These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

235 related articles for article (PubMed ID: 34927673)

  • 1. Forecasting stroke-like episodes and outcomes in mitochondrial disease.
    Ng YS; Lax NZ; Blain AP; Erskine D; Baker MR; Polvikoski T; Thomas RH; Morris CM; Lai M; Whittaker RG; Gebbels A; Winder A; Hall J; Feeney C; Farrugia ME; Hirst C; Roberts M; Lawthom C; Chrysostomou A; Murphy K; Baird T; Maddison P; Duncan C; Poulton J; Nesbitt V; Hanna MG; Pitceathly RDS; Taylor RW; Blakely EL; Schaefer AM; Turnbull DM; McFarland R; Gorman GS
    Brain; 2022 Apr; 145(2):542-554. PubMed ID: 34927673
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Stroke-like episodes in adult mitochondrial disease.
    Ng YS; Gorman GS
    Handb Clin Neurol; 2023; 194():65-78. PubMed ID: 36813321
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Anatomic & metabolic brain markers of the m.3243A>G mutation: A multi-parametric 7T MRI study.
    Haast RAM; Ivanov D; IJsselstein RJT; Sallevelt SCEH; Jansen JFA; Smeets HJM; de Coo IFM; Formisano E; Uludağ K
    Neuroimage Clin; 2018; 18():231-244. PubMed ID: 29868447
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ischemic optic neuropathy as first presentation in patient with m.3243 A > G MELAS classic mutation.
    Scarcella S; Dell'Arti L; Gagliardi D; Magri F; Govoni A; Velardo D; Mainetti C; Minorini V; Ronchi D; Piga D; Comi GP; Corti S; Meneri M
    BMC Neurol; 2023 Apr; 23(1):165. PubMed ID: 37095452
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Mitochondrial DNA mutation "m.3243A>G"-Heterogeneous clinical picture for cardiologists ("m.3243A>G": A phenotypic chameleon).
    Niedermayr K; Pölzl G; Scholl-Bürgi S; Fauth C; Schweigmann U; Haberlandt E; Albrecht U; Zlamy M; Sperl W; Mayr JA; Karall D
    Congenit Heart Dis; 2018 Sep; 13(5):671-677. PubMed ID: 30133155
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome.
    Chakrabarty S; Govindaraj P; Sankaran BP; Nagappa M; Kabekkodu SP; Jayaram P; Mallya S; Deepha S; Ponmalar JNJ; Arivinda HR; Meena AK; Jha RK; Sinha S; Gayathri N; Taly AB; Thangaraj K; Satyamoorthy K
    J Neurol; 2021 Jun; 268(6):2192-2207. PubMed ID: 33484326
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prediction of long-term prognosis by heteroplasmy levels of the m.3243A>G mutation in patients with the mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes syndrome.
    Fayssoil A; Laforêt P; Bougouin W; Jardel C; Lombès A; Bécane HM; Berber N; Stojkovic T; Béhin A; Eymard B; Duboc D; Wahbi K
    Eur J Neurol; 2017 Feb; 24(2):255-261. PubMed ID: 27869334
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Modeling Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes Syndrome Using Patient-Derived Induced Neurons Generated by Direct Reprogramming.
    Povea-Cabello S; Villanueva-Paz M; Villalón-García I; Talaverón-Rey M; Álvarez-Cordoba M; Suárez-Rivero JM; Montes MÁ; Rodríguez-Moreno A; Andrade-Talavera Y; Armengol JA; Sánchez-Alcázar JA
    Cell Reprogram; 2022 Oct; 24(5):294-303. PubMed ID: 35802497
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender?
    Mancuso M; Orsucci D; Angelini C; Bertini E; Carelli V; Comi GP; Donati A; Minetti C; Moggio M; Mongini T; Servidei S; Tonin P; Toscano A; Uziel G; Bruno C; Ienco EC; Filosto M; Lamperti C; Catteruccia M; Moroni I; Musumeci O; Pegoraro E; Ronchi D; Santorelli FM; Sauchelli D; Scarpelli M; Sciacco M; Valentino ML; Vercelli L; Zeviani M; Siciliano G
    J Neurol; 2014 Mar; 261(3):504-10. PubMed ID: 24375076
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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.
    Alenezi AF; Almelahi MA; Fekih-Romdhana F; Jahrami HA
    J Med Case Rep; 2022 Oct; 16(1):361. PubMed ID: 36210452
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Neuropathological hallmarks in autopsied cases with mitochondrial diseases caused by the mitochondrial 3243A>G mutation.
    Miyahara H; Tamai C; Inoue M; Sekiguchi K; Tahara D; Tahara N; Takeda K; Arafuka S; Moriyoshi H; Koizumi R; Akagi A; Riku Y; Sone J; Yoshida M; Ihara K; Iwasaki Y
    Brain Pathol; 2023 Nov; 33(6):e13199. PubMed ID: 37534760
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Impediments to Heart Transplantation in Adults With MELAS
    Di Toro A; Urtis M; Narula N; Giuliani L; Grasso M; Pasotti M; Pellegrini C; Serio A; Pilotto A; Antoniazzi E; Rampino T; Magrassi L; Valentini A; Cavallini A; Scelsi L; Ghio S; Abelli M; Olivotto I; Porcu M; Gavazzi A; Kodama T; Arbustini E
    J Am Coll Cardiol; 2022 Oct; 80(15):1431-1443. PubMed ID: 36202533
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Detection rates and phenotypic spectrum of m.3243A>G in the MT-TL1 gene: a molecular diagnostic laboratory perspective.
    Chin J; Marotta R; Chiotis M; Allan EH; Collins SJ
    Mitochondrion; 2014 Jul; 17():34-41. PubMed ID: 24846800
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Independent origin for m.3243A>G mitochondrial mutation in three Venezuelan cases of MELAS syndrome.
    Florez I; Pirrone I; Casique L; Domínguez CL; Mahfoud A; Rodríguez T; Rodríguez D; De Lucca M; Ramírez JL
    Clin Biochem; 2022; 109-110():98-101. PubMed ID: 36130631
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes with an
    Zheng H; Zhang X; Tian L; Liu B; He X; Wang L; Ding S; Guo Y; Cai J
    Front Neurosci; 2022; 16():1028762. PubMed ID: 36685235
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Lifestyle Changes Normalize Serum Lactate Levels in an m.3243A>G Carrier.
    Finsterer J
    Am J Case Rep; 2021 Apr; 22():e930175. PubMed ID: 33867519
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Renal manifestations in adults with mitochondrial disease from the mtDNA m.3243A>G pathogenic variant.
    Ferreira F; Gonçalves Bacelar C; Lisboa-Gonçalves P; Paulo N; Quental R; Nunes AT; Silva R; Tavares I
    Nefrologia (Engl Ed); 2023 Dec; 43 Suppl 2():1-7. PubMed ID: 38355238
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pseudo-obstruction, stroke, and mitochondrial dysfunction: A lethal combination.
    Ng YS; Feeney C; Schaefer AM; Holmes CE; Hynd P; Alston CL; Grady JP; Roberts M; Maguire M; Bright A; Taylor RW; Yiannakou Y; McFarland R; Turnbull DM; Gorman GS
    Ann Neurol; 2016 Nov; 80(5):686-692. PubMed ID: 27453452
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 12.