Clinical Characteristics Suggestive of a Genetic Cause in Cerebral Palsy: A Systematic Review

This publication has 145 references indexed in Scilit:

• Genetic insights into the causes and classification of the cerebral palsies
  The Lancet Neurology, 2012
• Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature
  The American Journal of Human Genetics, 2011
• Dopa-responsive Dystonia with a Novel Initiation Codon Mutation in the GCH1 Gene Misdiagnosed as Cerebral Palsy
  Journal of Korean Medical Science, 2011
• Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study
  The Lancet Neurology, 2011
• Free Sialic Acid Storage Disease Mimicking Cerebral Palsy and Revealed by Blood Smear Examination
  The Journal of Pediatrics, 2011
• Adaptor protein complex-4 (AP-4) deficiency causes a novel autosomal recessive cerebral palsy syndrome with microcephaly and intellectual disability
  Journal of Medical Genetics, 2010
• Mutation in the AP4M1 Gene Provides a Model for Neuroaxonal Injury in Cerebral Palsy
  The American Journal of Human Genetics, 2009
• Perinatal complications and socio-economic differences in cerebral palsy in Sweden – a national cohort study
  BMC Pediatrics, 2008
• Identification of Proteolipid Protein 1 Gene Duplication by Multiplex Ligation-Dependent Probe Amplification: First Report of Genetically Confirmed Family of Pelizaeus-Merzbacher Disease in Korea
  Journal of Korean Medical Science, 2008
• Functional analysis of a novel potassium channel (KCNA1) mutation in hereditary myokymia
  neurogenetics, 2006