Works matching IS 13646745 AND DT 2014 AND VI 15 AND IP 1

Results: 11

Rare variants in LRRK1 and Parkinson's disease.

Published in:

Neurogenetics, 2014, v. 15, n. 1, p. 49, doi. 10.1007/s10048-013-0383-8

By:

Schulte, Eva;
Ellwanger, Daniel;
Dihanich, Sybille;
Manzoni, Claudia;
Stangl, Katrin;
Schormair, Barbara;
Graf, Elisabeth;
Eck, Sebastian;
Mollenhauer, Brit;
Haubenberger, Dietrich;
Pirker, Walter;
Zimprich, Alexander;
Brücke, Thomas;
Lichtner, Peter;
Peters, Annette;
Gieger, Christian;
Trenkwalder, Claudia;
Mewes, Hans-Werner;
Meitinger, Thomas;
Lewis, Patrick

Publication type:

Article

Brain-derived neurotrophic factor: its impact upon neuroplasticity and neuroplasticity inducing transcranial brain stimulation protocols.

Published in:

Neurogenetics, 2014, v. 15, n. 1, p. 1, doi. 10.1007/s10048-014-0393-1

By:

Chaieb, L.;
Antal, A.;
Ambrus, G.;
Paulus, W.

Publication type:

Article

Repeat interruptions in spinocerebellar ataxia type 10 expansions are strongly associated with epileptic seizures.

Published in:

Neurogenetics, 2014, v. 15, n. 1, p. 59, doi. 10.1007/s10048-013-0385-6

By:

McFarland, Karen;
Liu, Jilin;
Landrian, Ivette;
Zeng, Desmond;
Raskin, Salmo;
Moscovich, Mariana;
Gatto, Emilia;
Ochoa, Adriana;
Teive, Hélio;
Rasmussen, Astrid;
Ashizawa, Tetsuo

Publication type:

Article

The documentation of consent and disclosure of neurogenetic testing outside clinical genetics.

Published in:

Neurogenetics, 2014, v. 15, n. 1, p. 19, doi. 10.1007/s10048-014-0391-3

By:

Lo, C.;
Martindale, J.;
Hadjivassiliou, M.;
Martin, P.;
Dalton, A.;
Bandmann, O.

Publication type:

Article

Expanding the spectrum of megalencephalic leukoencephalopathy with subcortical cysts in two patients with GLIALCAM mutations.

Published in:

Neurogenetics, 2014, v. 15, n. 1, p. 41, doi. 10.1007/s10048-013-0381-x

By:

Arnedo, Tanit;
Aiello, Chiara;
Jeworutzki, Elena;
Dentici, Maria;
Uziel, Graziella;
Simonati, Alessandro;
Pusch, Michael;
Bertini, Enrico;
Estévez, Raúl

Publication type:

Article

Founder effect and ancestral origin of the spinocerebellar ataxia type 7 (SCA7) mutation in Mexican families.

Published in:

Neurogenetics, 2014, v. 15, n. 1, p. 13, doi. 10.1007/s10048-013-0387-4

By:

García-Velázquez, Lizbeth;
Canizales-Quinteros, Samuel;
Romero-Hidalgo, Sandra;
Ochoa-Morales, Adriana;
Martínez-Ruano, Leticia;
Márquez-Luna, Carla;
Acuña-Alonzo, Víctor;
Villarreal-Molina, M.;
Alonso-Vilatela, M.;
Yescas-Gómez, Petra

Publication type:

Article

Genetic determinants of neuroglobin transcription.

Published in:

Neurogenetics, 2014, v. 15, n. 1, p. 65, doi. 10.1007/s10048-013-0388-3

By:

Wang, R.;
Halper-Stromberg, E.;
Szymanski-Pierce, M.;
Bassett, S.;
Avramopoulos, D.

Publication type:

Article

Mutations in MAPT give rise to aneuploidy in animal models of tauopathy.

Published in:

Neurogenetics, 2014, v. 15, n. 1, p. 31, doi. 10.1007/s10048-013-0380-y

By:

Rossi, Giacomina;
Conconi, Donatella;
Panzeri, Elena;
Paoletta, Laura;
Piccoli, Elena;
Ferretti, Maria;
Mangieri, Michela;
Ruggerone, Margherita;
Dalprà, Leda;
Tagliavini, Fabrizio

Publication type:

Article

SLC20A2 and THAP1 deletion in familial basal ganglia calcification with dystonia.

Published in:

Neurogenetics, 2014, v. 15, n. 1, p. 23, doi. 10.1007/s10048-013-0378-5

By:

Baker, Matt;
Strongosky, Audrey;
Sanchez-Contreras, Monica;
Yang, Shan;
Ferguson, Will;
Calne, Donald;
Calne, Susan;
Stoessl, A.;
Allanson, Judith;
Broderick, Daniel;
Hutton, Michael;
Dickson, Dennis;
Ross, Owen;
Wszolek, Zbigniew;
Rademakers, Rosa

Publication type:

Article

Evidence of a role for SNCA in impulse control in humans.

Published in:

2014

By:

Guillot, Casey;
Fanning, Jennifer;
Liang, Tiebing;
Berman, Mitchell

Publication type:

Letter

'Comment on the Paper "SLC20A2 and THAP1 deletion in familial basal ganglia calcification with dystonia" by Baker et al.'.

Published in:

2014

By:

Oliveira, João

Publication type:

Letter