Visual processing difficulties in children with NF1. A common but not widely recognized underlying cause of reading difficulties
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health
Reference5 articles.
1. Examination of the genetic factors underlying the cognitive variability associated with neurofibromatosis type 1;Ottenhoff;Genet. Med.,2020
2. A rare disease and education: neurofibriomatosis type 1 decreases educational attainment;Johansson;Clin. Genet.,2021
3. Simvastatin for cognitive deficits and behavioural problems in patients with neurofibromatosis type 1 (NF1-SIMCODA): a randomised, placebo-controlled trial;Van der Vaart;Lancet Neurol.,2013
4. Impact of neurofibromatosis type 1 on school performance;Krab;J. Child Neurol.,2008
5. Visual-processing deficits in children with neurofibromatosis type 1: a clinical marker of reading difficulties;Vernet;EJPN,2022
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