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DAVID VISKOCHIL, MD
MD
Clinical Genetics (M.D.) Physician
NPI: 1760561336IndividualAccepts Medicare
Specialties, Licenses & Credentials
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
174520-1205(UT)
CMS Specialties
PrimaryPEDIATRIC MEDICINE
Additional
MEDICAL GENETICS AND GENOMICS
Education
UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL SCHOOL OF MEDICINE
Class of 1985
Research & Publications (20)
Non-neurogenic sarcomas in four children and young adults with neurofibromatosis type 1.
PMID 15103715·Am J Med Genet A·2004
5-case
It takes two to tango: mast cell and Schwann cell interactions in neurofibromas.
PMID 14679174·J Clin Invest·2003
6-review
Analysis of radiographic characteristics of anterolateral bowing of the leg before fracture in neurofibromatosis type 1.
PMID 19461382·J Pediatr Orthop·2009
5-case
Familial occurrence of schwannomas and malignant rhabdoid tumour associated with a duplication in SMARCB1.
PMID 19124645·J Med Genet·2009
8-other
Tibial geometry in individuals with neurofibromatosis type 1 without anterolateral bowing of the lower leg using peripheral quantitative computed tomography.
PMID 19118659·Bone·2009
8-other
Evidence of increased bone resorption in neurofibromatosis type 1 using urinary pyridinium crosslink analysis.
PMID 18317233·Pediatr Res·2008
8-other
Neuroimaging findings in macrocephaly-capillary malformation: a longitudinal study of 17 patients.
PMID 18000912·Am J Med Genet A·2007
5-case
The use of anterolateral bowing of the lower leg in the diagnostic criteria for neurofibromatosis type 1.
PMID 17666887·Genet Med·2007
6-review
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders.
PMID 17564967·Am J Hum Genet·2007
8-other
The MPS I registry: design, methodology, and early findings of a global disease registry for monitoring patients with Mucopolysaccharidosis Type I.
PMID 17336562·Mol Genet Metab·2007
8-other
Bone mineral density in children and adolescents with neurofibromatosis type 1.
PMID 17188620·J Pediatr·2007
8-other
An absence of cutaneous neurofibromas associated with a 3-bp inframe deletion in exon 17 of the NF1 gene (c.2970-2972 delAAT): evidence of a clinically significant NF1 genotype-phenotype correlation.
PMID 17160901·Am J Hum Genet·2007
8-other
A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome.
PMID 17033969·Am J Hum Genet·2006
7-preclinical
Clinical and molecular aspects of an informative family with neurofibromatosis type 1 and Noonan phenotype.
PMID 16542390·Clin Genet·2006
5-case
Molecular, genetic, and cellular pathogenesis of neurofibromas and surgical implications.
PMID 16385324·Neurosurgery·2006
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
- 100 MARIO CAPECCHI DR
SALT LAKE CITY, UT 84113 - Phone
- (801) 213-3599
Quick Facts
- NPI
- 1760561336
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 41
- Publications
- 20
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