Physician

Pediatrics

Dr. David H. Viskochil, MD

David Viskochil is an expert in the field of Pediatrics. He attended University of Utah School of Medicine. He received 1 awards: "Fellow (FAAP)". David H. Viskochil, MD is also published. He has 50 publications published. The lastest publication: "Stress and coping in parents of children with Prader-Willi syndrome: Assessment of the impact of a structured plan of care.'

Publications

Evaluation of somatic mutations in tibial pseudarthrosis samples in neurofibromatosis type 1.
Stress and coping in parents of children with Prader-Willi syndrome: Assessment of the impact of a structured plan of care.
The Occurrence of Occult Acetabular Dysplasia in Relatives of Individuals With Developmental Dysplasia of the Hip.
The cyclic AMP pathway is a sex-specific modifier of glioma risk in type 1 neurofibromatosis patients.
Recent developments in neurofibromatoses and RASopathies: Management, diagnosis and current and future therapeutic avenues.
Sirolimus for progressive neurofibromatosis type 1-associated plexiform neurofibromas: a Neurofibromatosis Clinical Trials Consortium phase II study.
Neurofibromin Deficiency-Associated Transcriptional Dysregulation Suggests a Novel Therapy for Tibial Pseudoarthrosis in NF1.
Phenotype of a patient with contiguous deletion of TBX5 and TBX3: Expanding the disease spectrum.
Screening children with neurofibromatosis type 1 for autism spectrum disorder.
Low Bone Mineral Content and Challenges in Interpretation of Dual-Energy X-Ray Absorptiometry in Children With Mucopolysaccharidosis Types I, II, and VI.
Approaches to Treating NF1 Tibial Pseudarthrosis: Consensus From the Children's Tumor Foundation NF1 Bone Abnormalities Consortium.
Fractures in children with neurofibromatosis type 1 from two NF clinics.
A cost savings approach to SPRED1 mutational analysis in individuals at risk for neurofibromatosis type 1.
Peripheral muscle weakness in RASopathies.
Total hip arthroplasty, hip osteoarthritis, total knee arthroplasty, and knee osteoarthritis in patients with developmental dysplasia of the hip and their family membe...
Lower extremity strength and hopping and jumping ground reaction forces in children with neurofibromatosis type 1.
Disorders of the Ras pathway: An introduction.
Costello and cardio-facio-cutaneous syndromes: Moving toward clinical trials in RASopathies.
Multiple increased osteoclast functions in individuals with neurofibromatosis type 1.
Variable expression of neurofibromatosis 1 in monozygotic twins.
Back to the future: proceedings from the 2010 NF Conference.
NF1 exon 22 analysis of individuals with the clinical diagnosis of neurofibromatosis type 1.
Speech-language characteristics of children with neurofibromatosis type 1.
Proceedings from the 2009 genetic syndromes of the Ras/MAPK pathway: From bedside to bench and back.
Neurofibromatosis Type 1 and tumorigenesis: molecular mechanisms and therapeutic implications.
Motor proficiency in children with neurofibromatosis type 1.
Skeletal abnormalities in neurofibromatosis type 1: approaches to therapeutic options.
Familial predisposition to developmental dysplasia of the hip.
Analysis of radiographic characteristics of anterolateral bowing of the leg before fracture in neurofibromatosis type 1.
Tibial geometry in individuals with neurofibromatosis type 1 without anterolateral bowing of the lower leg using peripheral quantitative computed tomography.
Bone mineral density in children with neurofibromatosis type 1.
Evidence of increased bone resorption in neurofibromatosis type 1 using urinary pyridinium crosslink analysis.
Brain anomalies in encephalocraniocutaneous lipomatosis.
Neuroimaging findings in macrocephaly-capillary malformation: a longitudinal study of 17 patients.
Status of the human malformation map: 2007.
Neurofibromatosis type 1 is a genetic skeletal disorder.
The use of anterolateral bowing of the lower leg in the diagnostic criteria for neurofibromatosis type 1.
Bone mineral density in children and adolescents with neurofibromatosis type 1.
A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome.
Double inactivation of NF1 in tibial pseudarthrosis.
Pathologic and molecular analysis in a family with rare mixed supravalvar aortic and pulmonic stenosis.
Molecular, genetic, and cellular pathogenesis of neurofibromas and surgical implications.
Interstitial deletion 8q11.2-q13 with congenital anomalies of CHARGE association.
Elevated catecholamine metabolites in patients with Costello syndrome.
It takes two to tango: mast cell and Schwann cell interactions in neurofibromas.
Malignant peripheral nerve sheath tumor: a comparison of grade, immunophenotype, and cell cycle/growth activation marker expression in sporadic and neurofibromatosis 1...
Molecular characterization of a patient with central nervous system dysmyelination and cryptic unbalanced translocation between chromosomes 4q and 18q.
Status of the human malformation map: 2002.
Lost in translation: ambiguity in nerve sheath tumor nomenclature and its resultant treatment effect.

Schools

University of North Carolina At Chapel Hill
University Of Ut Med Center

Doctors Specialties

Clinical Genetics
Pediatrics

Accepted Insurances

Awards

Fellow (FAAP)

Education

University of Utah School of Medicine

Hospital

University of Utah Health Care - Hospital and Clinics

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