Hereditary demyelinating neuropathies: from gene to disease C.O. Hanemann Review article 31 January 2001 Pages: 53 - 57
Does (CUG)n repeat in DMPK mRNA ‘paint’ chromosome 19 to suppress distant genes to create the diverse phenotype of myotonic dystrophy?: R.P. JunghansA. EbralidzeB. Tiwari HYPOTHESIS 17 February 2001 Pages: 59 - 67
Nramp1 is expressed in neurons and is associated with behavioural and immune responses to stress Carlton A.W. EvansMichael S. HarbuzJenefer M. Blackwell Original Article 16 February 2001 Pages: 69 - 78
Dopamine D4 receptor (DRD4) polymorphism and adaptability trait during infancy: a longitudinal study in 1- to 5-month-old neonates Alessandro De LucaMario RizzardiGiuseppe Novelli Original Article 16 February 2001 Pages: 79 - 82
Ataxin-7 expression analysis in controls and spinocerebellar ataxia type 7 patients David D. EinumJeannette J. TownsendYing-Hui Fu Original Article 16 February 2001 Pages: 83 - 90
Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia Allison Ashley-KochErin R. BonnerMargaret A. Pericak-Vance Original Article 30 January 2001 Pages: 91 - 97
Mapping and sequencing rat dishevelled-1: a candidate gene for cerebral ischaemic insult in a rat model of stroke Robert P.J. De LangeKaren BurrDuncan J. Shaw Original Article 03 February 2001 Pages: 99 - 106
Denaturing high-performance liquid chromatography of the myotubularin-related 2 gene (MTMR2) in unrelated patients with Charcot-Marie-Tooth disease suggests a low frequency of mutation in inherited neuropathy Alessandra BolinoLorne J. LonieJames R. Lupski Short Communication 16 February 2001 Pages: 107 - 109
Autism: evidence of association with adenosine deaminase genetic polymorphism Nunzio BottiniDanila De LucaPaolo Curatolo Short Communication 16 February 2001 Pages: 111 - 113
