Annals of Neurology, 0364-5134

Journal

  1. 2020
  2. Peters, S., Broberg, K., Gallo, V., Levi, M., Kippler, M., Vineis, P., Veldink, J., Berg, L., Middleton, L., Travis, R. C., Bergmann, M. M., Palli, D., Grioni, S., Tumino, R., Elbaz, A., Vlaar, T., Mancini, F., Kühn, T., Katzke, V., ... Vermeulen, R. (2020). Blood metal levels and amyotrophic lateral sclerosis risk: A prospective cohort. Annals of Neurology, (1), 125-133. https://doi.org/10.1002/ana.25932
  3. Genomics England Research Consortium, Steel, D., Zech, M., Zhao, C., Barwick, K. E., Burke, D., Demailly, D., Kumar, K. R., Zorzi, G., Nardocci, N., Kaiyrzhanov, R., Wagner, M., Iuso, A., Berutti, R., Škorvánek, M., Necpál, J., Davis, R., Wiethoff, S., Mankad, K., ... Mencacci, N. E. (2020). Loss-of-function variants in HOPS complex genes VPS16 and VPS41 cause early-onset dystonia associated with lysosomal abnormalities. Annals of Neurology, 88(5), 867-877. https://doi.org/10.1002/ana.25879
  4. 2019
  5. Ruijter, B. J., Tjepkema-Cloostermans, M. C., Tromp, S. C., van den Bergh, W. M., Foudraine, N. A., Kornips, F. H. M., Drost, G., Scholten, E., Bosch, F. H., Beishuizen, A., van Putten, M. J. A. M., & Hofmeijer, J. (2019). Early electroencephalography for outcome prediction of postanoxic coma: A prospective cohort study. Annals of Neurology, 86(2), 203-214. https://doi.org/10.1002/ana.25518
  6. Giannini, L. A. A., Xie, S. X., McMillan, C. T., Liang, M., Williams, A., Jester, C., Rascovsky, K., Wolk, D. A., Ash, S., Lee, E. B., Trojanowski, J. Q., Grossman, M., & Irwin, D. J. (2019). Divergent patterns of TDP-43 and tau pathologies in primary progressive aphasia. Annals of Neurology, 85(5), 630-643. https://doi.org/10.1002/ana.25465
  7. 2018
  8. CAUSES Study, EuroEPINOMICS-RES-MAE Working Grp, Mulhern, M. S., Stumpel, C., Stong, N., Brunner, H. G., Bier, L., Lippa, N., Riviello, J., Rouhl, R. P. W., Kempers, M., Pfundt, R., Stegmann, A. P. A., Kukolich, M. K., Telegrafi, A., Lehman, A., Lopez-Rangel, E., Houcinat, N., Barth, M., ... Stevens, S. J. C. (2018). NBEA: Developmental disease gene with early generalized epilepsy phenotypes. Annals of Neurology, 84(5), 788-795. https://doi.org/10.1002/ana.25350
  9. 2017
  10. Seidel, K., Bouzrou, M., Heidemann, N., Kruger, R., Schöls, L., den Dunnen, W. F. A., Korf, H-W., & Rüb, U. (2017). Involvement of the Cerebellum in Parkinson Disease and Dementia with Lewy Bodies. Annals of Neurology, 81(6), 898-903. https://doi.org/10.1002/ana.24937
  11. 2016
  12. Olgiati, S., Quadri, M., Fang, M., Rood, J. P. M. A., Saute, J. A., Chien, H. F., Bouwkamp, C. G., Graafland, J., Minneboo, M., Breedveld, G. J., Zhang, J., Verheijen, F. W., Boon, A. J. W., Kievit, A. J. A., Jardim, L. B., Mandemakers, W., Barbosa, E. R., Rieder, C. R. M., Leenders, K. L., ... Int Parkinsonism Genetics Network (2016). DNAJC6 Mutations Associated With Early-Onset Parkinson's Disease. Annals of Neurology, 79(2), 244-256. https://doi.org/10.1002/ana.24553
  13. 2015
  14. Huizinga, R., van den Berg, B., van Rijs, W., Tio-Gillen, A. P., Fokkink, W. J. R., Bakker-Jonges, L. E., Geleijns, K., Samsom, J. N., van Doorn, P. A., Laman, J. D., & Jacobs, B. C. (2015). Innate Immunity to Campylobacter jejuni in Guillain-Barre Syndrome. Annals of Neurology, 78(3), 343-354. https://doi.org/10.1002/ana.24442
  15. 2014
  16. Wolf, N. I., Salomons, G. S., Rodenburg, R. J., Pouwels, P. J. W., Schieving, J. H., Derks, T. G. J., Fock, J. M., Rump, P., van Beek, D. M., van der Knaap, M. S., & Waisfisz, Q. (2014). Mutations in RARS cause hypomyelination. Annals of Neurology, 76(1), 134-139. https://doi.org/10.1002/ana.24167
  17. 2013
  18. Lohmann, K., Wilcox, R. A., Winkler, S., Ramirez, A., Rakovic, A., Park, J-S., Arns, B., Lohnau, T., Kasten, M., Brueggemann, N., Hagenah, J., Schmidt, A., Kaiser, F. J., Kumar, K. R., Zschiedrich, K., Alvarez-Fischer, D., Altenmueller, E., Ferbert, A., Lang, A. E., ... Groen, J. (2013). Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene. Annals of Neurology, 73(4), 537-545. https://doi.org/10.1002/ana.23829
  19. 2012
  20. Duarri, A., Jezierska, J., Fokkens, M., Meijer, M., Schelhaas, H. J., den Dunnen, W. F. A., van Dijk, F., Verschuuren - Bemelmans, C., Hageman, G., van de Vlies, P., Küsters, B., van de Warrenburg, B. P., Kremer, B., Wijmenga, C., Sinke, R. J., Swertz, M. A., Kampinga, H. H., Boddeke, H., & Verbeek, D. S. (2012). Mutations in Potassium Channel KCND3 Cause Spinocerebellar Ataxia Type 19. Annals of Neurology, 72(6), 870-880. https://doi.org/10.1002/ana.23700
  21. Friedman, J., Roze, E., Abdenur, J. E., Chang, R., Gasperini, S., Saletti, V., Wali, G. M., Eiroa, H., Neville, B., Felice, A., Parascandalo, R., Zafeiriou, D. I., Arrabal-Fernandez, L., Dill, P., Eichler, F. S., Echenne, B., Gutierrez-Solana, L. G., Hoffmann, G. F., Hyland, K., ... Blau, N. (2012). Sepiapterin reductase deficiency: A Treatable Mimic of Cerebral Palsy. Annals of Neurology, 71(4), 520-530. https://doi.org/10.1002/ana.22685
  22. 2011
  23. Koel-Simmelink, M. J. A., Teunissen, C. E., Behradkia, P., Blankenstein, M. A., & Petzold, A. (2011). The Neurofilament Light Chain is Not Stable in Vitro. Annals of Neurology, 69(6), 1065-1066. https://doi.org/10.1002/ana.22438
  24. Bralten, L. B. C., Kloosterhof, N. K., Balvers, R., Sacchetti, A., Lapre, L., Lamfers, M., Leenstra, S., de Jonge, H., Kros, J. M., Jansen, E. E. W., Struys, E. A., Jakobs, C., Salomons, G. S., Diks, S. H., Peppelenbosch, M., Kremer, A., Hoogenraad, C. C., Smitt, P. A. E. S., & French, P. J. (2011). IDH1 R132H Decreases Proliferation of Glioma Cell Lines In Vitro and In Vivo. Annals of Neurology, 69(3), 455-463. https://doi.org/10.1002/ana.22390
  25. Kreft, K. L., Verbraak, E., Wierenga-Wolf, A. F., Laman, J. D., & Hintzen, R. Q. (2011). Role of CD8 Regulatory T-Cells in Multiple Sclerosis. Annals of Neurology, 69(3), 593-593. https://doi.org/10.1002/ana.22288
  26. 2010
  27. Seidel, K., Schoels, L., Nuber, S., Petrasch-Parwez, E., Gierga, K., Wszolek, Z., Dickson, D., Gai, W. P., Bornemann, A., Riess, O., Rami, A., den Dunnen, W. F. A., Deller, T., Rueb, U., & Krueger, R. (2010). First Appraisal of Brain Pathology Owing to A30P Mutant Alpha-Synuclein. Annals of Neurology, 67(5), 684-689. https://doi.org/10.1002/ana.21966
  28. 2009
  29. Schirmer, L., Albert, M., Buss, A., Schulz-Schaeffer, W. J., Antel, J. P., Brueck, W., & Stadelmann, C. (2009). Substantial Early, But Nonprogressive Neuronal Loss in Multiple Sclerosis (MS) Spinal Cord. Annals of Neurology, 66(5), 698-704. https://doi.org/10.1002/ana.21799
  30. Verbeek, M. M., Kremer, B. P. H., Rikkert, M. O., Van Domburg, P. H. M. F., Skehan, M. E., & Greenberg, S. M. (2009). Cerebrospinal fluid amyloid beta(40) is decreased in cerebral amyloid angiopathy. Annals of Neurology, 66(2), 245-9. https://doi.org/10.1002/ana.21694
  31. Lindroos, M. M., Borra, R., Parkkola, R., Virtanen, S., Bucci, M., Rinne, J., Virta, J., Nuutila, P., & Majamaa, K. (2009). Cerebral Glucose and Oxygen Metabolism in Patients with Mitochondrial m.3243A > G Mutation. Annals of Neurology, 66, S56.
  32. 2008
  33. Pace, R. A., Peat, R. A., Baker, N. L., Zamurs, L., Moergelin, M., Irving, M., Adams, N. E., Bateman, J. F., Mowat, D., Smith, N. J. C., Lamont, P. J., Moore, S. A., Mathews, K. D., North, K. N., & Lamande, S. R. (2008). Collagen VI glycine mutations: Perturbed assembly and a spectrum of clinical severity. Annals of Neurology, 64(3), 294-303. https://doi.org/10.1002/ana.21439
  34. Verboon-Maciolek, M. A., Groenendaal, F., Hahn, C. D., Hellmann, J., van Loon, A. M., Boivin, G., & de Vries, L. S. (2008). Human parechovirus causes encephalitis with white matter injury in Neonates. Annals of Neurology, 64(3), 266-273. https://doi.org/10.1002/ana.21445
  35. Engbers, H. M., Berger, R., van Hasselt, P., de Koning, T., de Sain-van der Velden, M. G. M., Kroes, H. Y., & Visser, G. (2008). Yield of additional metabolic studies in neurodevelopmental disorders. Annals of Neurology, 64(2), 212-7. https://doi.org/10.1002/ana.21435
  36. Janssen, A. J. M., Schuelke, M., Smeitink, J. A. M., Trijbels, F. J. M., Sengers, R. C. A., Lucke, B., Wintjes, L. T. M., Morava, E., van Engelen, B. G. M., Struts, B. W., Hol, F. A., Siers, M. H., ter Laak, H., van der Knaap, M. S., van Spronsen, F. J., Rodenburg, R. J. T., & van den Heuvel, L. P. (2008). Muscle 3243A -> G mutation load and capacity of the mitochondrial energy-generating system. Annals of Neurology, 63(4), 473-481. https://doi.org/10.1002/ana.21328
  37. Koch, M., Mostert, J., De Keyser, J., Tremlett, H., & Filippini, G. (2008). Interferon-beta treatment and the natural history of relapsing-remitting multiple sclerosis. Annals of Neurology, 63(1), 125-126. https://doi.org/10.1002/ana.21185
  38. 2007
  39. Landwehrmeyer, G. B., Dubois, B., de Yébenes, J. G., Kremer, B., Gaus, W., Kraus, P. H., Przuntek, H., Dib, M., Doble, A., Fischer, W., Ludolph, A. C., & European Huntington's Disease Initiative Study Group (2007). Riluzole in Huntington's disease: a 3-year, randomized controlled study. Annals of Neurology, 62(3), 262-272. https://doi.org/10.1002/ana.21181
  40. 2006
  41. Ferdinandusse, S., Denis, S., Mooyer, PAW., Dekker, C., Duran, M., Soorani Yancheshmeh - Lunsing, R., Boltshauser, E., Macaya, A., Gartner, J., Majoie, CBLM., Barth, PG., Wanders, RJA., & Poll-The, BT. (2006). Clinical and biochemical spectrum of D-bifunctional protein deficiency. Annals of Neurology, 59(1), 92-104.
  42. Bartolomei, F., Bosma, I., Klein, M., Baayen, J. C., Reijneveld, J. C., Postma, T. J., Heimans, J. J., van Dijk, B. W., de Munck, J. C., de Jongh, A., Cover, K. S., & Stam, C. J. (2006). How do brain tumors alter functional connectivity? A magnetoencephalography study. Annals of Neurology, 59(1), 128-138. https://doi.org/10.1002/ana.20710
  43. Fuchs, S. A., Dorland, L., de Sain-van der Velden, M. G., Hendriks, M., Klomp, L. W. J., Berger, R., & de Koning, T. J. (2006). D-serine in the developing human central nervous system. Annals of Neurology, 60(4), 476-80. https://doi.org/10.1002/ana.20977
  44. Nyakas, C., Szabo, R., Penke, B., Banerjee, P. K., & Luiten, P. (2006). Memantine Rescues Cholinergic Neurons from the Neurotoxic Effects of β-Amyloid (Aβ1-42). Annals of Neurology, 60(3), S6-S6.
  45. 2005
  46. Verbeek, M. M., Pijnenburg, Y. A., Schoonenboom, N. S., Kremer, B. P. H., & Scheltens, P. (2005). Cerebrospinal fluid tau levels in frontotemporal dementia. Annals of Neurology, 58(4), 656-657 . https://doi.org/10.1002/ana.20642
  47. van de Warrenburg, B. P. C., Hendriks, H., Dürr, A., van Zuijlen, M. C. A., Stevanin, G., Camuzat, A., Sinke, R. J., Brice, A., & Kremer, B. P. H. (2005). Age at onset variance analysis in spinocerebellar ataxias: a study in a Dutch-French cohort. Annals of Neurology, 57(4), 505-12. https://doi.org/10.1002/ana.20424
  48. 2004
  49. Dobson-Stone, C., Velayos-Baeza, A., Filippone, LA., Westbury, S., Storch, A., Erdmann, T., Wroe, SJ., Leenders, KL., Lang, AE., Dotti, MT., Federico, A., Mohiddin, SA., Fananapazir, L., Daniels, G., Danek, A., & Monaco, AP. (2004). Chorein detection for the diagnosis of chorea-acanthocytosis. Annals of Neurology, 56(2), 299-302. https://doi.org/10.1002/ana.20200
  50. Winkel, LPF., Van den Hout, JMP., Kamphoven, JHJ., Disseldorp, JAM., Remmerswaal, M., Arts, WFM., Loonen, MCB., Vulto, AG., Van Doorn, PA., De Jong, G., Hop, W., Smit, GPA., Shapira, SK., Boer, MA., van Diggelen, OP., Reuser, AJJ., & Van der Ploeg, AT. (2004). Enzyme replacement therapy in late-onset Pompe's disease: A three-year follow-up. Annals of Neurology, 55(4), 495-502. https://doi.org/10.1002/ana.20019
  51. Schelhaas, H. J., Van de Warrenburg, B. P. C., Kremer, H. P. H., & Zwarts, M. J. (2004). Neuromuscular transmission in SCA6. Annals of Neurology, 55(3), 451-452. https://doi.org/10.1002/ana.20015
  52. 2003
  53. Geerlings, MI., Launer, LJ., de Jong, FH., Ruitenberg, A., Stijnen, T., van Swieten, JC., Hofman, A., Witteman, JCM., Pols, HAP., & Breteler, MMB. (2003). Endogenous estradiol and risk of dementia in women and men: The Rotterdam Study. Annals of Neurology, 53(5), 607-615. https://doi.org/10.1002/ana.10521
  54. 2002
  55. Badrising, UA., Maat-Schieman, MLC., Ferrari, MD., Zwinderman, AH., Wessels, JAM., Breedveld, FC., van Doorn, PA., van Engelen, BGM., Hoogendijk, JE., Howeler, CJ., de Jager, AE., Jennekens, FGI., Koehler, PJ., de Visser, M., Viddeleer, A., Verschuuren, JJ., & Wintzen, AR. (2002). Comparison of weakness progression in inclusion body myositis during treatment with methotrexate or placebo. Annals of Neurology, 51(3), 369-372. https://doi.org/10.1002/ana.10121
  56. Vermeer, SE., van Dijk, EJ., Koudstaal, PJ., Oudkerk, M., Hofman, A., Clarke, R., & Breteler, MMB. (2002). Homocysteine, silent brain infarcts, and white matter lesions: The Rotterdam scan study. Annals of Neurology, 51(3), 285-289. https://doi.org/10.1002/ana.10111
  57. 2001
  58. 2000
  59. Kunig, G., Leenders, KL., Sanchez-Pernaute, R., Antonini, A., Vontobel, P., Verhagen, A., & Günther, I. (2000). Benzodiazepine receptor binding in Huntington's disease: [C-11]flumazenil uptake measured using positron emission tomography. Annals of Neurology, 47(5), 644-648.
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