281 related articles for article (PubMed ID: 36362003)
1. Mitochondrial Epilepsy, a Challenge for Neurologists.
Lopriore P; Gomes F; Montano V; Siciliano G; Mancuso M
Int J Mol Sci; 2022 Oct; 23(21):. PubMed ID: 36362003
[TBL] [Abstract][Full Text] [Related]
2. Mitochondrial disease and epilepsy.
Rahman S
Dev Med Child Neurol; 2012 May; 54(5):397-406. PubMed ID: 22283595
[TBL] [Abstract][Full Text] [Related]
3. Mitochondrial diseases and epilepsy.
Bindoff LA; Engelsen BA
Epilepsia; 2012 Sep; 53 Suppl 4():92-7. PubMed ID: 22946726
[TBL] [Abstract][Full Text] [Related]
4. Mitochondrial dysfunction in epilepsy.
Khurana DS; Valencia I; Goldenthal MJ; Legido A
Semin Pediatr Neurol; 2013 Sep; 20(3):176-87. PubMed ID: 24331359
[TBL] [Abstract][Full Text] [Related]
5. Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease.
Blok MJ; Spruijt L; de Coo IF; Schoonderwoerd K; Hendrickx A; Smeets HJ
J Med Genet; 2007 Apr; 44(4):e74. PubMed ID: 17400793
[TBL] [Abstract][Full Text] [Related]
6. Mitochondrial respiratory chain disorders in the Old Order Amish population.
Ghaloul-Gonzalez L; Goldstein A; Walsh Vockley C; Dobrowolski SF; Biery A; Irani A; Ibarra J; Morton DH; Mohsen AW; Vockley J
Mol Genet Metab; 2016 Aug; 118(4):296-303. PubMed ID: 27344355
[TBL] [Abstract][Full Text] [Related]
7. Epilepsy in mitochondrial disorders.
Finsterer J; Zarrouk Mahjoub S
Seizure; 2012 Jun; 21(5):316-21. PubMed ID: 22459315
[TBL] [Abstract][Full Text] [Related]
8. Movement disorders in mitochondrial diseases.
Tranchant C; Anheim M
Rev Neurol (Paris); 2016; 172(8-9):524-529. PubMed ID: 27476418
[TBL] [Abstract][Full Text] [Related]
9. Genetic, pathogenetic, and phenotypic implications of the mitochondrial A3243G tRNALeu(UUR) mutation.
Finsterer J
Acta Neurol Scand; 2007 Jul; 116(1):1-14. PubMed ID: 17587249
[TBL] [Abstract][Full Text] [Related]
10. 8-year retrospective analysis of intravenous arginine therapy for acute metabolic strokes in pediatric mitochondrial disease.
Ganetzky RD; Falk MJ
Mol Genet Metab; 2018 Mar; 123(3):301-308. PubMed ID: 29428506
[TBL] [Abstract][Full Text] [Related]
11. The genetics of mitochondrial disease.
Davis RL; Sue CM
Semin Neurol; 2011 Nov; 31(5):519-30. PubMed ID: 22266889
[TBL] [Abstract][Full Text] [Related]
12. Mitochondrial syndromes with leukoencephalopathies.
Wong LJ
Semin Neurol; 2012 Feb; 32(1):55-61. PubMed ID: 22422207
[TBL] [Abstract][Full Text] [Related]
13. Mitochondrial function and pathology in status epilepticus.
Bindoff LA
Epilepsia; 2011 Oct; 52 Suppl 8():6-7. PubMed ID: 21967349
[TBL] [Abstract][Full Text] [Related]
14. Epilepsy in adults with mitochondrial disease: A cohort study.
Whittaker RG; Devine HE; Gorman GS; Schaefer AM; Horvath R; Ng Y; Nesbitt V; Lax NZ; McFarland R; Cunningham MO; Taylor RW; Turnbull DM
Ann Neurol; 2015 Dec; 78(6):949-57. PubMed ID: 26381753
[TBL] [Abstract][Full Text] [Related]
15. Metabolic rescue in pluripotent cells from patients with mtDNA disease.
Ma H; Folmes CD; Wu J; Morey R; Mora-Castilla S; Ocampo A; Ma L; Poulton J; Wang X; Ahmed R; Kang E; Lee Y; Hayama T; Li Y; Van Dyken C; Gutierrez NM; Tippner-Hedges R; Koski A; Mitalipov N; Amato P; Wolf DP; Huang T; Terzic A; Laurent LC; Izpisua Belmonte JC; Mitalipov S
Nature; 2015 Aug; 524(7564):234-8. PubMed ID: 26176921
[TBL] [Abstract][Full Text] [Related]
16. ADCK3 mutations with epilepsy, stroke-like episodes and ataxia: a POLG mimic?
Hikmat O; Tzoulis C; Knappskog PM; Johansson S; Boman H; Sztromwasser P; Lien E; Brodtkorb E; Ghezzi D; Bindoff LA
Eur J Neurol; 2016 Jul; 23(7):1188-94. PubMed ID: 27106809
[TBL] [Abstract][Full Text] [Related]
17. Recent Advances in Mitochondria-Targeted Gene Delivery.
Jang YH; Lim KI
Molecules; 2018 Sep; 23(9):. PubMed ID: 30208599
[TBL] [Abstract][Full Text] [Related]
18. Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease.
Martikainen MH; Ng YS; Gorman GS; Alston CL; Blakely EL; Schaefer AM; Chinnery PF; Burn DJ; Taylor RW; McFarland R; Turnbull DM
JAMA Neurol; 2016 Jun; 73(6):668-74. PubMed ID: 27111573
[TBL] [Abstract][Full Text] [Related]
19. Multisystem mitochondrial diseases due to mutations in mtDNA-encoded subunits of complex I.
Danhelovska T; Kolarova H; Zeman J; Hansikova H; Vaneckova M; Lambert L; Kucerova-Vidrova V; Berankova K; Honzik T; Tesarova M
BMC Pediatr; 2020 Jan; 20(1):41. PubMed ID: 31996177
[TBL] [Abstract][Full Text] [Related]
20. POLG-related disorders and their neurological manifestations.
Rahman S; Copeland WC
Nat Rev Neurol; 2019 Jan; 15(1):40-52. PubMed ID: 30451971
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
