Molecular cell biology of Charcot-Marie-Tooth disease Philipp BergerPeter YoungUeli Suter Review Article 06 March 2002 Pages: 1 - 15
A typical migraine susceptibility region localizes to chromosome 1q31 Rod A. LeaGraeme A. ShepherdLyn R. Griffiths Original Article 09 January 2002 Pages: 17 - 22
A new autosomal recessive non-progressive congenital cerebellar ataxia associated with mental retardation, optic atrophy, and skin abnormalities (CAMOS) maps to chromosome 15q24-q26 in a large consanguineous Lebanese Druze family Valérie DelagueCorinne BareilMireille Claustres Original Article 08 January 2002 Pages: 23 - 27
Expression of the survival of motor neuron (SMN) gene in primary neurons and increase in SMN levels by activation of the N-methyl-D-aspartate glutamate receptor Catia AndreassiAnna PatriziMaria Eboli Original Article 19 January 2002 Pages: 29 - 36
Search for mutations in the EGR2 corepressor proteins, NAB1 and NAB2, in human peripheral neuropathies Koen VenkenEmilio Di MariaJohn Svaren Original Article 12 December 2001 Pages: 37 - 41
A mannosyltransferase gene at 11q23 is disrupted by a translocation breakpoint that co-segregates with bipolar affective disorder in a small family Bora E. BaysalJoan E. Willett-BrozickSevilla D. Detera-Wadleigh Original Article 08 February 2002 Pages: 43 - 53
Sequence analysis of two nuclear encoded subunits (10 and 51 kDa) of mitochondrial complex I in Parkinson disease Eva M. Grasbon-FrodlP. Mehraein LETTER TO THE EDITOR 06 March 2002 Pages: 55 - 57
Identification of polymorphisms within the bovine prion protein gene (Prnp) by DNA sequencing and genotyping by MALDI-TOF-MS Andreas HumenyKatrin SchiebelCord-Michael Becker LETTER TO THE EDITOR 06 March 2002 Pages: 59 - 60