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45. The effect of nitisinone on homogentisic acid and tyrosine: a two-year survey of patients attending the National Alkaptonuria Centre, Liverpool. Milan AM; Hughes AT; Davison AS; Devine J; Usher J; Curtis S; Khedr M; Gallagher JA; Ranganath LR Ann Clin Biochem; 2017 May; 54(3):323-330. PubMed ID: 28081634 [TBL] [Abstract][Full Text] [Related]
46. Alkaptonuria is a novel human secondary amyloidogenic disease. Millucci L; Spreafico A; Tinti L; Braconi D; Ghezzi L; Paccagnini E; Bernardini G; Amato L; Laschi M; Selvi E; Galeazzi M; Mannoni A; Benucci M; Lupetti P; Chellini F; Orlandini M; Santucci A Biochim Biophys Acta; 2012 Nov; 1822(11):1682-91. PubMed ID: 22850426 [TBL] [Abstract][Full Text] [Related]
47. Alkaptonuria presenting with ochronotic spondyloarthropathy. Al-Mahfoudh R; Clark S; Buxton N Br J Neurosurg; 2008 Dec; 22(6):805-7. PubMed ID: 19085367 [TBL] [Abstract][Full Text] [Related]
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51. The Dark Side of the Heart: Cardiovascular Manifestation of Ochronosis. Planinc M; Unic D; Baric D; Blazekovic R; Sribar A; Sutlic Z; Rudez I Ann Thorac Surg; 2019 Oct; 108(4):e257-e259. PubMed ID: 30926473 [TBL] [Abstract][Full Text] [Related]
52. Conditional targeting in mice reveals that hepatic homogentisate 1,2-dioxygenase activity is essential in reducing circulating homogentisic acid and for effective therapy in the genetic disease alkaptonuria. Hughes JH; Liu K; Plagge A; Wilson PJM; Sutherland H; Norman BP; Hughes AT; Keenan CM; Milan AM; Sakai T; Ranganath LR; Gallagher JA; Bou-Gharios G Hum Mol Genet; 2019 Dec; 28(23):3928-3939. PubMed ID: 31600782 [TBL] [Abstract][Full Text] [Related]
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56. [Alkaptonuria. A brief outline of present-day knowledge of the biochemical aspects of the metabolic defect and pathogenesis of the disease (author's transl)]. Koska L; Srsen S Cas Lek Cesk; 1982 Jun; 121(22):673-6. PubMed ID: 7105116 [No Abstract] [Full Text] [Related]
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