Publikationen 2017

Publikationsliste 2017

Huse JT, Snuderl M, Jones DT, Brathwaite CD, Altman N, Lavi E, Saffery R, Sexton-Oates A, Blumcke I, Capper D, Karajannis MA, Benayed R, Chavez L, Thomas C, Serrano J, Borsu L, Ladanyi M, Rosenblum MK: (2017) Polymorphous low-grade neuroepithelial tumor of the young (PLNTY): an epileptogenic neoplasm with oligodendroglioma-like components, aberrant CD34 expression, and genetic alterations involving the MAP kinase pathway. Acta Neuropathol (Berl). 2017;133(3): 417-429
Unger A, Beckendorf L, Böhme P, Kley R, von Frieling-Salewsky M, Lochmüller H, Schröder R, Fürst DO, Vorgerd M, Linke WA: (2017) Translocation of molecular chaperones to the titin springs is common in skeletal myopathy patients and affects sarcomere function. Acta Neuropathol Commun. 2017;5(1): 72
Kiese K, Jablonski J, Hackenbracht J, Wrosch JK, Groemer TW, Kornhuber J, Blümcke I, Kobow K: (2017) Epigenetic control of epilepsy target genes contributes to a cellular memory of epileptogenesis in cultured rat hippocampal neurons. Acta Neuropathol Commun. 2017;5(1): 79
Schurr J, Coras R, Rössler K, Pieper T, Kudernatsch M, Holthausen H, Winkler P, Woermann F, Bien CG, Polster T, Schulz R, Kalbhenn T, Urbach H, Becker A, Grunwald T, Huppertz HJ, Gil-Nagel A, Toledano R, Feucht M, Mühlebner A, Czech T, Blümcke I: (2017) Mild Malformation of Cortical Development with Oligodendroglial Hyperplasia in Frontal Lobe Epilepsy: A New Clinico-Pathological Entity. Brain Pathol. 2017;27(1): 26-35
Hölsken A, Buslei R: (2017) Models of human adamantinomatous craniopharyngioma tissue: Steps toward an effective adjuvant treatment. Brain Pathol. 2017;27(3): 358-363
Bernreuther C, Illies C, Flitsch J, Buchfelder M, Buslei R, Glatzel M, Saeger W: (2017) IgG4-related hypophysitis is highly prevalent among cases of histologically confirmed hypophysitis. Brain Pathol. 2017;27(6): 839-845
D'Gama AM, Woodworth MB, Hossain AA, Bizzotto S, Hatem NE, LaCoursiere CM, Najm I, Ying Z, Yang E, Barkovich AJ, Kwiatkowski DJ, Vinters HV, Madsen JR, Mathern GW, Blümcke I, Poduri A, Walsh CA: (2017) Somatic Mutations Activating the mTOR Pathway in Dorsal Telencephalic Progenitors Cause a Continuum of Cortical Dysplasias. Cell Rep. 2017;21(13): 3754-3766
Sharma S, Conover GM, Elliott JL, Der Perng M, Herrmann H, Quinlan RA: (2017) ?B-crystallin is a sensor for assembly intermediates and for the subunit topology of desmin intermediate filaments. Cell Stress Chaperones. 2017;22(4): 613-626
Mende KC, Matschke J, Burkhardt T, Saeger W, Buslei R, Buchfelder M, Fahlbusch R, Westphal M, Flitsch J: (2017) Pituicytoma-An outlook on possible targeted therapies. CNS Neurosci Ther. 2017;23(7): 620-626
Kreitschmann-Andermahr I, Buchfelder M, Kleist B, Kohlmann J, Menzel C, Buslei R, Ko?towska-Häggsträm M, Strasburger C, Siegel S: (2017) PREDICTORS OF QUALITY OF LIFE IN 165 PATIENTS WITH ACROMEGALY: RESULTS FROM A SINGLE-CENTER STUDY. Endocr Pract. 2017;23(1): 79-88
Siegel S, Weber Carneiro R, Buchfelder M, Kleist B, Grzywotz A, Buslei R, Bingel U, Brabant G, Schenk T, Kreitschmann-Andermahr I: (2017) Presence of headache and headache types in patients with tumors of the sellar region-can surgery solve the problem? Results of a prospective single center study. Endocrine. 2017;56(2): 325-335
Li J, Blumcke I: (2017) International summer school for neuropathology and epilepsy surgery in Chengdu, China, August 29-September 1, 2016. Epilepsia. 2017;58(1): 172-174
Uckermann O, Galli R, Leupold S, Coras R, Meinhardt M, Hallmeyer-Elgner S, Mayer T, Storch A, Schackert G, Koch E, Blümcke I, Steiner G, Kirsch M: (2017) Label-free multiphoton microscopy reveals altered tissue architecture in hippocampal sclerosis. Epilepsia. 2017;58(1): e1-e5
Wang DD, Piao YS, Blumcke I, Coras R, Zhou WJ, Gui QP, Liu CC, Hu JX, Cao LZ, Zhang GJ, Lu DH: (2017) A distinct clinicopathological variant of focal cortical dysplasia IIId characterized by loss of layer 4 in the occipital lobe in 12 children with remote hypoxic-ischemic injury. Epilepsia. 2017;58(10): 1697-1705
Jozwiak S, Becker A, Cepeda C, Engel J, Gnatkovsky V, Huberfeld G, Kaya M, Kobow K, Simonato M, Loeb JA: (2017) WONOEP appraisal: Development of epilepsy biomarkers-What we can learn from our patients? Epilepsia. 2017;58(6): 951-961
Roessler K, Kasper B, Coras R, Sommer B, Blumcke I, Hamer H, Buchfelder M: (2017) MODIFIED SUBPIAL Epilepsia. 2017;58 5: S171-S171
Neupert LM, May P, Kobow K, Nothnagel M, Nurnberg P, Freiman T, Harter P, Klein KM, Weber Y, Blumcke I, Lal D: (2017) DISCOVERY AND PATHOGENICITY ASSESSMENT OF NEUROPATHOLOGY-ASSOCIATED GENE VARIANTS Epilepsia. 2017;58 5: S174-S174
Huang C, Zhang H, Chi XS, Chen N, Zhou Q, Blumcke I, Zhou D, Li JM: (2017) THE PRACTICE OF REVISED CLASSIFICATION OF FOCAL CORTICAL DYSPLASIA ON DRUG-RESISTANT EPILEPSY IN WEST CHINA: AN URGENT DIAGNOSTIC GAP FOR FILLING Epilepsia. 2017;58 5: S198-S198
Roessler K, Kasper B, Heynold E, Coras R, Rampp S, Sommer B, Hamer H, Blumcke I, Buchfelder M: (2017) FOCAL CORTICAL DYSPLASIA TYPE II IS MEG, MULTIMODAL NEURONAVIGATION AND INTRAOPERATIVE MR IMAGING HELPFUL FOR SURGERY? Epilepsia. 2017;58 5: S29-S29
Argente-Escrig H, Gomez NM, Gomez L, Turk M, Thiel CT, Schroder R, Vilchez JJ: (2017) Ephedrine and 3,4 diaminopyridine responsive myasthenic syndrome in plectin-related epidermolysis bullosa simplex with muscular dystrophy Eur J Neurol. 2017;24 1: 205-205
Thümecke S, Beermann A, Klingler M, Schröder R: (2017) The flipflop orphan genes are required for limb bud eversion in the Tribolium embryo. Front Zool. 2017;14: 48
Foit NA, van Velthoven V, Schulz R, Blümcke I, Urbach H, Woermann FG, Bien CG: (2017) Lesional cerebellar epilepsy: a review of the evidence. J Neurol. 2017;264(1): 1-10
Wang ZI, McBride A, Grinenko O, Blümcke I, Overmyer M, Bingaman W, Alexopoulos AV, Najm IM, Jones SE: (2017) Utility of CISS sequence in detecting anteroinferior temporal encephalocele. J Neurol Sci. 2017;381: 59-61
Blumcke I, Spreafico R, Haaker G, Coras R, Kobow K, Bien CG, Pfäfflin M, Elger C, Widman G, Schramm J, Becker A, Braun KP, Leijten F, Baayen JC, Aronica E, Chassoux F, Hamer H, Stefan H, Rössler K, Thom M, Walker MC, Sisodiya SM, Duncan JS, McEvoy AW, Pieper T, Holthausen H, Kudernatsch M, Meencke HJ, Kahane P, Schulze-Bonhage A, Zentner J, Heiland DH, Urbach H, Steinhoff BJ, Bast T, Tassi L, Lo Russo G, Özkara C, Oz B, Krsek P, Vogelgesang S, Runge U, Lerche H, Weber Y, Honavar M, Pimentel J, Arzimanoglou A, Ulate-Campos A, Noachtar S, Hartl E, Schijns O, Guerrini R, Barba C, Jacques TS, Cross JH, Feucht M, Mühlebner A, Grunwald T, Trinka E, Winkler PA, Gil-Nagel A, Toledano Delgado R, Mayer T, Lutz M, Zountsas B, Garganis K, Rosenow F, Hermsen A, von Oertzen TJ, Diepgen TL, Avanzini G, EEBB Consortium , Aparicio J, Bento C, Beckervordersandforth J, Buccoliero A, Cabral P, Chamadoira C, Colon A, Chabardès S, Carpenter S, Czech T, Dressler A, Deleo F, Dílio A, Dings J, Devaux B, De Tisi J, De Bellescize J, Ebner A, Franke K, Groeppel G, Giordano F, Gozzo F, Garbelli R, Guenot M, García-Morales I, Gómez-Angulo JC, Garcia G, Hainfellner JA, Höfler J, Hoogland G, Hendriks M, Hofman P, Harding B, Huppertz H, Herms J, Hilkman DMW, Hamelin S, Idema S, Jansen FE, Jahodova A, Keeley A, Kalss G, Kudr M, Kroell J, Kokkinos V, Keo Kosal P, Kalbhenn T, Leitinger M, Landré E, Melo Pires M, Matas A, Mann MW, Ostrowsky-Coste K, Prinz M, Puttinger G, Peraud A, Rangel Pinho R, Romero C, Rego R, Rouhl R, Ryvlin P, Rumia J, Rampp S, Scholl T, Schulz R, Stone TJ, Streichenberger N, Tisdall M, Turak B, Taipa R, Uzan M, Van Kranen-Mastenbroek V, Varlet P, Vlooswijk M, Wagner L, Weis S: (2017) Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery. N Engl J Med. 2017;377(17): 1648-1656
Türk M, Schröder R, Khuller K, Hofmann A, Berwanger C, Ludolph AC, Dekomien G, Müller K, Weishaupt JH, Thiel CT, Clemen CS: (2017) Genetic analysis of VCP and WASH complex genes in a German cohort of sporadic ALS-FTD patients. Neurobiol Aging. 2017;56: 213.e1-213.e5
Diermeier S, Buttgereit A, Schürmann S, Winter L, Xu H, Murphy RM, Clemen CS, Schröder R, Friedrich O: (2017) Preaged remodeling of myofibrillar cytoarchitecture in skeletal muscle expressing R349P mutant desmin. Neurobiol Aging. 2017;58: 77-87
Steve TA, Yasuda CL, Coras R, Lail M, Blumcke I, Livy DJ, Malykhin N, Gross DW: (2017) Development of a histologically validated segmentation protocol for the hippocampal body. Neuroimage. 2017;157: 219-232
Regensburger M, Türk M, Pagenstecher A, Schröder R, Winkler J: (2017) VCP-related multisystem proteinopathy presenting as early-onset Parkinson disease. Neurology. 2017;89(7): 746-748
Bongaarts A, Giannikou K, Reinten RJ, Anink JJ, Mills JD, Jansen FE, Spliet GMW, den Dunnen WFA, Coras R, Blümcke I, Paulus W, Scholl T, Feucht M, Kotulska K, Jozwiak S, Buccoliero AM, Caporalini C, Giordano F, Genitori L, Söylemezo?lu F, Pimentel J, Nellist M, Schouten-van Meeteren AYN, Nag A, Mühlebner A, Kwiatkowski DJ, Aronica E: (2017) Subependymal giant cell astrocytomas in Tuberous Sclerosis Complex have consistent TSC1/TSC2 biallelic inactivation, and no BRAF mutations. Oncotarget. 2017;8(56): 95516-95529
Hagel C, Buslei R, Buchfelder M, Fahlbusch R, Bergmann M, Giese A, Flitsch J, Lüdecke DK, Glatzel M, Saeger W: (2017) Immunoprofiling of glial tumours of the neurohypophysis suggests a common pituicytic origin of neoplastic cells. Pituitary. 2017;20(2): 211-217
Premchandar A, Kupniewska A, Bonna A, Faure G, Fraczyk T, Roldan A, Hoffmann B, Faria da Cunha M, Herrmann H, Lukacs GL, Edelman A, Dadlez M: (2017) New insights into interactions between the nucleotide-binding domain of CFTR and keratin 8. Protein Sci. 2017;26(2): 343-354
Diermeier S, Iberl J, Vetter K, Haug M, Pollmann C, Reischl B, Buttgereit A, Schürmann S, Spörrer M, Goldmann WH, Fabry B, Elhamine F, Stehle R, Pfitzer G, Winter L, Clemen CS, Herrmann H, Schröder R, Friedrich O: (2017) Early signs of architectural and biomechanical failure in isolated myofibers and immortalized myoblasts from desmin-mutant knock-in mice. Sci Rep. 2017;7(1): 1391
Thimsen V, John N, Buchfelder M, Flitsch J, Fahlbusch R, Stefanits H, Knosp E, Losa M, Buslei R, Hölsken A: (2017) Expression of SRY-related HMG Box Transcription Factors (Sox) 2 and 9 in Craniopharyngioma Subtypes and Surrounding Brain Tissue. Sci Rep. 2017;7(1): 15856
Huang C, Zhang H, Chi XS, Chen N, Gong J, Zhou Q, Blümcke I, Zhou D, Li JM: (2017) Putting the new ILAE classification of focal cortical dysplasia into practice in western China. Seizure. 2017;51: 133-138

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