Methodological note: Video analysis of the early development of Rett syndrome—one method for many disciplines

Rett syndrome is a profoundly disabling X-linked neurodevelopmental disorder that predominantly, but not exclusively, occurs in females. It is mainly caused by mutations in the gene MECP2 for methy...

[1]  Alessandra Renieri,et al.  FOXG1 is responsible for the congenital variant of Rett syndrome. , 2008, American journal of human genetics.

[2]  W. Kaufmann,et al.  Development of a Video-based Evaluation Tool in Rett Syndrome , 2007, Journal of autism and developmental disorders.

[3]  Christa Einspieler,et al.  Prechtl's assessment of general movements: a diagnostic tool for the functional assessment of the young nervous system. , 2005, Mental retardation and developmental disabilities research reviews.

[4]  V. Slonims,et al.  Regression in individuals with Rett syndrome , 2002, Brain and Development.

[5]  Sally Ozonoff,et al.  Autism and family home movies: a comprehensive review. , 2006, Journal of developmental and behavioral pediatrics : JDBP.

[6]  H. Leonard,et al.  Is the girl with Rett syndrome normal at birth? , 2008, Developmental medicine and child neurology.

[7]  G. Cioni,et al.  Role of vision on early motor development: lessons from the blind. , 2001 .

[8]  M. Chetouani,et al.  What studies of family home movies can teach us about autistic infants: A literature review , 2010 .

[9]  A. Kerr,et al.  Nurse recognition of early deviation in development in home videos of infants with Rett disorder. , 2003, Journal of intellectual disability research : JIDR.

[10]  S. Skinner,et al.  Rett Syndrome: North American Database , 2007, Journal of child neurology.

[11]  W. Kaufmann,et al.  Rett syndrome: Revised diagnostic criteria and nomenclature , 2010, Annals of neurology.

[12]  G. Cioni,et al.  Role of vision on early motor development: lessons from the blind , 2001, Developmental medicine and child neurology.

[13]  H. Zoghbi,et al.  Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 , 1999, Nature Genetics.

[14]  D. Armstrong.  Neuropathology of Rett syndrome. , 2002, Mental retardation and developmental disabilities research reviews.

[15]  N. Boddaert,et al.  Key clinical features to identify girls with CDKL5 mutations. , 2008, Brain : a journal of neurology.

[16]  P. Marschik,et al.  Case Report: Retracing Atypical Development: A Preserved Speech Variant of Rett Syndrome , 2009, Journal of autism and developmental disorders.

[17]  C. Einspieler,et al.  Is the Early Development of Girls with Rett Disorder Really Normal? , 2005, Pediatric Research.

[18]  Filippo Muratori,et al.  Early Behavioral Development in Autistic Children: The First 2 Years of Life through Home Movies , 2001, Psychopathology.

[19]  C. Einspieler,et al.  Abnormal general movements in girls with Rett disorder: The first four months of life , 2005, Brain and Development.

[20]  Russell Lang,et al.  Communication assessment for individuals with Rett syndrome: A systematic review , 2011 .

[21]  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.

[22]  P. Marschik,et al.  ‘Relabelling the preserved speech variant of Rett syndrome?’ , 2010, Developmental medicine and child neurology.