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MICHAEL HALEY, MD
MD
Internal Medicine Physician
NPI: 1720003429IndividualAccepts Medicare
Specialties, Licenses & Credentials
Cardiovascular Disease Physician
Internal Medicine — Cardiovascular Disease
Code: 207RC0000X
200100545(NC)
Critical Care Medicine (Internal Medicine) Physician
Internal Medicine — Critical Care Medicine
Code: 207RC0200X
200100545(NC)
Pulmonary Disease Physician
Internal Medicine — Pulmonary Disease
Code: 207RP1001X
200100545(NC)
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
200100545(NC)
Education
UNIVERSITY OF SOUTH CAROLINA SCHOOL OF MEDICINE
Class of 1999
Research & Publications (20)
Stereotactic radiosurgery in the management of cancer pain.
PMID 19586590·Curr Pain Headache Rep·2009
6-review
Multivariate model for predicting recurrence in congenital diaphragmatic hernia.
PMID 19524735·J Pediatr Surg·2009
8-other
Emission from regioisomeric bis(phenylethynyl)benzenes during pulse radiolysis.
PMID 19366233·J Org Chem·2009
8-other
Gastric tube-pericardial fistula: a remote complication of esophageal replacement for long gap esophageal atresia.
PMID 19573675·J Pediatr Surg·2009
5-case
Synthesis of alpha-ketoester- and alpha-hydroxyester-substituted isoindazoles via the thermodynamic coarctate cyclization of ester-terminated azo-ene-yne systems.
PMID 19642649·J Org Chem·2009
8-other
Percutaneous distal perfusion of the lower extremity after femoral cannulation for venoarterial extracorporeal membrane oxygenation in a small child.
PMID 19231552·J Pediatr Surg·2009
5-case
Norepinephrine increases blood pressure but not survival with anthrax lethal toxin in rats.
PMID 19242337·Crit Care Med·2009
7-preclinical
Protonation activates anion binding and alters binding selectivity in new inherently fluorescent 2,6-bis(2-anilinoethynyl)pyridine bisureas.
PMID 19532876·Chem Commun (Camb)·2009
8-other
Reactions in the conjugated 'ene-ene-yne' manifold: five-membered ring fragmentation and ring formation via coarctate/pseudocoarctate mechanisms.
PMID 18197350·Chem Soc Rev·2008
8-other
Synthesis and properties of butyl-capped dehydrothieno[14]annulenes and their conversion into terthiophenes.
PMID 18712877·Org Lett·2008
8-other
Synthesis and structure-property relationships of donor/acceptor-functionalized bis(dehydrobenzo[18]annuleno)benzenes.
PMID 18421388·Org Biomol Chem·2008
8-other
Structure-property relationships of fluorinated donor/acceptor tetrakis(phenylethynyl)benzenes and bis(dehydrobenzoannuleno)benzenes.
PMID 18278934·J Org Chem·2008
8-other
Fine-tuning of radiolysis induced emission by variable substitution of donor-/acceptor-substituted tetrakis(arylethynyl)benzenes.
PMID 18380481·J Org Chem·2008
8-other
Computational analysis on the dual reactivity of conjugated "ene-ene-yne" systems.
PMID 18928321·J Org Chem·2008
8-other
Structure-property investigations of conjugated thiophenes fused onto a dehydro[14]annulene scaffold.
PMID 18507443·J Org Chem·2008
8-other
Water and hydrogen halides serve the same structural role in a series of 2+2 hydrogen-bonded dimers based on 2,6-bis(2-anilinoethynyl)pyridine sulfonamide receptors.
PMID 17992675·Angew Chem Int Ed Engl·2008
8-other
Synthesis of 1-substituted benzo[c]isoxazol-3(1H)-imines via tandem nitroso-ene/intramolecular cyclizations of 2-nitrosobenzonitrile.
PMID 18358045·J Org Chem·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 · 5 locations total
- Address
- 1350 S KINGS DR
CHARLOTTE, NC 28207 - Phone
- (704) 446-1242
Locations (5)
Practice Location
1350 S KINGS DR, CHARLOTTE, NC
(704) 446-1242
Practice Location
1100 BLYTHE BLVD, CHARLOTTE, NC
(704) 355-4300
Practice Location
1000 BLYTHE BLVD, CHARLOTTE, NC
(704) 355-2000
Practice Location
1350 S KINGS DR, CHARLOTTE, NC
(704) 446-4490
Practice Location
2301 US HIGHWAY 74 W, WADESBORO, NC
(704) 994-4500
Quick Facts
- NPI
- 1720003429
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 4
- Locations
- 5
- Years in Practice
- 27
- Publications
- 20
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