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 *

177 related articles for article (PubMed ID: 8026131)

  • 61. Renal complications in a patient with A-to-G mutation of mitochondrial DNA at the 3243 position of leucine tRNA.
    Hirano M; Konishi K; Arata N; Iyori M; Saruta T; Kuramochi S; Akizuki M
    Intern Med; 2002 Feb; 41(2):113-8. PubMed ID: 11868597
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Congenital encephalomyopathy and adult-onset myopathy and diabetes mellitus: different phenotypic associations of a new heteroplasmic mtDNA tRNA glutamic acid mutation.
    Hanna MG; Nelson I; Sweeney MG; Cooper JM; Watkins PJ; Morgan-Hughes JA; Harding AE
    Am J Hum Genet; 1995 May; 56(5):1026-33. PubMed ID: 7726155
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Multiple deletions of the mitochondrial DNA in polymyalgia rheumatica.
    Reynier P; Pellissier JF; Harle JR; Malthiéry Y
    Biochem Biophys Res Commun; 1994 Nov; 205(1):375-80. PubMed ID: 7999051
    [TBL] [Abstract][Full Text] [Related]  

  • 64. [Myoclonus epilepsy associated with ragged-red fibers--report of a patient with negative myoclonus].
    Iwanga K; Mori K; Inoue M; Yoshimura T; Tanno Y
    Rinsho Shinkeigaku; 1992 Aug; 32(8):870-3. PubMed ID: 1490314
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Familial mitochondrial encephalomyopathy with deaf-mutism, ophthalmoplegia and leukodystrophy.
    Nakagawa M; Kaminishi Y; Isashiki Y; Yamada H; Higuchi I; Uchida Y; Osame M
    Acta Neurol Scand; 1995 Jul; 92(1):102-8. PubMed ID: 7572054
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Mitochondrial encephalomyopathy with 15915 mutation: clinical report.
    Seki A; Nishino I; Goto Y; Maegaki Y; Koeda T
    Pediatr Neurol; 1997 Sep; 17(2):161-4. PubMed ID: 9367299
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Diabetes mellitus associated with 3243 mitochondrial tRNA(Leu(UUR)) mutation: clinical features and coenzyme Q10 treatment.
    Suzuki Y; Taniyama M; Muramatsu T; Atsumi Y; Hosokawa K; Asahina T; Shimada A; Murata C; Matsuoka K
    Mol Aspects Med; 1997; 18 Suppl():S181-8. PubMed ID: 9266520
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Coexistence of mitochondrial and nuclear DNA mutations in a woman with mitochondrial encephalomyopathy and double cortex.
    Scuderi C; Borgione E; Castello F; Lo Giudice M; Fichera M; Elia M; Amato C; Savio M; Di Blasi FD; Vitello GA; Romano S; DiMauro S; Musumeci SA
    Mitochondrion; 2010 Aug; 10(5):548-54. PubMed ID: 20433951
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Presence of mitochondrial tRNA(Leu(UUR)) A to G 3243 mutation in DNA extracted from serum and plasma of patients with type 2 diabetes mellitus.
    Zhong S; Ng MC; Lo YM; Chan JC; Johnson PJ
    J Clin Pathol; 2000 Jun; 53(6):466-9. PubMed ID: 10911806
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Clinical and cellular consequences of the mutation m.12300G>A in the mitochondrial tRNA(Leu(CUN)) gene.
    Martín-Jiménez R; Martín-Hernández E; Cabello A; García-Silva MT; Arenas J; Campos Y
    Mitochondrion; 2012 Mar; 12(2):288-93. PubMed ID: 22094595
    [TBL] [Abstract][Full Text] [Related]  

  • 71. [Neuroleptanesthesia for a patient with mitochondrial encephalomyopathy].
    Matsuno S; Hashimoto H; Matsuki A
    Masui; 1994 Jul; 43(7):1038-40. PubMed ID: 7933472
    [TBL] [Abstract][Full Text] [Related]  

  • 72. [A case of mitochondrial cardiomyopathy with heart failure, sick sinus syndrome and diabetes mellitus: mitochondrial DNA adenine-to-guanine transition at 3243 of mitochondrial tRNA(LEU)(UUR) gene].
    Inamori M; Ishigami T; Takahashi N; Hibi K; Ashino K; Sumita S; Tamura K; Ochiai H; Umemura S; Ishii M; Tanaka S; Sekihara H; Inayama Y
    J Cardiol; 1997 Dec; 30(6):341-7. PubMed ID: 9436076
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Japanese case of diabetes mellitus and deafness with mutation in mitochondrial tRNA(Leu(UUR)) gene.
    Awata T; Matsumoto T; Iwamoto Y; Matsuda A; Kuzuya T; Saito T
    Lancet; 1993 May; 341(8855):1291-2. PubMed ID: 8098444
    [No Abstract]   [Full Text] [Related]  

  • 74. A new mitochondrial DNA mutation associated with progressive dementia and chorea: a clinical, pathological, and molecular genetic study.
    Nelson I; Hanna MG; Alsanjari N; Scaravilli F; Morgan-Hughes JA; Harding AE
    Ann Neurol; 1995 Mar; 37(3):400-3. PubMed ID: 7695240
    [TBL] [Abstract][Full Text] [Related]  

  • 75. A new mtDNA mutation associated with a progressive encephalopathy and cytochrome c oxidase deficiency.
    Silvestri G; Mongini T; Odoardi F; Modoni A; deRosa G; Doriguzzi C; Palmucci L; Tonali P; Servidei S
    Neurology; 2000 Apr; 54(8):1693-6. PubMed ID: 10762520
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Mitochondrial DNA [tRNA(Leu)(UUR)] mutation in a southern Italian diabetic population.
    Rigoli L; Di Benedetto A; Romano G; Corica F; Cucinotta D
    Diabetes Care; 1997 Apr; 20(4):674-5. PubMed ID: 9097002
    [No Abstract]   [Full Text] [Related]  

  • 77. Mitochondrial encephalomyopathy: towards diagnosis. A case report.
    Gaweł M; Kierdaszuk B; Tońska K; Kaliszewska M; Kubiszewska J; Jamrozik Z; Bartnik E; Kwieciński H; Kamińska AM
    Neurol Neurochir Pol; 2014; 48(1):76-80. PubMed ID: 24636775
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Mitochondrial encephalomyopathy associated with diabetes mellitus, cataract, and corpus callosum atrophy.
    Oishi M; Miki K; Morita A; Fujioka K; Aoki S; Nishino I; Nonaka I; Goto Y; Mizutani T
    Intern Med; 2008; 47(5):441-4. PubMed ID: 18310979
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Maternally inherited mitochondrial cardiomyopathy associated with a C-to-T transition at nucleotide 3303 of mitochondrial DNA in the tRNA(Leu(UUR)) gene.
    Goldstein JD; Shanske S; Bruno C; Perszyk AA
    Pediatr Dev Pathol; 1999; 2(1):78-85. PubMed ID: 9841711
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Mitochondrial myopathy with predominant respiratory dysfunction in a patient with A3243G mutation in the mitochondrial tRNA(Leu(UUR))gene.
    Yang CC; Hwang CC; Pang CY; Wei YH
    J Formos Med Assoc; 1998 Oct; 97(10):715-9. PubMed ID: 9830283
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.