Works matching IS 13646745 AND DT 2009 AND VI 10 AND IP 3

Results: 11

A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype.

Published in:

Neurogenetics, 2009, v. 10, n. 3, p. 271, doi. 10.1007/s10048-009-0173-5

By:

Pirkevi, C.;
Lesage, S.;
Condroyer, C.;
Tomiyama, H.;
Hattori, N.;
Ertan, S.;
Brice, A.;
Başak, A.

Publication type:

Article

Association between migraine and a functional polymorphism at the dopamine β-hydroxylase locus.

Published in:

Neurogenetics, 2009, v. 10, n. 3, p. 199, doi. 10.1007/s10048-009-0176-2

By:

Fernandez, F.;
Colson, N.;
Quinlan, S.;
MacMillan, J.;
Lea, R.;
Griffiths, L.

Publication type:

Article

Examination of association of genes in the serotonin system to autism.

Published in:

Neurogenetics, 2009, v. 10, n. 3, p. 209, doi. 10.1007/s10048-009-0171-7

By:

Anderson, B.;
Schnetz-Boutaud, N.;
Bartlett, J.;
Wotawa, A.;
Wright, H.;
Abramson, R.;
Cuccaro, M.;
Gilbert, J.;
Pericak-Vance, M.;
Haines, J.

Publication type:

Article

Interaction of the SPG21 protein ACP33/maspardin with the aldehyde dehydrogenase ALDH16A1.

Published in:

Neurogenetics, 2009, v. 10, n. 3, p. 217, doi. 10.1007/s10048-009-0172-6

By:

Hanna, Michael;
Blackstone, Craig

Publication type:

Article

A new complex homozygous large rearrangement of the PINK1 gene in a Sudanese family with early onset Parkinson’s disease.

Published in:

Neurogenetics, 2009, v. 10, n. 3, p. 265, doi. 10.1007/s10048-009-0174-4

By:

Cazeneuve, Cécile;
Sân, Channkanira;
Ibrahim, Salah;
Mukhtar, Maowia;
Kheir, Musa;
LeGuern, Eric;
Brice, Alexis;
Salih, Mustafa

Publication type:

Article

The spectrum of somatic and germline NF1 mutations in NF1 patients with spinal neurofibromas.

Published in:

Neurogenetics, 2009, v. 10, n. 3, p. 251, doi. 10.1007/s10048-009-0178-0

By:

Upadhyaya, Meena;
Spurlock, Gill;
Kluwe, Lan;
Chuzhanova, Nadia;
Bennett, Emma;
Thomas, Nick;
Guha, Abhijit;
Mautner, Victor

Publication type:

Article

Novel mutations in the CDKL5 gene, predicted effects and associated phenotypes.

Published in:

Neurogenetics, 2009, v. 10, n. 3, p. 241, doi. 10.1007/s10048-009-0177-1

By:

Russo, S.;
Marchi, M.;
Cogliati, F.;
Bonati, M.;
Pintaudi, M.;
Veneselli, E.;
Saletti, V.;
Balestrini, M.;
Ben-Zeev, B.;
Larizza, L.

Publication type:

Article

Extended tracts of homozygosity identify novel candidate genes associated with late-onset Alzheimer’s disease.

Published in:

Neurogenetics, 2009, v. 10, n. 3, p. 183, doi. 10.1007/s10048-009-0182-4

By:

Nalls, M.;
Guerreiro, R.;
Simon-Sanchez, J.;
Bras, J.;
Traynor, B.;
Gibbs, J.;
Launer, L.;
Hardy, J.;
Singleton, A.

Publication type:

Article

Molecular analysis of NPC1 and NPC2 gene in 34 Niemann–Pick C Italian Patients: identification and structural modeling of novel mutations.

Published in:

Neurogenetics, 2009, v. 10, n. 3, p. 229, doi. 10.1007/s10048-009-0175-3

By:

Fancello, Tatiana;
Dardis, Andrea;
Rosano, Camillo;
Tarugi, Patrizia;
Tappino, Barbara;
Zampieri, Stefania;
Pinotti, Elisa;
Corsolini, Fabio;
Fecarotta, Simona;
D’Amico, Adele;
Rocco, Maja;
Uziel, Graziella;
Calandra, Sebastiano;
Bembi, Bruno;
Filocamo, Mirella

Publication type:

Article

Familial hemiplegic migraine: linkage to chromosome 14q32 in a Spanish kindred.

Published in:

Neurogenetics, 2009, v. 10, n. 3, p. 191, doi. 10.1007/s10048-008-0169-6

By:

Cuenca-León, Ester;
Corominas, Roser;
Montfort, Magda;
Artigas, Josep;
Roig, Manuel;
Bayés, Mònica;
Cormand, Bru;
Macaya, Alfons

Publication type:

Article

Whole-genome conditional two-locus analysis identifies novel candidate genes for late-onset Parkinson’s disease.

Published in:

Neurogenetics, 2009, v. 10, n. 3, p. 173, doi. 10.1007/s10048-009-0170-8

By:

González-Pérez, A.;
Gayán, J.;
Marín, J.;
Galán, J.;
Sáez, M.;
Real, L.;
Antúnez, C.;
Ruiz, A.

Publication type:

Article