The Cost of Raising Individuals with Fragile X or Chromosome 15 Imprinting Disorders in Australia
暂无分享,去创建一个
J. Slee | D. Amor | S. Arora | S. Goodall | C. Rogers | E. Baker | D. Godler | M. Cross | C. Simons | P. Date | James O'Brien | Christina Cahir | James O’Brien
[1] M. Field,et al. DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X Syndrome , 2020, International journal of molecular sciences.
[2] Meghan T. Miller,et al. Measuring What Matters to Individuals with Angelman Syndrome and Their Families: Development of a Patient-Centered Disease Concept Model , 2020, Child psychiatry and human development.
[3] A. Franzese,et al. Caring and living with Prader-Willi syndrome in Italy: integrating children, adults and parents’ experiences through a multicentre narrative medicine research , 2020, BMJ Open.
[4] R. Viney,et al. Societal cost of childhood intellectual disability in Australia. , 2020, Journal of intellectual disability research : JIDR.
[5] Rujuta B. Wilson,et al. Behavioral characterization of dup15q syndrome: Toward meaningful endpoints for clinical trials , 2019, American journal of medical genetics. Part A.
[6] S. A. Vera,et al. Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome , 2019, Journal of Neurodevelopmental Disorders.
[7] H. Moll,et al. An overview of health issues and development in a large clinical cohort of children with Angelman syndrome , 2019, American journal of medical genetics. Part A.
[8] D. J. Driscoll,et al. Early Diagnosis in Prader–Willi Syndrome Reduces Obesity and Associated Co-Morbidities , 2019, Genes.
[9] L. Bird,et al. Healthcare burden among individuals with Angelman syndrome: Findings from the Angelman Syndrome Natural History Study , 2019, Molecular genetics & genomic medicine.
[10] J. Schweitzer,et al. Cognitive training for children and adolescents with fragile X syndrome: a randomized controlled trial of Cogmed , 2019, Journal of neurodevelopmental disorders.
[11] D. Amor,et al. Exploring autism symptoms in an Australian cohort of patients with Prader-Willi and Angelman syndromes , 2018, Journal of Neurodevelopmental Disorders.
[12] C. Dissanayake,et al. Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile X , 2018, Scientific Reports.
[13] C. Dissanayake,et al. Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile X , 2018, Scientific Reports.
[14] M. Raspa,et al. Public Health Literature Review of Fragile X Syndrome , 2017, Pediatrics.
[15] M. Butler,et al. Causes of Death in Prader-Willi Syndrome: Prader-Willi Syndrome Association (USA) 40-Year Mortality Survey , 2016, Genetics in Medicine.
[16] M. Butler,et al. The High Direct Medical Costs of Prader-Willi Syndrome , 2016, The Journal of pediatrics.
[17] G. Iskrov,et al. Social/economic costs and health-related quality of life in patients with fragile X syndrome in Europe , 2016, The European Journal of Health Economics.
[18] T. Nazareth,et al. Burden of illness among patients with fragile X syndrome (FXS): a Medicaid perspective , 2016, Current medical research and opinion.
[19] L. Zwaigenbaum,et al. Autism spectrum disorder in Prader–Willi syndrome: A systematic review , 2015, American journal of medical genetics. Part A.
[20] Chris Oliver,et al. Prevalence of autism spectrum disorder phenomenology in genetic disorders: a systematic review and meta-analysis. , 2015, The lancet. Psychiatry.
[21] Stormy J. Chamberlain,et al. Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes. , 2015, Pediatric clinics of North America.
[22] J. Loeber,et al. Current status of newborn screening worldwide: 2015. , 2015, Seminars in perinatology.
[23] J. Brazier,et al. Developing a utility index for the Aberrant Behavior Checklist (ABC-C) for fragile X syndrome , 2014, Quality of Life Research.
[24] Dalyir I. Pretto,et al. Clinical and molecular implications of mosaicism in FMR1 full mutations , 2014, Front. Genet..
[25] D. Loesch,et al. Early detection of fragile X syndrome: applications of a novel approach for improved quantitative methylation analysis in venous blood and newborn blood spots. , 2014, Clinical chemistry.
[26] S. Spence,et al. A survey of seizures and current treatments in 15q duplication syndrome , 2014, Epilepsia.
[27] John O. Willis,et al. Wechsler Intelligence Scale for Children–Fourth Edition , 2014 .
[28] John O. Willis,et al. Wechsler Adult Intelligence Scale–Fourth Edition , 2014 .
[29] D. Wechsler,et al. Wechsler Adult Intelligence Scale - fourth edition , 2012 .
[30] D H Geschwind,et al. Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts , 2012, Molecular Psychiatry.
[31] Allan L. Reiss,et al. Psychometric Study of the Aberrant Behavior Checklist in Fragile X Syndrome and Implications for Targeted Treatment , 2012, Journal of autism and developmental disorders.
[32] C. Doran,et al. How much does intellectual disability really cost? First estimates for Australia , 2012, Journal of intellectual & developmental disability.
[33] D. Bailey,et al. Employment impact and financial burden for families of children with fragile X syndrome: findings from the National Fragile X Survey. , 2010, Journal of intellectual disability research : JIDR.
[34] E. Scholte,et al. Maternal parenting stress in families with a child with Angelman syndrome or Prader–Willi syndrome , 2010, Journal of intellectual & developmental disability.
[35] Клинические дисциплины. Autism Diagnostic Observation Schedule , 2010 .
[36] M. Tauber,et al. Endocrine Disorders in Children with Prader-Willi Syndrome – Data from 142 Children of the French Database , 2010, Hormone Research in Paediatrics.
[37] A. Salvatoni,et al. The Italian National Survey for Prader–Willi syndrome: An epidemiologic study , 2008, American journal of medical genetics. Part A.
[38] A. Thomson,et al. A long-term population-based clinical and morbidity profile of Angelman syndrome in Western Australia: 1953–2003 , 2006, Disability and rehabilitation.
[39] S. Bradley-Johnson. Mullen Scales of Early Learning , 1997 .
[40] E. Thiele,et al. Angelman syndrome in adulthood , 1996, American journal of medical genetics. Part A.
[41] V. Wright,et al. Endocrine disorders , 1991, Current opinion in rheumatology.
[42] M. Aman,et al. The aberrant behavior checklist: a behavior rating scale for the assessment of treatment effects. , 1985, American journal of mental deficiency.
[43] S. Freeman. Wechsler Preschool and Primary Scale of Intelligence , 2021, Encyclopedia of Autism Spectrum Disorders.
[44] E. Dykens,et al. Cognitive and adaptive advantages of growth hormone treatment in children with Prader‐Willi syndrome , 2017, Journal of child psychology and psychiatry, and allied disciplines.
[45] A. Thomsona,et al. A long-term population-based clinical and morbidity profile of Angelman syndrome in Western Australia : 1953 – 2003 , 2006 .
[46] Martin Knapp,et al. Costing psychiatric interventions. , 1992 .
[47] P. Feros. Pharmaceutical benefits scheme. , 1986, The Medical journal of Australia.