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Journal Abstract Search

125 related items for PubMed ID: 3085790

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  • 2. Thiosulphate-sulphur transferase (rhodanese) deficiency in Leber's hereditary optic atrophy.
    Cagianut B, Rhyner K, Furrier W, Schnebli HP.
    Lancet; 1981 Oct 31; 2(8253):981-2. PubMed ID: 6117741
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  • 9. Leber's optic neuropathy. New observations.
    Lopez PF, Smith JL.
    J Clin Neuroophthalmol; 1986 Sep 31; 6(3):144-52. PubMed ID: 2946720
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  • 10. The metabolomic signature of Leber's hereditary optic neuropathy reveals endoplasmic reticulum stress.
    Chao de la Barca JM, Simard G, Amati-Bonneau P, Safiedeen Z, Prunier-Mirebeau D, Chupin S, Gadras C, Tessier L, Gueguen N, Chevrollier A, Desquiret-Dumas V, Ferré M, Bris C, Kouassi Nzoughet J, Bocca C, Leruez S, Verny C, Miléa D, Bonneau D, Lenaers G, Martinez MC, Procaccio V, Reynier P.
    Brain; 2016 Nov 01; 139(11):2864-2876. PubMed ID: 27633772
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  • 15. Histochemical detection of thiosulphate sulphurtransferase (rhodanese) activity.
    Tanka D, Gátai K.
    Histochemistry; 1983 Nov 01; 77(2):285-8. PubMed ID: 6573305
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  • 16. The effect of cAMP and some sulphur compounds upon the activity of mercaptopyruvate sulphurtransferase and rhodanese in mouse liver.
    Wróbel M, Frendo J.
    Folia Biol (Krakow); 1992 Nov 01; 40(1-2):11-4. PubMed ID: 1333420
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  • 17. [The influence of smoking on thiosulphate sulphurtransferase (rhodanese) activity in mixed saliva].
    Bartelik S.
    Czas Stomatol; 1988 Jul 01; 41(7):421-3. PubMed ID: 3270418
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  • 18. Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis.
    Kellar-Wood H, Robertson N, Govan GG, Compston DA, Harding AE.
    Ann Neurol; 1994 Jul 01; 36(1):109-12. PubMed ID: 8024249
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