-
1
Leighs disease: powerhouse failure
Published 2018-01-01Subjects: “…leigh disease…”
Get full text
Article -
2
Differential diagnosis of Acute Flaccid Paralysis in children: clinical case of Leigh disease
Published 2014-12-01Get full text
Article -
3
Leigh's Disease: The Acute Clinical Course of a Two-Year-Old Child with Subacute Necrotizing Encephalomyelopathy
Published 2010-01-01“…On the basis of the characteristic neuropathological findings in combination with the age of the child, we had to take into consideration that the child might have died from subacute necrotizing encephalomyelopathy (Leigh's Disease) despite the untypical, fulminant clinical course.…”
Get full text
Article -
4
-
5
How to mitigate neurological and cardiac decompensation in Leigh syndrome: Can nicotinamide riboside be an answer?
Published 2022-09-01Subjects: “…Leigh disease…”
Get full text
Article -
6
-
7
Evaluation of the Genetically Diagnosed Mitochondrial Disease Cases with Neuromuscular Involvement
Published 2022-04-01Subjects: Get full text
Article -
8
Leigh syndrome global patient registry: uniting patients and researchers worldwide
Published 2023-09-01Subjects: Get full text
Article -
9
Anesthetic Management of a Pediatric Patient with Leigh Syndrome
Published 2013-03-01“…Intensive care and breathing support for the patient with LS, under sedation with an analgesic combination during the early postoperative period, minimized the stress response due to pain after surgery. Keywords: Leigh Disease, Anesthesia, General, Monitoring, Physiologic, Intensive Care…”
Get full text
Article -
10
Reliability of MRI in detection and differentiation of acute neonatal/pediatric encephalopathy causes among neonatal/pediatric intensive care unit patients
Published 2020-04-01“…The final diagnosis of the study group patients were hypoxic ischemia injury (HII) in 39 patients (65%), metachromatic leukodystrophy in 6 patients (10%), biotin-thiamine-responsive basal ganglia disease (BTBGD) and Leigh disease each in 4 patients (6.7%), periventricular leukomalacia (PVL) in 3 patients (5%), and mitochondrial encephalopathy with lactic acidosis and stroke-like episodes syndrome (MELAS) and non-ketotic hyperglycinemia (NKH) each in 2 patients (3.3%). …”
Get full text
Article -
11
Mitochondrial complex I deficiency leads to the retardation of early embryonic development in Ndufs4 knockout mice
Published 2017-05-01“…In our study, we attempted to investigate embryonic development in Ndufs4 KO mice, which can be regarded as a Leigh disease model and were created through the CRISPR (clustered regularly interspaced short palindromic repeat) and Cas9 (CRISPR associated)-mediated genome editing system. …”
Get full text
Article