Works matching IS 13646745 AND DT 2008 AND VI 9 AND IP 4

Results: 11

Founder effect and recurrent mutational events in fatal familial insomnia.

Published in:

2008

By:

Peña, José;
Alfonso-Sánchez, Miguel;
Rodríguez-Martínez, Ana;
Pancorbo, Marian

Publication type:

Letter

Global distribution of Fatal familial insomnia: founder or recurrent mutations.

Published in:

2008

By:

Lee, H.-S.;
Goldfarb, L.

Publication type:

Letter

The LRRK2 Arg1628Pro variant is a risk factor for Parkinson’s disease in the Chinese population.

Published in:

Neurogenetics, 2008, v. 9, n. 4, p. 271, doi. 10.1007/s10048-008-0140-6

By:

Lu, Chin-Song;
Wu-Chou, Yah-Huei;
Doeselaar, Marina;
Simons, Erik;
Chang, Hsiu-Chen;
Breedveld, Guido;
Fonzo, Alessio;
Chen, Rou-Shayn;
Weng, Yi-Hsin;
Lai, Szu-Chia;
Oostra, Ben;
Bonifati, Vincenzo

Publication type:

Article

Behavioral effects of a deletion in Kcnn2, the gene encoding the SK2 subunit of small-conductance Ca<sup>2+</sup>-activated K<sup>+</sup> channels.

Published in:

Neurogenetics, 2008, v. 9, n. 4, p. 237, doi. 10.1007/s10048-008-0136-2

By:

Szatanik, Marek;
Vibert, Nicolas;
Vassias, Isabelle;
Guénet, Jean-Louis;
Eugène, Daniel;
Waele, Catherine;
Jaubert, Jean

Publication type:

Article

Nitric oxide synthase genes and their interactions with environmental factors in Parkinson’s disease.

Published in:

Neurogenetics, 2008, v. 9, n. 4, p. 249, doi. 10.1007/s10048-008-0137-1

By:

Hancock, Dana;
Martin, Eden;
Vance, Jeffery;
Scott, William

Publication type:

Article

Identification and characterisation of a large Senataxin ( SETX) gene duplication in ataxia with ocular apraxia type 2 (AOA2).

Published in:

Neurogenetics, 2008, v. 9, n. 4, p. 295, doi. 10.1007/s10048-008-0139-z

By:

Arning, Larissa;
Schöls, Ludger;
Cin, Huriye;
Souquet, Manfred;
Epplen, Jörg;
Timmann, Dagmar

Publication type:

Article

The location of DCX mutations predicts malformation severity in X-linked lissencephaly.

Published in:

Neurogenetics, 2008, v. 9, n. 4, p. 277, doi. 10.1007/s10048-008-0141-5

By:

Leger, Pierre-Louis;
Souville, Isabelle;
Boddaert, Nathalie;
Elie, Caroline;
Pinard, Jean;
Plouin, Perrine;
Moutard, Marie;
Portes, Vincent;
Esch, Hilde;
Joriot, Sylvie;
Renard, Jean;
Chelly, Jamel;
Francis, Fiona;
Beldjord, Cherif;
Bahi-Buisson, Nadia

Publication type:

Article

A novel locus for autosomal recessive primary torsion dystonia (DYT17) maps to 20p11.22–q13.12.

Published in:

Neurogenetics, 2008, v. 9, n. 4, p. 287, doi. 10.1007/s10048-008-0142-4

By:

Chouery, E.;
Kfoury, J.;
Delague, V.;
Jalkh, N.;
Bejjani, P.;
Serre, J.;
Mégarbané, A.

Publication type:

Article

Analysis of PARK genes in a Korean cohort of early-onset Parkinson disease.

Published in:

Neurogenetics, 2008, v. 9, n. 4, p. 263, doi. 10.1007/s10048-008-0138-0

By:

Choi, Jung;
Woo, Myoung;
Ma, Hyeo-Il;
Kang, Suk;
Sung, Young-Hee;
Yong, Seok;
Chung, Sun;
Kim, Joong-Seok;
Shin, Hae-won;
Lyoo, Chul;
Lee, Phil;
Baik, Jong;
Kim, Sang-Jin;
Park, Mee;
Sohn, Young;
Kim, Jin-Ho;
Kim, Jae;
Lee, Myung;
Lee, Myoung;
Kim, Dong-Hyun

Publication type:

Article

Induced pluripotent stem (iPS) cells as in vitro models of human neurogenetic disorders.

Published in:

Neurogenetics, 2008, v. 9, n. 4, p. 227, doi. 10.1007/s10048-008-0147-z

By:

Chamberlain, Stormy;
Li, Xue-Jun;
Lalande, Marc

Publication type:

Article

Acknowledgement to Referees 2007/2008.

Published in:: Neurogenetics, 2008, v. 9, n. 4, p. 305, doi. 10.1007/s10048-008-0146-0
Publication type:: Article