Zobrazeno 1 - 10
of 104
pro vyhledávání: '"Jørgen Erik, Nielsen"'
Autor:
Gunver Skytte
Publikováno v:
Linguistica, Vol 37, Iss 1 (1997)
È un tratto positivo della linguistica di oggi l'interesse rinnovato per la storia della linguistica e per i grandi classici della linguistica, molti dei quali sono oggetto di un vero revival scientifico. Basti ricordare ii caso di Lucien Tesnière,
Externí odkaz:
https://doaj.org/article/ada6611fd48646baaea3ce4a2742ecfe
Autor:
McCawley, James D.
Publikováno v:
Language, 1998 Dec 01. 74(4), 861-863.
Externí odkaz:
https://www.jstor.org/stable/417013
Autor:
Philipp, Marthe
Publikováno v:
Zeitschrift für Dialektologie und Linguistik, 1997 Jan 01. 64(3), 321-323.
Externí odkaz:
https://www.jstor.org/stable/40504341
Autor:
Henriette Haukedal, Giulia I. Corsi, Veerendra P. Gadekar, Nadezhda T. Doncheva, Shekhar Kedia, Noortje de Haan, Abinaya Chandrasekaran, Pia Jensen, Pernille Schiønning, Sarah Vallin, Frederik Ravnkilde Marlet, Anna Poon, Carlota Pires, Fawzi Khoder Agha, Hans H. Wandall, Susanna Cirera, Anja Hviid Simonsen, Troels Tolstrup Nielsen, Jørgen Erik Nielsen, Poul Hyttel, Ravi Muddashetty, Blanca I. Aldana, Jan Gorodkin, Deepak Nair, Morten Meyer, Martin Røssel Larsen, Kristine Freude
Publikováno v:
Frontiers in Neuroscience, Vol 17 (2023)
Alzheimer’s disease (AD) is the most common cause of dementia, with no current cure. Consequently, alternative approaches focusing on early pathological events in specific neuronal populations, besides targeting the well-studied amyloid beta (Aβ)
Externí odkaz:
https://doaj.org/article/4d6bdc2e3ad742debbe8defab51f61f4
Autor:
Anders Toft, Simon Sjödin, Anja Hviid Simonsen, Patrick Ejlerskov, Peter Roos, Christian Sandøe Musaeus, Emil Elbæk Henriksen, Troels Tolstrup Nielsen, Ann Brinkmalm, Kaj Blennow, Henrik Zetterberg, Jørgen Erik Nielsen
Publikováno v:
Alzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring, Vol 15, Iss 1, Pp n/a-n/a (2023)
Abstract Introduction Increasing evidence implicates proteostatic dysfunction as an early event in the development of frontotemporal dementia (FTD). This study aimed to explore potential cerebrospinal fluid (CSF) biomarkers associated with the proteo
Externí odkaz:
https://doaj.org/article/1fe201e7a3b54b478027a96c40786b76
Autor:
Ober, Kenneth H.
Publikováno v:
The Journal of English and Germanic Philology, 1979 Apr 01. 78(2), 286-288.
Externí odkaz:
https://www.jstor.org/stable/27708488
Autor:
Birna Ásbjörnsdóttir, Otto Mølby Henriksen, Suzanne Lindquist, Lisbeth Birk Møller, Annette Sidaros, Jørgen Erik Nielsen
Publikováno v:
BMJ case reports. 15(3)
Biallelic pathogenic variants in theANO10gene cause spinocerebellar ataxia recessive type 10. We report two patients, both compound heterozygous forANO10variants, including two novel variants. Both patients had onset of cerebellar ataxia in adulthood
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce1ae335983ce530987998c0d8f3f84d
https://pubmed.ncbi.nlm.nih.gov/35256372
https://pubmed.ncbi.nlm.nih.gov/35256372
Autor:
Christian Sandøe Musaeus, Jette Stokholm Pedersen, Troels Wesenberg Kjær, Peter Johannsen, Gunhild Waldemar, Maria Joy Normann Haverberg, Theis Bacher, Jørgen Erik Nielsen, Peter Roos, The FReJA Consortium, S Gydesen, J Brown, AM Isaacs, J Collinge, A Gade, E Englund, E Fisher, TT Nielsen, T Thusgaard, I Holm
Publikováno v:
Frontiers in Aging Neuroscience, Vol 13 (2021)
A rare cause of inherited frontotemporal dementia (FTD) is a mutation in the CHMP2B gene on chromosome 3 leading to the autosomal dominantly inherited FTD (CHMP2B-FTD). Since CHMP2B-FTD is clinically well-characterized, and patients show a distinct p
Externí odkaz:
https://doaj.org/article/cc78cd044125440b9c28ce0618e30014
Autor:
Birna Ásbjörnsdóttir, Christian Sandøe Musaeus, Marie NN Hellem, Tua Vinther-Jensen, Lena E Hjermind, Anja Hviid Simonsen, Marina R von Essen, Finn Sellebjerg, Jørgen Erik Nielsen
Publikováno v:
D: Wet biomarkers.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df9f531b0b13ff67910bfe8707f560a3
https://doi.org/10.1136/jnnp-2022-ehdn.71
https://doi.org/10.1136/jnnp-2022-ehdn.71
Autor:
Emilie Neerup, Nielsen, Birna, Ásbjörnsdóttir, Lisbeth Birk, Møller, Jørgen Erik, Nielsen, Suzanne Granhøj, Lindquist
Publikováno v:
Cold Spring Harbor molecular case studies. 8(6)
Episodic ataxia type 1 and 2 (EA1 and EA2) are the most well-described of the episodic ataxias. They are autosomal dominantly inherited early-onset diseases characterized by attacks of cerebellar dysfunction. EA1 is clinically characterized by short
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e4e6cbe792287ca52f21fe9968e4c3e7
https://pubmed.ncbi.nlm.nih.gov/36307210
https://pubmed.ncbi.nlm.nih.gov/36307210