Neuroimaging findings in patient series with mucopolysaccharidosis.

[1]  N. Boddaert,et al.  Cognitive and neuroradiological improvement in three patients with attenuated MPS I treated by laronidase. , 2010, Molecular genetics and metabolism.

[2]  J. Abdenur,et al.  Treatment reduces or stabilizes brain imaging abnormalities in patients with MPS I and II. , 2009, Molecular genetics and metabolism.

[3]  U. Matte,et al.  Guidelines for the management of mucopolysaccharidosis type I. , 2009, The Journal of pediatrics.

[4]  P. Landrieu,et al.  Developmental dilatation of Virchow-Robin spaces: a genetic disorder? , 2009, Pediatric neurology.

[5]  E. Mayatepek,et al.  Neurological findings in Hunter disease: Pathology and possible therapeutic effects reviewed , 2008, Journal of Inherited Metabolic Disease.

[6]  Gutiérrez Solana.  Manifestaciones neurológicas del síndrome de Hunter , 2008 .

[7]  L. de Meirleir,et al.  Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy , 2007, European Journal of Pediatrics.

[8]  R. Giugliani,et al.  Brain MRI in mucopolysaccharidosis , 2007, Neurology.

[9]  R. Greenstein,et al.  When is enlargement of the subarachnoid spaces not benign? A genetic perspective. , 2007, Pediatric neurology.

[10]  R. Giugliani,et al.  Correlation of MR Imaging and MR Spectroscopy Findings with Cognitive Impairment in Mucopolysaccharidosis II , 2007, American Journal of Neuroradiology.

[11]  L. G. Gutiérrez-Solana.  Avances en el tratamiento de las enfermedades lisosomales en la infancia , 2006 .

[12]  P. Dechent,et al.  Magnetic resonance imaging and proton magnetic resonance spectroscopy of megalencephaly and dilated Virchow-Robin spaces. , 2006, Pediatric neurology.

[13]  O. Gabrielli,et al.  Correlation between cerebral MRI abnormalities and mental retardation in patients with mucopolysaccharidoses , 2004, American journal of medical genetics. Part A.

[14]  T. Nagayama,et al.  MRI in the mild type of mucopolysaccharidosis II (Hunter's syndrome) , 1996, Neuroradiology.

[15]  K. Kono,et al.  Brain magnetic resonance imaging in 23 patients with mucopolysaccharidoses and the effect of bone marrow transplantation , 2001, Annals of neurology.

[16]  J. B. Williamson,et al.  Spinal problems in mucopolysaccharidosis I (Hurler syndrome). , 1996, The Journal of bone and joint surgery. British volume.

[17]  R. Adams,et al.  Neurology of hereditary metabolic diseases of children , 1996 .

[18]  E. Shapiro,et al.  Dementia in Childhood: Issues in Neuropsychological Assessment with Application to the Natural History and Treatment of Degenerative Storage Diseases , 1994 .

[19]  L. Whitaker.  Treatment and Prevention , 1992 .

[20]  P. Narayana,et al.  Magnetic resonance imaging in the diagnosis of the cranio-cervical manifestations of the mucopolysaccharidoses. , 1987, Magnetic resonance imaging.

[21]  L. Ment.  Neurology of Hereditary Metabolic Diseases of Children , 1983, The Yale Journal of Biology and Medicine.