Early development in Rett syndrome – the benefits and difficulties of a birth cohort approach
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[1] S. Brage,et al. Criterion validity of the Physical Activity Scale (PAS2) in Danish adults , 2018, Scandinavian journal of public health.
[2] W. Kaufmann,et al. Parents’ initial concerns about the development of their children later diagnosed with fragile X syndrome , 2017, Journal of intellectual & developmental disability.
[3] M. Lauritsen,et al. Early development in children that are later diagnosed with disorders of attention and activity: a longitudinal study in the Danish National Birth Cohort , 2016, European Child & Adolescent Psychiatry.
[4] A. Bisgaard,et al. Is it possible to diagnose Rett syndrome before classical symptoms become obvious? Review of 24 Danish cases born between 2003 and 2012. , 2015, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
[5] S. Ozonoff. Editorial: Early detection of mental health and neurodevelopmental disorders: the ethical challenges of a field in its infancy. , 2015, Journal of Child Psychology and Psychiatry and Allied Disciplines.
[6] S. Bölte,et al. Comparing social reciprocity in preserved speech variant and typical Rett syndrome during the early years of life. , 2015, Research in developmental disabilities.
[7] Heather M. O'Leary,et al. Age of diagnosis in Rett syndrome: patterns of recognition among diagnosticians and risk factors for late diagnosis. , 2015, Pediatric neurology.
[8] S. Girdler,et al. Aspects of speech‐language abilities are influenced by MECP2 mutation type in girls with Rett syndrome , 2015, American journal of medical genetics. Part A.
[9] A. Antonietti,et al. Recent insights into genotype-phenotype relationships in patients with Rett syndrome using a fine grain scale. , 2014, Research in developmental disabilities.
[10] Hye-Seung Lee,et al. Developmental delay in Rett syndrome: data from the natural history study , 2014, Journal of Neurodevelopmental Disorders.
[11] Larah van der Meer,et al. Developmental profile of speech-language and communicative functions in an individual with the Preserved Speech Variant of Rett syndrome , 2014, Developmental neurorehabilitation.
[12] J. Sigafoos,et al. Monozygotic Twins with Rett Syndrome: Phenotyping the First Two Years of Life , 2014, Journal of developmental and physical disabilities.
[13] Florian B. Pokorny,et al. Three different profiles: Early socio-communicative capacities in typical Rett syndrome, the preserved speech variant and normal development , 2014, Developmental neurorehabilitation.
[14] P. Marschik. The Pivotal Role of Parents in Documenting Early Development , 2014, North American Journal of Medicine and Science.
[15] H. Leonard,et al. Early development and regression in Rett syndrome , 2013, Clinical genetics.
[16] Jeff Sigafoos,et al. Early socio-communicative forms and functions in typical Rett syndrome. , 2013, Research in developmental disabilities.
[17] Lonnie Zwaigenbaum,et al. Early identification of autism spectrum disorders , 2013, Behavioural Brain Research.
[18] Jeff Sigafoos,et al. Changing the perspective on early development of Rett syndrome , 2013, Research in developmental disabilities.
[19] Erik T Parner,et al. Early Signs of Autism in Toddlers: A Follow-Up Study in the Danish National Birth Cohort , 2013, Journal of Autism and Developmental Disorders.
[20] Tony Charman,et al. Infants at risk for autism: a European perspective on current status, challenges and opportunities , 2013, European Child & Adolescent Psychiatry.
[21] W. Kaufmann,et al. Profiling early socio-communicative development in five young girls with the preserved speech variant of Rett syndrome , 2012, Research in developmental disabilities.
[22] W. Kaufmann,et al. Peculiarities in the gestural repertoire: An early marker for Rett syndrome? , 2012, Research in developmental disabilities.
[23] P. Marschik,et al. Differences between girls and boys in emerging language skills: evidence from 10 language communities. , 2012, The British journal of developmental psychology.
[24] Markus Gugatschka,et al. Early speech–language development in females with Rett syndrome: focusing on the preserved speech variant , 2012, Developmental medicine and child neurology.
[25] Christa Einspieler,et al. Methodological note: Video analysis of the early development of Rett syndrome—one method for many disciplines , 2011, Developmental neurorehabilitation.
[26] P. Bech,et al. Increasing prevalence of depression from 2000 to 2006 , 2011, Scandinavian journal of public health.
[27] C. Pedersen,et al. The Danish Civil Registration System , 2011, Scandinavian journal of public health.
[28] A. Nybo Andersen,et al. The Danish National Birth Cohort: Selected scientific contributions within perinatal epidemiology and future perspectives , 2011, Scandinavian journal of public health.
[29] Elsebeth Lynge,et al. The Danish National Patient Register , 2011, Scandinavian journal of public health.
[30] H. Leonard,et al. Altered Attainment of Developmental Milestones Influences the Age of Diagnosis of Rett Syndrome , 2011, Journal of child neurology.
[31] W. Kaufmann,et al. Rett syndrome: Revised diagnostic criteria and nomenclature , 2010, Annals of neurology.
[32] H. Leonard,et al. Atypical presentations and specific genotypes are associated with a delay in diagnosis in females with Rett syndrome , 2010, American journal of medical genetics. Part A.
[33] A. Rozga,et al. A prospective study of the emergence of early behavioral signs of autism. , 2010, Journal of the American Academy of Child and Adolescent Psychiatry.
[34] Jane E. Roberts,et al. Trajectories and predictors of the development of very young boys with fragile X syndrome. , 2009, Journal of pediatric psychology.
[35] Deborah D. Hatton,et al. Developmental trajectories of young girls with fragile x syndrome. , 2009, American journal on intellectual and developmental disabilities.
[36] P. Marschik,et al. Case Report: Retracing Atypical Development: A Preserved Speech Variant of Rett Syndrome , 2009, Journal of autism and developmental disorders.
[37] H. Leonard,et al. Is the girl with Rett syndrome normal at birth? , 2008, Developmental medicine and child neurology.
[38] M. Spence,et al. Use of Home Videotapes to Confirm Parental Reports of Regression in Autism , 2008, Journal of autism and developmental disorders.
[39] W. Kaufmann,et al. Investigating genotype–phenotype relationships in Rett syndrome using an international data set , 2008, Neurology.
[40] P. Marschik,et al. Events at early development: are they associated with early word production and neurodevelopmental abilities at the preschool age? , 2007, Early human development.
[41] Sally Ozonoff,et al. Autism and family home movies: a comprehensive review. , 2006, Journal of developmental and behavioral pediatrics : JDBP.
[42] J. Christodoulou,et al. Genotype and early development in Rett syndrome: The value of international data , 2005, Brain and Development.
[43] B. Burford. Perturbations in the development of infants with Rett disorder and the implications for early diagnosis , 2005, Brain and Development.
[44] R. Prescott,et al. Predictive value of the early clinical signs in Rett disorder , 2005, Brain and Development.
[45] C. Einspieler,et al. Is the Early Development of Girls with Rett Disorder Really Normal? , 2005, Pediatric Research.
[46] Frances Page Glascoe,et al. Parents' Evaluation of Developmental Status: How Well Do Parents' Concerns Identify Children With Behavioral and Emotional Problems? , 2003, Clinical pediatrics.
[47] Henrik Toft Sørensen,et al. The Danish National Birth Cohort - its background, structure and aim , 2001, Scandinavian journal of public health.
[48] Jane E. Roberts,et al. Family Experiences and Factors Associated with the Diagnosis of Fragile X Syndrome , 2000, Journal of developmental and behavioral pediatrics : JDBP.
[49] H. Zoghbi,et al. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 , 1999, Nature Genetics.
[50] E. Fombonne,et al. Parental recognition of developmental abnormalities in autism , 1998, European Child & Adolescent Psychiatry.
[51] B. Hagberg,et al. Rett variants: a suggested model for inclusion criteria. , 1994, Pediatric neurology.
[52] W. Altemeier,et al. The importance of parents' concerns about their child's development. , 1989, American journal of diseases of children.
[53] Jean Aicardi,et al. A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: Report of 35 cases , 1983, Annals of neurology.
[54] A Rett,et al. [On a unusual brain atrophy syndrome in hyperammonemia in childhood]. , 1966, Wiener medizinische Wochenschrift.
[55] B. Hagberg. Clinical manifestations and stages of Rett syndrome. , 2002, Mental retardation and developmental disabilities research reviews.