Correlations between genotype, ultrastructural morphology and clinical phenotype in the neuronal ceroid lipofuscinoses Sara E. MoleRuth E. WilliamsHans H. Goebel Review Article 18 June 2005 Pages: 107 - 126
The Gem interacting protein (GMIP) gene is associated with major depressive disorder Kazuyuki TadokoroRyota HashimotoHiroshi Kunugi Original Article 06 August 2005 Pages: 127 - 133
Subcellular localization of spastin: implications for the pathogenesis of hereditary spastic paraplegia Ingrid K. SvensonMark T. KloosDouglas A. Marchuk Original Article 13 May 2005 Pages: 135 - 141
Genetic heterogeneity for autosomal recessive pyridoxine-dependent seizures C. L. BennettH. M. HuynhS. M. Gospe Jr Original Article 02 August 2005 Pages: 143 - 149
Identification of a VPS13A founder mutation in French Canadian families with chorea-acanthocytosis Carol Dobson-StoneAntonio Velayos-BaezaAnthony P. Monaco Original Article 26 May 2005 Pages: 151 - 158
Two missense mutations of EGR2 R359W and GJB1 V136A in a Charcot–Marie–Tooth disease family K. W. ChungI. N. SunwooB. O. Choi Short Communication 10 June 2005 Pages: 159 - 163
X-linked creatine transporter deficiency Maria C. SchiaffinoCarlo BelliniEugenio Bonioli Short Communication 06 August 2005 Pages: 165 - 168
A G301R Na+/K+-ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs Maria SpadaroSimona UrsuKarin Jurkat-Rott Erratum 26 August 2005 Pages: 169 - 169