BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

863 related articles for article (PubMed ID: 27476418)

  • 1. 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]  

  • 2. Retinal ganglion cell neurodegeneration in mitochondrial inherited disorders.
    Carelli V; La Morgia C; Valentino ML; Barboni P; Ross-Cisneros FN; Sadun AA
    Biochim Biophys Acta; 2009 May; 1787(5):518-28. PubMed ID: 19268652
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The expanding clinical spectrum of mitochondrial diseases.
    De Vivo DC
    Brain Dev; 1993; 15(1):1-22. PubMed ID: 8338207
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Defects of mitochondrial DNA.
    Zeviani M; Antozzi C
    Brain Pathol; 1992 Apr; 2(2):121-32. PubMed ID: 1341953
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mitochondrial disease and epilepsy.
    Rahman S
    Dev Med Child Neurol; 2012 May; 54(5):397-406. PubMed ID: 22283595
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Eye diseases in mitochondrial encephalomyopathies].
    Mojon D
    Ther Umsch; 2001 Jan; 58(1):49-55. PubMed ID: 11217487
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Mitochondrial encephalopathy, lactic acidosis and stroke-like episodes / myoclonus epilepsy with ragged-red fibers /Leigh overlap syndrome caused by mitochondrial DNA 8344A>G mutation].
    Hou Y; Zhao XT; Xie ZY; Yuan Y; Wang ZX
    Beijing Da Xue Xue Bao Yi Xue Ban; 2020 Oct; 52(5):851-855. PubMed ID: 33047718
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular epidemiologic study of mitochondrial DNA mutations in patients with mitochondrial diseases in Taiwan.
    Pang CY; Huang CC; Yen MY; Wang EK; Kao KP; Chen SS; Wei YH
    J Formos Med Assoc; 1999 May; 98(5):326-34. PubMed ID: 10420700
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cognitive dysfunction in mitochondrial disorders.
    Finsterer J
    Acta Neurol Scand; 2012 Jul; 126(1):1-11. PubMed ID: 22335339
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A MELAS-associated ND1 mutation causing leber hereditary optic neuropathy and spastic dystonia.
    Spruijt L; Smeets HJ; Hendrickx A; Bettink-Remeijer MW; Maat-Kievit A; Schoonderwoerd KC; Sluiter W; de Coo IF; Hintzen RQ
    Arch Neurol; 2007 Jun; 64(6):890-3. PubMed ID: 17562939
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Diagnosis of mitochondrial disorders in children with next generation sequencing].
    Liu Z; Fang F; Ding C; Zhang W; Li J; Yang X; Wang X; Wu Y; Wang H; Liu L; Han T; Wang X; Chen C; Lyu J; Wu H
    Zhonghua Er Ke Za Zhi; 2015 Oct; 53(10):747-53. PubMed ID: 26758110
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mitochondrial Retinopathies.
    Zeviani M; Carelli V
    Int J Mol Sci; 2021 Dec; 23(1):. PubMed ID: 35008635
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Mitochondrial diseases].
    Radelfahr F; Klopstock T
    Nervenarzt; 2019 Feb; 90(2):121-130. PubMed ID: 30643957
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Diagnostic screening of mitochondrial DNA mutations in Australian adults 1990-2001.
    Marotta R; Chin J; Quigley A; Katsabanis S; Kapsa R; Byrne E; Collins S
    Intern Med J; 2004; 34(1-2):10-9. PubMed ID: 14748908
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Human mitochondrial diseases: answering questions and questioning answers.
    Howell N
    Int Rev Cytol; 1999; 186():49-116. PubMed ID: 9770297
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) - A Polish family with novel SACS mutations.
    Krygier M; Konkel A; Schinwelski M; Rydzanicz M; Walczak A; Sildatke-Bauer M; Płoski R; Sławek J
    Neurol Neurochir Pol; 2017; 51(6):481-485. PubMed ID: 28843771
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Inherited peripheral neuropathies due to mitochondrial disorders.
    Cassereau J; Codron P; Funalot B
    Rev Neurol (Paris); 2014 May; 170(5):366-74. PubMed ID: 24768438
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Spastic ataxias.
    Bereznyakova O; Dupré N
    Handb Clin Neurol; 2018; 155():191-203. PubMed ID: 29891058
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Retinal manifestations in mitochondrial diseases associated with mitochondrial DNA mutation.
    Isashiki Y; Nakagawa M; Ohba N; Kamimura K; Sakoda Y; Higuchi I; Izumo S; Osame M
    Acta Ophthalmol Scand; 1998 Feb; 76(1):6-13. PubMed ID: 9541428
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 44.