In vitro contracture test results and anaesthetic management of a patient with emery-dreifuss muscular dystrophy for cardiac transplantation
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
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In: Case Reports in Anesthesiology. 2012:349046. doi:10.1155/2012/349046
- Keyword
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Anästhesiologie
- Event
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Veröffentlichung
- (where)
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Würzburg
- (who)
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Universität Würzburg
- (when)
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2015
- Creator
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Schuster, Frank
Wessig, Carsten
Schimmer, Christoph
Johannsen, Stephan
Lazarus, Marc
Aleksic, Ivan
Leyh, Rainer
Roewer, Norbert
- URN
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urn:nbn:de:bvb:20-opus-123413
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:54 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Schuster, Frank
- Wessig, Carsten
- Schimmer, Christoph
- Johannsen, Stephan
- Lazarus, Marc
- Aleksic, Ivan
- Leyh, Rainer
- Roewer, Norbert
- Universität Würzburg
Time of origin
- 2015
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Impairment of Lamin A/C-Polycomb crosstalk as a possible epigenetic cause of Emery Dreifuss Muscular Dystrophy (EDMD)
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Perinatal Management of Pregnancy Complicated by Autosomal Dominant Emery–Dreifuss Muscular Dystrophy
Isolated Right Atrial Enhancement with Atrial Standstill: An Uncommon Presentation of Emery–Dreifuss Muscular Dystrophy
A novel SYNE1 gene mutation in a Chinese family of Emery-Dreifuss muscular dystrophy-like
Lamin A and lamin C are differentially dysfunctional in autosomal dominant Emery-Dreifuss muscular dystrophy
Impairment of Lamin A/C-Polycomb crosstalk as a possible epigenetic cause of Emery Dreifuss Muscular Dystrophy (EDMD)
Occurrence of Emery-Dreifuss muscular dystrophy in a rural setting of Cameroon: a case report and review of the literature
Emerin deficiency does not exacerbate cardiomyopathy in a murine model of Emery–Dreifuss muscular dystrophy caused by an LMNA gene mutation
Autosomal dominant Emery-Dreifuss muscular dystrophy caused by a mutation in the lamin A/C gene identified by exome sequencing: a case report
Mutationsanalyse von Kandidatengenen für die Emery-Dreifuss Muskeldystrophie in der Region Xq 28