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ALISA GUTMAN, MD
MD
Neurology Physician
NPI: 1255566733Individual
Specialties, Licenses & Credentials
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
MD443156(PA)
Research & Publications (20)
The role of neuropeptide Y in the expression and extinction of fear-potentiated startle.
PMID 19036961·J Neurosci·2008
7-preclinical
A novel PEX12 mutation identified as the cause of a peroxisomal biogenesis disorder with mild clinical phenotype, mild biochemical abnormalities in fibroblasts and a mosaic catalase immunofluorescence pattern, even at 40 degrees C.
PMID 17534573·J Hum Genet·2007
5-case
Functional interactions between endocannabinoid and CCK neurotransmitter systems may be critical for extinction learning.
PMID 18580872·Neuropsychopharmacology·2009
7-preclinical
Glutaric aciduria type 1: clinical, biochemical and molecular findings in patients from Israel.
PMID 17188916·Eur J Paediatr Neurol·2007
8-other
Severe infantile type of carnitine palmitoyltransferase II (CPT II) deficiency due to homozygous R503C mutation.
PMID 17372854·J Inherit Metab Dis·2007
5-case
A novel SLC25A20 splicing mutation in patients of different ethnic origin with neonatally lethal carnitine-acylcarnitine translocase (CACT) deficiency.
PMID 16919490·Mol Genet Metab·2006
5-case
TAT gene mutation analysis in three Palestinian kindreds with oculocutaneous tyrosinaemia type II; characterization of a silent exonic transversion that causes complete missplicing by exon 11 skipping.
PMID 16917729·J Inherit Metab Dis·2006
8-other
Treatment from birth of nonketotic hyperglycinemia due to a novel GLDC mutation.
PMID 16404748·Ann Neurol·2006
5-case
Central oxytocin, vasopressin, and corticotropin-releasing factor receptor densities in the basal forebrain predict isolation potentiated startle in rats.
PMID 16339041·J Neurosci·2005
4-observational
Patients' attitudes toward resident participation in dermatology outpatient clinics.
PMID 16198803·J Am Acad Dermatol·2005
8-other
Novel metabolic and molecular findings in hepatic carnitine palmitoyltransferase I deficiency.
PMID 16146704·Mol Genet Metab·2005
5-case
2-ethylhydracrylic aciduria in short/branched-chain acyl-CoA dehydrogenase deficiency: application to diagnosis and implications for the R-pathway of isoleucine oxidation.
PMID 15615815·Clin Chem·2005
8-other
Persistent NKH with transient or absent symptoms and a homozygous GLDC mutation.
PMID 15236413·Ann Neurol·2004
8-other
Prenatal diagnosis for arginase deficiency by second-trimester fetal erythrocyte arginase assay and first-trimester ARG1 mutation analysis.
PMID 15565656·Prenat Diagn·2004
5-case
D-2-hydroxyglutaric aciduria and glutaric aciduria type 1 in siblings: coincidence, or linked disorders?
PMID 15248096·Neuropediatrics·2004
8-other
N-acetyl tyrosyluria caused by parenteral or enteral administration of N-acetyl-L-tyrosine: differentiation from hereditary and acquired tyrosinemias.
PMID 15187789·J Pediatr Gastroenterol Nutr·2004
5-case
Homozygosity for a severe novel medium-chain acyl-CoA dehydrogenase (MCAD) mutation IVS3-1G > C that leads to introduction of a premature termination codon by complete missplicing of the MCAD mRNA and is associated with phenotypic diversity ranging from sudden neonatal death to asymptomatic status.
PMID 15171999·Mol Genet Metab·2004
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
- 800 SPRUCE ST, 4TH FLOOR
PHILADELPHIA, PA 19107 - Phone
- (215) 829-3474
Quick Facts
- NPI
- 1255566733
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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