Medical complications, clinical findings, and educational outcomes in adults with Noonan syndrome

Sudden onset of Chiari malformation Type I in previously asymptomatic patients

(2011) Luca Massimi et al.   Journal of Neurosurgery-Pediatrics

Orthopaedic Conditions in Ras/MAPK Related Disorders

(2011) Kent A. Reinker et al.   JOURNAL OF PEDIATRIC ORTHOPAEDICS

High incidence of progressive postnatal cerebellar enlargement in Costello syndrome: Brain overgrowth associated withHRASmutations as the likely cause of structural brain and spinal cord abnormalities

(2010) Karen W. Gripp et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Bone resorption in syndromes of the Ras/MAPK pathway

(2010) DA Stevenson et al.   CLINICAL GENETICS

Skeletal abnormalities in neurofibromatosis type 1: Approaches to therapeutic options

(2009) Florent Elefteriou et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

The Rising Prevalence of Chronic Low Back Pain

(2009) Janet K. Freburger et al.   ARCHIVES OF INTERNAL MEDICINE

Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair

(2009) Viviana Cordeddu et al.   NATURE GENETICS

LEOPARD Syndrome and Chiari Type I Malformation

(2009) Alexandra D. Beier et al.   NEUROLOGIST

Prevalence of Refractive Error in the United States, 1999-2004

(2008) Susan Vitale   ARCHIVES OF OPHTHALMOLOGY

Generalized metabolic bone disease in Neurofibromatosis type I

(2008) Nicola Brunetti-Pierri et al.   MOLECULAR GENETICS AND METABOLISM