BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

107 related articles for article (PubMed ID: 9091196)

  • 1. [Mitochondrial encephalopathies: clinical considerations].
    DiMauro S
    Rev Neurol; 1997 Jan; 25(137):126-30. PubMed ID: 9091196
    [No Abstract]   [Full Text] [Related]  

  • 2. [Mitochondrial encephalopathies: where are we going?].
    DiMauro S; Andreu AL; Bonilla E
    Rev Neurol; 1999 Jan 16-31; 28(2):164-8. PubMed ID: 10101786
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Mitochondrial encephalomyopathies starting in childhood and adolescence].
    Castro-Gago M; Novo-Rodríguez MI; Eirís-Puñal J
    Rev Neurol; 1998 Apr; 26 Suppl 1():S61-71. PubMed ID: 9810592
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [The study of point mutation of muscular mitochondrial DNA from patients with mitochondrial encephalomyopathies].
    Song D; Zhang Y; Shi J
    Zhonghua Yi Xue Za Zhi; 2001 Jun; 81(11):659-61. PubMed ID: 11798943
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Point mutations of muscle mitochondrial DNA from patients with mitochondrial encephalomyopathies.
    Song D; Zhang Y; Shi J; Lü Q; Chen J; Zhang H; Zhang W; Wang H; Cai Q
    Chin Med J (Engl); 2001 Dec; 114(12):1273-5. PubMed ID: 11793851
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Mitochondrial encephalomyopathies and mitochondrial DNA].
    Wang WY; Zhang JW
    Sheng Li Ke Xue Jin Zhan; 1997 Jan; 28(1):70-2. PubMed ID: 10921085
    [No Abstract]   [Full Text] [Related]  

  • 7. [Hypopituitarism].
    Miyake I; Hiromatsu Y
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():575-8. PubMed ID: 12013946
    [No Abstract]   [Full Text] [Related]  

  • 8. [Mitochondrial encephalopathies].
    Castro-Gago M; Novo-Rodríguez MI; Pintos-Martínez E; Campos Y; Arenas J; Eirís-Puñal J
    Rev Neurol; 2000 Aug 1-15; 31(3):263-82. PubMed ID: 10996928
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial encephalomyopathies: gene mutation.
    Neuromuscul Disord; 1997 Sep; 7(6-7):XIII-XIX. PubMed ID: 9327409
    [No Abstract]   [Full Text] [Related]  

  • 10. Mitochondrial encephalomyopathy associated with a novel mutation in the mitochondrial tRNA(leu)(UUR) gene (A3243T).
    Shaag A; Saada A; Steinberg A; Navon P; Elpeleg ON
    Biochem Biophys Res Commun; 1997 Apr; 233(3):637-9. PubMed ID: 9168904
    [TBL] [Abstract][