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MEGHAN GERAGHTY, MD
MD
Hospitalist Physician
NPI: 1609167584IndividualAccepts Medicare
Specialties, Licenses & Credentials
Hospitalist PhysicianPrimary
Hospitalist
Code: 208M00000X
0101269034(VA)
Education
OTHER
Class of 2011
Research & Publications (20)
High-frequency detection of deletions and variable rearrangements at the ornithine transcarbamylase (OTC) locus by oligonucleotide array CGH.
PMID 19138872·Mol Genet Metab·2009
8-other
Patient mobile telephone 'text' reminder: a novel way to reduce non-attendance at the ENT out-patient clinic.
PMID 17470313·J Laryngol Otol·2008
8-other
Utility of oligonucleotide array-based comparative genomic hybridization for detection of target gene deletions.
PMID 18487280·Clin Chem·2008
5-case
Assessment of techniques used to evaluate the effect of posture and cardiac output on cerebral autoregulation.
PMID 19163083·Annu Int Conf IEEE Eng Med Biol Soc·2008
8-other
Discrepant DNA analysis in three patients with inherited arrhythmia: molecular genetic test results deserve a second glance.
PMID 18449933·Am J Med Genet A·2008
5-case
Genetic and clinical heterogeneity in eIF2B-related disorder.
PMID 18263758·J Child Neurol·2008
8-other
Hypoglycaemia in an adult male: a surprising finding in pursuit of insulinoma.
PMID 18318091·Surgeon·2008
5-case
Cultural perceptions of health and diabetes among Native American men.
PMID 19029735·J Health Care Poor Underserved·2008
8-other
Three novel mutations in KIF21A highlight the importance of the third coiled-coil stalk domain in the etiology of CFEOM1.
PMID 17511870·BMC Genet·2007
8-other
Effects of sequential changes from conventional ventilation to high-frequency oscillatory ventilation at increasing mean airway pressures in an ovine model of combined lung and head injury.
PMID 17261210·Eur J Anaesthesiol·2007
7-preclinical
Molecular autopsy in the sudden cardiac death of a young woman: a first Canadian report.
PMID 17876385·Can J Cardiol·2007
5-case
Development of a clinical assay for detection of GAA mutations and characterization of the GAA mutation spectrum in a Canadian cohort of individuals with glycogen storage disease, type II.
PMID 17723315·Mol Genet Metab·2007
8-other
Neuroimaging and serologic markers of neurologic injury after cardiac arrest.
PMID 16443133·Neurol Clin·2006
6-review
Identification of a recurrent mutation in the human hairless gene underlying atrichia with papular lesions.
PMID 15953070·Clin Exp Dermatol·2005
5-case
Effects of carotid or vertebrobasilar stent placement on cerebral perfusion and cognition.
PMID 16091529·AJNR Am J Neuroradiol·2005
8-other
Co-proxamol and suicide: Availability of co-proxamol has been successfully reduced in Doncaster.
PMID 12896948·BMJ·2003
8-other
The relationship of plasma glutamine to ammonium and of glycine to acid-base balance in propionic acidaemia.
PMID 12872849·J Inherit Metab Dis·2003
8-other
Mode of anti-fungal activity of 1,10-phenanthroline and its Cu(II), Mn(II) and Ag(I) complexes.
PMID 12572690·Biometals·2003
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
- 1215 LEE ST
CHARLOTTESVILLE, VA 22908 - Phone
- (434) 243-4288
Quick Facts
- NPI
- 1609167584
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 15
- Publications
- 20
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