Works matching IS 13646745 AND DT 2006 AND VI 7 AND IP 3

Results: 8

Spastic paraplegia with thin corpus callosum: description of 20 new families, refinement of the SPG11 locus, candidate gene analysis and evidence of genetic heterogeneity.

Published in:

Neurogenetics, 2006, v. 7, n. 3, p. 149, doi. 10.1007/s10048-006-0044-2

By:

Stevanin, Giovanni;
Montagna, Giorgia;
Azzedine, Hamid;
Valente, Enza Maria;
Durr, Alexandra;
Scarano, Valentina;
Bouslam, Naima;
Cassandrini, Denise;
Denora, Paola S.;
Criscuolo, Chiara;
Belarbi, Soraya;
Orlacchio, Antonio;
Jonveaux, Philippe;
Silvestri, Gabriella;
Ouvard Hernandez, Anne Marie;
De Michele, Giuseppe;
Tazir, Meriem;
Mariotti, Caterina;
Brockmann, Knut;
Malandrini, Alessandro

Publication type:

Article

Transcriptome analysis reveals link between proteasomal and mitochondrial pathways in Parkinson’s disease.

Published in:

Neurogenetics, 2006, v. 7, n. 3, p. 139, doi. 10.1007/s10048-006-0033-5

By:

Duke, D. C.;
Moran, L. B.;
Kalaitzakis, M. E.;
Deprez, M.;
Dexter, D. T.;
Pearce, R. K. B.;
Graeber, M. B.

Publication type:

Article

Investigation of autism and GABA receptor subunit genes in multiple ethnic groups.

Published in:

Neurogenetics, 2006, v. 7, n. 3, p. 167, doi. 10.1007/s10048-006-0045-1

By:

Collins, Ann L.;
Deqiong Ma;
Whitehead, Patrice L.;
Martin, Eden R.;
Wright, Harry H.;
Abramson, Ruth K.;
Hussman, John P.;
Haines, Jonathan L.;
Cuccaro, Michael L.;
Gilbert, John R.;
Pericak-Vance, Margaret A.

Publication type:

Article

Founder effect for the Ala431Glu mutation of the presenilin 1 gene causing early-onset Alzheimer’s disease in Mexican families.

Published in:

Neurogenetics, 2006, v. 7, n. 3, p. 195, doi. 10.1007/s10048-006-0043-3

By:

Yescas, Petra;
Huertas-Vazquez, Adriana;
Villarreal-Molina, María;
Rasmussen, Astrid;
Tusié-Luna, María Teresa;
López, Marisol;
Canizales-Quinteros, Samuel;
Alonso, María Elisa

Publication type:

Article

A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson’s disease risk in Taiwan.

Published in:

Neurogenetics, 2006, v. 7, n. 3, p. 133, doi. 10.1007/s10048-006-0041-5

By:

Di Fonzo, Alessio;
Yah-Huei Wu-Chou;
Chin-Song Lu;
van Doeselaar, Marina;
Simons, Erik J.;
Rohé, Christan F.;
Hsiu-Chen Chang;
Rou-Shayn Chen;
Yi-Hsin Weng;
Vanacore, Nicola;
Breedveld, Guido J.;
Oostra, Ben A.;
Bonifati, Vincenzo

Publication type:

Article

Molecular mechanism of rigid spine with muscular dystrophy type 1 caused by novel mutations of selenoprotein N gene.

Published in:

Neurogenetics, 2006, v. 7, n. 3, p. 175, doi. 10.1007/s10048-006-0046-0

By:

Okamoto, Yuji;
Takashima, Hiroshi;
Higuchi, Itsuro;
Matsuyama, Wataru;
Suehara, Masahito;
Nishihira, Yasushi;
Hashiguchi, Akihiro;
Hirano, Ryuki;
Ng, Arlene;
Nakagawa, Masanori;
Izumo, Shuji;
Osame, Mitsuhiro;
Arimura, Kimiyoshi

Publication type:

Article

Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL.

Published in:

Neurogenetics, 2006, v. 7, n. 3, p. 185, doi. 10.1007/s10048-006-0049-x

By:

Annunen-Rasila, Johanna;
Finnilä, Saara;
Mykkänen, Kati;
Moilanen, Jukka S.;
Veijola, Johanna;
Pöyhönen, Minna;
Viitanen, Matti;
Kalimo, Hannu;
Majamaa, Kari

Publication type:

Article

Parsing the genetic heterogeneity of chromosome 12q susceptibility genes for Alzheimer disease by family-based association analysis.

Published in:

Neurogenetics, 2006, v. 7, n. 3, p. 157, doi. 10.1007/s10048-006-0047-z

By:

Ping-I Lin;
Martin, Eden R.;
Browning-Large, Carrie A.;
Schmechel, Donald E.;
Welsh-Bohmer, Kathleen A.;
Murali Doraiswamy, P.;
Gilbert, John R.;
Haines, Jonathan L.;
Pericak-Vance, Margaret A.

Publication type:

Article