Neurogenetics
Collection
Collection
- ISSN: 13646745
Published by Springer
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A novel presenilin 1 mutation (L174M) in a large Cuban family with early onset Alzheimer disease. Article
Neurogenetics, 4(2), 97-104.B. Marcheco Teruel, J.J. Llibre Rodriguez, N. Gomez Viera, I. Borrajero Martinez, E.A.W.F.M. Severijnen (Lies-Anne), M. Joosse (Marijke), C.M. van Duijn (Cornelia), L. Heredero-Baute, P. Heutink (Peter) and A.M. Bertoli Avella (Aida)
October 2002
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Absence of pathogenic mutations in presenilin homologue 2 in a conclusively 17-linked tau-negative dementia family Article
Neurogenetics, 5(1), 79-80.R. Rademakers (Rosa), M. van den Broeck (Marleen), K. Sleegers (Kristel), C.M. van Duijn (Cornelia), C. van Broeckhoven (Christine) and M. Cruts (Marc)
February 2004
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Homozygosity for the p.K136E mutation in the SLC17A5 gene as cause of an Italian severe Salla disease Article
Neurogenetics, 6(4), 195-199.R. Biancheri, A. Rossi (Andrea), J.H.A.M. Verbeek (Jos), R. Schot (Rachel), F. Corsolini, S. Assereto, G.M.S. Mancini (Grazia), F.W. Verheijen (Frans), C. Minetti and M. Filocamo (Mirella)
December 2005 -
Early-onset Parkinson's disease caused by a novel parkin mutation in a genetic isolate from north-eastern Brazil Article
Neurogenetics, 7(1), 13-19.H.F. Chien (Hsin), C.F. Rohe, M.D.L. Costa (Maria D.), G.J. Breedveld (Guido), B.A. Oostra (Ben), E.R. Barbosa (Egberto) and V. Bonifati (Vincenzo)
March 2006 -
A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan Article
Neurogenetics, 7(3), 133-138.A. Di Fonzo (Alessio), Y.H. Wu-Chou (Yah-Huei), C.S. Lu (Chin-Song), M. van Doeselaar (Marina), E.J. Simons (Erik), C.F. Rohe, H.C. Chang (Hsiu-Chen), R.S. Chen (Rou-Shayn), Y.H. Weng (Yi Hsin), N. Vanacore (Nicola), et al. G.J. Breedveld (Guido), B.A. Oostra (Ben) and V. Bonifati (Vincenzo)
July 2006 -
Microcephaly and simplified gyral pattern of the brain associated with early onset insulin-dependent diabetes mellitus Article
Neurogenetics, 7(4), 259-263.M.C.Y. de Wit (Marie Claire), I.F.M. de Coo (René), C. Julier (C.), M. Delepine (Marc), M.H. Lequin (Maarten), I.M.B.H. van de Laar (Ingrid), B. Sibbles (Barbara), G.J. Bruining and G.M.S. Mancini (Grazia)
November 2006 -
Biological effects of the PINK1 c.1366C>T mutation: Implications in Parkinson disease pathogenesis Article
Neurogenetics, 8(2), 103-109.A. Grünewald (Anne), G.J. Breedveld (Guido), K. Lohmann-Hedrich (Katja), C.F. Rohe, I.R. König (Inke), J. Hagenah, N. Vanacore (Nicola), G. Meco (Giuseppe), A. Antonini (Angelo), S. Goldwurm (Stefano), et al. S. Lesage (Suzanne), A. Durr, F. Binkofski (Ferdinand), H. Siebner (Hartwig), A. Münchau (Alexander), A. Brice, B.A. Oostra (Ben), C. Klein (Christoph) and V. Bonifati (Vincenzo)
April 2007 -
The cholesteryl ester transfer protein (CETP) gene and the risk of Alzheimer's disease Article
Neurogenetics, 8(3), 189-193.A. Arias-Vásquez (Alejandro), A.J. Isaacs (Aaron), Y.S. Aulchenko (Yurii), A. Hofman (Albert), B.A. Oostra (Ben), M.M.B. Breteler (Monique) and P. Tikka-Kleemola (Päivi)
August 2007