MELAS (Mitochondrial Encephalopathy, Lactic Acidosis and Stroke-Like Episodes)—Usual and Unusual MRI Finding
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
MELAS (Mitochondrial Encephalopathy, Lactic Acidosis and Stroke-Like Episodes)—Usual and Unusual MRI Finding ; day:30 ; month:08 ; year:2022
The Indian journal of radiology and imaging ; (30.08.2022)
- Contributor
-
Prabhu, Sameeta M.
Banerjee, Bidisha
Acharya, Ullas
Hegde, Poonam P.
Shetty, Mitesh
- DOI
-
10.1055/s-0042-1755241
- URN
-
urn:nbn:de:101:1-2022111011020394924312
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:34 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
- Prabhu, Sameeta M.
- Banerjee, Bidisha
- Acharya, Ullas
- Hegde, Poonam P.
- Shetty, Mitesh
Other Objects (12)
Initial manifestations of mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) at an infant
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
Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome
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
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
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes with coexisting nemaline myopathy: a case report
Metformin-Associated Lactic Acidosis: A Case Report
Materno-fetal lactic acid mediated infusion acidosis
Metformin-induced lactic acidosis: a case series
Combined metformin-associated lactic acidosis and euglycemic ketoacidosis
Salbutamol-induced lactic acidosis in status asthmaticus survivor
Initial manifestations of mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) at an infant
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
Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome
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
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
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes with coexisting nemaline myopathy: a case report
Metformin-Associated Lactic Acidosis: A Case Report
Materno-fetal lactic acid mediated infusion acidosis
Metformin-induced lactic acidosis: a case series
Combined metformin-associated lactic acidosis and euglycemic ketoacidosis
Salbutamol-induced lactic acidosis in status asthmaticus survivor
Initial manifestations of mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) at an infant
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
Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome
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
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
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes with coexisting nemaline myopathy: a case report
Metformin-Associated Lactic Acidosis: A Case Report
Materno-fetal lactic acid mediated infusion acidosis
Metformin-induced lactic acidosis: a case series
Combined metformin-associated lactic acidosis and euglycemic ketoacidosis