Works matching IS 03645134 AND DT 2018 AND VI 84 AND IP 5

Results: 21

Neural basis of induced phantom limb pain relief.

Published in:

2018

By:

Kikkert, Sanne;
Mezue, Melvin;
O'Shea, Jacinta;
Henderson Slater, David;
Johansen-Berg, Heidi;
Tracey, Irene;
Makin, Tamar R

Publication type:

journal article

Evidence of dysfunction in the visual association cortex in visual snow syndrome.

Published in:

2018

By:

Eren, Ozan;
Rauschel, Veronika;
Ruscheweyh, Ruth;
Straube, Andreas;
Schankin, Christoph J

Publication type:

journal article

Genome-wide meta-analysis identifies 3 novel loci associated with stroke.

Published in:

2018

By:

Malik, Rainer;
Rannikmäe, Kristiina;
Traylor, Matthew;
Georgakis, Marios K;
Sargurupremraj, Muralidharan;
Markus, Hugh S;
Hopewell, Jemma C;
Debette, Stephanie;
Sudlow, Cathie L M;
Dichgans, Martin;
MEGASTROKE consortium and the International Stroke Genetics Consortium

Publication type:

journal article

Annals of Neurology: Volume 84, Number 5, November 2018.

Published in:: 2018
Publication type:: Cover Art

Issue Information.

Published in:: Annals of Neurology, 2018, v. 84, n. 5, p. i, doi. 10.1002/ana.25381
Publication type:: Article

Fingolimod enhances the efficacy of delayed alteplase administration in acute ischemic stroke by promoting anterograde reperfusion and retrograde collateral flow.

Published in:

2018

By:

Tian, De‐Cai;
Shi, Kaibin;
Zhu, Zilong;
Yao, Jia;
Yang, Xiaoxia;
Su, Lei;
Zhang, Sheng;
Zhang, Meixia;
Gonzales, Rayna J.;
Liu, Qiang;
Huang, DeRen;
Waters, Michael F.;
Sheth, Kevin N.;
Ducruet, Andrew F.;
Fu, Ying;
Lou, Min;
Shi, Fu‐Dong;
Tian, De-Cai;
Shi, Fu-Dong

Publication type:

journal article

KCTD7 deficiency defines a distinct neurodegenerative disorder with a conserved autophagy-lysosome defect.

Published in:

2018

By:

Metz, Kyle A.;
Teng, Xinchen;
Coppens, Isabelle;
Lamb, Heather M.;
Wagner, Bart E.;
Rosenfeld, Jill A.;
Chen, Xianghui;
Zhang, Yu;
Kim, Hee Jong;
Meadow, Michael E.;
Wang, Tim Sen;
Haberlandt, Edda D.;
Anderson, Glenn W.;
Leshinsky‐Silver, Esther;
Bi, Weimin;
Markello, Thomas C.;
Pratt, Marsha;
Makhseed, Nawal;
Garnica, Adolfo;
Danylchuk, Noelle R.

Publication type:

journal article

NBEA: Developmental disease gene with early generalized epilepsy phenotypes.

Published in:

2018

By:

Mulhern, Maureen S.;
Stumpel, Constance;
Stong, Nicholas;
Brunner, Han G.;
Bier, Louise;
Lippa, Natalie;
Riviello, James;
Rouhl, Rob P. W.;
Kempers, Marlies;
Pfundt, Rolph;
Stegmann, Alexander P. A.;
Kukolich, Mary K.;
Telegrafi, Aida;
Lehman, Anna;
Lopez‐Rangel, Elena;
Houcinat, Nada;
Barth, Magalie;
den Hollander, Nicolette;
Hoffer, Mariette J. V.;
Weckhuysen, Sarah

Publication type:

journal article

Development of a cerebrovascular magnetic resonance imaging biomarker for cognitive aging.

Published in:

2018

By:

Vemuri, Prashanthi;
Lesnick, Timothy G.;
Przybelski, Scott A.;
Graff‐Radford, Jonathan;
Reid, Robert I.;
Lowe, Val J.;
Zuk, Samantha M.;
Senjem, Matthew L.;
Schwarz, Christopher G.;
Gunter, Jeffrey L.;
Kantarci, Kejal;
Machulda, Mary M.;
Mielke, Michelle M.;
Petersen, Ronald C.;
Knopman, David S.;
Jack, Clifford R.;
Graff-Radford, Jonathan;
Jack, Clifford R Jr

Publication type:

journal article

Disease progression and outcome measures in spinobulbar muscular atrophy.

Published in:

2018

By:

Dahlqvist, Julia R.;
Fornander, Freja;
de Stricker Borch, Josefine;
Oestergaard, Sofie T.;
Poulsen, Nanna S.;
Vissing, John

Publication type:

journal article

Relative neuron loss in hippocampal sclerosis of aging and Alzheimer's disease.

Published in:

2018

By:

Ihara, Ryoko;
Vincent, Benjamin D.;
Baxter, Michael R.;
Franklin, Erin E.;
Hassenstab, Jason J.;
Xiong, Chengjie;
Morris, John C.;
Cairns, Nigel J.

Publication type:

journal article

Human pegivirus-1 associated leukoencephalitis: Clinical and molecular features.

Published in:

2018

By:

Balcom, Erin F.;
Doan, Matthew A.L.;
Branton, William G.;
Jovel, Juan;
Blevins, Gregg;
Edguer, Beste;
Hobman, Tom C.;
Yacyshyn, Elaine;
Emery, Derek;
Box, Adrian;
van Landeghem, Frank K.H.;
Power, Christopher

Publication type:

journal article

Neuroimaging and clinical outcomes of oral anticoagulant-associated intracerebral hemorrhage.

Published in:

2018

By:

Tsivgoulis, Georgios;
Wilson, Duncan;
Katsanos, Aristeidis H.;
Sargento‐Freitas, João;
Marques‐Matos, Cláudia;
Azevedo, Elsa;
Adachi, Tomohide;
Brelie, Christian;
Aizawa, Yoshifusa;
Abe, Hiroshi;
Tomita, Hirofumi;
Okumura, Ken;
Hagii, Joji;
Seiffge, David J.;
Lioutas, Vasileios‐Arsenios;
Traenka, Christopher;
Varelas, Panayiotis;
Basir, Ghazala;
Krogias, Christos;
Purrucker, Jan C.

Publication type:

journal article

Prevalence of amyloid-β pathology in distinct variants of primary progressive aphasia.

Published in:

2018

By:

Bergeron, David;
Gorno‐Tempini, Maria L.;
Rabinovici, Gil D.;
Santos‐Santos, Miguel A.;
Seeley, William;
Miller, Bruce L.;
Pijnenburg, Yolande;
Keulen, M. Antoinette;
Groot, Colin;
van Berckel, Bart N. M.;
van der Flier, Wiesje M.;
Scheltens, Philip;
Rohrer, Jonathan D.;
Warren, Jason D.;
Schott, Jonathan M.;
Fox, Nick C.;
Sanchez‐Valle, Raquel;
Grau‐Rivera, Oriol;
Gelpi, Ellen;
Seelaar, Harro

Publication type:

journal article

Efficacy of Botulinum Toxin A for Treating Cramps in Diabetic Neuropathy.

Published in:

2018

By:

Restivo, Domenico A.;
Casabona, Antonino;
Frittitta, Lucia;
Belfiore, Antonino;
Le Moli, Rosario;
Gullo, Damiano;
Vigneri, Riccardo

Publication type:

journal article

ETFDH Mutations and Flavin Adenine Dinucleotide Homeostasis Disturbance Are Essential for Developing Riboflavin-Responsive Multiple Acyl-Coenzyme A Dehydrogenation Deficiency.

Published in:

2018

By:

Xu, Jingwen;
Li, Duoling;
Lv, Jingwei;
Xu, Xuebi;
Wen, Bing;
Lin, Pengfei;
Liu, Fuchen;
Ji, Kunqian;
Shan, Jingli;
Li, Honghao;
Li, Wei;
Zhao, Yuying;
Zhao, Dandan;
Pok, Joo Y.;
Yan, Chuanzhu

Publication type:

journal article

Correction: An extremely severe phenotype attributed to WDR81 nonsense mutations.

Published in:: 2018
Publication type:: corrected article

Plasma Amyloid as Prescreener for the Earliest Alzheimer Pathological Changes.

Published in:

2018

By:

Verberk, Inge M. W.;
Slot, Rosalinde E.;
Verfaillie, Sander C. J.;
Heijst, Hans;
Prins, Niels D.;
van Berckel, Bart N. M.;
Scheltens, Philip;
Teunissen, Charlotte E.;
van der Flier, Wiesje M.

Publication type:

journal article

β2-adrenoreceptor medications and risk of Parkinson disease.

Published in:

2018

By:

Searles Nielsen, Susan;
Gross, Anat;
Camacho‐Soto, Alejandra;
Willis, Allison W.;
Racette, Brad A.;
Camacho-Soto, Alejandra

Publication type:

journal article

Loss of Protocadherin-12 Leads to Diencephalic-Mesencephalic Junction Dysplasia Syndrome.

Published in:

2018

By:

Guemez‐Gamboa, Alicia;
Çağlayan, Ahmet Okay;
Stanley, Valentina;
Gregor, Anne;
Zaki, Maha S.;
Saleem, Sahar N.;
Musaev, Damir;
McEvoy‐Venneri, Jennifer;
Belandres, Denice;
Akizu, Naiara;
Silhavy, Jennifer L.;
Schroth, Jana;
Rosti, Rasim Ozgur;
Copeland, Brett;
Lewis, Steven M.;
Fang, Rebecca;
Issa, Mahmoud Y.;
Per, Huseyin;
Gumus, Hakan;
Bayram, Ayse Kacar

Publication type:

journal article

Facioscapulohumeral Dystrophy in Childhood: A Nationwide Natural History Study.

Published in:

2018

By:

Goselink, Rianne J.M.;
Schreuder, Tim H.A.;
van Alfen, Nens;
de Groot, Imelda J.M.;
Jansen, Merel;
Lemmers, Richard J.L.F.;
van der Vliet, Patrick J.;
van der Stoep, Nienke;
Theelen, Thomas;
Voermans, Nicol C.;
van der Maarel, Silvère M.;
van Engelen, Baziel G.M.;
Erasmus, Corrie E.

Publication type:

journal article