Zentrum für Neuropathologie und Prionforschung
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Dr. med. Sigrun Roeber

[2019] [2018] [2017] [2015] [2014] [2013] [2012] [2011] [2010] [2009] [2008] [2007] [2006] [2005]

2019

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 Mar 18

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

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 Feb 09

2018

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

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

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

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 NC, 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 JP, 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 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

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

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