Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Matthias, Lindenau"'
Autor:
Olivia Foesleitner, Karl Christian Knop, Matthias Lindenau, Fabian Preisner, Philipp Bäumer, Sabine Heiland, Martin Bendszus, Moritz Kronlage
Publikováno v:
Diagnostics, Vol 13, Iss 7, p 1237 (2023)
Background: The aim of this study was to assess the phenotype of multifocal motor neuropathy (MMN) and amyotrophic lateral sclerosis (ALS) in quantitative MR neurography. Methods: In this prospective study, 22 patients with ALS, 8 patients with MMN,
Externí odkaz:
https://doaj.org/article/617c3b496e20440697047de88c2230e7
Autor:
Ralph Buchert, Tobias Martens, Matthias Lindenau, Susanne Klutmann, Jila Taherpour, Ivayla Apostolova, Berthold Voges, Stefan Stodieck, Mariam Jaber, Patrick M. House, Michael Lanz, Thomas Sauvigny
Publikováno v:
Clinical nuclear medicine. 46(11)
PURPOSE Ictal brain perfusion SPECT with the tracer 99mTc-HMPAO or 99mTc-ECD is widely used for identification of the epileptic seizure onset zone (SOZ) in presurgical evaluation if standard pointers are uncertain or inconsistent. For both tracers, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dd0a1bbfc074205cc53f0bc6c6d7e77
https://pubmed.ncbi.nlm.nih.gov/34238801
https://pubmed.ncbi.nlm.nih.gov/34238801
Autor:
Matthias Lindenau, Berthold Voges, Ivayla Apostolova, Marian Jaber, Jila Taherpour, Thomas Sauvigny, Susanne Klutmann, Ralph Buchert, Michael Lanz, Stefan Stodieck, Tobias Martens, Patrick M. House
Publikováno v:
Journal of nuclear medicine : official publication, Society of Nuclear Medicine. 63(6)
Previous studies on the utility of specific perfusion patterns in ictal brain perfusion SPECT for predicting the outcome of temporal lobe epilepsy surgery used qualitative visual pattern classification, semi-quantitative region-of-interest analysis o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b87e8dbd8a9e145ddd2f8d6755ad1ed3
https://pubmed.ncbi.nlm.nih.gov/34593599
https://pubmed.ncbi.nlm.nih.gov/34593599
Autor:
Mariam Jaber, Jila Taherpour, Berthold Voges, Ralph Buchert, Thomas Sauvigny, Michael Lanz, Stefan Stodieck, Tobias Martens, Matthias Lindenau, Ivayla Apostolova, Patrick M. House, Susanne Klutmann
Background: The chemical microspheres 99mTc-HMPAO and 99mTc-ECD are widely used as tracers in ictal brain perfusion SPECT for identification of the seizure onset zone (SOZ) in presurgical evaluation of patients with drug-resistant epilepsy and uncert
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10415b6475bf548cb36957ee34eb57e7
https://doi.org/10.21203/rs.3.rs-104415/v1
https://doi.org/10.21203/rs.3.rs-104415/v1
Autor:
Frederick Andermann, Zaid Afawi, Krystyna Spodar, Laura Licchetta, Francesca Bisulli, Rachel Straussberg, Laura Canafoglia, Snezana Maljevic, Bernt A. Engelsen, Silvana Franceschetti, Simone Mandelstam, Samuel F. Berkovic, Rikke S. Møller, Annette Wulf, Eva Andermann, João Massano, Francesca Ragona, Elena Gardella, Carlo Di Bonaventura, Steven Petrou, Patrizia Riguzzi, Guido Rubboli, Carol J. Milligan, Anna-Elina Lehesjoki, Karen Oliver, Ferruccio Panzica, Elena Pasini, Amos D. Korczyn, Mikko Muona, Roberto Michelucci, Daniel Friedman, Anna M. Boguszewska-Chachulska, Holger Lerche, Matthias Lindenau, Felix Benninger, Christopher A. Reid, Bruria Ben-Zeev, Paolo Tinuper, Arielle Crespel, Anetta Lasek-Bal
Publikováno v:
Oliver, K L, Franceschetti, S, Milligan, C J, Muona, M, Mandelstam, S A, Canafoglia, L, Boguszewska-Chachulska, A M, Korczyn, A D, Bisulli, F, Di Bonaventura, C, Ragona, F, Michelucci, R, Ben-Zeev, B, Straussberg, R, Panzica, F, Massano, J, Friedman, D, Crespel, A, Engelsen, B A, Andermann, F, Andermann, E, Spodar, K, Lasek-Bal, A, Riguzzi, P, Pasini, E, Tinuper, P, Licchetta, L, Gardella, E, Lindenau, M, Wulf, A, Møller, R S, Benninger, F, Afawi, Z, Rubboli, G, Reid, C A, Maljevic, S, Lerche, H, Lehesjoki, A-E, Petrou, S & Berkovic, S F 2017, ' Myoclonus epilepsy and ataxia due to KCNC1 mutation : Analysis of 20 cases and K(+) channel properties ', Annals of Neurology, vol. 81, no. 5, pp. 677-689 . https://doi.org/10.1002/ana.24929
OBJECTIVE: To comprehensively describe the new syndrome of myoclonus epilepsy and ataxia due to potassium channel mutation (MEAK), including cellular electrophysiological characterization of observed clinical improvement with fever.METHODS: We analyz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e24095de7d217867a83d748eead4731
https://doi.org/10.1002/ana.24929
https://doi.org/10.1002/ana.24929
Autor:
Stefan Stodieck, Matthias Lindenau, Brigitte Holst, Patrick M. House, Bernhard Kohl, Hans-Jürgen Huppertz, Michael Lanz, Tobias Martens, Berthold Voges
Publikováno v:
Epilepsy Research. 117:29-34
Purpose Focal cortical dysplasias (FCD) type IIb and cortical tubers in tuberous sclerosis complex (TSC) are histopathologically similar and are both epileptogenic lesions frequently causing pharmacoresistant epilepsies. Morphometric analysis of T1-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e73fed38ca87e57321b23bc52efab620
https://doi.org/10.1016/j.eplepsyres.2015.08.002
https://doi.org/10.1016/j.eplepsyres.2015.08.002
Autor:
Karen L, Oliver, Silvana, Franceschetti, Carol J, Milligan, Mikko, Muona, Simone A, Mandelstam, Laura, Canafoglia, Anna M, Boguszewska-Chachulska, Amos D, Korczyn, Francesca, Bisulli, Carlo, Di Bonaventura, Francesca, Ragona, Roberto, Michelucci, Bruria, Ben-Zeev, Rachel, Straussberg, Ferruccio, Panzica, João, Massano, Daniel, Friedman, Arielle, Crespel, Bernt A, Engelsen, Frederick, Andermann, Eva, Andermann, Krystyna, Spodar, Anetta, Lasek-Bal, Patrizia, Riguzzi, Elena, Pasini, Paolo, Tinuper, Laura, Licchetta, Elena, Gardella, Matthias, Lindenau, Annette, Wulf, Rikke S, Møller, Felix, Benninger, Zaid, Afawi, Guido, Rubboli, Christopher A, Reid, Snezana, Maljevic, Holger, Lerche, Anna-Elina, Lehesjoki, Steven, Petrou, Samuel F, Berkovic
Publikováno v:
Annals of neurology. 81(5)
To comprehensively describe the new syndrome of myoclonus epilepsy and ataxia due to potassium channel mutation (MEAK), including cellular electrophysiological characterization of observed clinical improvement with fever.We analyzed clinical, electro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::37102853278507196f841f5281fe2c2e
https://pubmed.ncbi.nlm.nih.gov/28380698
https://pubmed.ncbi.nlm.nih.gov/28380698
Autor:
Steven Petrou, Aarno Palotie, Danielle M. Andrade, Marta A. Bayly, Laura Licchetta, Ingrid E. Scheffer, Rikke S. Møller, Frederick Andermann, Laura Canafoglia, Arielle Crespel, Silvana Franceschetti, Veronica Saletti, Michael Duchowny, Michael S. Hildebrand, Ebba Lohmann, Antonio Gambardella, Eva Andermann, Chiara Criscuolo, Salla Markkinen, Bernt A. Engelsen, Cigdem Ozkara, Meral Topçu, Adeel Ahmad, Edoardo Ferlazzo, Holger Lerche, João Massano, Edith Said, Mary D. King, Paolo Tinuper, Alessandro Filla, Mikko Muona, Samuel F. Berkovic, Betül Baykan, Alberto J. Espay, Karen Oliver, Matthias Lindenau, Michael Privitera, Zaid Afawi, Tarja Joensuu, Leanne M. Dibbens, Bruria Ben-Zeev, Snezana Maljevic, Patrizia Riguzzi, Kaitlin E. Samocha, Birgit Kauffmann, Mark J. Daly, Roberto Michelucci, Rachel Straussberg, Sarah E. Heron, Anna-Elina Lehesjoki, Jamil Ahmad
Publikováno v:
Nature genetics 47(1), 39-46 (2014). doi:10.1038/ng.3144
Muona, M, Berkovic, S F, Dibbens, L M, Oliver, K L, Maljevic, S, Bayly, M A, Joensuu, T, Canafoglia, L, Franceschetti, S, Michelucci, R, Markkinen, S, Heron, S E, Hildebrand, M S, Andermann, E, Andermann, F, Gambardella, A, Tinuper, P, Licchetta, L, Scheffer, I E, Criscuolo, C, Filla, A, Ferlazzo, E, Ahmad, J, Ahmad, A, Baykan, B, Said, E, Topcu, M, Riguzzi, P, King, M D, Ozkara, C, Andrade, D M, Engelsen, B A, Crespel, A, Lindenau, M, Lohmann, E, Saletti, V, Massano, J, Privitera, M, Espay, A J, Kauffmann, B, Duchowny, M, Moller, R S, Straussberg, R, Afawi, Z, Ben-Zeev, B, Samocha, K E, Daly, M J, Petrou, S, Lerche, H, Palotie, A & Lehesjoki, A E 2015, ' A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy ', Nature Genetics, vol. 47, no. 1, pp. 39-46 . https://doi.org/10.1038/ng.3144
Muona, M, Berkovic, S F, Dibbens, L M, Oliver, K L, Maljevic, S, Bayly, M A, Joensuu, T, Canafoglia, L, Franceschetti, S, Michelucci, R, Markkinen, S, Heron, S E, Hildebrand, M S, Andermann, E, Andermann, F, Gambardella, A, Tinuper, P, Licchetta, L, Scheffer, I E, Criscuolo, C, Filla, A, Ferlazzo, E, Ahmad, J, Ahmad, A, Baykan, B, Said, E, Topcu, M, Riguzzi, P, King, M D, Ozkara, C, Andrade, D M, Engelsen, B A, Crespel, A, Lindenau, M, Lohmann, E, Saletti, V, Massano, J, Privitera, M, Espay, A J, Kauffmann, B, Duchowny, M, Moller, R S, Straussberg, R, Afawi, Z, Ben-Zeev, B, Samocha, K E, Daly, M J, Petrou, S, Lerche, H, Palotie, A & Lehesjoki, A E 2015, ' A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy ', Nature Genetics, vol. 47, no. 1, pp. 39-46 . https://doi.org/10.1038/ng.3144
Progressive myoclonus epilepsies (PMEs) are a group of rare, inherited disorders manifesting with action myoclonus, tonic-clonic seizures and ataxia. We sequenced the exomes of 84 unrelated individuals with PME of unknown cause and molecularly solved
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa4050a358a032c2d80f76710ccd788f
https://hdl.handle.net/11541.2/111719
https://hdl.handle.net/11541.2/111719
Autor:
Thomas Bengner, Einar Goebell, Stefan Stodieck, B. Voges, Matthias Lindenau, C. Fortmeier, Thomas Malina
Publikováno v:
Epilepsy & Behavior. 9:593-600
The influence of sex on face recognition memory was studied in 49 patients with temporal lobe epilepsy, 20 patients with generalized epilepsy, and 32 healthy controls. After learning 20 faces, serially presented for 5 seconds each, subjects had to re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21dbe380ed27fce4e3c10c722d35f985
https://doi.org/10.1016/j.yebeh.2006.08.021
https://doi.org/10.1016/j.yebeh.2006.08.021
Autor:
Matthias Lindenau, Johanna Schröder, Ulf Köther, Eik Vettorazzi, Anja Fischer, Katja Brückner, Steffen Moritz
Publikováno v:
Epilepsia. 55(12)
OBJECTIVE: \ud \ud Depression is the most prevalent psychiatric disorder in persons with epilepsy (PWEs). Despite its major impact on quality of life and risk of suicide, most PWEs are not treated for depression. A current challenge in mental health
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9263e3e4c1aef7153250779bd15b665
https://pubmed.ncbi.nlm.nih.gov/25410633
https://pubmed.ncbi.nlm.nih.gov/25410633