SEARCH

SEARCH BY CITATION

Reference

  • Aron M. (1990) The use and effectiveness of elbow splints in Rett syndrome. Brain Dev 12:1623.
  • Amir RE, Van den Veyber IB, Wan M, Tran CQ, Francke U, Zoghbi HY. (1999) Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG binding protein 2. Nat Genet 23:1858.
  • Budden S. (1995) Management of Rett syndrome: a ten year experience. Neuropediatrics 26: 757.
  • Budden S, Meek MM, Henighan C. (1990) Communication and oral-motor function in Rett syndrome. Dev Med Child Neurol 32: 515.
  • Charman T, Cass H, Owen L, Wisbeach A, Weekes L, Slonims V, Wigram T, Reilly S. (2002) Regression in individuals with Rett syndrome. Brain Dev 24: 2813.
  • Coleman M, Brubaker J, Hunter K, Smith G. (1988) Rett syndrome: a survey of the North American patients. J Mental Defic Res 32:11724.
  • Cooper RA, Kerr AM, Amos PM. (1998) Rett syndrome: critical examination of clinical features, serial EEG and video-monitoring in understanding and management. Europ J Paediatr Neurol 2:12735.
  • Dahlgren SO, Sandberg AD, Ehlers S, Hagberg B, Gillberg C. (2000) The Rett syndrome complex: communicative functions in relation to developmental level. Autism 4: 24967.
  • Dragich J, Houwink-Manville I, Schanen C. (2000) Rett syndrome: a surprising result of mutation in MECP2. Hum Mol Genet 9: 236575.
  • Elian M, Rudolf ND. (1996) Observations on hand movements in Rett syndrome: a pilot study. Acta Neurol Scand 94: 2124.
  • Fombonne E, Simmon H, Ford T, Meltzer H, Goodman R. (2001) Prevalence of pervasive developmental disorders in the British nationwide survey of child mental health. J Am Acad Child Adolesc Psychiatry 40: 8207.
  • Fontanesi J, Hass RH. (1988) Cognitive profile of Rett syndrome. J Child Neurol 3: S204.
  • Glaze DG, Schltz RJ, Frost JD. (1998) Rett syndrome: characterization of seizures versus non-seizures. Electroencephalogr Clin Neurophysiol 106: 7983.
  • Hagberg B. (1993) Clinical criteria, stages and natural history. In: Hagberg B, Anvret M, Wahlstrom J, editors. Rett Syndrome: Clinical and Biological Aspects. Clinics in Developmental Medicine No. 127. London : Mac Keith Press. p 420.
  • Hagberg B. (1995) Rett syndrome: clinical peculiarities and biological mysteries. Acta Paediatr 84: 9716.
  • Hagberg B, Hagberg G. (1997) Rett syndrome: epidemiology and geographical variability. Eur Child Adolesc Psychiatry 6 (Suppl 1): 57.
  • Hagberg BA, Skjeldal OH. (1994) Rett variants: a suggested model for inclusion criteria. Pediatr Neurol 11: 511.
  • Hagberg B, Witt Engerström I (1986) Rett syndrome: a suggested staging system for describing impairment profile with increasing age towards adolescence. Am J Med Genet 24: 4759.
  • Hagberg B, Aicardi J, Dias K, Ramos O. (1983) A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand movements in girls: Rett syndrome: report of 3 5 cases. Ann Neurol 14: 4719.
  • Hagberg B, Goutieres F, Hanefeld, Rett A, Wilson J. (1985) Rett syndrome: criteria for inclusion and exclusion. Brain Dev 7:3723.
  • Harrison DJ, Webb PJ. (1990) Scoliosis in the Rett syndrome: natural history and treatment. Brain Dev 12:1546.
  • Hoffbuhr KC, Moses LM, Jerdonek MA, Naidu S, Hoffman EP. (2002) Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype. Ment Retard Dev Disabil Res Rev 8:99105.
  • Julu POO, Kerr AM, Hansen S, Apartopoulos SF, Jamal GA. (1997) Functional evidence of brain stem immaturity in Rett syndrome. Eur Child Adolesc Psychiatry 6: 4754.
  • Julu POO, Kerr AM, Apartopoulos F, Al-Rawas S, Witt Engerström I, Engerström L, Jamal GA, Hansen S. (2001) Characterisation of breathing and associated central autonomic dysfunction in the Rett disorder. Arch Dis Child 85: 2937.
  • Kerr A. (1992) Rett syndrome: British longitudinal study (1982–1990). In: Rosendaal JJ, editors. MentalRetardation and Medical Care. Zeist , the Netherlands : Uitgeverij Kerckebosch. P 1435.
  • Kerr AM, Julu POO. (1999) Recent insights into hyperventilation for the study of Rett syndrome. Arch Dis Child 80: 3847.
  • Kerr AM, Witt Engerström I (2001) The clinical background to the Rett disorder. In: KerrAM, Witt Engerström I, editors. Rett Disorder and the Developing Brain. Oxford : Oxford University Press. p 126.
  • Kerr AM, Montague J, Stephenson JB. (1987) The hands, and the mind, pre- and post-regression, in Rett syndrome. Brain Dev 9:48790.
  • Kerr AM, Nomura Y, Armstrong D, Anvret M, Belichenko PV, Budden S, Cass H, Christodoulou J, Clarke A, Ellaway C, D'esposito M, Francke U, Hulten M, Julu P, Leonare H, Naidu S, Schanen C, Webb T, Witt Engerström I, Yamashita Y, Segawa M. (2001) Guidelines for reporting clinical features in cases with MECP2 mutations. Brain Dev 23: 20811.
  • Kozinetz CA, Skender ML, MacNaughton N, Almes MJ, Schultz RJ, Percy AK, Glaze DG. (1993) Epidemiology of Rett syndrome: a population-based registry. Pediatrics 91: 44550.
  • Kubas E. (1992) Use of splints to develop hand skills in awoman with Rett syndrome. Am J Occup Ther 46: 3648.
  • Leonard H, Fyfe S, Leonard S, Msall M. (2001) Functional status, medical impairments, and rehabilitation resources in 84 females with Rett syndrome: a snapshot across the world from the parental perspective. Disabil Rehabil 23:10717.
  • Morton RE, Bonas R, Minford J, Kerr A, Ellis RE. (1997) Feeding ability in Rett syndrome. Dev Med Child Neuro 139: 3315.
  • Morton RE, Bonas R, Minford J, Tarrant SC, Ellis RE. (1997) Respiration patterns during feeding in Rett syndrome. Dev Med Child Neurol 39: 60713.
  • Motil KR, Schultz R, Brown B, Glaze DG, Percy AL. (1994) Altered energy balance may account for growth failure in Rett syndrome. J Child Neurol 9: 3159.
  • Motil KR, Schultz R, Wong WW, Glaze DG. (1998) Increased energy expenditure associated with repetitive involuntary movement does not contribute to growth failure in girls with Rett syndrome. J Pediatr 132: 22833.
  • Motil KR, Schultz R, Glaze DG, Armstrong D. (2001) Orophraryngeal dysfunction and upper gastrointestinal dysmotility, a reflection of disturbances in the autonomic nervous system in Rett syndrome. In: Kerr AM, Witt Engerström I, editors. Rett Disorder and the Developing Brain. Oxford : Oxford University Press. p 25963.
  • Mount RH, Hastings RP, Reilly S, Cass H, Charman T. (2001) Behavioural and emotional features in Rett syndrome. Disabil Rehabil 23:12938.
  • Naganuma GM, Billingsley FF. (1988) Effect of hand splints on stereotypic hand behavior of three girls with Rett syndrome. Phys Ther 68: 66471.
  • Nomura Y, Segawa M. (1992) Motor symptoms of the Rett syndrome: abnormal muscle tone, posture, locomotion and stereotyped movement. Brain Dev 14: S218.
  • Perry A, Sarlo McGarvey N, Haddad C. (1991) Brief report: cognitive and adaptive functioning in 28 girls with Rett syndrome. J Autism Dev Disord 21: 5516.
  • Piazza CC, Anderson C, Fisher W. (1993) Teaching self-feeding skills to patients with Rett syndrome. Dev Med Child Neurol 35: 9916.
  • Poutney TE, Creek L, Green E, Mulcahy C, Nelham R. (1999) Content and validation of the Chailey levels of ability. Physioherapy 85: 4106.
  • Reilly S, Cass H. (2001) Growth and nutrition in Rett syndrome. Disabil Rehabil 23: 11828.
  • Reilly S, Skuse D, Mathisen B, Wolke D. (1995) The objective rating of oral motor functions during feeding. Dysphagia 10: 17791.
  • Reilly S, Skuse D, Poblete X. (1996) Prevalence of feeding problems and oral motor dysfunction in children with cerebral palsy: a community survey. J Pediatr 129: 87782.
  • Reilly S, Skuse D, Wolke D. (2000) The Schedule for Oral Motor Assessment. London : Whurr Publishers.
  • Rett A. (1966) Über ein eigenartiges hirnatrophisches syndrome bei hyperammonamie im kindsalter. Wien Med Wochenschr 116: 7236. (In German).
  • Rett Syndrome Diagnostic Criteria Working Group. (1988) Diagnostic criteria for Rett syndrome. Ann Neurol 23: 4258.
  • Rice MA, Haas RH. (1988) The nutritional aspects of Rett syndrome. J Child Neurol S3542.
  • Schultz RJ, Glaze DG, Motil KJ, Armstrong DD, del Junco DJ, Hubbard CR, Percy AK. (1993) The pattern of growth failure in Rett syndrome. Am J Dis Child 147: 6337.
  • Shahbazian MD, Zoghbi HY. (2001) Molecular genetics of Rett syndrome and the clinical spectrum of MECP2 mutations. Curr Opin Neurol 14: 1716.
  • Sharpe PA, Ottenbacher KJ. (1988) Use of an elbow restraint to improve finger-feeding skills in a child with Rett syndrome. Am J Occup Ther 44: 32832.
  • Skuse D, Stephenson J, Reilly S, Mathisen B. (1995) Schedule for oral motor assessment (SOMA): methods of validation. Dysphagia 10:192202.
  • Steffenburg U, Hagberg G, Hagberg B. (2001) Epilepsy in a representative series of Rett syndrome. Acta Paediatr 90: 349.
  • Stenbom Y, Witt Engerström I, Hagberg G. (1995) Gross motor disability and head growth in Rett syndrome: a preliminary report. Neuropediatrics 26: 856.
  • Tanguy A. (1993) Orthopaedic aspects of Rett syndrome. Ann Pediatr 40: 23741.
  • Uchino J, Suzuki M, Hoshino K, Nomura Y, Segawa M. (2001) Development of language in Rett syndrome. Brain Dev 23: S2335.
  • von Tetzchner S (1997) Communication skills among females with Rett syndrome. Eur J Child Adolesc Psychiat 6: 337.
  • Wan M, Sung Jae, Lee S, Zhang X, Houwink Manville I, Song HR, Amir R, Budden S, Naidu S, Pereira JL, Lo IF, Zoghbi HY, Schanen NC, Francke U. (1999) Rett Syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots. Am J Hum Genet 65: 15209.
  • Witt Engerström I (1990) Rett syndrome in Sweden. Acta Paediatr Scand 369S: 160.
  • Witt Engerström I (1992) Age-related occurrence of signs and symptoms in the Rett syndrome. Brain Dev 14: S1120.
  • Witt Engerström I, Hagberg B. (1990) The Rett syndrome: gross motor disability and neural impairment in adults. Brain Dev 12: 236.
  • Witt Engerström I, Hagberg B. (1993) Evolution of clinical signs. In: Hagberg B, Anvret M, Wahlstrom J, editors. Rett Syndrome: Clinical and Biological Aspects. Clinics in Developmental Medicine No. 127. London : Mac Keith Press. p 2639.
  • Woodyatt GC, Ozanne AE. (1992) Communication abilities and Rett syndrome. J Autism Dev Disord 37: 41935.
  • Woodyatt GC, Ozanne AE. (1993) A longitudinal study of cognitive skills and communication behaviours in children with Rett syndrome. J Intellect Disabil Res 37: 41935.
  • Woodyatt GC, Ozanne AE. (1997) Rett syndrome (RS) and profound intellectual disability: cognitive and communicative similarities and differences. Eur Child Adolesc Psychiat 6:312.
  • Zappella M, Gillberg C, Ehlers S. (1998) The preserved speech variant: a subgroup of the Rett complex: a clinical report of 30 cases. J Autism Dev Disord 28: 51926.