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 *

236 related articles for article (PubMed ID: 25978847)

  • 21. MR findings in Leigh syndrome with COX deficiency and SURF-1 mutations.
    Farina L; Chiapparini L; Uziel G; Bugiani M; Zeviani M; Savoiardo M
    AJNR Am J Neuroradiol; 2002 Aug; 23(7):1095-100. PubMed ID: 12169463
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Clinical and magnetic resonance imaging findings in patients with Leigh syndrome and SURF1 mutations.
    Sonam K; Khan NA; Bindu PS; Taly AB; Gayathri N; Bharath MM; Govindaraju C; Arvinda HR; Nagappa M; Sinha S; Thangaraj K
    Brain Dev; 2014 Oct; 36(9):807-12. PubMed ID: 24262866
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Leigh-like subacute necrotising encephalopathy in Yorkshire Terriers: neuropathological characterisation, respiratory chain activities and mitochondrial DNA.
    Baiker K; Hofmann S; Fischer A; Gödde T; Medl S; Schmahl W; Bauer MF; Matiasek K
    Acta Neuropathol; 2009 Nov; 118(5):697-709. PubMed ID: 19466433
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A novel mutation in the human complex I NDUFS7 subunit associated with Leigh syndrome.
    Lebon S; Rodriguez D; Bridoux D; Zerrad A; Rötig A; Munnich A; Legrand A; Slama A
    Mol Genet Metab; 2007 Apr; 90(4):379-82. PubMed ID: 17275378
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Clinical and laboratory survey of 65 Chinese patients with Leigh syndrome.
    Yang YL; Sun F; Zhang Y; Qian N; Yuan Y; Wang ZX; Qi Y; Xiao JX; Wang XY; Qi ZY; Zhang YH; Jiang YW; Bao XH; Qin J; Wu XR
    Chin Med J (Engl); 2006 Mar; 119(5):373-7. PubMed ID: 16542579
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The neuroimaging of Leigh syndrome: case series and review of the literature.
    Bonfante E; Koenig MK; Adejumo RB; Perinjelil V; Riascos RF
    Pediatr Radiol; 2016 Apr; 46(4):443-51. PubMed ID: 26739140
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Leigh syndrome: One disorder, more than 75 monogenic causes.
    Lake NJ; Compton AG; Rahman S; Thorburn DR
    Ann Neurol; 2016 Feb; 79(2):190-203. PubMed ID: 26506407
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Late-onset Leigh syndrome with myoclonic epilepsy with ragged-red fibers.
    Monden Y; Mori M; Kuwajima M; Goto T; Yamagata T; Momoi MY
    Brain Dev; 2013 Jun; 35(6):582-5. PubMed ID: 22981260
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Clinico-neuropathological study of a Chinese case of familial adult Leigh syndrome.
    Piao YS; Tang GC; Yang H; Lu DH
    Neuropathology; 2006 Jun; 26(3):218-21. PubMed ID: 16771178
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T>C.
    Dermaut B; Seneca S; Dom L; Smets K; Ceulemans L; Smet J; De Paepe B; Tousseyn S; Weckhuysen S; Gewillig M; Pals P; Parizel P; De Bleecker JL; Boon P; De Meirleir L; De Jonghe P; Van Coster R; Van Paesschen W; Santens P
    J Neurol Neurosurg Psychiatry; 2010 Jan; 81(1):90-3. PubMed ID: 20019223
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mitochondrial DNA mutations in late-onset Leigh syndrome.
    Wei Y; Cui L; Peng B
    J Neurol; 2018 Oct; 265(10):2388-2395. PubMed ID: 30128709
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Clinical and genetic characteristics of children with Leigh syndrome].
    Fang F; Shen Y; Shen DM; Liu ZM; Ding CH; Zhang WC; Sun SZ; Lyu JL; Han TL; Wang XH; Zhang WH; Yang XY; Li JW; Wu HS
    Zhonghua Er Ke Za Zhi; 2017 Mar; 55(3):205-209. PubMed ID: 28273704
    [No Abstract]   [Full Text] [Related]  

  • 33. [Clinical characteristics and genetic analysis of two cases with Leigh syndrome with acute pulmonary hemorrhage as predominant manifestation].
    Danqun J; Jie D; Wenjia T; Kefei H
    Zhonghua Er Ke Za Zhi; 2015 Apr; 53(4):290-5. PubMed ID: 26182505
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A novel NDUFV1 gene mutation in complex I deficiency in consanguineous siblings with brainstem lesions and Leigh syndrome.
    Vilain C; Rens C; Aeby A; Balériaux D; Van Bogaert P; Remiche G; Smet J; Van Coster R; Abramowicz M; Pirson I
    Clin Genet; 2012 Sep; 82(3):264-70. PubMed ID: 21696386
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Genetic heterogeneity of mitochondrial genome in thiamine deficient Leigh syndrome patients.
    Mani S; Rao SN; Kranthi Kumar MV
    J Neurol Sci; 2019 Sep; 404():91-100. PubMed ID: 31352295
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Leigh syndrome: Resolving the clinical and genetic heterogeneity paves the way for treatment options.
    Gerards M; Sallevelt SC; Smeets HJ
    Mol Genet Metab; 2016 Mar; 117(3):300-12. PubMed ID: 26725255
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A novel mitochondrial m.14430A>G (MT-ND6, p.W82R) variant causes complex I deficiency and mitochondrial Leigh syndrome.
    Du M; Wei X; Xu P; Xie A; Zhou X; Yang Y; Li D; Lyu J; Fang H
    Clin Chem Lab Med; 2020 Oct; 58(11):1809-1817. PubMed ID: 32432562
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Leigh syndrome in individuals bearing m.9185T>C MTATP6 variant. Is hyperventilation a factor which starts its development?
    Piekutowska-Abramczuk D; Rutyna R; Czyżyk E; Jurkiewicz E; Iwanicka-Pronicka K; Rokicki D; Stachowicz S; Strzemecka J; Guz W; Gawroński M; Kosierb A; Ligas J; Puchala M; Drelich-Zbroja A; Bednarska-Makaruk M; Dąbrowski W; Ciara E; Książyk JB; Pronicka E
    Metab Brain Dis; 2018 Feb; 33(1):191-199. PubMed ID: 29116603
    [TBL] [Abstract][Full Text] [Related]  

  • 39. FOXRED1 silencing in mice: a possible animal model for Leigh syndrome.
    Salama M; El-Desouky S; Alsayed A; El-Hussiny M; Moustafa A; Taalab Y; Mohamed W
    Metab Brain Dis; 2019 Feb; 34(1):367-372. PubMed ID: 30392038
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Sudden death in Leigh syndrome: an autopsy case.
    Ventura F; Rocca G; Gentile R; De Stefano F
    Am J Forensic Med Pathol; 2012 Sep; 33(3):259-61. PubMed ID: 22441409
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.