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CAROL VANCE, M.D.
M.D.
Pediatric Neurodevelopmental Disabilities Physician
NPI: 1417012022Individual
Specialties, Licenses & Credentials
Pediatric Neurodevelopmental Disabilities PhysicianPrimary
Pediatrics — Neurodevelopmental Disabilities
Code: 2080P0008X
M9751(ID)
Research & Publications (20)
Perceived challenges to obtaining informed consent for a time-sensitive emergency department study of pediatric status epilepticus: results of two focus groups.
PMID 19673713·Acad Emerg Med·2009
8-other
Three-dimensional MRI volumetric measurements of the normal fetal colon.
PMID 19234275·AJR Am J Roentgenol·2009
8-other
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6.
PMID 19251628·Science·2009
7-preclinical
Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotype.
PMID 19459885·Clin Genet·2009
5-case
Integrating microarray analysis and the soybean genome to understand the soybeans iron deficiency response.
PMID 19678937·BMC Genomics·2009
8-other
Artificial fertilization for amphibian conservation: current knowledge and future considerations.
PMID 19026442·Theriogenology·2009
6-review
Applied reproductive technologies and genetic resource banking for amphibian conservation.
PMID 19567216·Reprod Fertil Dev·2009
6-review
Arabidopsis UDP-sugar pyrophosphorylase: evidence for two isoforms.
PMID 18768324·Plant Physiol Biochem·2008
8-other
Essential role of MYB transcription factor: PvPHR1 and microRNA: PvmiR399 in phosphorus-deficiency signalling in common bean roots.
PMID 18771575·Plant Cell Environ·2008
8-other
Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis.
PMID 18802454·PLoS Genet·2008
8-other
Effectiveness of transcutaneous electrical nerve stimulation for treatment of hyperalgesia and pain.
PMID 19007541·Curr Rheumatol Rep·2008
6-review
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis.
PMID 18309045·Science·2008
7-preclinical
CHMP2B mutations are not a common cause of familial or sporadic amyotrophic lateral sclerosis.
PMID 18270236·J Neurol Neurosurg Psychiatry·2008
8-other
Ultrasound-assisted peripheral venous access in young children: a randomized controlled trial and pilot feasibility study.
PMID 19561750·West J Emerg Med·2008
8-other
Molecular cloning, characterization and regulation of two different NADH-glutamate synthase cDNAs in bean nodules.
PMID 18182018·Plant Cell Environ·2008
8-other
Corticosteroid-induced suppression of in vitro lymphocyte proliferation in four captive rhinoceros species.
PMID 18229856·J Zoo Wildl Med·2007
7-preclinical
Differences between forest type and vertical strata in the diversity and composition of hymenopteran families and mymarid genera in northeastern temperate forests.
PMID 18284731·Environ Entomol·2007
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1619 CURLEW DR STE 6
AMMON, ID 83406 - Phone
- (208) 523-4688
Quick Facts
- NPI
- 1417012022
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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