Zobrazeno 1 - 10
of 242
pro vyhledávání: '"Berendse HW"'
Autor:
Jansen, IE, Ye, H, Heetveld, S, Lechler, MC, Michels, H, Seinstra, RI, Lubbe, SJ, Drouet, V, Lesage, S, Majounie, E, Gibbs, JR, Nalls, MA, Ryten, M, Botia, JA, Vandrovcova, J, Simon-Sanchez, J, Castillo-Lizardo, M, Rizzu, P, Blauwendraat, C, Chouhan, AK, Li, Y, Yogi, P, Amin, N, van Duijn, CM, Morris, HR, Brice, A, Singleton, AB, David, DC, Nollen, EA, Jain, S, Shulman, JM, Heutink, P, Hernandez, DG, Arepalli, S, Brooks, J, Price, R, Nicolas, A, Chong, S, Cookson, MR, Dillman, A, Moore, M, Traynor, BJ, Plagnol, V, Nicholas, WW, Sheerin, UM, Jose, MB, Charlesworth, G, Gardner, M, Guerreiro, R, Trabzuni, D, Hardy, J, Sharma, M, Saad, M, Javier, S-S, Schulte, C, Corvol, JC, Dürr, A, Vidailhet, M, Sveinbjörnsdóttir, S, Barker, R, Caroline, HW-G, Ben-Shlomo, Y, Berendse, HW, van Dijk, KD, Berg, D, Brockmann, K, Wurster, I, Mätzler, W, Gasser, T, Martinez, M, de Bie, RMA, Biffi, A, Velseboer, D
Background: Whole-exome sequencing (WES) has been successful in identifying genes that cause familial Parkinson's disease (PD). However, until now this approach has not been deployed to study large cohorts of unrelated participants. To discover rare
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::6898845d66f7113c3c3c6fc803df251a
https://eprints.whiterose.ac.uk/112351/1/art%3A10.1186%2Fs13059-017-1147-9.pdf
https://eprints.whiterose.ac.uk/112351/1/art%3A10.1186%2Fs13059-017-1147-9.pdf
Autor:
De Jongh, T.O.H., Berendse, HW
Publikováno v:
De Jongh, T O H & Berendse, HW 2017, Trillende handen (essentiële tremor). in In ‘Therapie van alledaagse klachten: handreiking voor rationeel symptomatisch behandelen’ . Bohn Stafleu, Van Loghum .
Therapie van alledaagse klachten ISBN: 9789036819213
In ‘Therapie van alledaagse klachten: handreiking voor rationeel symptomatisch behandelen’
Therapie van alledaagse klachten ISBN: 9789036819213
In ‘Therapie van alledaagse klachten: handreiking voor rationeel symptomatisch behandelen’
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d21d5d7038d9a0103832ad27fc961207
https://research.vumc.nl/en/publications/20c311c0-2c8d-4d2e-aa26-6943f4010e0a
https://research.vumc.nl/en/publications/20c311c0-2c8d-4d2e-aa26-6943f4010e0a
Publikováno v:
Bek-Tol, MC, Elting, MW & Berendse, HW 2016, ' PHARC: zeldzame oorzaak van polyneuropathie met ataxie ', Tijdschrift voor Neurologie & Neurochirurgie, vol. 117, no. 3, pp. 103-108 . < http://www.ariez.nl/artikelen.1206.lynkx?edition=&author=Elting&title=&keyword=&free=&event=search&tijdschrift=tnn >
Tijdschrift voor Neurologie & Neurochirurgie, 117(3), 103-108
Tijdschrift voor Neurologie & Neurochirurgie, 117(3), 103-108
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::cc684e068e4124dacabd7f6bf9186de2
https://research.vumc.nl/en/publications/7da52fcd-0edf-49fd-a289-28694222d323
https://research.vumc.nl/en/publications/7da52fcd-0edf-49fd-a289-28694222d323
Autor:
Pichler I, Del Greco M. F, Gögele M, Lill CM, Bertram L, Do CB, Eriksson N, Foroud T, Myers RH, PD GWAS Consortium, Nalls M, Keller MF, International Parkinson's Disease Genomics Consortium, Wellcome Trust Case Control Consortium 2, Benyamin B, Whitfield JB, Genetics of Iron Status Consortium, Pramstaller PP, Hicks AA, Thompson JR, Minelli C., Plagnol V, Hernandez DG, Sharma M, Sheerin UM, Saad M, Simón Sánchez J, Schulte C, Lesage S, Arepalli S, Barker R, Ben Shlomo Y, Berendse HW, Berg D, Bhatia K, de Bie RM, Biffi A, Bloem B, Bochdanovits Z, Bonin M, Bras JM, Brockmann K, Brooks J, Burn DJ, Charlesworth G, Chen H, Chinnery PF, Chong S, Clarke CE, Cookson MR, Cooper JM, Corvol JC, Counsell C, Damier P, Dartigues JF, Deloukas P, Deuschl G, Dexter DT, van Dijk KD, Dillman A, Durif F, Dürr A, Edkins S, Evans JR, Foltynie T, Gao J, Gardner M, Gibbs JR, Goate A, Gray E, Guerreiro R, Harris C, van Hilten JJ, Hofman A, Hollenbeck A, Holton J, Hu M, Huang X, Huber H, Hudson G, Hunt SE, Illig T, Lambert JC, Langford C, Lees A, Lichtner P, Limousin P, Lopez G, Lorenz D, McNeill A, Moorby C, Moore M, Morris HR, Morrison KE, Mudanohwo E, O'Sullivan SS, Pearson J, Perlmutter JS, Pollak P, Post B, Potter S, Ravina B, Revesz T, Riess O, Rivadeneira F, Rizzu P, Ryten M, Sawcer S, Schapira A, Scheffer H, Shaw K, Shoulson I, Sidransky E, Smith C, Spencer CC, Stockton JD, Strange A, Talbot K, Tanner CM, Tashakkori Ghanbaria A, Trabzuni D, Traynor BJ, Uitterlinden AG, Velseboer D, Vidailhet M, Walker R, van de Warrenburg B, Wickremaratchi M, Williams N, Williams Gray CH, Winder Rhodes S, Martinez M, Hardy J, Heutink P, Brice A, Gasser T, Singleton AB, Wood NW, Donnelly P, Barroso I, Blackwell JM, Bramon E, Brown MA, Casas JP, Corvin A, Duncanson A, Jankowski J, Markus HS, Mathew CG, Palmer CN, Plomin R, Rautanen A, Sawcer SJ, Trembath RC, Viswanathan AC, Band G, Bellenguez C, Freeman C, Hellenthal G, Giannoulatou E, Pirinen M, Pearson R, Su Z, Vukcevic D, Gwilliam R, Blackburn H, Bumpstead SJ, Dronov S, Gillman M, Hammond N, Jayakumar A, McCann OT, Liddle J, Potter SC, Ravindrarajah R, Ricketts M, Waller M, Weston P, Widaa S, Whittaker P, McCarthy MI, Ouwehand WH, Radhakrishnan A, Sambrook J, Toniolo D, Camaschella C, Metspalu A, Esko T, Gieger C, Ried J, Meitinger T, Oexle K, Winkelmann J, Swinkels D, Vermeulen S, van Duijn C, Broer L, Beilby J, Hui J, Anderson D, Visscher P, Martin N., TRAGLIA, MICHELA
Publikováno v:
Pichler, I, Del Greco, M F, Gögele, M, Lill, C M, Bertram, L, Do, C B, Eriksson, N, Foroud, T, Myers, R H, Benyamin, B, Withfield, J B, Pramstaller, P P, Hicks, A A, Thompson, J R, Minelli, C & Bochdanovits, Z 2013, ' Serum iron levels and the risk of Parkinson disease: a mendelian randomization study ', PLoS Medicine, vol. 10, no. 6, e1001462, pp. 1-13 . https://doi.org/10.1371/journal.pmed.1001462
PLOS Medicine, Vol. 10, No 6 (2013) P. e1001462
PLoS Medicine, 10(6):e1001462, 1-13. Nature Publishing Group
PLoS Medicine, Vol 10, Iss 6, p e1001462 (2013)
PLoS Medicine, 10(6):e1001462, 1-13. Public Library of Science
PLoS medicine, 10(6). Public Library of Science
PLoS Medicine
PLOS Medicine, Vol. 10, No 6 (2013) P. e1001462
PLoS Medicine, 10(6):e1001462, 1-13. Nature Publishing Group
PLoS Medicine, Vol 10, Iss 6, p e1001462 (2013)
PLoS Medicine, 10(6):e1001462, 1-13. Public Library of Science
PLoS medicine, 10(6). Public Library of Science
PLoS Medicine
In this study, Mendelian randomization was used to study genes known to modify iron levels, and the effect of iron on Parkinson's disease (PD) risk was estimated. Based on estimates of the genetic effects on both iron and PD obtained from the largest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a1ff83d9ac49e91aea223736fdcdb62
https://hdl.handle.net/11541.2/130162
https://hdl.handle.net/11541.2/130162
Autor:
van Dijk KD, Persichetti, Emanuele, Chiasserini, Davide, Eusebi, Paolo, Beccari, Tommaso, Calabresi, Paolo, Berendse, Hw, Parnetti, Lucilla, van de Berg WD
Publikováno v:
Movement Disorders, 28(6), 747-754. John Wiley and Sons Inc.
van Dijk, K D, Persichetti, E, Chiasserini, D, Eusebi, P, Beccari, T, Calabresi, P, Berendse, H W, Parnetti, L & van de Berg, W D J 2013, ' Changes in endolysosomal enzyme activities in cerebrospinal fluid of patients with Parkinson's disease ', Movement Disorders, vol. 28, no. 6, pp. 747-754 . https://doi.org/10.1002/mds.25495
van Dijk, K D, Persichetti, E, Chiasserini, D, Eusebi, P, Beccari, T, Calabresi, P, Berendse, H W, Parnetti, L & van de Berg, W D J 2013, ' Changes in endolysosomal enzyme activities in cerebrospinal fluid of patients with Parkinson's disease ', Movement Disorders, vol. 28, no. 6, pp. 747-754 . https://doi.org/10.1002/mds.25495
Parkinson's disease (PD) is characterized neuropathologically by the cytoplasmic accumulation of misfolded α-synuclein in specific brain regions. The endolysosomal pathway appears to be involved in α-synuclein degradation and, thus, may be relevant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::eec0f9bba3846f555f482e338feee85a
https://research.vumc.nl/en/publications/a7bd4688-f0ab-4756-a467-232442c149e8
https://research.vumc.nl/en/publications/a7bd4688-f0ab-4756-a467-232442c149e8
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.