المؤلفون: Schols, L, Rattay, TW, Martus, P, Meisner, C, Baets, J, Fischer, I, Jagle, C, Fraidakis, MJ, Martinuzzi, A, Saute, JA, Scarlato, M, Antenora, A, Stendel, C, Hoflinger, P, Lourenco, CM, Abreu, L, Smets, K, Paucar, M, Deconinck, T, Bis, DM, Wiethoff, S, Bauer, P, Arnoldi, A, Marques, W, Jardim, LB, Hauser, S, Criscuolo, C, Filla, A, Zuchner, S, Bassi, MT, Klopstock, T, De Jonghe, P, Bjorkhem, I, Schule, R

المصدر: Brain : a journal of neurology. 140(12):3112-3127

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:137155329

المؤلفون: Lerche, S, Schulte, C, Srulijes, K, Pilotto, A, Rattay, TW, Hauser, A-K, Stransky, E, Deuschle, C, Csoti, I, Lachmann, I, Zetterberg, H, Liepelt-Scarfone, I, Gasser, T, Maetzler, W, Berg, D, Brockmann, K

المصدر: Movement Disorders , 32 (12) pp. 1780-1783. (2017)

مصطلحات موضوعية: Parkinson, GBA, Abeta, Tau, alpha‐synuclein, CSF

Relation: https://discovery.ucl.ac.uk/id/eprint/10057927/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/10057927/

المؤلفون: Minnerop M, Kurzwelly D, Rattay TW, Timmann D, Hengel H, Synofzik M, Stendel C, Horvath R, Schule R, Ramirez A

المصدر: Brain, 1 January 2018

Relation: https://eprints.ncl.ac.uk/245538

الاتاحة: https://eprints.ncl.ac.uk/245538

المؤلفون: Rattay, TW, Lindig, T, Baets, J, Smets, K, Deconinck, T, Söhn, AS, Hörtnagel, K, Eckstein, KN, Wiethoff, S, Reichbauer, J, Döbler-Neumann, M, Krägeloh-Mann, I, Auer-Grumbach, M, Plecko, B, Münchau, A, Wilken, B, Janauschek, M, Giese, AK, De Bleecker, Jan, Ortibus, E, Debyser, M, Lopez de Munain, A, Pujol, A, Bassi, MT, D'Angelo, MG, De Jonghe, P, Züchner, S, Bauer, P, Schöls, L, Schüle, R

المصدر: BRAIN ; ISSN: 0006-8950 ; ISSN: 1460-2156

مصطلحات موضوعية: Medicine and Health Sciences, SPG35, FAHN, FA2H, imaging biomarker, hereditary spastic paraplegia: HEREDITARY SPASTIC PARAPLEGIA, FATTY-ACID 2-HYDROXYLASE, IRON ACCUMULATION, COMPLICATED FORM, MUTATIONS, NEURODEGENERATION, PARAPARESIS, DISORDERS, DIAGNOSIS

وصف الملف: application/pdf

Relation: https://biblio.ugent.be/publication/8618343; http://hdl.handle.net/1854/LU-8618343; http://dx.doi.org/10.1093/brain/awz102; https://biblio.ugent.be/publication/8618343/file/8618344

الاتاحة: https://biblio.ugent.be/publication/8618343
http://hdl.handle.net/1854/LU-8618343
https://doi.org/10.1093/brain/awz102
https://biblio.ugent.be/publication/8618343/file/8618344

المؤلفون: Minnerop M, Kurzwelly D, Wagner H, Soehn AS, Reichbauer J, Tao F, Rattay TW, Peitz M, Rehbach K, Giorgetti A, Pyle A, Thiele H, Altmuller J, Timmann D, Karaca I, Lennarz M, Baets J, Hengel H, Synofzik M, Atasu B, Feely S, Kennerson M, Stendel C, Lindig T, Gonzalez MA, Stirnberg R, Sturm M, Roeske S, Jung J, Bauer P, Lohmann E, Herms S, Heilmann-Heimbach S, Nicholson G, Mahanjah M, Sharkia R, Carloni P, Brustle O, Klopstock T, Mathews KD, Shy ME, De Jonghe P, Chinnery PF, Horvath R, Kohlhase J, Schmitt I, Wolf M, Greschus S, Amunts K, Maier W, Schols L, Nurnberg P, Zuchner S, Klockgether T, Ramirez A, Schule R

المصدر: Brain, 2017

Relation: https://eprints.ncl.ac.uk/239953

الاتاحة: https://eprints.ncl.ac.uk/239953

المؤلفون: Hauser, S, Hoflinger, P, Theurer, Y, Rattay, TW, Bjorkhem, I, Schule, R, Schols, L

المصدر: HUMAN GENE THERAPY. 27(11):A76-A77

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:134625975