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Home Fascicolo n.1/2021 Bibliografia
Bibliografia
Sindromi dismorfogenetiche: valore predittivo dei movimenti generalizzati
pubblicato nel Gennaio - Febbraio 2021 ne Il Fisioterapista - fascicolo n.1

Bibliografia

  1. Einspieler C, Prechtl HF. Prechtl‘s assessment of general movements: a diagnostic tool for the functional assessment of the young nervous system. Ment Retard Dev Disabil Res Rev. 2005;11(1):61-7.
  2. Einspieler C, Prechtl HFR, Bos AF et al. Prechtl’s method of qualitative assessment of general movements in preterm, term and young infants. London: Mac-Keith Press, 2008.
  3. Prechtl HF, Einspieler C, Cioni G et al. An early marker for neurological deficits after perinatal brain lesions. Lancet. 1997;349:1361-3.
  4. Marschik PB, Soloveichick M, Windpassinger C, Einspieler C. General movements in genetic disorders: A first look into Cornelia de Lange syndrome. Dev Neurorehabil. 2015;18(4):280-2.
  5. Einspieler C, Kerr AM, Prechtl HFR. Abnormal general movements in girls with Rett disorder: The first months of life. Brain Dev. 2005; 27(Supplement 1): S8-S13.
  6. Einspieler C, Hirota H, Yuge M et al. Early behavioural manifestation of Smith-Magenis syndrome (del 17p11.2) in a 4-month-old boy. Dev Neurorehabil. 2012;15(3):313-6.
  7. Herrero D, Einspieler C, Panvequio Aizawa CY et al. The motor repertoire in 3- to 5-month old infants with Downsyndrome. Res Devel Disab. 2017;67:1-8.
  8. Splitte AJ, Olsen J, Kwong A et al. The Baby Moves prospective cohort study protocol: using a smartphone application with the General Movements Assessment to predict neurodevelopmental outcomes at age 2 years for extremely preterm or extremely low birth birthweight infants. BMJ Open. 2016; 6(10):e013446.
  9. Einspieler C, Peharz R, Marschik. Fidgety movements - tiny in appearance, but huge in impact. J Pediatr (Rio J). 2016;92(3Suppl 1):S64-70.