Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Ernst Hund"'
Publikováno v:
Neurological Research and Practice, Vol 3, Iss 1, Pp 1-11 (2021)
Abstract Hereditary transthyretin (TTR) amyloidosis (ATTRv) is an autosomal dominant, systemic disease transmitted by amyloidogenic mutations in the TTR gene. To prevent the otherwise fatal disease course, TTR stabilizers and mRNA silencing antisense
Externí odkaz:
https://doaj.org/article/9fb44f289ffd423bb7e7aa14a4bebefc
Autor:
Jennifer Kollmer, Ute Hegenbart, Christoph Kimmich, Ernst Hund, Jan C. Purrucker, John M. Hayes, Stephen I. Lentz, Georges Sam, Johann M. E. Jende, Stefan O. Schönland, Martin Bendszus, Sabine Heiland, Markus Weiler
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 7, Iss 5, Pp 799-807 (2020)
Abstract Objective To quantify peripheral nerve lesions in symptomatic and asymptomatic hereditary transthyretin amyloidosis with polyneuropathy (ATTRv‐PNP) by analyzing the magnetization transfer ratio (MTR) of the sciatic nerve, and to test its p
Externí odkaz:
https://doaj.org/article/9e22a57b5bc84ab196b434c089e25a39
Autor:
Ute Hegenbart, Tilmann Bochtler, Axel Benner, Natalia Becker, Christoph Kimmich, Arnt V. Kristen, Jörg Beimler, Ernst Hund, Markus Zorn, Anja Freiberger, Marianne Gawlik, Hartmut Goldschmidt, Dirk Hose, Anna Jauch, Anthony D. Ho, Stefan O. Schönland
Publikováno v:
Haematologica, Vol 102, Iss 8 (2017)
Chemotherapy in light chain amyloidosis aims to normalize the involved free light chain in serum, which leads to an improvement, or at least stabilization of organ function in most responding patients. We performed a prospective single center phase 2
Externí odkaz:
https://doaj.org/article/db58a56d0ef04bf3bbffeebdde94ab6e
Autor:
F. Escolano-Lozano, Ernst Hund, C. Sommer, Wilhelm Schulte-Mattler, Jens Schmidt, C. Geber, M. Auer-Grumbach, Ralf Baron, M. Schilling, J. Sachau, Markus Weiler, H. C. Lehmann, Maike F. Dohrn, N. Grether, F. Birklein, Katrin Hahn, T. Hagenacker
Publikováno v:
DGNeurologie. 3:369-383
Autor:
Sabine Heiland, Johann M E Jende, Martin Bendszus, Ernst Hund, John M. Hayes, Markus Weiler, Christoph Kimmich, Georges Sam, Jan C. Purrucker, Jennifer Kollmer, Stephen I. Lentz, Ute Hegenbart, Stefan Schönland
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 7, Iss 5, Pp 799-807 (2020)
Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology
Objective To quantify peripheral nerve lesions in symptomatic and asymptomatic hereditary transthyretin amyloidosis with polyneuropathy (ATTRv‐PNP) by analyzing the magnetization transfer ratio (MTR) of the sciatic nerve, and to test its potential
Publikováno v:
Neurological Research and Practice, Vol 3, Iss 1, Pp 1-11 (2021)
Neurological Research and Practice
Neurological research and practice 3, 57 (2021). doi:10.1186/s42466-021-00155-8
Neurological Research and Practice
Neurological research and practice 3, 57 (2021). doi:10.1186/s42466-021-00155-8
Neurological research and practice 3, 57 (2021). doi:10.1186/s42466-021-00155-8
Published by BioMed Central, [London]
Published by BioMed Central, [London]
Publikováno v:
Neuroinfektiologie ISBN: 9783662616680
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed15b0a451582a756106967760b66880
https://doi.org/10.1007/978-3-662-61669-7_14
https://doi.org/10.1007/978-3-662-61669-7_14
Autor:
Christian Geber, Claudia Sommer, Katrin Hahn, Juliane Sachau, Markus Weiler, Ernst Hund, Gilbert Wunderlich, Wilhelm J. Schulte-Mattler, Jens Schmidt, Tim Hagenacker, Michaela Auer-Grumbach, Ralf Baron, Matthias Schilling, Maike F. Dohrn, Nicolai B Grether, Fabiola Escolano-Lozano, Frank Birklein
Publikováno v:
Journal of Neurology
Journal of neurology 268(10), 3610-3625 (2021). doi:10.1007/s00415-020-09962-6
Journal of neurology 268(10), 3610-3625 (2021). doi:10.1007/s00415-020-09962-6
Journal of neurology 268(10), 3610-3625 (2021). doi:10.1007/s00415-020-09962-6
Published by Steinkopff, [Darmstadt]
Published by Steinkopff, [Darmstadt]
Autor:
Christoph Kimmich, Laura Huber, Fabian aus dem Siepen, Selina Hein, Stefan Schönland, Matthias N. Ungerer, Jan C. Purrucker, Katrin Hinderhofer, Ute Hegenbart, Ernst Hund, Jennifer Kollmer, Markus Weiler, Arnt V. Kristen
Hereditary transthyretin amyloidosis is caused by pathogenic variants in the TTR gene and typically manifests, alongside cardiac and other organ dysfunctions, with a rapidly progressive sensorimotor and autonomic polyneuropathy (ATTRv-PN) leading to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ece3f24016fede160a36737d2ce34237
Autor:
Christian Geber, Arnt V. Kristen, Frank Birklein, Christoph Röcken, Wilhelm Schulte-Mattler, Claudia Sommer, Michaela Auer-Grumbach, Hartmut Schmidt, Ernst Hund
Publikováno v:
Aktuelle Neurologie. 45:605-616
ZusammenfassungDie Transthyretin-Amyloidose (ATTR-Amyloidose) ist eine seltene, rasch verlaufende neurodegenerative Erkrankung, verursacht durch Mutationen im Transthyretin-Gen. Aufgrund der Seltenheit ist sie wenig bekannt mit der Folge, dass die Di