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Journal Abstract Search

128 related items for PubMed ID: 7993661

  • 41.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 42. Mitochondrial myopathy with progressive decrease in mitochondrial tRNA(Leu)(UUR) mutant genomes.
    Kawakami Y, Sakuta R, Hashimoto K, Fujino O, Fujita T, Hida M, Horai S, Goto Y, Nonaka I.
    Ann Neurol; 1994 Mar; 35(3):370-3. PubMed ID: 8122892
    [Abstract] [Full Text] [Related]

  • 43. Leigh syndrome and hypertrophic cardiomyopathy in an infant with a mitochondrial DNA point mutation (T8993G).
    Pastores GM, Santorelli FM, Shanske S, Gelb BD, Fyfe B, Wolfe D, Willner JP.
    Am J Med Genet; 1994 Apr 15; 50(3):265-71. PubMed ID: 8042671
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  • 44.
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  • 45. The phenotypic spectrum of fifty Czech m.3243A>G carriers.
    Dvorakova V, Kolarova H, Magner M, Tesarova M, Hansikova H, Zeman J, Honzik T.
    Mol Genet Metab; 2016 Aug 15; 118(4):288-95. PubMed ID: 27296531
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  • 46.
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  • 47. Familial recurrence of atypical symptoms in an extended pedigree with the syndrome of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Dougherty FE, Ernst SG, Aprille JR.
    J Pediatr; 1994 Nov 15; 125(5 Pt 1):758-61. PubMed ID: 7965431
    [Abstract] [Full Text] [Related]

  • 48. Heterogeneous presentation in A3243G mutation in the mitochondrial tRNA(Leu(UUR)) gene.
    Koga Y, Akita Y, Takane N, Sato Y, Kato H.
    Arch Dis Child; 2000 May 15; 82(5):407-11. PubMed ID: 10799437
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  • 49.
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  • 50. Mitochondrial angiopathy in a family with MELAS.
    Förster C, Hübner G, Müller-Höcker J, Pongratz D, Baierl P, Senger R, Ruitenbeek W.
    Neuropediatrics; 1992 Jun 15; 23(3):165-8. PubMed ID: 1322508
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  • 51.
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  • 52. Severe lactic acidosis secondary to minocycline in a teenager with infectious mononucleosis and mitochondrial myopathy.
    Zoraster RM, Rison RA.
    Clin Neurol Neurosurg; 2008 Jun 15; 110(6):627-30. PubMed ID: 18440128
    [Abstract] [Full Text] [Related]

  • 53. MELAS syndrome involving a mother and two children.
    Driscoll PF, Larsen PD, Gruber AB.
    Arch Neurol; 1987 Sep 15; 44(9):971-3. PubMed ID: 3619716
    [Abstract] [Full Text] [Related]

  • 54. Mitochondrial diseases.
    Nonaka I.
    Curr Opin Neurol Neurosurg; 1992 Oct 15; 5(5):622-32. PubMed ID: 1392136
    [Abstract] [Full Text] [Related]

  • 55. Prenatal diagnosis of myopathy, encephalopathy, lactic acidosis, and stroke-like syndrome: contribution to understanding mitochondrial DNA segregation during human embryofetal development.
    Bouchet C, Steffann J, Corcos J, Monnot S, Paquis V, Rötig A, Lebon S, Levy P, Royer G, Giurgea I, Gigarel N, Benachi A, Dumez Y, Munnich A, Bonnefont JP.
    J Med Genet; 2006 Oct 15; 43(10):788-92. PubMed ID: 16690729
    [Abstract] [Full Text] [Related]

  • 56.
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  • 57. Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes: basic concepts, clinical phenotype, and therapeutic management of MELAS syndrome.
    Sproule DM, Kaufmann P.
    Ann N Y Acad Sci; 2008 Oct 15; 1142():133-58. PubMed ID: 18990125
    [Abstract] [Full Text] [Related]

  • 58. Α rare case of myopathy, lactic acidosis, and severe rhabdomyolysis, due to a homozygous mutation of the ferredoxin-2 (FDX2) gene.
    Gkiourtzis N, Tramma D, Papadopoulou-Legbelou K, Moutafi M, Evangeliou A.
    Am J Med Genet A; 2023 Dec 15; 191(12):2843-2849. PubMed ID: 37565517
    [Abstract] [Full Text] [Related]

  • 59. [Mitochondrial encephalopathy, lactic acidosis and stroke-like episodes / myoclonus epilepsy with ragged-red fibers /Leigh overlap syndrome caused by mitochondrial DNA 8344A>G mutation].
    Hou Y, Zhao XT, Xie ZY, Yuan Y, Wang ZX.
    Beijing Da Xue Xue Bao Yi Xue Ban; 2020 Oct 18; 52(5):851-855. PubMed ID: 33047718
    [Abstract] [Full Text] [Related]

  • 60.
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