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KENTON HOLDEN, M.D.
M.D.
Pediatric Neurodevelopmental Disabilities Physician
NPI: 1780640839Individual
Specialties, Licenses & Credentials
Pediatric Neurodevelopmental Disabilities PhysicianPrimary
Pediatrics — Neurodevelopmental Disabilities
Code: 2080P0008X
C47743(SC)
Research & Publications (20)
X-linked MCT8 gene mutations: characterization of the pediatric neurologic phenotype.
PMID 16417886·J Child Neurol·2005
5-case
Dietary intake and blood folate levels in Honduran women of childbearing age.
PMID 12150580·J Child Neurol·2002
8-other
Serum leptin level and cognition in the elderly: Findings from the Health ABC Study.
PMID 18358569·Neurobiol Aging·2009
8-other
Co-detection of Bartonella henselae, Borrelia burgdorferi, and Anaplasma phagocytophilum in Ixodes pacificus ticks from California, USA.
PMID 16584332·Vector Borne Zoonotic Dis·2006
4-observational
Inhibition of dengue virus translation and RNA synthesis by a morpholino oligomer targeted to the top of the terminal 3' stem-loop structure.
PMID 16214197·Virology·2006
7-preclinical
Enhancement of dengue virus translation: role of the 3' untranslated region and the terminal 3' stem-loop domain.
PMID 15476880·Virology·2004
7-preclinical
Detection of Borrelia burgdorferi, Ehrlichia chaffeensis, and Anaplasma phagocytophilum in ticks (Acari: Ixodidae) from a coastal region of California.
PMID 14680123·J Med Entomol·2003
7-preclinical
Adherence and complementary and alternative medicine use among Honduran people with epilepsy.
PMID 19435580·Epilepsy Behav·2009
8-other
A questionnaire study of the approach to the anorexia-cachexia syndrome in patients with cancer by staff in a district general hospital.
PMID 18663481·Support Care Cancer·2009
8-other
Expanding the neurologic phenotype of oculodentodigital dysplasia in a 4-generation Hispanic family.
PMID 18660473·J Child Neurol·2008
5-case
Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome.
PMID 18674751·Am J Hum Genet·2008
7-preclinical
The modified Atkins diet: a potential treatment for developing countries.
PMID 18782218·Epilepsia·2008
5-case
Humour experience in schizophrenia: relationship with executive dysfunction and psychosocial impairment.
PMID 18177530·Psychol Med·2008
8-other
Finding new etiologies of mental retardation and hypotonia: X marks the spot.
PMID 18190539·Dev Med Child Neurol·2008
6-review
Audit of symptoms and prescribing in patients with the anorexia-cachexia syndrome.
PMID 18246443·Pharm World Sci·2008
8-other
Persistence of Borrelia burgdorferi following antibiotic treatment in mice.
PMID 18316520·Antimicrob Agents Chemother·2008
7-preclinical
Persistent growth failure in Prader-Willi syndrome associated with short-chain acyl-CoA dehydrogenase gene variant.
PMID 18184946·J Child Neurol·2008
5-case
A novel GLRA1 mutation associated with an atypical hyperekplexia phenotype.
PMID 19073849·J Child Neurol·2008
8-other
FIRST: a practical approach to the causes and management of febrile seizures.
PMID 19073858·J Child Neurol·2008
6-review
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 101 GREGOR MENDEL CIR
GREENWOOD, SC 29646 - Phone
- (864) 941-8100
Quick Facts
- NPI
- 1780640839
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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