Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Sima Canaan–Kühl"'
Autor:
Isabel Mattig, Tilman Steudel, Karin Klingel, Gina Barzen, David Frumkin, Sebastian Spethmann, Elena Romero Dorta, Karl Stangl, Bettina Heidecker, Ulf Landmesser, Fabian Knebel, Sima Canaan-Kühl, Katrin Hahn, Anna Brand
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract Echocardiographic differentiation of cardiac amyloidosis (CA) and Fabry disease (FD) is often challenging using standard echocardiographic parameters. We retrospectively analyzed the diagnostic accuracy of right heart and left atrial strain
Externí odkaz:
https://doaj.org/article/7dc75468acb04b7eaf31c2724c076ab3
Autor:
Dilara Kersebaum, Manon Sendel, Josephine Lassen, Sophie-Charlotte Fabig, Julia Forstenpointner, Maren Reimer, Sima Canaan-Kühl, Jens Gaedeke, Stefanie Rehm, Janne Gierthmühlen, Ralf Baron, Philipp Hüllemann
Publikováno v:
Frontiers in Pain Research, Vol 5 (2024)
BackgroundFabry disease (FD) causes cold-evoked pain and impaired cold perception through small fiber damage, which also occurs in polyneuropathies (PNP) of other origins. The integrity of thinly myelinated fibers and the spinothalamic tract is asses
Externí odkaz:
https://doaj.org/article/1a43342f2de14e36941f85032a5667f2
Autor:
Julia Forstenpointner, Manon Sendel, Paul Moeller, Maren Reimer, Sima Canaan-Kühl, Jens Gaedeke, Stefanie Rehm, Philipp Hüllemann, Janne Gierthmühlen, Ralf Baron
Publikováno v:
Frontiers in Neuroscience, Vol 14 (2020)
PurposeFabry disease frequently includes pain as an early disease feature, which was characterized as a dysfunctional processing of somatosensory information in various studies. The pathomechanism involves the mutation in the x-chromosomal GLA-gene a
Externí odkaz:
https://doaj.org/article/5f754615fe2545bf8a35c49301825552
Autor:
Tim Godel, Katharina von Cossel, Reinhard E. Friedrich, Markus Glatzel, Sima Canaan-Kühl, Thomas Duning, Moritz Kronlage, Sabine Heiland, Martin Bendszus, Nicole Muschol, Victor-Felix Mautner
Publikováno v:
Diagnostics, Vol 10, Iss 12, p 1027 (2020)
The purpose of this study is to examine alterations of the peripheral nervous system (PNS) in oligo-symptomatic patients carrying the Fabry related GLA-gene variant p.A143T by Magnetic Resonance Neurography (MRN) and skin biopsy. This prospective stu
Externí odkaz:
https://doaj.org/article/37ba789758d7418cbfe7ad32ca85c46e
Autor:
Maamoun Al Daas, Sima Canaan-Kühl, Karl Stangl, Fabian Knebel, Anna Brand, Isabel Mattig, David Frumkin, Nina Laule
Publikováno v:
Echocardiography. 38:1870-1878
Background ‘Classical’ echocardiographic signs of Fabry cardiomyopathy (FC), such as left ventricular hypertrophy (LVH), posterolateral strain deficiency (PLSD) and papillary muscle hypertrophy may have a limited diagnostic accuracy in clinical p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bccd450c898f1209631b429d3aad702f
https://doi.org/10.1111/echo.15224
https://doi.org/10.1111/echo.15224
Autor:
Fabian Knebel, Sima Canaan-Kühl, Christian Tillmanns, Isa bel Mattig, Tarek Bekfani, Norman Mangner, Rüdiger C. Braun-Dullaeus
Publikováno v:
Der Kardiologe. 15:299-314
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5bd430f8f07f79f4aab2a5ee9a5c648
https://doi.org/10.1007/s12181-021-00484-7
https://doi.org/10.1007/s12181-021-00484-7
Autor:
Malte Lenders, Christian Pogoda, Christoph Wanner, Eva Brand, Lora Lorenz, Thomas Duning, Peter Nordbeck, Lukas Kreul, Stefan-Martin Brand, Sima Canaan-Kühl
Publikováno v:
Journal of Medical Genetics. 58:342-350
BackgroundPatients with Fabry disease (FD) on reduced dose of agalsidase-beta or after switch to agalsidase-alfa show a decline in chronic kidney disease epidemiology collaboration-based estimated glomerular filtration rate (eGFR) and a worsened plas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9afa0709fdfc0dc22d2d1ec20631825e
https://doi.org/10.1136/jmedgenet-2020-106874
https://doi.org/10.1136/jmedgenet-2020-106874
Autor:
Manon Sendel, Ralf Baron, Sima Canaan-Kühl, Maren Reimer, Stefanie Rehm, Jens Gaedeke, Philipp Hüllemann, Paul Moeller, Janne Gierthmühlen, Julia Forstenpointner
Publikováno v:
Frontiers in Neuroscience
Frontiers in Neuroscience, Vol 14 (2020)
Frontiers in Neuroscience, Vol 14 (2020)
Purpose Fabry disease frequently includes pain as an early disease feature, which was characterized as a dysfunctional processing of somatosensory information in various studies. The pathomechanism involves the mutation in the x-chromosomal GLA-gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3195f9507e477b855363a327c2c6a52
https://pubmed.ncbi.nlm.nih.gov/32612493
https://pubmed.ncbi.nlm.nih.gov/32612493
Autor:
Thomas Rauen, Stephanie Wied, Christina Fitzner, Frank Eitner, Claudia Sommerer, Martin Zeier, Britta Otte, Ulf Panzer, Klemens Budde, Urs Benck, Peter R. Mertens, Uwe Kuhlmann, Oliver Witzke, Oliver Gross, Volker Vielhauer, Johannes F.E. Mann, Ralf-Dieter Hilgers, Jürgen Floege, Marcus J. Moeller, Horst Weihprecht, Harm Peters, Saban Elitok, Markus Bieringer, Ralf Schindler, Ulrich Frei, Sima Canaan–Kühl, Christiane Erley, Karsten Schlieps, Frans Zandvoort, Bernd Hohenstein, Christian Hugo, Catrin Palm, Karl Hilgers, Hermann Haller, Anna Bertram, Gunter Wolf, Martin Busch, Thomas Rath, Stephan Ziefle, Thomas Benzing, Franziska Grundmann, Stefan Westphalen, Uwe Göttmann, Michael Fischereder, Oliver Sarkar, Marianna Stefanidou, Hermann Pavenstädt, Bernhard Banas, Alexander Boeger, Nils Heyne, Ferruh Artunc, Helmut Reichel, Thomas Mettang, Christoph Wanner, Thomas Metzger
The randomized, controlled STOP-IgAN trial in patients with IgA nephropathy (IgAN) and substantial proteinuria showed no benefit of immunosuppression added on top of supportive care on renal function over three years. As a follow-up we evaluated rena
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf5bce68f00692dedc833b4298d37fb1
https://opus.bibliothek.uni-augsburg.de/opus4/frontdoor/index/index/docId/87939
https://opus.bibliothek.uni-augsburg.de/opus4/frontdoor/index/index/docId/87939
Autor:
Nicole Muschol, Katharina Stumpfe, Sima Canaan-Kühl, Claudia Sommer, Thomas Duning, Eva Brand, Daniela Blaschke, W. Alexander Mann, Christine Kurschat, Nurcan Üçeyler, Nesrin Karabul, Dan Liu, Stefanie Reiermann, Peter Nordbeck, Anibh M. Das, Malte Lenders, Monica Patten, Jessica Kaufeld, Christoph Kampmann, Jens Gaedeke, Jonas Müntze, Stefan-Martin Brand, Markus Cybulla, Christian Pogoda, Julia B. Hennermann
Publikováno v:
Clinical pharmacology and therapeutics. 108(2)
Fabry's disease (FD) is an X-linked lysosomal storage disorder caused by the deficient activity of the lysosomal enzyme alpha-galactosidase A (alpha-Gal A) leading to intracellular accumulation of globotriaosylceramide (Gb3). Patients with amenable m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5adac12f2836176d39f9cf2fbe9beed8
https://pubmed.ncbi.nlm.nih.gov/32198894
https://pubmed.ncbi.nlm.nih.gov/32198894