Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Holm, Ida Elisabeth"'
Autor:
Andersen, Olav Michael, Bøgh, Nikolaj Hvidt, Landau, Anne, Pløen, Gro Grunnet, Jensen, Anne Mette Gissel, Monti, Giulia, Ulhøi, Benedicte Parm, Nyengaard, Jens Randel, Jacobsen, Kirsten Rosenmay, Jørgensen, Margarita Melnikova, Holm, Ida Elisabeth, Kristensen, Marianne Lundsgaard, Alstrup, Aage Kristian Olsen, Søvsø Szocska Hansen, Esben, Teunissen, Charlotte E, Breidenbach, Laura, Droescher, Mathias, Liu, Ying, Pedersen, Hanne Skovsgaard, Callesen, Henrik, Luo, Yonglun, Bolund, Lars, Brooks, David J, Laustsen, Christoffer, Small, Scott A, Mikkelsen, Lars F., Sørensen, Charlotte Brandt
Publikováno v:
Andersen, O M, Bøgh, N H, Landau, A, Pløen, G G, Jensen, A M G, Monti, G, Ulhøi, B P, Nyengaard, J R, Jacobsen, K R, Jørgensen, M M, Holm, I E, Kristensen, M L, Alstrup, A K O, Søvsø Szocska Hansen, E, Teunissen, C E, Breidenbach, L, Droescher, M, Liu, Y, Pedersen, H S, Callesen, H, Luo, Y, Bolund, L, Brooks, D J, Laustsen, C, Small, S A, Mikkelsen, L F & Sørensen, C B 2022, ' In vivo evidence that SORL1, encoding the endosomal recycling receptor SORLA, can function as a causal gene in Alzheimer’s Disease ', Cell Reports Medicine .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pure_au_____::dc969e87fc6c15f6aae59681524861ec
https://pure.au.dk/portal/da/publications/in-vivo-evidence-that-sorl1-encoding-the-endosomal-recycling-receptor-sorla-can-function-as-a-causal-gene-in-alzheimers-disease(8f324037-02ad-4236-91a3-8da398a58cf0).html
https://pure.au.dk/portal/da/publications/in-vivo-evidence-that-sorl1-encoding-the-endosomal-recycling-receptor-sorla-can-function-as-a-causal-gene-in-alzheimers-disease(8f324037-02ad-4236-91a3-8da398a58cf0).html
Autor:
Axelsen, Trine Veje, Holm, Arne, Birkelund, Svend, Christiansen, Gunna, Ploug, Michael, Holm, Ida Elisabeth
Publikováno v:
In Molecular Immunology 2009 46(11):2267-2273
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Melnikova, M S, Dorph-Petersen, K-A & Holm, I E 2015, ' Frontotemporal lobar degeneration: Neuropathological classification of cases from the Brain collection at Aarhus University Hospital, Risskov ', Risskov, Denmark, 05/11/2015-05/11/2015, .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pure_au_____::3cec96b794ab291dbd69f854b9b71d78
https://pure.au.dk/portal/da/publications/frontotemporal-lobar-degeneration-neuropathological-classification-of-cases-from-the-brain-collection-at-aarhus-university-hospital-risskov(cfaf03b2-3fbe-4975-976d-7b783d8eade6).html
https://pure.au.dk/portal/da/publications/frontotemporal-lobar-degeneration-neuropathological-classification-of-cases-from-the-brain-collection-at-aarhus-university-hospital-risskov(cfaf03b2-3fbe-4975-976d-7b783d8eade6).html
Publikováno v:
Holm, I E, Rosenberg, R & Dorph-Petersen, K-A 2013, ' Frontotemporal lobær degeneration. Neuropatologisk undersøgelse af cases fra Hjernesamlingen på Aarhus Universitetshospital, Risskov” (“Frontotemporal lobar degeneration. Neuropathological examination of cases from the Brain Collection at Aarhus University Hospital, Risskov) ' Psykiatriens 8. forskningsdag, Risskov, Denmark, 07/11/2013-07/11/2013, .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pure_au_____::40ff0e6091330ce57a029171e955884c
https://pure.au.dk/portal/da/publications/frontotemporal-lobaer-degeneration-neuropatologisk-undersoegelse-af-cases-fra-hjernesamlingen-paa-aarhus-universitetshospital-risskov-frontotemporal-lobar-degeneration-neuropathological-examination-of-cases-from-the-brain-collection-at-aarhus-university-hospital-risskov(20fa5e95-345e-40cc-b254-3a2b798d7e69).html
https://pure.au.dk/portal/da/publications/frontotemporal-lobaer-degeneration-neuropatologisk-undersoegelse-af-cases-fra-hjernesamlingen-paa-aarhus-universitetshospital-risskov-frontotemporal-lobar-degeneration-neuropathological-examination-of-cases-from-the-brain-collection-at-aarhus-university-hospital-risskov(20fa5e95-345e-40cc-b254-3a2b798d7e69).html
Autor:
Al-Hamdany, Saad, Holm, Ida Elisabeth
Publikováno v:
Al-Hamdany, S & Holm, I E 2010, ' Sjælden form for Creutzfeldt-Jakobs sygdom ', Ugeskrift for Laeger, bind 172, nr. 40, s. 2772-3 .
Creutzfeldt-Jakob disease (CJD) is the most common type of prion disease. A considerable variation in disease phenotype is seen, primarily influenced by a naturally occurring polymorphism in the prion protein gene. We present a case of sporadic CJD o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pure_au_____::e76752f85f51f3941d9f021182d0eae8
https://pure.au.dk/portal/da/publications/sjaelden-form-for-creutzfeldtjakobs-sygdom(85a2249e-9da4-4d70-9d91-37f09499573c).html
https://pure.au.dk/portal/da/publications/sjaelden-form-for-creutzfeldtjakobs-sygdom(85a2249e-9da4-4d70-9d91-37f09499573c).html
Autor:
Kragh, Peter, Nielsen, Anders Lade, Li, Juan, Du, Yutao, Lin, Lin, Mette, schmidt, Holm, Ida Elisabeth, Jakobsen, Jannik E., Johansen, Marianne Gregers, Purup, Stig, Bolund, Lars, Vajta, Gabor, Jørgensen, Arne Lund
Publikováno v:
Kragh, P, Nielsen, A L, Li, J, Du, Y, Lin, L, Mette, S, Holm, I E, Jakobsen, J E, Johansen, M G, Purup, S, Bolund, L, Vajta, G & Jørgensen, A L 2009, ' Hemizygous minipigs produced by random gene insertion and handmade cloning express the Alzheimer's disease-causing dominant mutation APPsw. ', Transgenic Research, bind 18, nr. 4 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pure_au_____::e74b3272b29cd211571835f0cd701476
https://pure.au.dk/portal/da/publications/hemizygous-minipigs-produced-by-random-gene-insertion-and-handmade-cloning-express-the-alzheimers-diseasecausing-dominant-mutation-appsw(ec8ed3b3-3d7e-4423-b6e0-e7f114c7ced8).html
https://pure.au.dk/portal/da/publications/hemizygous-minipigs-produced-by-random-gene-insertion-and-handmade-cloning-express-the-alzheimers-diseasecausing-dominant-mutation-appsw(ec8ed3b3-3d7e-4423-b6e0-e7f114c7ced8).html
Autor:
Holm, Ida Elisabeth, Englund, Elisabeth, R. Mackenzie, Ian, Johannesen, Peter, M. Issacs, Adrian
Publikováno v:
Holm, I E, Englund, E, R. Mackenzie, I, Johannesen, P & M. Issacs, A 2007, ' A Reassessment of the Neuropathology of Frontotemporal Dementia Linked to Chromosome 3 ', Journal of Neuropathology and Experimental Neurology, vol. 66, no. 10, pp. 884-91 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pure_au_____::07428062588bc9f48009cff775b45e2d
https://pure.au.dk/portal/da/publications/a-reassessment-of-the-neuropathology-of-frontotemporal-dementia-linked-to-chromosome-3(5131a710-aee3-11dc-89ab-000ea68e967b).html
https://pure.au.dk/portal/da/publications/a-reassessment-of-the-neuropathology-of-frontotemporal-dementia-linked-to-chromosome-3(5131a710-aee3-11dc-89ab-000ea68e967b).html
Autor:
Cairns, Nigel J., Neumann, Manuela, Bigio, Eileen H., Holm, Ida Elisabeth, Troost, Dirk, Hatanpaa, Kimmo J., Foong, Chan, White III, Charles L., Schneider, Julia A., Kretzschmar, Hans A., Carter, Deborah, Taylor-Reinwald, Lisa, Paulsmeyer, Katherine, Strider, Jeffrey, Gitcho, Michael, Goate, Alison M., Morris, John C., Mishra, Manjari, Kwong, Linda K., Stieber, Anna, Xu, Yan, Forman, Mark S., Trojanowski, John Q., Lee, Virginia M.-Y., Mackenzie, Ian R.A.
Publikováno v:
Cairns, N J, Neumann, M, Bigio, E H, Holm, I E, Troost, D, Hatanpaa, K J, Foong, C, White III, C L, Schneider, J A, Kretzschmar, H A, Carter, D, Taylor-Reinwald, L, Paulsmeyer, K, Strider, J, Gitcho, M, Goate, A M, Morris, J C, Mishra, M, Kwong, L K, Stieber, A, Xu, Y, Forman, M S, Trojanowski, J Q, Lee, V M-Y & Mackenzie, I R A 2007, ' TDP-43 in Familial and Sporadic Frontotemporal Lobar Degeneration wih Ubiquitin Inclusions ', The American Journal of Pathology, vol. 171, no. 1, pp. 227-40 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pure_au_____::92aad8d6d250055a6c5e9ba214efd9bb
https://pure.au.dk/portal/da/publications/tdp43-in-familial-and-sporadic-frontotemporal-lobar-degeneration-wih-ubiquitin-inclusions(b7c688f0-9f3f-11dc-bee9-02004c4f4f50).html
https://pure.au.dk/portal/da/publications/tdp43-in-familial-and-sporadic-frontotemporal-lobar-degeneration-wih-ubiquitin-inclusions(b7c688f0-9f3f-11dc-bee9-02004c4f4f50).html
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.