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I. NELSON, MD,PC
MD,PC
Otolaryngology Physician
NPI: 1972517043Individual
Specialties, Licenses & Credentials
Otolaryngology PhysicianPrimary
Otolaryngology
Code: 207Y00000X
1526791205(UT)
Research & Publications (20)
Clinical outcomes and fusion success associated with the use of BoneSave in spinal surgery.
PMID 19629506·Arch Orthop Trauma Surg·2010
8-other
Street ball, swim team and the sour cream machine: a cluster analysis of out of school time participation portfolios.
PMID 19669898·J Youth Adolesc·2009
8-other
The value of radiographs obtained during forced traction under general anaesthesia in predicting flexibility in idiopathic scoliosis with Cobb angles exceeding 60 degree.
PMID 18978268·J Bone Joint Surg Br·2008
8-other
A novel locus for autosomal dominant "uncomplicated" hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3.
PMID 17605047·Hum Genet·2007
8-other
PTA testing, the Westmead post traumatic amnesia scale and opiate analgesia: a cautionary note.
PMID 18066941·Brain Inj·2007
8-other
Helical tomotherapy: image guidance and adaptive dose guidance.
PMID 17641508·Front Radiat Ther Oncol·2007
6-review
Exercise when young provides lifelong benefits to bone structure and strength.
PMID 17129172·J Bone Miner Res·2007
7-preclinical
SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years.
PMID 16401858·Neurology·2006
8-other
Anterior transvertebral transposition of the spinal cord for the relief of paraplegia associated with congenital cervicothoracic kyphoscoliosis. Technical note.
PMID 17048777·J Neurosurg Spine·2006
5-case
A founder effect and mutational hot spots may contribute to the most frequent mutations in the SPG3A gene.
PMID 16612642·Neurogenetics·2006
8-other
A new phenotype linked to SPG27 and refinement of the critical region on chromosome.
PMID 16511635·J Neurol·2006
4-observational
New phenotypic diversity associated with the mitochondrial tRNA(SerUCN) gene mutation.
PMID 15833431·Neuromuscul Disord·2005
5-case
Community-based screening for cardiovascular disease and diabetes using HbA1c.
PMID 15110052·Am J Prev Med·2004
8-other
Cervical spondyloptosis caused by an aneurysmal bone cyst: a case report.
PMID 12590221·Spine (Phila Pa 1976)·2003
5-case
Classical mitochondrial phenotypes without mtDNA mutations: the possible role of nuclear genes.
PMID 14581685·Neurology·2003
5-case
Six novel connexin32 (GJB1) mutations in X-linked Charcot-Marie-Tooth disease.
PMID 12185164·J Neurol Neurosurg Psychiatry·2002
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
- 556 E 4020 N
PROVO, UT 84604 - Phone
- (801) 225-5881
Quick Facts
- NPI
- 1972517043
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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