Dystrophinopathies

This publication has 46 references indexed in Scilit:

• Motor and cognitive assessment of infants and young boys with Duchenne Muscular Dystrophy: results from the Muscular Dystrophy Association DMD Clinical Research Network
  Neuromuscular Disorders, 2013
• Newborn bloodspot screening for Duchenne Muscular Dystrophy: 21 years experience in Wales (UK)
  European Journal of Human Genetics, 2013
• Long-term benefits and adverse effects of intermittent versus daily glucocorticoids in boys with Duchenne muscular dystrophy
  Journal of Neurology, Neurosurgery & Psychiatry, 2012
• Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management
  The Lancet Neurology, 2010
• Dystrophin expression in the human retina is required for normal function as defined by electroretinography
  Nature Genetics, 1993
• Enhanced sensitivity of hippocampal pyramidal neurons from mdx mice to hypoxia-induced loss of synaptic transmission.
  Proceedings of the National Academy of Sciences, 1992
• Dystrophin: The protein product of the duchenne muscular dystrophy locus
  Cell, 1987
• Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals
  Cell, 1987
• Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene
  Nature, 1986
• Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion.
  Proceedings of the National Academy of Sciences, 1985