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 *

122 related articles for article (PubMed ID: 10641610)

  • 1. Neurologic presentations of mitochondrial disorders.
    Nissenkorn A; Zeharia A; Lev D; Watemberg N; Fattal-Valevski A; Barash V; Gutman A; Harel S; Lerman-Sagie T
    J Child Neurol; 2000 Jan; 15(1):44-8. PubMed ID: 10641610
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Mitochondrial myopathy and mitochondrial encephalomyopathy].
    Song D; Liu C; Lu Q; Shi J; Chen J; Zhang H; Zhang Y; Wang H; Zhang W; Li G
    Zhonghua Yi Xue Za Zhi; 2002 Feb; 82(3):158-60. PubMed ID: 11953149
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 74th ENMC international workshop: mitochondrial diseases 19-20 november 1999, Naarden, the netherlands.
    Poulton J; Turnbull DM
    Neuromuscul Disord; 2000 Aug; 10(6):460-2. PubMed ID: 10899455
    [No Abstract]   [Full Text] [Related]  

  • 4. Multiple presentation of mitochondrial disorders.
    Nissenkorn A; Zeharia A; Lev D; Fatal-Valevski A; Barash V; Gutman A; Harel S; Lerman-Sagie T
    Arch Dis Child; 1999 Sep; 81(3):209-14. PubMed ID: 10451392
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mitochondrial respiratory-chain defects presenting as nonspecific features in children.
    Tsao CY; Mendell JR; Lo WD; Luquette M; Rusin J
    J Child Neurol; 2000 Jul; 15(7):445-8. PubMed ID: 10921514
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Rapid and noninvasive screening of patients with mitochondrial myopathy.
    Kotsimbos N; Jean-Francois MJ; Huizing M; Kapsa RM; Lertrit P; Siregar NC; Marzuki S; Sue C; Byrne E
    Hum Mutat; 1994; 4(2):132-5. PubMed ID: 7981717
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Clinical and investigative approaches in mitochondrial diseases. A review of 15 cases].
    Arpa J; Campos Y; Cruz Martínez A; Gutiérrez Molina M; Arenas J; Alonso M; Plaza I; Morales C; Palomo F; Barreiro P
    Neurologia; 1994 Oct; 9(8):324-36. PubMed ID: 7803049
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Diagnosis and therapy of mitochondriopathies].
    Sperl W
    Wien Klin Wochenschr; 1997 Feb; 109(3):93-9. PubMed ID: 9139466
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Long-term outcome and clinical spectrum of 73 pediatric patients with mitochondrial diseases.
    Debray FG; Lambert M; Chevalier I; Robitaille Y; Decarie JC; Shoubridge EA; Robinson BH; Mitchell GA
    Pediatrics; 2007 Apr; 119(4):722-33. PubMed ID: 17403843
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Neurological mitochondrial cytopathies.
    Mehndiratta MM; Agarwal P; Tatke M; Krishnamurthy M
    Neurol India; 2002 Jun; 50(2):162-7. PubMed ID: 12134180
    [TBL] [Abstract][Full Text] [Related]  

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

  • 12. Clinical manifestation of mitochondrial diseases.
    Magner M; Kolářová H; Honzik T; Švandová I; Zeman J
    Dev Period Med; 2015; 19(4):441-9. PubMed ID: 26982751
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mitochondrial diseases.
    Nonaka I
    Curr Opin Neurol Neurosurg; 1992 Oct; 5(5):622-32. PubMed ID: 1392136
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Update in molecular genetics: mitochondrial energy transduction disorders.
    Marzuki S; Sudoyo H; Lertrit P
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():155-61. PubMed ID: 8629096
    [No Abstract]   [Full Text] [Related]  

  • 15. MERRF/MELAS overlap syndrome in a family with A3243G mtDNA mutation.
    Mongini T; Doriguzzi C; Chiadò-Piat L; Silvestri G; Servidei S; Palmucci L
    Clin Neuropathol; 2002; 21(2):72-6. PubMed ID: 12005255
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Therapy of metabolic myopathies].
    Reichmann H
    Nervenarzt; 1993 Oct; 64(10):627-32. PubMed ID: 8232675
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Maternal inheritance and the evaluation of oxidative phosphorylation diseases.
    Shoffner JM
    Lancet; 1996 Nov; 348(9037):1283-8. PubMed ID: 8909383
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Neurologic course of congenital disorders of glycosylation.
    Pearl PL; Krasnewich D
    J Child Neurol; 2001 Jun; 16(6):409-13. PubMed ID: 11417605
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Neuromuscular and systemic presentations in adults: diagnoses beyond MERRF and MELAS.
    Cohen BH
    Neurotherapeutics; 2013 Apr; 10(2):227-42. PubMed ID: 23549648
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Mitochondrial myopathy, deafness and type 2 diabetes mellitus with tRNALeu(UUR) point mutation in mitochondrial DNA].
    Stratilová L; Zeman J; Hansíková H; Houstĕk J; Hermanská J; Dudková Z; Konrádová V; Hůlková H; Elleder M
    Cas Lek Cesk; 1998 Jul; 137(14):430-3. PubMed ID: 9748738
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.