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TORBJOERN NYGAARD, M.D.
M.D.
Neurology Physician
NPI: 1417961830Individual
Specialties, Licenses & Credentials
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
25MA04261100(NJ)
Research & Publications (17)
The SaeR/S gene regulatory system is essential for innate immune evasion by Staphylococcus aureus.
PMID 19374556·J Infect Dis·2009
7-preclinical
Community-associated methicillin-resistant Staphylococcus aureus skin infections: advances toward identifying the key virulence factors.
PMID 18317037·Curr Opin Infect Dis·2008
6-review
Ammonium recruitment and ammonia transport by E. coli ammonia channel AmtB.
PMID 17012311·Biophys J·2006
8-other
Identification and characterization of the heme-binding proteins SeShp and SeHtsA of Streptococcus equi subspecies equi.
PMID 17007644·BMC Microbiol·2006
8-other
The mechanism of direct heme transfer from the streptococcal cell surface protein Shp to HtsA of the HtsABC transporter.
PMID 16717094·J Biol Chem·2006
8-other
High mutation rate in dopa-responsive dystonia: detection with comprehensive GCHI screening.
PMID 15753436·Neurology·2005
8-other
Imaging of dopamine transporters and D2 receptors in patients with Parkinson's disease and multiple system atrophy.
PMID 15583914·Eur J Nucl Med Mol Imaging·2004
3-trial
Phenylalanine loading as a diagnostic test for DRD: interpreting the utility of the test.
PMID 15542391·Mol Genet Metab·2004
4-observational
Toxic pediatric parkinsonism: report of a child with metabolic studies and response to treatment.
PMID 14696914·J Child Neurol·2003
5-case
A novel autosomal dominant limb-girdle muscular dystrophy (LGMD 1F) maps to 7q32.1-32.2.
PMID 12913210·Neurology·2003
8-other
Brain biopterin and tyrosine hydroxylase in asymptomatic dopa-responsive dystonia.
PMID 12112113·Ann Neurol·2002
5-case
Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex. 1994.
PMID 11775599·Neurology·2001
8-other
Complications of femoral artery closure devices.
PMID 11146512·Catheter Cardiovasc Interv·2001
4-observational
Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutations.
PMID 10852545·Ann Neurol·2000
8-other
Gaucher disease: the origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutations.
PMID 10777718·Am J Hum Genet·2000
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
- 385 TREMONT AVE, 112
EAST ORANGE, NJ 07018 - Phone
- (973) 676-1000
Quick Facts
- NPI
- 1417961830
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 17
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