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Sensitivity and specificity of a seed amplification assay for diagnosis of multiple system atrophy: a multicentre cohort study.
Ma Y, Farris CM, Weber S, Schade S, Nguyen H, Pérez-Soriano A, Giraldo DM, Fernández M, Soto M, Cámara A, Painous C, Muñoz E, Valldeoriola F, Martí MJ, Clarimon J, Kallunki P, Ma TC, Alcalay RN, Gomes BF, Blennow K, Zetterberg H, Constantinescu J, Mengel D, Kadam V, Parchi P, Brockmann K, Tropea TF, Siderowf A, Synofzik M, Kang UJ, Compta Y, Svenningsson P, Mollenhauer B, Concha-Marambio L. Ma Y, et al. Among authors: kallunki p. Lancet Neurol. 2024 Dec;23(12):1225-1237. doi: 10.1016/S1474-4422(24)00395-8. Lancet Neurol. 2024. PMID: 39577923
Randomized Phase I Trial of the α-Synuclein Antibody Lu AF82422.
Buur L, Wiedemann J, Larsen F, Ben Alaya-Fourati F, Kallunki P, Ditlevsen DK, Sørensen MH, Meulien D. Buur L, et al. Among authors: kallunki p. Mov Disord. 2024 Jun;39(6):936-944. doi: 10.1002/mds.29784. Epub 2024 Mar 17. Mov Disord. 2024. PMID: 38494847 Clinical Trial.
New prospects for 89Zr-immuno-PET in brain applications - Alpha-synucleinopathies.
Wuensche TE, Pereira PM, Windhorst AD, Bjerregaard-Andersen K, Sotty F, Kallunki P, Jensen A, Bang-Andersen B, van Dongen GAMS, Beaino W, Vugts DJ. Wuensche TE, et al. Among authors: kallunki p. Nucl Med Biol. 2024 Nov 12;140-141:108969. doi: 10.1016/j.nucmedbio.2024.108969. Online ahead of print. Nucl Med Biol. 2024. PMID: 39591759 Free article.
Corrigendum to: DYRK1A interacts with the REST/NRSF-SWI/SNF chromatin remodelling complex to deregulate gene clusters involved in the neuronal phenotypic traits of Down syndrome.
Lepagnol-Bestel AM, Zvara A, Maussion G, Quignon F, Ngimbous B, Ramoz N, Imbeaud S, Loe-Mie Y, Benihoud K, Agier N, Salin PA, Cardona A, Khung-Savatovsky S, Kallunki P, Delabar JM, Puskas LG, Delacroix H, Aggerbeck L, Delezoide AL, Delattre O, Gorwood P, Moalic JM, Simonneau M. Lepagnol-Bestel AM, et al. Among authors: kallunki p. Hum Mol Genet. 2022 Jun 22;31(12):2106-2107. doi: 10.1093/hmg/ddab346. Hum Mol Genet. 2022. PMID: 34918050 No abstract available.
A mouse model of the schizophrenia-associated 1q21.1 microdeletion syndrome exhibits altered mesolimbic dopamine transmission.
Nielsen J, Fejgin K, Sotty F, Nielsen V, Mørk A, Christoffersen CT, Yavich L, Lauridsen JB, Clausen D, Larsen PH, Egebjerg J, Werge TM, Kallunki P, Christensen KV, Didriksen M. Nielsen J, et al. Among authors: kallunki p. Transl Psychiatry. 2017 Nov 30;7(11):1261. doi: 10.1038/s41398-017-0011-8. Transl Psychiatry. 2017. PMID: 29187755 Free PMC article.
Antibodies against the C-terminus of α-synuclein modulate its fibrillation.
Sahin C, Lorenzen N, Lemminger L, Christiansen G, Møller IM, Vesterager LB, Pedersen LØ, Fog K, Kallunki P, Otzen DE. Sahin C, et al. Among authors: kallunki p. Biophys Chem. 2017 Jan;220:34-41. doi: 10.1016/j.bpc.2016.11.002. Epub 2016 Nov 10. Biophys Chem. 2017. PMID: 27863716
Persistent gating deficit and increased sensitivity to NMDA receptor antagonism after puberty in a new mouse model of the human 22q11.2 microdeletion syndrome: a study in male mice.
Didriksen M, Fejgin K, Nilsson SR, Birknow MR, Grayton HM, Larsen PH, Lauridsen JB, Nielsen V, Celada P, Santana N, Kallunki P, Christensen KV, Werge TM, Stensbøl TB, Egebjerg J, Gastambide F, Artigas F, Bastlund JF, Nielsen J. Didriksen M, et al. Among authors: kallunki p. J Psychiatry Neurosci. 2017 Jan;42(1):48-58. doi: 10.1503/jpn.150381. J Psychiatry Neurosci. 2017. PMID: 27391101 Free PMC article.
35 results