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BRADLEY HAYWARD, M.D.
M.D.
Pulmonary Disease Physician
NPI: 1245466051IndividualAccepts Medicare
Specialties, Licenses & Credentials
Pulmonary Disease PhysicianPrimary
Internal Medicine — Pulmonary Disease
Code: 207RP1001X
267061(NY)
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
MD443688(PA)267061(NY)
Critical Care Medicine (Internal Medicine) Physician
Internal Medicine — Critical Care Medicine
Code: 207RC0200X
267061(NY)
Hospice and Palliative Medicine (Internal Medicine) Physician
Internal Medicine — Hospice and Palliative Medicine
Code: 207RH0002X
267061(NY)
CMS Specialties
PrimaryPULMONARY DISEASE
Education
OTHER
Class of 2009
Research & Publications (20)
Clinical evaluation of moroctocog alfa (AF-CC), a new generation of B-domain deleted recombinant factor VIII (BDDrFVIII) for treatment of haemophilia A: demonstration of safety, efficacy, and pharmacokinetic equivalence to full-length recombinant factor VIII.
PMID 19473411·Haemophilia·2009
8-other
IBDfinder and SNPsetter: tools for pedigree-independent identification of autozygous regions in individuals with recessive inherited disease.
PMID 19405095·Hum Mutat·2009
8-other
Ketohexokinase: expression and localization of the principal fructose-metabolizing enzyme.
PMID 19365088·J Histochem Cytochem·2009
7-preclinical
Gas bubbles in seals, dolphins, and porpoises entangled and drowned at depth in gillnets.
PMID 19176498·Vet Pathol·2009
7-preclinical
A novel TNFRSF1A splice mutation associated with increased nuclear factor kappaB (NF-kappaB) transcription factor activation in patients with tumour necrosis factor receptor associated periodic syndrome (TRAPS).
PMID 18086728·Ann Rheum Dis·2008
5-case
Clinical and molecular phenotype of Aicardi-Goutieres syndrome.
PMID 17846997·Am J Hum Genet·2007
8-other
Extensive gene conversion at the PMS2 DNA mismatch repair locus.
PMID 17253626·Hum Mutat·2007
7-preclinical
Cluster A personality disorders: considering the 'odd-eccentric' in psychiatric nursing.
PMID 17229270·Int J Ment Health Nurs·2007
6-review
Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection.
PMID 16845400·Nat Genet·2006
4-observational
Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus.
PMID 16845398·Nat Genet·2006
7-preclinical
A multiple PCR-primer approach to access the microeukaryotic diversity in environmental samples.
PMID 16431157·Protist·2006
7-preclinical
Side-hole to anti-hole conversion in time-resolved transient spectral hole-burning of emerald: ground state level versus excited state population storage in low magnetic fields.
PMID 16189567·Phys Chem Chem Phys·2005
8-other
Phenotype associated with recessively inherited mutations in DNA mismatch repair (MMR) genes.
PMID 16042583·Biochem Soc Trans·2005
6-review
Prognostic significance of DCC and p27Kip1 in colorectal cancer.
PMID 15722793·Appl Immunohistochem Mol Morphol·2005
8-other
Identifying SNPs predictive of phenotype using random forests.
PMID 15593090·Genet Epidemiol·2005
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 · 2 locations total
- Address
- 525 E 68TH ST
NEW YORK, NY 10065 - Phone
- (212) 746-2898
Quick Facts
- NPI
- 1245466051
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 5
- Locations
- 2
- Years in Practice
- 17
- Publications
- 20
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