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 *

130 related articles for article (PubMed ID: 1447652)

  • 1. Fatal infantile liver failure associated with mitochondrial DNA depletion.
    Mazziotta MR; Ricci E; Bertini E; Dionisi Vici C; Servidei S; Burlina AB; Sabetta G; Bartuli A; Manfredi G; Silvestri G
    J Pediatr; 1992 Dec; 121(6):896-901. PubMed ID: 1447652
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Depletion of mitochondrial DNA in the liver of a patient with lactic acidemia and hypoketotic hypoglycemia.
    Maaswinkel-Mooij PD; Van den Bogert C; Scholte HR; Onkenhout W; Brederoo P; Poorthuis BJ
    J Pediatr; 1996 May; 128(5 Pt 1):679-83. PubMed ID: 8627441
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Defects of the mitochondrial respiratory chain complexes in three pediatric cases with hypotonia and cardiac involvement.
    Figarella-Branger D; Pellissier JF; Scheiner C; Wernert F; Desnuelle C
    J Neurol Sci; 1992 Mar; 108(1):105-13. PubMed ID: 1320661
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Liver failure associated with mitochondrial DNA depletion.
    Morris AA; Taanman JW; Blake J; Cooper JM; Lake BD; Malone M; Love S; Clayton PT; Leonard JV; Schapira AH
    J Hepatol; 1998 Apr; 28(4):556-63. PubMed ID: 9566823
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Early-onset fatal encephalomyopathy associated with severe mtDNA depletion.
    Paquis-Flucklinger V; Pellissier JF; Camboulives J; Chabrol B; Saunières A; Monfort MF; Giudicelli H; Desnuelle C
    Eur J Pediatr; 1995 Jul; 154(7):557-62. PubMed ID: 7556323
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mitochondrial respiratory chain defect: a new etiology for neonatal cholestasis and early liver insufficiency.
    Goncalves I; Hermans D; Chretien D; Rustin P; Munnich A; Saudubray JM; Van Hoof F; Reding R; de Ville de Goyet J; Otte JB
    J Hepatol; 1995 Sep; 23(3):290-4. PubMed ID: 8550993
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Inter- and/or intra-organ distribution of mitochondrial C3303T or A3243G mutation in mitochondrial cytopathy.
    Iwanaga R; Koga Y; Aramaki S; Kato S; Kato H
    Acta Neuropathol; 2001 Feb; 101(2):179-84. PubMed ID: 11271374
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Zidovudine-induced mitochondrial disorder with massive liver steatosis, myopathy, lactic acidosis, and mitochondrial DNA depletion.
    Chariot P; Drogou I; de Lacroix-Szmania I; Eliezer-Vanerot MC; Chazaud B; Lombès A; Schaeffer A; Zafrani ES
    J Hepatol; 1999 Jan; 30(1):156-60. PubMed ID: 9927163
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Depletion of mitochondrial DNA in the liver of an infant with neonatal giant cell hepatitis.
    Müller-Höcker J; Muntau A; Schäfer S; Jaksch M; Staudt F; Pongratz D; Taanman JW
    Hum Pathol; 2002 Feb; 33(2):247-53. PubMed ID: 11957153
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mitochondrial DNA depletion in children.
    Tsao CY; Mendell JR; Luquette M; Dixon B; Morrow G
    J Child Neurol; 2000 Dec; 15(12):822-4. PubMed ID: 11198501
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Abnormal fatty acid metabolism in spinal muscular atrophy may predispose to perioperative risks.
    Zolkipli Z; Sherlock M; Biggar WD; Taylor G; Hutchison JS; Peliowski A; Alman BA; Ling SC; Tein I
    Eur J Paediatr Neurol; 2012 Sep; 16(5):549-53. PubMed ID: 22264649
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hereditary mitochondrial hypertrophic cardiomyopathy with mitochondrial myopathy of skeletal muscle, congenital cataract and lactic acidosis.
    van Ekeren GJ; Stadhouders AM; Egberink GJ; Sengers RC; Daniëls O; Kubat K
    Virchows Arch A Pathol Anat Histopathol; 1987; 412(1):47-52. PubMed ID: 3120403
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Deficiency of the reduced nicotinamide adenine dinucleotide dehydrogenase component of complex I of mitochondrial electron transport. Fatal infantile lactic acidosis and hypermetabolism with skeletal-cardiac myopathy and encephalopathy.
    Hoppel CL; Kerr DS; Dahms B; Roessmann U
    J Clin Invest; 1987 Jul; 80(1):71-7. PubMed ID: 3110216
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Liver failure in mitochondrial DNA depletion syndrome: the importance of serial neuroimaging in liver transplantation evaluation.
    deBruyn JC; Chan AK; Bhargava R; Idikio H; Huynh HQ
    J Pediatr Gastroenterol Nutr; 2007 Aug; 45(2):252-6. PubMed ID: 17667724
    [No Abstract]   [Full Text] [Related]  

  • 15. Mitochondrial DNA polymerase gamma deficiency and mtDNA depletion in a child with Alpers' syndrome.
    Naviaux RK; Nyhan WL; Barshop BA; Poulton J; Markusic D; Karpinski NC; Haas RH
    Ann Neurol; 1999 Jan; 45(1):54-8. PubMed ID: 9894877
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblasts.
    Procaccio V; Mousson B; Beugnot R; Duborjal H; Feillet F; Putet G; Pignot-Paintrand I; Lombès A; De Coo R; Smeets H; Lunardi J; Issartel JP
    J Clin Invest; 1999 Jul; 104(1):83-92. PubMed ID: 10393702
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Depletion of mitochondrial deoxyribonucleic acid in a family with fatal neonatal liver disease.
    Bakker HD; Scholte HR; Dingemans KP; Spelbrink JN; Wijburg FA; Van den Bogert C
    J Pediatr; 1996 May; 128(5 Pt 1):683-7. PubMed ID: 8627442
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical, biochemical and morphological features of hepatocerebral syndrome with mitochondrial DNA depletion due to deoxyguanosine kinase deficiency.
    Labarthe F; Dobbelaere D; Devisme L; De Muret A; Jardel C; Taanman JW; Gottrand F; Lombès A
    J Hepatol; 2005 Aug; 43(2):333-41. PubMed ID: 15964659
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mitochondrial cytochrome deficiency presenting as a myopathy with hypotonia, external ophthalmoplegia, and lactic acidosis in an infant and as fatal hepatopathy in a second cousin.
    Boustany RN; Aprille JR; Halperin J; Levy H; DeLong GR
    Ann Neurol; 1983 Oct; 14(4):462-70. PubMed ID: 6314875
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mitochondrial dysfunction in liver failure requiring transplantation.
    Lane M; Boczonadi V; Bachtari S; Gomez-Duran A; Langer T; Griffiths A; Kleinle S; Dineiger C; Abicht A; Holinski-Feder E; Schara U; Gerner P; Horvath R
    J Inherit Metab Dis; 2016 May; 39(3):427-436. PubMed ID: 27053192
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.