Back to Search
WILLIAM NEWMAN, M.D.
M.D.
Neurological Surgery Physician
NPI: 1578825097IndividualAccepts Medicare
Specialties, Licenses & Credentials
Neurological Surgery PhysicianPrimary
Neurological Surgery
Code: 207T00000X
323761(LA)297797(NY)
CMS Specialties
PrimaryNEUROSURGERY
Education
UNIVERSITY OF FLORIDA COLLEGE OF MEDICINE
Class of 2012
Research & Publications (20)
Breast cancer susceptibility variants alter risks in familial disease.
PMID 19617217·J Med Genet·2010
8-other
Randomized comparison of everolimus-eluting and paclitaxel-eluting stents: two-year clinical follow-up from the Clinical Evaluation of the Xience V Everolimus Eluting Coronary Stent System in the Treatment of Patients with de novo Native Coronary Artery Lesions (SPIRIT) III trial.
PMID 19171853·Circulation·2009
4-observational
Improving pharmacovigilance in Europe: TPMT genotyping and phenotyping in the UK and Spain.
PMID 19223932·Eur J Hum Genet·2009
4-observational
UGT1A1*28 genotype predicts gastrointestinal toxicity in patients treated with intermediate-dose irinotecan.
PMID 19450125·Pharmacogenomics·2009
8-other
Gender-based evaluation of the XIENCE V everolimus-eluting coronary stent system: clinical and angiographic results from the SPIRIT III randomized trial.
PMID 19530147·Catheter Cardiovasc Interv·2009
4-observational
Reply to Clare and Høeg 2008. Balanus amphitrite or Amphibalanus amphitrite? A note on barnacle nomenclature.
PMID 19021015·Biofouling·2009
7-preclinical
The SPINK1 N34S variant is associated with acute pancreatitis.
PMID 19369834·Eur J Gastroenterol Hepatol·2009
8-other
CTLA4/ICOS gene variants and haplotypes are associated with rheumatoid arthritis and primary biliary cirrhosis in the Canadian population.
PMID 19333938·Arthritis Rheum·2009
8-other
Impaired tamoxifen metabolism reduces survival in familial breast cancer patients.
PMID 18794105·Clin Cancer Res·2008
8-other
Geroderma osteodysplastica maps to a 4 Mb locus on chromosome 1q24.
PMID 19006212·Am J Med Genet A·2008
8-other
Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golgin.
PMID 18997784·Nat Genet·2008
8-other
Molecular characterisation of SMARCB1 and NF2 in familial and sporadic schwannomatosis.
PMID 18285426·J Med Genet·2008
8-other
Re: Pharmacogenomic variation of CYP2D6 and the choice of optimal adjuvant endocrine therapy for postmenopausal breast cancer: a modeling analysis.
PMID 18780871·J Natl Cancer Inst·2008
8-other
Impaired glycocalyx barrier properties and increased capillary tube haematocrit.
PMID 18703574·J Physiol·2008
7-preclinical
Chiari I malformation without hydrocephalus: acute intracranial hypertension managed with endoscopic third ventriculostomy (ETV).
PMID 18626650·Childs Nerv Syst·2008
5-case
Comparison of an everolimus-eluting stent and a paclitaxel-eluting stent in patients with coronary artery disease: a randomized trial.
PMID 18430909·JAMA·2008
4-observational
Atrial fibrillation with QRS voltage low in the limb leads and high in the precordial leads.
PMID 18982091·Proc (Bayl Univ Med Cent)·2008
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 3 locations total
- Address
- 1275 YORK AVE
NEW YORK, NY 10065 - Phone
- (212) 639-8557
Quick Facts
- NPI
- 1578825097
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 3
- Years in Practice
- 14
- Publications
- 20
Are you this provider?
Claim Your Profile