Zentrum für Neuropathologie und Prionforschung
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Dr. med. Sigrun Roeber

[2024] [2023] [2022] [2021] [2020] [2019] [2018] [2017] [2015] [2014] [2013] [2012] [2011] [2010] [2009] [2008] [2007] [2006] [2005]

2024

Wang H, Chang TS, Dombroski BA, Cheng PL, Si YQ, Tucci A, Patil V, Valiente-Banuet L, Farrell K, Mclean C, Molina-Porcel L, Alex R, Paul De Deyn P, Le Bastard N, Gearing M, Donker Kaat L, Van Swieten JC, Dopper E, Ghetti BF, Newell KL, Troakes C, G de Yébenes J, Rábano-Gutierrez A, Meller T, Oertel WH, Respondek G, Stamelou M, Arzberger T, Roeber S, Müller U, Hopfner F, Pastor P, Brice A, Durr A, Le Ber I, Beach TG, Serrano GE, Hazrati LN, Litvan I, Rademakers R, Ross OA, Galasko D, Boxer AL, Miller BL, Seeley WW, Van Deerlin VM, Lee EB, White CL, Morris HR, de Silva R, Crary JF, Goate AM, Friedman JS, Leung YY, Coppola G, Naj AC, Wang LS, PSP genetics study group, Dickson DW, Höglinger GU, Tzeng JY, Geschwind DH, Schellenberg GD & Lee WP
Association of Structural Forms of 17q21.31 with the Risk of Progressive Supranuclear Palsy and MAPT Sub-haplotypes.
medRxiv : the preprint server for health sciences, 2024 Feb 28

Wang H, Chang TS, Dombroski BA, Cheng PL, Patil V, Valiente-Banuet L, Farrell K, Mclean C, Molina-Porcel L, Rajput A, De Deyn PP, Bastard NL, Gearing M, Kaat LD, Swieten JCV, Dopper E, Ghetti BF, Newell KL, Troakes C, de Yébenes JG, Rábano-Gutierrez A, Meller T, Oertel WH, Respondek G, Stamelou M, Arzberger T, Roeber S, Müller U, Hopfner F, Pastor P, Brice A, Durr A, Ber IL, Beach TG, Serrano GE, Hazrati LN, Litvan I, Rademakers R, Ross OA, Galasko D, Boxer AL, Miller BL, Seeley WW, Deerlin VMV, Lee EB, White CL, Morris H, de Silva R, Crary JF, Goate AM, Friedman JS, Leung YY, Coppola G, Naj AC, Wang LS, PSP genetics study group, Dickson DW, Höglinger GU, Schellenberg GD, Geschwind DH & Lee WP
Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear Palsy.
medRxiv : the preprint server for health sciences, 2024 Jan 30

Chemparathy A, Le Guen Y, Chen S, Lee EG, Leong L, Gorzynski JE, Jensen TD, Ferrasse A, Xu G, Xiang H, Belloy ME, Kasireddy N, Peña-Tauber A, Williams K, Stewart I, Talozzi L, Wingo TS, Lah JJ, Jayadev S, Hales CM, Peskind E, Child DD, Roeber S, Keene CD, Cong L, Ashley EA, Yu CE & Greicius MD
APOE loss-of-function variants: Compatible with longevity and associated with resistance to Alzheimer's disease pathology.
Neuron, 2024 Jan 29

Diehl-Schmid J, Ellerbrock P, Winkler T, Zwanzger P, Ledderose S, Herms J & Roeber S
[Neoplastic meningitis as differential diagnosis of a rapidly progressive dementia].
Der Nervenarzt, 2024 Jan, 95 (1) 53-56

2023

Harrer P, Mirza-Schreiber N, Mandel V, Roeber S, Stefani A, Naher S, Wagner M, Gieger C, Waldenberger M, Peters A, Högl B, Herms J, Schormair B, Zhao C, Winkelmann J & Oexle K
Epigenetic Association Analyses and Risk Prediction of RLS.
Movement disorders : official journal of the Movement Disorder Society, 2023 Aug, 38 (8) 1410-1418

Valentino RR, Scotton WJ, Roemer SF, Lashley T, Heckman MG, Shoai M, Martinez-Carrasco A, Tamvaka N, Walton RL, Baker MC, Macpherson HL, Real R, Soto-Beasley AI, Mok K, Revesz T, Warner TT, Jaunmuktane Z, Boeve BF, Christopher EA, DeTure M, Duara R, Graff-Radford NR, Josephs KA, Knopman DS, Koga S, Murray ME, Lyons KE, Pahwa R, Parisi JE, Petersen RC, Whitwell J, Grinberg LT, Miller B, Schlereth A, Seeley WW, Spina S, Grossman M, Irwin DJ, Lee EB, Suh E, Trojanowski JQ, Van Deerlin VM, Wolk DA, Connors TR, Dooley PM, Frosch MP, Oakley DH, Aldecoa I, Balasa M, Gelpi E, Borrego-Écija S, de Eugenio Huélamo RM, Gascon-Bayarri J, Sánchez-Valle R, Sanz-Cartagena P, Piñol-Ripoll G, Molina-Porcel L, Bigio EH, Flanagan ME, Gefen T, Rogalski EJ, Weintraub S, Redding-Ochoa J, Chang K, Troncoso JC, Prokop S, Newell KL, Ghetti B, Jones M, Richardson A, Robinson AC, Roncaroli F, Snowden J, Allinson K, Green O, Rowe JB, Singh P, Beach TG, Serrano GE, Flowers XE, Goldman JE, Heaps AC, Leskinen SP, Teich AF, Black SE, Keith JL, Masellis M, Bodi I, King A, Sarraj SA, Troakes C, Halliday GM, Hodges JR, Kril JJ, Kwok JB, Piguet O, Gearing M, Arzberger T, Roeber S, Attems J, Morris CM, Thomas AJ, Evers BM, White CL, Mechawar N, Sieben AA, Cras PP, De Vil BB, De Deyn PPPP, Duyckaerts C, Le Ber I, Seihean D, Turbant-Leclere S, MacKenzie IR, McLean C, Cykowski MD, Ervin JF, Wang SJ, Graff C, Nennesmo I, Nagra RM, Riehl J, Kovacs GG, Giaccone G, Nacmias B, Neumann M, Ang LC, Finger EC, Blauwendraat C, Nalls MA, Singleton AB, Vitale D, Cunha C, Carvalho A, Wszolek ZK, Morris HR, Rademakers R, Hardy JA, Dickson DW, Rohrer JD & Ross OA
Creating the Pick's disease International Consortium: Association study of MAPT H2 haplotype with risk of Pick's disease.
medRxiv : the preprint server for health sciences, 2023 Apr 24

2022

Messerschmidt K, Barthel H, Brendel M, Scherlach C, Hoffmann KT, Rauchmann BS, Rullmann M, Marek K, Villemagne VL, Rumpf JJ, Saur D, Schroeter ML, Schildan A, Patt M, Beyer L, Song M, Palleis C, Katzdobler S, Fietzek UM, Respondek G, Scheifele M, Nitschmann A, Zach C, Barret O, Madonia J, Russell D, Stephens AW, Koglin N, Roeber S, Herms J, Bötzel K, Bartenstein P, Levin J, Seibyl JP, Höglinger G, Classen J, Sabri O & German Imaging Initiative for Tauopathies (GII4T)
18F-PI-2620 Tau PET Improves the Imaging Diagnosis of Progressive Supranuclear Palsy.
Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 2022 Nov, 63 (11) 1754-1760

Lukic MJ, Respondek G, Kurz C, Compta Y, Gelpi E, Ferguson LW, Rajput A, Troakes C, MDS-endorsed PSP study group, van Swieten JC, Giese A, Roeber S, Herms J, Arzberger T & Höglinger G
Long-Duration Progressive Supranuclear Palsy: Clinical Course and Pathological Underpinnings.
Annals of neurology, 2022 Oct, 92 (4) 637-649

Perez-Rivas LG, Simon J, Albani A, Tang S, Roeber S, Assié G, Deutschbein T, Fassnacht M, Gadelha MR, Hermus AR, Stalla GK, Tichomirowa MA, Rotermund R, Flitsch J, Buchfelder M, Nasi-Kordhishti I, Honegger J, Thorsteinsdottir J, Saeger W, Herms J, Reincke M & Theodoropoulou M
TP53 mutations in functional corticotroph tumors are linked to invasion and worse clinical outcome.
Acta neuropathologica communications, 2022 Sep 19, 10 (1) 139

Albani A, Perez-Rivas LG, Tang S, Simon J, Lucia KE, Colón-Bolea P, Schopohl J, Roeber S, Buchfelder M, Rotermund R, Flitsch J, Thorsteinsdottir J, Herms J, Stalla G, Reincke M & Theodoropoulou M
Improved pasireotide response in USP8 mutant corticotroph tumours in vitro.
Endocrine-related cancer, 2022 Aug 01, 29 (8) 503-511

Charidimou A, Boulouis G, Frosch MP, Baron JC, Pasi M, Albucher JF, Banerjee G, Barbato C, Bonneville F, Brandner S, Calviere L, Caparros F, Casolla B, Cordonnier C, Delisle MB, Deramecourt V, Dichgans M, Gokcal E, Herms J, Hernandez-Guillamon M, Jäger HR, Jaunmuktane Z, Linn J, Martinez-Ramirez S, Martínez-Sáez E, Mawrin C, Montaner J, Moulin S, Olivot JM, Piazza F, Puy L, Raposo N, Rodrigues MA, Roeber S, Romero JR, Samarasekera N, Schneider JA, Schreiber S, Schreiber F, Schwall C, Smith C, Szalardy L, Varlet P, Viguier A, Wardlaw JM, Warren A, Wollenweber FA, Zedde M, van Buchem MA, Gurol ME, Viswanathan A, Al-Shahi Salman R, Smith EE, Werring DJ & Greenberg SM
The Boston criteria version 2.0 for cerebral amyloid angiopathy: a multicentre, retrospective, MRI-neuropathology diagnostic accuracy study.
The Lancet. Neurology, 2022 Aug, 21 (8) 714-725

Franzmeier N, Brendel M, Beyer L, Slemann L, Kovacs GG, Arzberger T, Kurz C, Respondek G, Lukic MJ, Biel D, Rubinski A, Frontzkowski L, Hummel S, Müller A, Finze A, Palleis C, Joseph E, Weidinger E, Katzdobler S, Song M, Biechele G, Kern M, Scheifele M, Rauchmann BS, Perneczky R, Rullman M, Patt M, Schildan A, Barthel H, Sabri O, Rumpf JJ, Schroeter ML, Classen J, Villemagne V, Seibyl J, Stephens AW, Lee EB, Coughlin DG, Giese A, Grossman M, McMillan CT, Gelpi E, Molina-Porcel L, Compta Y, van Swieten JC, Laat LD, Troakes C, Al-Sarraj S, Robinson JL, Xie SX, Irwin DJ, Roeber S, Herms J, Simons M, Bartenstein P, Lee VM, Trojanowski JQ, Levin J, Höglinger G & Ewers M
Tau deposition patterns are associated with functional connectivity in primary tauopathies.
Nature communications, 2022 Mar 15, 13 (1) 1362

Vöglein J, Kostova I, Arzberger T, Noachtar S, Dieterich M, Herms J, Schmitz P, Ruf V, Windl O, Roeber S, Simons M, Höglinger GU, Danek A, Giese A & Levin J
Seizure prevalence in neurodegenerative diseases-a study of autopsy proven cases.
European journal of neurology, 2022 Jan, 29 (1) 12-18

2021

Song M, Beyer L, Kaiser L, Barthel H, van Eimeren T, Marek K, Nitschmann A, Scheifele M, Palleis C, Respondek G, Kern M, Biechele G, Hammes J, Bischof G, Barbe M, Onur Ö, Jessen F, Saur D, Schroeter ML, Rumpf JJ, Rullmann M, Schildan A, Patt M, Neumaier B, Barret O, Madonia J, Russell DS, Stephens AW, Mueller A, Roeber S, Herms J, Bötzel K, Danek A, Levin J, Classen J, Höglinger GU, Bartenstein P, Villemagne V, Drzezga A, Seibyl J, Sabri O, Boening G, Ziegler S & Brendel M
Binding characteristics of [18F]PI-2620 distinguish the clinically predicted tau isoform in different tauopathies by PET.
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, 2021 Nov, 41 (11) 2957-2972

Vöglein J, Kostova I, Arzberger T, Roeber S, Schmitz P, Simons M, Ruf V, Windl O, Herms J, Dieterich M, Danek A, Höglinger GU, Giese A & Levin J
First symptom guides diagnosis and prognosis in neurodegenerative diseases-a retrospective study of autopsy proven cases.
European journal of neurology, 2021 Jun, 28 (6) 1801-1811

Yamamoto Y, Hase Y, Ihara M, Khundakar A, Roeber S, Duering M & Kalaria RN
Neuronal densities and vascular pathology in the hippocampal formation in CADASIL.
Neurobiology of aging, 2021 Jan, 97 33-40

Willroider M, Roeber S, Horn AKE, Arzberger T, Scheifele M, Respondek G, Sabri O, Barthel H, Patt M, Mishchenko O, Schildan A, Mueller A, Koglin N, Stephens A, Levin J, Höglinger GU, Bartenstein P, Herms J, Brendel M & Beyer L
Superiority of Formalin-Fixed Paraffin-Embedded Brain Tissue for in vitro Assessment of Progressive Supranuclear Palsy Tau Pathology With [ 18 F]PI-2620.
Frontiers in neurology, 2021, 12 684523

2020

Grimm MJ, Respondek G, Stamelou M, Arzberger T, Ferguson L, Gelpi E, Giese A, Grossman M, Irwin DJ, Pantelyat A, Rajput A, Roeber S, van Swieten JC, Troakes C, Meissner WG, Nilsson C, Piot I, Compta Y, Rowe JB, Höglinger GU & Movement Disorder Society-Endorsed PSP Study Group
Clinical Conditions "Suggestive of Progressive Supranuclear Palsy"-Diagnostic Performance.
Movement disorders : official journal of the Movement Disorder Society, 2020 Dec, 35 (12) 2301-2313

Beyer L, Nitschmann A, Barthel H, van Eimeren T, Unterrainer M, Sauerbeck J, Marek K, Song M, Palleis C, Respondek G, Hammes J, Barbe MT, Onur Ö, Jessen F, Saur D, Schroeter ML, Rumpf JJ, Rullmann M, Schildan A, Patt M, Neumaier B, Barret O, Madonia J, Russell DS, Stephens AW, Roeber S, Herms J, Bötzel K, Levin J, Classen J, Höglinger GU, Bartenstein P, Villemagne V, Drzezga A, Seibyl J, Sabri O & Brendel M
Early-phase [18F]PI-2620 tau-PET imaging as a surrogate marker of neuronal injury.
European journal of nuclear medicine and molecular imaging, 2020 Nov, 47 (12) 2911-2922

Brendel M, Barthel H, van Eimeren T, Marek K, Beyer L, Song M, Palleis C, Gehmeyr M, Fietzek U, Respondek G, Sauerbeck J, Nitschmann A, Zach C, Hammes J, Barbe MT, Onur O, Jessen F, Saur D, Schroeter ML, Rumpf JJ, Rullmann M, Schildan A, Patt M, Neumaier B, Barret O, Madonia J, Russell DS, Stephens A, Roeber S, Herms J, Bötzel K, Classen J, Bartenstein P, Villemagne V, Levin J, Höglinger GU, Drzezga A, Seibyl J & Sabri O
Assessment of 18F-PI-2620 as a Biomarker in Progressive Supranuclear Palsy.
JAMA neurology, 2020 Nov 01, 77 (11) 1408-1419

Dinkelbach L, Südmeyer M, Hartmann CJ, Roeber S, Arzberger T, Felsberg J, Ferrea S, Moldovan AS, Amunts K, Schnitzler A & Caspers S
Somatosensory area 3b is selectively unaffected in corticobasal syndrome: combining MRI and histology.
Neurobiology of aging, 2020 Oct, 94 89-100

Nibbe L, Jungehülsing M, Röber S, Ripberger G & Oppert M
["Hybrid tracheostomy": a low risk procedure for tracheostomy in COVID-19 patients].
Medizinische Klinik, Intensivmedizin und Notfallmedizin, 2020 Oct, 115 (7) 585-590

Kovacs GG, Lukic MJ, Irwin DJ, Arzberger T, Respondek G, Lee EB, Coughlin D, Giese A, Grossman M, Kurz C, McMillan CT, Gelpi E, Compta Y, van Swieten JC, Laat LD, Troakes C, Al-Sarraj S, Robinson JL, Roeber S, Xie SX, Lee VM, Trojanowski JQ & Höglinger GU
Distribution patterns of tau pathology in progressive supranuclear palsy.
Acta neuropathologica, 2020 Aug, 140 (2) 99-119

Jecmenica Lukic M, Kurz C, Respondek G, Grau-Rivera O, Compta Y, Gelpi E, Troakes C, Barcelona Brain Bank collaborative group, the MDS-endorsed PSP study group, van Swieten JC, Giese A, Roeber S, Arzberger T & Höglinger G
Copathology in Progressive Supranuclear Palsy: Does It Matter?
Movement disorders : official journal of the Movement Disorder Society, 2020 Jun, 35 (6) 984-993

Respondek G, Grimm MJ, Piot I, Arzberger T, Compta Y, Englund E, Ferguson LW, Gelpi E, Roeber S, Giese A, Grossman M, Irwin DJ, Meissner WG, Nilsson C, Pantelyat A, Rajput A, van Swieten JC, Troakes C, Höglinger GU & Movement Disorder Society-Endorsed Progressive Supranuclear Palsy Study Group
Validation of the movement disorder society criteria for the diagnosis of 4-repeat tauopathies.
Movement disorders : official journal of the Movement Disorder Society, 2020 Jan, 35 (1) 171-176

2019

Cali CP, Patino M, Tai YK, Ho WY, McLean CA, Morris CM, Seeley WW, Miller BL, Gaig C, Vonsattel JPG, White CL, Roeber S, Kretzschmar H, Troncoso JC, Troakes C, Gearing M, Ghetti B, Van Deerlin VM, Lee VM, Trojanowski JQ, Mok KY, Ling H, Dickson DW, Schellenberg GD, Ling SC & Lee EB
C9orf72 intermediate repeats are associated with corticobasal degeneration, increased C9orf72 expression and disruption of autophagy.
Acta neuropathologica, 2019 Nov, 138 (5) 795-811

Grimm MJ, Respondek G, Stamelou M, Arzberger T, Ferguson L, Gelpi E, Giese A, Grossman M, Irwin DJ, Pantelyat A, Rajput A, Roeber S, van Swieten JC, Troakes C, Antonini A, Bhatia KP, Colosimo C, van Eimeren T, Kassubek J, Levin J, Meissner WG, Nilsson C, Oertel WH, Piot I, Poewe W, Wenning GK, Boxer A, Golbe LI, Josephs KA, Litvan I, Morris HR, Whitwell JL, Compta Y, Corvol JC, Lang AE, Rowe JB, Höglinger GU & Movement Disorder Society-endorsed PSP Study Group
How to apply the movement disorder society criteria for diagnosis of progressive supranuclear palsy.
Movement disorders : official journal of the Movement Disorder Society, 2019 Aug, 34 (8) 1228-1232

Pottier C, Ren Y, Perkerson RB, Baker M, Jenkins GD, van Blitterswijk M, DeJesus-Hernandez M, van Rooij JGJ, Murray ME, Christopher E, McDonnell SK, Fogarty Z, Batzler A, Tian S, Vicente CT, Matchett B, Karydas AM, Hsiung GR, Seelaar H, Mol MO, Finger EC, Graff C, Öijerstedt L, Neumann M, Heutink P, Synofzik M, Wilke C, Prudlo J, Rizzu P, Simon-Sanchez J, Edbauer D, Roeber S, Diehl-Schmid J, Evers BM, King A, Mesulam MM, Weintraub S, Geula C, Bieniek KF, Petrucelli L, Ahern GL, Reiman EM, Woodruff BK, Caselli RJ, Huey ED, Farlow MR, Grafman J, Mead S, Grinberg LT, Spina S, Grossman M, Irwin DJ, Lee EB, Suh E, Snowden J, Mann D, Ertekin-Taner N, Uitti RJ, Wszolek ZK, Josephs KA, Parisi JE, Knopman DS, Petersen RC, Hodges JR, Piguet O, Geier EG, Yokoyama JS, Rissman RA, Rogaeva E, Keith J, Zinman L, Tartaglia MC, Cairns NJ, Cruchaga C, Ghetti B, Kofler J, Lopez OL, Beach TG, Arzberger T, Herms J, Honig LS, Vonsattel JP, Halliday GM, Kwok JB, White CL, Gearing M, Glass J, Rollinson S, Pickering-Brown S, Rohrer JD, Trojanowski JQ, Van Deerlin V, Bigio EH, Troakes C, Al-Sarraj S, Asmann Y, Miller BL, Graff-Radford NR, Boeve BF, Seeley WW, Mackenzie IRA, van Swieten JC, Dickson DW, Biernacka JM & Rademakers R
Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD.
Acta neuropathologica, 2019 Jun, 137 (6) 879-899

Yin C, Ackermann S, Ma Z, Mohanta SK, Zhang C, Li Y, Nietzsche S, Westermann M, Peng L, Hu D, Bontha SV, Srikakulapu P, Beer M, Megens RTA, Steffens S, Hildner M, Halder LD, Eckstein HH, Pelisek J, Herms J, Roeber S, Arzberger T, Borodovsky A, Habenicht L, Binder CJ, Weber C, Zipfel PF, Skerka C & Habenicht AJR
ApoE attenuates unresolvable inflammation by complex formation with activated C1q.
Nature medicine, 2019 Mar, 25 (3) 496-506

Yin C, Ackermann S, Ma Z, Mohanta SK, Zhang C, Li Y, Nietzsche S, Westermann M, Peng L, Hu D, Bontha SV, Srikakulapu P, Beer M, Megens RTA, Steffens S, Hildner M, Halder LD, Eckstein HH, Pelisek J, Herms J, Roeber S, Arzberger T, Borodovsky A, Habenicht L, Binder CJ, Weber C, Zipfel PF, Skerka C & Habenicht AJR
Publisher Correction: ApoE attenuates unresolvable inflammation by complex formation with activated C1q.
Nature medicine, 2019 Mar, 25 (3) 529

2018

Gasparoni G, Bultmann S, Lutsik P, Kraus TFJ, Sordon S, Vlcek J, Dietinger V, Steinmaurer M, Haider M, Mulholland CB, Arzberger T, Roeber S, Riemenschneider M, Kretzschmar HA, Giese A, Leonhardt H & Walter J
DNA methylation analysis on purified neurons and glia dissects age and Alzheimer's disease-specific changes in the human cortex.
Epigenetics & chromatin, 2018 Jul 25, 11 (1) 41

Albani A, Pérez-Rivas LG, Dimopoulou C, Zopp S, Colón-Bolea P, Roeber S, Honegger J, Flitsch J, Rachinger W, Buchfelder M, Stalla GK, Herms J, Reincke M & Theodoropoulou M
The USP8 mutational status may predict long-term remission in patients with Cushing's disease.
Clinical endocrinology, 2018 Jun 29

Steinacker P, Verde F, Fang L, Feneberg E, Oeckl P, Roeber S, Anderl-Straub S, Danek A, Diehl-Schmid J, Fassbender K, Fliessbach K, Foerstl H, Giese A, Jahn H, Kassubek J, Kornhuber J, Landwehrmeyer GB, Lauer M, Pinkhardt EH, Prudlo J, Rosenbohm A, Schneider A, Schroeter ML, Tumani H, von Arnim CAF, Weishaupt J, Weydt P, Ludolph AC, Yilmazer Hanke D, Otto M & FTLDc study group
Chitotriosidase (CHIT1) is increased in microglia and macrophages in spinal cord of amyotrophic lateral sclerosis and cerebrospinal fluid levels correlate with disease severity and progression.
Journal of neurology, neurosurgery, and psychiatry, 2018 Mar, 89 (3) 239-247

2017

Saal KA, Galter D, Roeber S, Bähr M, Tönges L & Lingor P
Altered Expression of Growth Associated Protein-43 and Rho Kinase in Human Patients with Parkinson's Disease.
Brain pathology (Zurich, Switzerland), 2017 Jan, 27 (1) 13-25

Kattah JC, Saber Tehrani AS, Roeber S, Gujrati M, Bach SE, Newman Toker DE, Blitz AM & Horn AKE
Transient Vestibulopathy in Wallenberg's Syndrome: Pathologic Analysis.
Frontiers in neurology, 2017, 8 191

2015

Roeber S, Müller-Sarnowski F, Kress J, Edbauer D, Kuhlmann T, Tüttelmann F, Schindler C, Winter P, Arzberger T, Müller U, Danek A & Kretzschmar HA
Three novel presenilin 1 mutations marking the wide spectrum of age at onset and clinical patterns in familial Alzheimer's disease.
Journal of neural transmission (Vienna, Austria : 1996), 2015 Dec, 122 (12) 1715-9

Roeber , Schludi MH, May S, Grässer FA, Rentzsch K, Kremmer E, Küpper C, Klopstock T, German Consortium for Frontotemporal Lobar Degeneration, Bavarian Brain Banking Alliance, Arzberger T & Edbauer D
Distribution of dipeptide repeat proteins in cellular models and C9orf72 mutation cases suggests link to transcriptional silencing.
Acta neuropathologica, 2015 Oct, 130 (4) 537-55

Henz S, Ackl N, Knels C, Rominger A, Flatz W, Teipel S, Huppertz HJ, Roeber S, Neumann M & Danek A
[A Pair of Siblings with a rare R5H-Mutation in Exon 1 of the MAPT-Gene].
Fortschritte der Neurologie-Psychiatrie, 2015 Jul, 83 (7) 397-401

Kouri N, Ross OA, Dombroski B, Younkin CS, Serie DJ, Soto-Ortolaza A, Baker M, Finch NCA, Yoon H, Kim J, Fujioka S, McLean CA, Ghetti B, Spina S, Cantwell LB, Farlow MR, Grafman J, Huey ED, Ryung Han M, Beecher S, Geller ET, Kretzschmar HA, Roeber S, Gearing M, Juncos JL, Vonsattel JPG, Van Deerlin VM, Grossman M, Hurtig HI, Gross RG, Arnold SE, Trojanowski JQ, Lee VM, Wenning GK, White CL, Höglinger GU, Müller U, Devlin B, Golbe LI, Crook J, Parisi JE, Boeve BF, Josephs KA, Wszolek ZK, Uitti RJ, Graff-Radford NR, Litvan I, Younkin SG, Wang LS, Ertekin-Taner N, Rademakers R, Hakonarsen H, Schellenberg GD & Dickson DW
Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy.
Nature communications, 2015 Jun 16, 6 7247

Eggers SD, Horn AK, Roeber S, Härtig W, Nair G, Reich DS & Leigh RJ
Saccadic palsy following cardiac surgery: a review and new hypothesis.
Annals of the New York Academy of Sciences, 2015 Apr, 1343 (1) 113-9

Eggers SD, Horn AK, Roeber S, Härtig W, Nair G, Reich DS & Leigh RJ
Saccadic Palsy following Cardiac Surgery: Possible Role of Perineuronal Nets.
PloS one, 2015, 10 (7) e0132075

2014

Respondek G, Stamelou M, Kurz C, Ferguson LW, Rajput A, Chiu WZ, van Swieten JC, Troakes C, Al Sarraj S, Gelpi E, Gaig C, Tolosa E, Oertel WH, Giese A, Roeber S, Arzberger T, Wagenpfeil S, Höglinger GU & Movement Disorder Society-endorsed PSP Study Group
The phenotypic spectrum of progressive supranuclear palsy: a retrospective multicenter study of 100 definite cases.
Movement disorders : official journal of the Movement Disorder Society, 2014 Dec, 29 (14) 1758-66

Craggs LJ, Yamamoto Y, Ihara M, Fenwick R, Burke M, Oakley AE, Roeber S, Duering M, Kretzschmar H & Kalaria RN
White matter pathology and disconnection in the frontal lobe in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
Neuropathology and applied neurobiology, 2014 Aug, 40 (5) 591-602

2013

Sundal C, Fujioka S, Van Gerpen JA, Wider C, Nicholson AM, Baker M, Shuster EA, Aasly J, Spina S, Ghetti B, Roeber S, Garbern J, Tselis A, Swerdlow RH, Miller BB, Borjesson-Hanson A, Uitti RJ, Ross OA, Stoessl AJ, Rademakers R, Josephs KA, Dickson DW, Broderick D & Wszolek ZK
Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutations.
Parkinsonism & related disorders, 2013 Oct, 19 (10) 869-77

Roeber , Stutzbach LD, Xie SX, Naj AC, Albin R, Gilman S, PSP Genetics Study Group, Lee VM, Trojanowski JQ, Devlin B & Schellenberg GD
The unfolded protein response is activated in disease-affected brain regions in progressive supranuclear palsy and Alzheimer's disease.
Acta neuropathologica communications, 2013 Jul 06, 1 31

Kastrup M, Powollik R, Balzer F, Röber S, Ahlborn R, von Dossow-Hanfstingl V, Wernecke KD & Spies CD
Predictive ability of the stability and workload index for transfer score to predict unplanned readmissions after ICU discharge.
Critical care medicine, 2013 Jul, 41 (7) 1608-15

Respondek G, Roeber S, Kretzschmar H, Troakes C, Al-Sarraj S, Gelpi E, Gaig C, Chiu WZ, van Swieten JC, Oertel WH & Höglinger GU
Accuracy of the National Institute for Neurological Disorders and Stroke/Society for Progressive Supranuclear Palsy and neuroprotection and natural history in Parkinson plus syndromes criteria for the diagnosis of progressive supranuclear palsy.
Movement disorders : official journal of the Movement Disorder Society, 2013 Apr, 28 (4) 504-9

Birnbaum T, Langer S, Roeber S, von Baumgarten L & Straube A
Expression of B-cell activating factor, a proliferating inducing ligand and its receptors in primary central nervous system lymphoma.
Neurology international, 2013 Feb 11, 5 (1) e4

2012

Sundal C, Van Gerpen JA, Nicholson AM, Wider C, Shuster EA, Aasly J, Spina S, Ghetti B, Roeber S, Garbern J, Borjesson-Hanson A, Tselis A, Swerdlow RH, Miller BB, Fujioka S, Heckman MG, Uitti RJ, Josephs KA, Baker M, Andersen O, Rademakers R, Dickson DW, Broderick D & Wszolek ZK
MRI characteristics and scoring in HDLS due to CSF1R gene mutations.
Neurology, 2012 Aug 07, 79 (6) 566-74

Martins-de-Souza D, Guest PC, Mann DM, Roeber S, Rahmoune H, Bauder C, Kretzschmar H, Volk B, Baborie A & Bahn S
Proteomic analysis identifies dysfunction in cellular transport, energy, and protein metabolism in different brain regions of atypical frontotemporal lobar degeneration.
Journal of proteome research, 2012 Apr 06, 11 (4) 2533-43

Sundal C, Lash J, Aasly J, Øygarden S, Roeber S, Kretzschman H, Garbern JY, Tselis A, Rademakers R, Dickson DW, Broderick D & Wszolek ZK
Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): a misdiagnosed disease entity.
Journal of the neurological sciences, 2012 Mar 15, 314 (1-2) 130-7

Martins-de-Souza D, Guest PC, Guest FL, Bauder C, Rahmoune H, Pietsch S, Roeber S, Kretzschmar H, Mann D, Baborie A & Bahn S
Characterization of the human primary visual cortex and cerebellum proteomes using shotgun mass spectrometry-data-independent analyses.
Proteomics, 2012 Feb, 12 (3) 500-4

Schmidt C, Haïk S, Satoh K, Rábano A, Martinez-Martin P, Roeber S, Brandel JP, Calero-Lara M, de Pedro-Cuesta J, Laplanche JL, Hauw JJ, Kretzschmar H & Zerr I
Rapidly progressive Alzheimer's disease: a multicenter update.
Journal of Alzheimer's disease : JAD, 2012, 30 (4) 751-6

2011

Rademakers R, Baker M, Nicholson AM, Rutherford NJ, Finch N, Soto-Ortolaza A, Lash J, Wider C, Wojtas A, DeJesus-Hernandez M, Adamson J, Kouri N, Sundal C, Shuster EA, Aasly J, MacKenzie J, Roeber S, Kretzschmar HA, Boeve BF, Knopman DS, Petersen RC, Cairns NJ, Ghetti B, Spina S, Garbern J, Tselis AC, Uitti R, Das P, Van Gerpen JA, Meschia JF, Levy S, Broderick DF, Graff-Radford N, Ross OA, Miller BB, Swerdlow RH, Dickson DW & Wszolek ZK
Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids.
Nature genetics, 2011 Dec 25, 44 (2) 200-5

de Boni L, Tierling S, Roeber S, Walter J, Giese A & Kretzschmar HA
Next-generation sequencing reveals regional differences of the α-synuclein methylation state independent of Lewy body disease.
Neuromolecular medicine, 2011 Dec, 13 (4) 310-20

Eigenbrod S, Roeber S, Thon N, Giese A, Krieger A, Grasbon-Frodl E, Egensperger R, Tonn JC, Kreth FW & Kretzschmar HA
α-Internexin in the diagnosis of oligodendroglial tumors and association with 1p/19q status.
Journal of neuropathology and experimental neurology, 2011 Nov, 70 (11) 970-8

Hartig MB, Iuso A, Haack T, Kmiec T, Jurkiewicz E, Heim K, Roeber S, Tarabin V, Dusi S, Krajewska-Walasek M, Jozwiak S, Hempel M, Winkelmann J, Elstner M, Oexle K, Klopstock T, Mueller-Felber W, Gasser T, Trenkwalder C, Tiranti V, Kretzschmar H, Schmitz G, Strom TM, Meitinger T & Prokisch H
Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation.
American journal of human genetics, 2011 Oct 07, 89 (4) 543-50

Neumann M, Bentmann E, Dormann D, Jawaid A, DeJesus-Hernandez M, Ansorge O, Roeber S, Kretzschmar HA, Munoz DG, Kusaka H, Yokota O, Ang LC, Bilbao J, Rademakers R, Haass C & Mackenzie IR
FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations.
Brain : a journal of neurology, 2011 Sep, 134 (Pt 9) 2595-609

Kummer MP, Hermes M, Delekarte A, Hammerschmidt T, Kumar S, Terwel D, Walter J, Pape HC, König S, Roeber S, Jessen F, Klockgether T, Korte M & Heneka MT
Nitration of tyrosine 10 critically enhances amyloid β aggregation and plaque formation.
Neuron, 2011 Sep 08, 71 (5) 833-44

Roeber , Höglinger GU, Melhem NM, Dickson DW, Sleiman PM, Wang LS, Klei L, Rademakers R, de Silva R, Litvan I, Riley DE, van Swieten JC, Heutink P, Wszolek ZK, Uitti RJ, Vandrovcova J, Hurtig HI, Gross RG, Maetzler W, Goldwurm S, Tolosa E, Borroni B, Pastor P, PSP Genetics Study Group, Cantwell LB, Han MR, Dillman A, van der Brug MP, Gibbs JR, Cookson MR, Hernandez DG, Singleton AB, Farrer MJ, Yu CE, Golbe LI, Revesz T, Hardy J, Lees AJ, Devlin B, Hakonarson H, Müller U & Schellenberg GD
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
Nature genetics, 2011 Jun 19, 43 (7) 699-705

Mollenhauer B, Esselmann H, Roeber S, Schulz-Schaeffer WJ, Trenkwalder C, Bibl M, Steinacker P, Kretzschmar HA, Wiltfang J & Otto M
Different CSF β-amyloid processing in Alzheimer's and Creutzfeldt-Jakob disease.
Journal of neural transmission (Vienna, Austria : 1996), 2011 May, 118 (5) 691-7

Mackenzie IR, Munoz DG, Kusaka H, Yokota O, Ishihara K, Roeber S, Kretzschmar HA, Cairns NJ & Neumann M
Distinct pathological subtypes of FTLD-FUS.
Acta neuropathologica, 2011 Feb, 121 (2) 207-18

2010

Sostak P, Padovan CS, Eigenbrod S, Roeber S, Segerer S, Schankin C, Siegert S, Saam T, Theil D, Kolb HJ, Kretzschmar H & Straube A
Cerebral angiitis in four patients with chronic GVHD.
Bone marrow transplantation, 2010 Jul, 45 (7) 1181-8

Schmidt C, Redyk K, Meissner B, Krack L, von Ahsen N, Roeber S, Kretzschmar H & Zerr I
Clinical features of rapidly progressive Alzheimer's disease.
Dementia and geriatric cognitive disorders, 2010, 29 (4) 371-8

2009

Neumann M, Roeber S, Kretzschmar HA, Rademakers R, Baker M & Mackenzie IR
Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease.
Acta neuropathologica, 2009 Nov, 118 (5) 605-16

Neumann M, Rademakers R, Roeber S, Baker M, Kretzschmar HA & Mackenzie IR
A new subtype of frontotemporal lobar degeneration with FUS pathology.
Brain : a journal of neurology, 2009 Nov, 132 (Pt 11) 2922-31

2008

Roeber S, Mackenzie IR, Kretzschmar HA & Neumann M
TDP-43-negative FTLD-U is a significant new clinico-pathological subtype of FTLD.
Acta neuropathologica, 2008 Aug, 116 (2) 147-57

Roeber S, Grasbon-Frodl EM, Windl O, Krebs B, Xiang W, Vollmert C, Illig T, Schröter A, Arzberger T, Weber P, Zerr I & Kretzschmar HA
Evidence for a pathogenic role of different mutations at codon 188 of PRNP.
PloS one, 2008 May 14, 3 (5) e2147

2007

Sostak P, Theil D, Stepp H, Roeber S, Kretzschmar HA & Straube A
Detection of bone marrow-derived cells expressing a neural phenotype in the human brain.
Journal of neuropathology and experimental neurology, 2007 Feb, 66 (2) 110-6

2006

Krasnianski A, Schulz-Schaeffer WJ, Kallenberg K, Meissner B, Collie DA, Roeber S, Bartl M, Heinemann U, Varges D, Kretzschmar HA & Zerr I
Clinical findings and diagnostic tests in the MV2 subtype of sporadic CJD.
Brain : a journal of neurology, 2006 Sep, 129 (Pt 9) 2288-96

Roeber S, Bäzner H, Hennerici M, Porstmann R & Kretzschmar HA
Neurodegeneration with features of NIFID and ALS--extended clinical and neuropathological spectrum.
Brain pathology (Zurich, Switzerland), 2006 Jul, 16 (3) 228-34

2005

Koch HJ, Roeber S, Zimmermann UW, Schäfer C, Villarrubia V, Kuchelmeister K, Schachenmayr W, Bogdahn U & Steinbrecher A
[Spinal and cerebral leptomeningeal seeding from a melanocytoma of the cerebello-pontine angle].
Wiener medizinische Wochenschrift (1946), 2005 Aug, 155 (15-16) 360-4

Roeber S, Krebs B, Neumann M, Windl O, Zerr I, Grasbon-Frodl EM & Kretzschmar HA
Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragment.
Acta neuropathologica, 2005 Apr, 109 (4) 443-8