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RICHARD BOLES, D.M.D.
D.M.D.
General Practice Dentistry
NPI: 1730234584Individual
Specialties, Licenses & Credentials
General Practice DentistryPrimary
Dentist — General Practice
Code: 1223G0001X
DS024036-L(PA)
Research & Publications (20)
Mitochondrial DNA and gastrointestinal motor and sensory functions in health and functional gastrointestinal disorders.
PMID 19147801·Am J Physiol Gastrointest Liver Physiol·2009
8-other
Two common mitochondrial DNA polymorphisms are highly associated with migraine headache and cyclic vomiting syndrome.
PMID 19220304·Cephalalgia·2009
8-other
A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiency.
PMID 19157942·Mol Genet Metab·2009
6-review
Are pediatric and adult-onset cyclic vomiting syndrome (CVS) biologically different conditions? Relationship of adult-onset CVS with the migraine and pediatric CVS-associated common mtDNA polymorphisms 16519T and 3010A.
PMID 19368653·Neurogastroenterol Motil·2009
8-other
Symptoms of somatization as a rapid screening tool for mitochondrial dysfunction in depression.
PMID 18294386·Biopsychosoc Med·2008
8-other
Mitochondrial energy depletion in depression with somatization.
PMID 18230947·Psychother Psychosom·2008
8-other
Reflex sympathetic dystrophy: complex regional pain syndrome type I in children with mitochondrial disease and maternal inheritance.
PMID 18192313·Arch Dis Child·2008
8-other
North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition consensus statement on the diagnosis and management of cyclic vomiting syndrome.
PMID 18728540·J Pediatr Gastroenterol Nutr·2008
8-other
The additive and interactive effects of parenting style and temperament in obese youth seeking treatment.
PMID 18698318·Int J Obes (Lond)·2008
8-other
Supervising children during parental distractions.
PMID 18334495·J Pediatr Psychol·2008
4-observational
Mutations in the MPV17 gene are responsible for rapidly progressive liver failure in infancy.
PMID 17694548·Hepatology·2007
5-case
National threatened species listing based on IUCN criteria and regional guidelines: current status and future perspectives.
PMID 17531047·Conserv Biol·2007
7-preclinical
A patient with arginase deficiency and episodic hyperammonemia successfully treated with menses cessation.
PMID 16963300·Mol Genet Metab·2006
5-case
Individual human hair mitochondrial DNA control region heteroplasmy proportions in mothers and children.
PMID 16412703·Mitochondrion·2006
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
- 16000 PERRY HWY
WARRENDALE, PA 15086 - Phone
- (724) 935-9966
Quick Facts
- NPI
- 1730234584
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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