Výsledky vyhledávání - Lena E. Hjermind
- Zobrazuji výsledky 1 - 9 z 9
-
1
Generation of a gene-corrected isogenic control hiPSC line derived from a familial Alzheimer's disease patient carrying a L150P mutation in presenilin 1 Autor Anna Poon, Benjamin Schmid, Carlota Pires, Troels T. Nielsen, Lena E. Hjermind, Jørgen E. Nielsen, Bjørn Holst, Poul Hyttel, Kristine Freude
Vydáno 2016Artigo -
2
A clinical classification acknowledging neuropsychiatric and cognitive impairment in Huntington’s disease Autor Tua Vinther‐Jensen, Ida Unmack Larsen, Lena E. Hjermind, Esben Budtz‐Jørgensen, Troels T. Nielsen, Anne Nørremølle, Jørgen E. Nielsen, Asmus Vogel
Vydáno 2014Artigo -
3
Selected CSF biomarkers indicate no evidence of early neuroinflammation in Huntington disease Autor Tua Vinther‐Jensen, Lars Börnsen, Esben Budtz‐Jørgensen, Cecilie Ammitzbøll, Ida Unmack Larsen, Lena E. Hjermind, Finn Sellebjerg, Jørgen E. Nielsen
Vydáno 2016Artigo -
4
A germline chromothripsis event stably segregating in 11 individuals through three generations Autor Birgitte Bertelsen, Lusine Nazaryan‐Petersen, Wei Sun, Mana M. Mehrjouy, Gangcai Xie, Wei Chen, Lena E. Hjermind, Peter E.M. Taschner, Zeynep Tümer
Vydáno 2015Artigo -
5
Generation of a gene-corrected isogenic control cell line from an Alzheimer's disease patient iPSC line carrying a A79V mutation in PSEN1 Autor Carlota Pires, Benjamin Schmid, Carina Petræus, Anna Poon, Natakarn Nimsanor, Troels T. Nielsen, Gunhild Waldemar, Lena E. Hjermind, Jørgen E. Nielsen, Poul Hyttel, Kristine Freude
Vydáno 2016Artigo -
6
Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY Autor Michael Orth, Olivia Handley, Carsten Schwenke, Stephen B. Dunnett, Edward J. Wild, Sarah J. Tabrizi, G. Bernhard Landwehrmeyer, Lis Hasholt, Lena E. Hjermind, Anne Nørremølle, Jørgen Erik Nielsen
Vydáno 2010Artigo -
7
Diagnostic genetic testing for Huntington's disease Autor David Craufurd, Rhona MacLeod, Marina Frontali, Oliver Quarrell, Emilia K. Bijlsma, Mary B. Davis, Lena E. Hjermind, Nayana Lahiri, Paola Mandich, A. Martinez, Aad Tibben, Raymund A.C. Roos
Vydáno 2014Revisão -
8
Missense dopamine transporter mutations associate with adult parkinsonism and ADHD Autor Freja Herborg, Tina Skjørringe, Saiqa Yasmeen, Natascha V. Arends, Michelle A. Sahai, Kevin Erreger, Thorvald F. Andreassen, Marion Holy, Peter J. Hamilton, Viruna Neergheen, Merete Karlsborg, Amy Hauck Newman, Simon Pope, Simon J.R. Heales, Lars Friberg, Ian Law, Lars H. Pinborg, Harald H. Sitte, Claus J. Løland, Lei Shi, Harel Weinstein, Aurelio Galli, Lena E. Hjermind, Lisbeth Birk Møller, Ulrik Gether
Vydáno 2014Artigo -
9
Frontotemporal dementia and its subtypes: a genome-wide association study Autor Raffaele Ferrari, Dena G. Hernandez, Michael A. Nalls, Jonathan D. Rohrer, Adaikalavan Ramasamy, John B. Kwok, Carol Dobson‐Stone, William S. Brooks, Peter R. Schofield, Glenda M. Halliday, John R. Hodges, Olivier Piguet, Lauren Bartley, Elizabeth Thompson, Eric Haan, Isabel Hernández, Agustı́n Ruiz, Merçé Boada, Barbara Borroni, Alessandro Padovani, Carlos Cruchaga, Nigel J. Cairns, Luisa Benussi, Giuliano Binetti, Roberta Ghidoni, Gianluigi Forloni, Daniela Galimberti, Chiara Fenoglio, María Serpente, Elio Scarpini, Jordi Clarimón, Alberto Lleó, Rafael Blesa, María Landqvist Waldö, Karin Nilsson, Christer Nilsson, Ian R. Mackenzie, Ging‐Yuek Robin Hsiung, David Mann, Jordan Grafman, Christopher M. Morris, Johannes Attems, Timothy D. Griffiths, Ian G. McKeith, Alan Thomas, Pietro Pietrini, Edward D. Huey, Eric M. Wassermann, Atik Baborie, Evelyn Jaros, Michael Tierney, Pau Pástor, Cristina Razquín, Sara Ortega‐Cubero, Elena Alonso, Robert Perneczky, Janine Diehl‐Schmid, Panagiotis Alexopoulos, Alexander Kurz, Innocenzo Rainero, Elisa Rubino, Lorenzo Pinessi, Ekaterina Rogaeva, Peter St George‐Hyslop, Giacomina Rossi, Fabrizio Tagliavini, Giorgio Giaccone, James B. Rowe, Johannes C. M. Schlachetzki, James Uphill, John Collinge, Simon Mead, Adrian Danek, Vivianna M. Van Deerlin, Murray Grossman, John Q. Trojanowski, Julie van der Zee, William Deschamps, Tim Van Langenhove, Marc Cruts, Christine Van Broeckhoven, Stefano F. Cappa, Isabelle Le Ber, Didier Hannequin, Véronique Golfier, Martine Vercelletto, Alexis Brice, Benedetta Nacmias, Sandro Sorbi, Silvia Bagnoli, Irene Piaceri, Jørgen E. Nielsen, Lena E. Hjermind, Markus J. Riemenschneider, Manuel Mayhaus, Bernd Ibach, Gilles Gasparoni, Sabrina Pichler, Wei Gu, Martin N. Rossor
Vydáno 2014Artigo
Vyhledávací nástroje:
Související témata
Biology
Medicine
Disease
Genetics
Gene
Internal medicine
Huntington's disease
Psychology
Mutation
Neuroscience
Psychiatry
Alzheimer's disease
Dementia
Embryonic stem cell
Induced pluripotent stem cell
PSEN1
Pathology
Phenotype
Point mutation
Presenilin
Allele
Anxiety
Apathy
Association (psychology)
CRISPR
Cancer research
Chorea
Chromothripsis
Cognition
Cognitive decline