Works matching IS 13646745 AND DT 2006 AND VI 7 AND IP 4

Results: 11

Genetic susceptibility to Parkinson’s disease among South and North Indians: I. Role of polymorphisms in dopamine receptor and transporter genes and association of DRD4 120-bp duplication marker.

Published in:

Neurogenetics, 2006, v. 7, n. 4, p. 223, doi. 10.1007/s10048-006-0048-y

By:

Juyal, Ramesh;
Das, Mitashree;
Punia, Sohan;
Behari, Madhuri;
Nainwal, Geetika;
Singh, Sumit;
Swaminath, Pazhayannur;
Govindappa, Shyla;
Jayaram, Sachi;
Muthane, Uday;
Thelma, B.

Publication type:

Article

Spinal muscular atrophy genotyping by gene dosage using multiple ligation-dependent probe amplification.

Published in:

Neurogenetics, 2006, v. 7, n. 4, p. 269, doi. 10.1007/s10048-006-0051-3

By:

Scarciolla, Oronzo;
Stuppia, Liborio;
Angelis, Maria;
Murru, Stefania;
Palka, Chiara;
Giuliani, Rossella;
Pace, Marta;
Muzio, Antonio;
Torrente, Isabella;
Morella, Annunziata;
Grammatico, Paola;
Giacanelli, Manlio;
Rosatelli, Maria;
Uncini, Antonino;
Dallapiccola, Bruno

Publication type:

Article

The A431E mutation in PSEN1 causing Familial Alzheimer’s Disease originating in Jalisco State, Mexico: an additional fifteen families.

Published in:

Neurogenetics, 2006, v. 7, n. 4, p. 277, doi. 10.1007/s10048-006-0053-1

By:

Murrell, Jill;
Ghetti, Bernardino;
Cochran, Elizabeth;
Macias-Islas, Miguel;
Medina, Luis;
Varpetian, Arousiak;
Cummings, Jeffrey;
Mendez, Mario;
Kawas, Claudia;
Chui, Helena;
Ringman, John

Publication type:

Article

Interaction between the dopamine D4 receptor and the serotonin transporter promoter polymorphisms in alcohol and tobacco use among 15-year-olds.

Published in:

Neurogenetics, 2006, v. 7, n. 4, p. 239, doi. 10.1007/s10048-006-0050-4

By:

Skowronek, M.;
Laucht, M.;
Hohm, E.;
Becker, K.;
Schmidt, M.

Publication type:

Article

Behavior of mice with mutations in the conserved region deleted in velocardiofacial/DiGeorge syndrome.

Published in:

Neurogenetics, 2006, v. 7, n. 4, p. 247, doi. 10.1007/s10048-006-0054-0

By:

Long, Jeffrey;
LaPorte, Patricia;
Merscher, Sandra;
Funke, Birgit;
Saint-Jore, Bruno;
Puech, Anne;
Kucherlapati, Raju;
Morrow, Bernice;
Skoultchi, Arthur;
Wynshaw-Boris, Anthony

Publication type:

Article

Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes.

Published in:

Neurogenetics, 2006, v. 7, n. 4, p. 265, doi. 10.1007/s10048-006-0057-x

By:

Stogmann, E.;
Lichtner, P.;
Baumgartner, C.;
Schmied, M.;
Hotzy, C.;
Asmus, F.;
Leutmezer, F.;
Bonelli, S.;
Assem-Hilger, E.;
Vass, K.;
Hatala, K.;
Strom, T.;
Meitinger, T.;
Zimprich, F.;
Zimprich, A.

Publication type:

Article

Current perspectives on the genetic causes of neural tube defects.

Published in:

Neurogenetics, 2006, v. 7, n. 4, p. 201, doi. 10.1007/s10048-006-0052-2

By:

Marco, Patrizia;
Merello, Elisa;
Mascelli, Samantha;
Capra, Valeria

Publication type:

Article

Microcephaly and simplified gyral pattern of the brain associated with early onset insulin-dependent diabetes mellitus.

Published in:

Neurogenetics, 2006, v. 7, n. 4, p. 259, doi. 10.1007/s10048-006-0061-1

By:

Wit, M.;
Coo, I.;
Julier, C.;
Delépine, M.;
Lequin, M.;
Laar, I.;
Sibbles, B.;
Bruining, G.;
Mancini, G.

Publication type:

Article

Familial risks of hospitalization for Parkinson’s disease in first-degree relatives: a nationwide follow-up study from Sweden.

Published in:

Neurogenetics, 2006, v. 7, n. 4, p. 231, doi. 10.1007/s10048-006-0055-z

By:

Sundquist, Kristina;
Xinjun Li;
Hemminki, Kari

Publication type:

Article

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

Published in:

2006

By:

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

Publication type:

Correction Notice

Acknowledgement to Referees 2005–2006.

Published in:: Neurogenetics, 2006, v. 7, n. 4, p. 283, doi. 10.1007/s10048-006-0064-y
Publication type:: Article