Remimazolam anesthesia for transcatheter mitral valve repair in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome: a case report
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2363-9024
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Remimazolam anesthesia for transcatheter mitral valve repair in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome: a case report ; volume:8 ; number:1 ; day:1 ; month:6 ; year:2022 ; pages:1-4 ; date:12.2022
JA clinical reports ; 8, Heft 1 (1.6.2022), 1-4, 12.2022
- Creator
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Kitaura, Atsuhiro
Kosumi, Reiko
Iwamoto, Tatsushige
Nakao, Shinichi
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s40981-022-00528-1
- URN
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urn:nbn:de:101:1-2022073111005542399632
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:24 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
- Kitaura, Atsuhiro
- Kosumi, Reiko
- Iwamoto, Tatsushige
- Nakao, Shinichi
- SpringerLink (Online service)
Other Objects (12)
Initial manifestations of mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) at an infant
MELAS (Mitochondrial Encephalopathy, Lactic Acidosis and Stroke-Like Episodes)—Usual and Unusual MRI Finding
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes with coexisting nemaline myopathy: a case report
An anesthetic experience with remimazolam for MELAS patients
Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome
Delay in diagnosing a patient with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome who presented with status epilepticus and lactic acidosis: a case report
Assessing the anesthetic effectiveness of remimazolam in MELAS patients requires careful investigations
Mitochondrial disease in a heteroplasmic MT DNA mutation causing mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) and leigh syndrome phenotypes
A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report
General anesthesia with remimazolam for a pediatric patient with MELAS and recurrent epilepsy: a case report
Acidosis
Mela Panaia o Mela Flagellata
Initial manifestations of mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) at an infant
MELAS (Mitochondrial Encephalopathy, Lactic Acidosis and Stroke-Like Episodes)—Usual and Unusual MRI Finding
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes with coexisting nemaline myopathy: a case report
An anesthetic experience with remimazolam for MELAS patients
Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome
Delay in diagnosing a patient with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome who presented with status epilepticus and lactic acidosis: a case report
Assessing the anesthetic effectiveness of remimazolam in MELAS patients requires careful investigations
Mitochondrial disease in a heteroplasmic MT DNA mutation causing mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) and leigh syndrome phenotypes
A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report
General anesthesia with remimazolam for a pediatric patient with MELAS and recurrent epilepsy: a case report
Acidosis
Mela Panaia o Mela Flagellata
Initial manifestations of mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) at an infant
MELAS (Mitochondrial Encephalopathy, Lactic Acidosis and Stroke-Like Episodes)—Usual and Unusual MRI Finding
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes with coexisting nemaline myopathy: a case report
An anesthetic experience with remimazolam for MELAS patients
Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome
Delay in diagnosing a patient with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome who presented with status epilepticus and lactic acidosis: a case report
Assessing the anesthetic effectiveness of remimazolam in MELAS patients requires careful investigations
Mitochondrial disease in a heteroplasmic MT DNA mutation causing mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) and leigh syndrome phenotypes
A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report
General anesthesia with remimazolam for a pediatric patient with MELAS and recurrent epilepsy: a case report
Acidosis