Detalhe da pesquisa
1.
Coupling MoSe2 with Non-Stoichiometry Ni0.85 Se in Carbon Hollow Nanoflowers for Efficient Electrocatalytic Synergistic Effect on Li-O2 Batteries.
Small
; 20(10): e2304882, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-37890468
2.
Mitochondrial Dysfunction due to Novel COQ8A Variation with Poor Response to CoQ10 Treatment: A Comprehensive Study and Review of Literatures.
Cerebellum
; 2024 Mar 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38429489
3.
Shedding Light on Lysosomal Malondialdehyde Affecting Vitamin B12 Transport during Cerebral Ischemia/Reperfusion Injury.
J Am Chem Soc
; 145(41): 22609-22619, 2023 10 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-37803879
4.
MELAS-associated m.5541C>T mutation caused instability of mitochondrial tRNATrp and remarkable mitochondrial dysfunction.
J Med Genet
; 59(1): 79-87, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33208382
5.
Leber's hereditary optic neuropathy plus dystonia caused by the mitochondrial ND1 gene m.4160 T > C mutation.
Neurol Sci
; 43(9): 5581-5592, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-35699829
6.
Novel biallelic mutations in POLG gene: large deletion and missense variant associated with PEO.
Neurol Sci
; 42(10): 4271-4280, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34189666
7.
Leber hereditary optic neuropathy and dystonia overlapping mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes due to m.14459G>A mutation.
Neurol Sci
; 42(12): 5123-5130, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-33779865
8.
Unraveling the Diagnostic Puzzle: Minor Stroke-Like Lesions and Normal Muscle Histopathology in MELAS Syndrome.
Stroke
; 55(4): e127-e130, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38362757
9.
ETFDH Mutations and Flavin Adenine Dinucleotide Homeostasis Disturbance Are Essential for Developing Riboflavin-Responsive Multiple Acyl-Coenzyme A Dehydrogenation Deficiency.
Ann Neurol
; 84(5): 659-673, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30232818
10.
Seven-and-a-half syndrome.
Pract Neurol
; 2024 Feb 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38326019
11.
Fluctuating ataxia caused by mitochondrial tRNA (Lys) gene m.8363G > A variant.
Neurol Sci
; 43(11): 6589-6591, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35821181
12.
Idebenone protects against oxidized low density lipoprotein induced mitochondrial dysfunction in vascular endothelial cells via GSK3ß/ß-catenin signalling pathways.
Biochem Biophys Res Commun
; 465(3): 548-55, 2015 Sep 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-26284974
13.
[Expression of retinoic acid-I nducible gene I in the muscle tissues of idiopathic inflammatory myopathies].
Zhonghua Yi Xue Za Zhi
; 95(23): 1823-8, 2015 Jun 16.
Artigo
em Zh
| MEDLINE | ID: mdl-26712399
14.
Mesenchymal stem cells rescue injured endothelial cells in an in vitro ischemia-reperfusion model via tunneling nanotube like structure-mediated mitochondrial transfer.
Microvasc Res
; 92: 10-8, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24486322
15.
Twinkle mutations in two Chinese families with autosomal dominant progressive external ophthalmoplegia.
Neurol Sci
; 35(3): 443-8, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24091712
16.
MERRF/MELAS overlap syndrome due to the m.3291T>C mutation.
Metab Brain Dis
; 29(1): 139-44, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24338029
17.
Mitochondrial myopathy without extraocular muscle involvement: a unique clinicopathologic profile.
J Neurol
; 271(2): 864-876, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37847292
18.
Clinical features of epileptic seizures in patients with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes.
Seizure
; 106: 110-116, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36827862
19.
A Missense Variant in AIFM1 Caused Mitochondrial Dysfunction and Intolerance to Riboflavin Deficiency.
Neuromolecular Med
; 25(4): 489-500, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37603145
20.
A different pattern of clinical, muscle pathology and brain MRI findings in MELAS with mt-ND variants.
Ann Clin Transl Neurol
; 10(6): 1035-1045, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37221696