG1 mutations: EEG and MRI features.
PMID 19054397·Epilepsia·2009
8-other
Influences of opioids and nanoparticles on in vitro wound healing models.
PMID 19344759·Eur J Pharm Biopharm·2009
4-observational
Ataxia, delayed dentition and hypomyelination: a novel leukoencephalopathy.
PMID 17712733·Neuropediatrics·2007
5-case
Development of a high-throughput screen for soluble epoxide hydrolase inhibition.
PMID 16729954·Anal Biochem·2006
8-other
Sedation with 4-hydroxybutyric acid: a potential pitfall in the diagnosis of SSADH deficiency.
PMID 15243989·J Inherit Metab Dis·2004
5-case
Severe hypomyelination associated with increased levels of N-acetylaspartylglutamate in CSF.
PMID 15136672·Neurology·2004
5-case
Combination of caudal myxopapillary ependymoma and dermal sinus: a single shared embryologic lesion?
PMID 12882537·Dev Med Child Neurol·2003
5-case
New pattern of brain MRI lesions in isolated complex I deficiency.
PMID 12910441·Neuropediatrics·2003
5-case
Impact of selenite and selenate on differentially expressed genes in rat liver examined by microarray analysis.
PMID 19681755·Biosci Rep·2010
7-preclinical
Myelin basic protein-reactive T cells persist in an inactive state in the bone marrow of Lewis rats that have recovered from autoimmune encephalomyelitis.
PMID 19211156·J Neuroimmunol·2009
7-preclinical
Analysis of mutant DNA polymerase gamma in patients with mitochondrial DNA depletion.
PMID 18828154·Hum Mutat·2009
8-other
Isotopic ecology ten years after a call for more laboratory experiments.
PMID 19046398·Biol Rev Camb Philos Soc·2009
6-review
Combining subproteome enrichment and Rubisco depletion enables identification of low abundance proteins differentially regulated during plant defense.
PMID 19053141·Proteomics·2009
8-other
A rapid protocol for construction and production of high-capacity adenoviral vectors.
PMID 19373227·Nat Protoc·2009
8-other
Maternal uniparental heterodisomy with partial isodisomy of a chromosome 2 carrying a splice acceptor site mutation (IVS9-2A>T) in ALS2 causes infantile-onset ascending spastic paralysis (IAHSP).
PMID 18810511·Neurogenetics·2009
5-case
Disruption of protein kinase A in mice enhances healthy aging.
PMID 19536287·PLoS One·2009
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
- 230 W 17TH ST
NEW YORK, NY 10011 - Phone
- (212) 604-1970
Quick Facts
- NPI
- 1497191670
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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