Affiliation: University of California
- Social impairments in chromosome 22q11.2 deletion syndrome (22q11.2DS): autism spectrum disorder or a different endophenotype?Kathleen Angkustsiri
Department of Pediatrics, University of California at Davis Medical Center, Sacramento, CA, USA
J Autism Dev Disord 44:739-46. 2014..2DS. Differences in methodology, along with comorbid conditions such as anxiety, likely contribute to false elevations in ASD prevalence and information from multiple sources should be included in the evaluation of ASD. ..
- An examination of the relationship of anxiety and intelligence to adaptive functioning in children with chromosome 22q11.2 deletion syndromeKathleen Angkustsiri
Department of Pediatrics, University of California at Davis Medical Center, Sacramento, USA
J Dev Behav Pediatr 33:713-20. 2012..This study investigates the relationship between anxiety symptoms and adaptive function in children with chromosome 22q11.2 deletion syndrome (22q11.2DS)...
- Minor physical anomalies in children with autism spectrum disordersKathleen Angkustsiri
University of California, Davis, USA
Autism 15:746-60. 2011..This study employs an adaptation of Miles and Hillman's (2000) classifications by using photographs to identify a subgroup with significant dysmorphology among children with ASD, typical development (TYP), and developmental delay (DD)...
- Fragile X syndrome with anxiety disorder and exceptional verbal intelligenceKathleen Angkustsiri
M I N D Institute, University of California Davis Medical Center, Sacramento, California 95817, USA
Am J Med Genet A 146:376-9. 2008..Women with FXS can present primarily with learning and emotional problems, and clinicians should consider FXS in these women regardless of their IQ...
- Two boys with fragile x syndrome and hepatic tumorsJuthamas Wirojanan
Medical Investigation of Neurodevelopmental Disorders, University of California Davis Health System, Sacramento, CA 95817, USA
J Pediatr Hematol Oncol 30:239-41. 2008..We speculate regarding molecular pathways that might explain the cooccurrence of the 2 conditions. Further examination of a possible functional link between hepatic neoplasia and loss of FMRP is warranted...
- A girl with fragile X premutation from sperm donationJuthamas Wirojanan
MIND Institute, University of California Davis Medical Center, Sacramento, California 95817, USA
Am J Med Genet A 146:888-92. 2008..We suggest fragile X DNA screening in gamete donor candidates to decrease the chance of fragile X involvement in their offspring...
- Utilization patterns of conventional and complementary/alternative treatments in children with autism spectrum disorders and developmental disabilities in a population-based studyRoger S Akins
Department of Pediatrics, School of Medicine, University of California, Davis, CA MIND Medical Investigation of Neurodevelopmental Disorders Institute, University of California, Davis, CA Department of Pediatrics, Naval Medical Center Portsmouth, Portsmouth, VA Divisions of Epidemiology and Environmental and Occupational Health, Department of Public Health Sciences, School of Medicine, University of California, Davis, CA
J Dev Behav Pediatr 35:1-10. 2014..To compare the utilization of conventional treatments and utilization of complementary and alternative medicine in preschoolers with autism spectrum disorders (ASD) and other developmental disabilities (DD)...
- Regression in autism: prevalence and associated factors in the CHARGE StudyRobin L Hansen
Medical Investigation of Neurodevelopmental Disorders Institute, University of California, Davis, Sacramento 95817, USA
Ambul Pediatr 8:25-31. 2008..The aim of this study was to examine the prevalence of regressive autism and associated demographic, medical, and developmental factors by using 2 different definitions of regression based on the Autism Diagnostic Interview, Revised...
- Mapping the deletion endpoints in individuals with 22q11.2 deletion syndrome by droplet digital PCRVicki J Hwang
Department of Biochemistry and Molecular Medicine, UC Davis, 2700 Stockton Blvd, Suite 2102, Sacramento 95817, CA, USA
BMC Med Genet 15:106. 2014....