Mitochondrial Neurogastrointestinal Encephalopathy Disease: A Rare Disease Diagnosed in Siblings with Double Vision
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
Mitochondrial Neurogastrointestinal Encephalopathy Disease: A Rare Disease Diagnosed in Siblings with Double Vision ; volume:12 ; number:1 ; year:2021 ; pages:174-181 ; extent:8
Case reports in ophthalmology ; 12, Heft 1 (2021), 174-181 (gesamt 8)
- Creator
-
Farahvash, Armin
Kassardjian, Charles D.
Micieli, Jonathan A.
- DOI
-
10.1159/000514098
- URN
-
urn:nbn:de:101:1-2021051301164665931199
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:44 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
- Farahvash, Armin
- Kassardjian, Charles D.
- Micieli, Jonathan A.
Other Objects (12)
Mitochondrial Disease Masquerading as Recurrent Encephalopathy
Mitochondrial neurogastrointestinal encephalopathy: a clinicopathological mimic of Crohn’s disease
Chronic traumatic encephalopathy in a former Australian rules football player diagnosed with Alzheimer’s disease
Synchronous disease onset and flares in siblings with PFAPA
Dystonia and mitochondrial disease: the movement disorder connection revisited in 900 genetically diagnosed patients
Mitochondrial neurogastrointestinal encephalopathy: a case report
A recurrent homozygous NHLRC1 variant in siblings with Lafora disease
International Paediatric Mitochondrial Disease Scale
Left ventricular noncompaction diagnosed following Graves′ disease
Co-occurrence of chronic traumatic encephalopathy and prion disease
Management of Hepatic Encephalopathy Associated with Advanced Liver Disease
A Case Report of Familial Extramammary Paget's Disease in Female Siblings
Mitochondrial Disease Masquerading as Recurrent Encephalopathy
Mitochondrial neurogastrointestinal encephalopathy: a clinicopathological mimic of Crohn’s disease
Chronic traumatic encephalopathy in a former Australian rules football player diagnosed with Alzheimer’s disease
Synchronous disease onset and flares in siblings with PFAPA
Dystonia and mitochondrial disease: the movement disorder connection revisited in 900 genetically diagnosed patients
Mitochondrial neurogastrointestinal encephalopathy: a case report
A recurrent homozygous NHLRC1 variant in siblings with Lafora disease
International Paediatric Mitochondrial Disease Scale
Left ventricular noncompaction diagnosed following Graves′ disease
Co-occurrence of chronic traumatic encephalopathy and prion disease
Management of Hepatic Encephalopathy Associated with Advanced Liver Disease
A Case Report of Familial Extramammary Paget's Disease in Female Siblings
Mitochondrial Disease Masquerading as Recurrent Encephalopathy
Mitochondrial neurogastrointestinal encephalopathy: a clinicopathological mimic of Crohn’s disease
Chronic traumatic encephalopathy in a former Australian rules football player diagnosed with Alzheimer’s disease
Synchronous disease onset and flares in siblings with PFAPA
Dystonia and mitochondrial disease: the movement disorder connection revisited in 900 genetically diagnosed patients
Mitochondrial neurogastrointestinal encephalopathy: a case report
A recurrent homozygous NHLRC1 variant in siblings with Lafora disease
International Paediatric Mitochondrial Disease Scale
Left ventricular noncompaction diagnosed following Graves′ disease
Co-occurrence of chronic traumatic encephalopathy and prion disease
Management of Hepatic Encephalopathy Associated with Advanced Liver Disease