BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

197 related articles for article (PubMed ID: 38505790)

  • 21. Phenotype, genotype, and outcome of 25 Palestinian patients with hereditary tyrosinemia type 1.
    Dweikat I; Qawasmi N; Najeeb A; Radwan M
    Metabol Open; 2021 Mar; 9():100083. PubMed ID: 33598652
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Effect of nitisinone (NTBC) treatment on the clinical course of hepatorenal tyrosinemia in Québec.
    Larochelle J; Alvarez F; Bussières JF; Chevalier I; Dallaire L; Dubois J; Faucher F; Fenyves D; Goodyer P; Grenier A; Holme E; Laframboise R; Lambert M; Lindstedt S; Maranda B; Melançon S; Merouani A; Mitchell J; Parizeault G; Pelletier L; Phan V; Rinaldo P; Scott CR; Scriver C; Mitchell GA
    Mol Genet Metab; 2012 Sep; 107(1-2):49-54. PubMed ID: 22885033
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Fumarylacetoacetate Hydrolase Knock-out Rabbit Model for Hereditary Tyrosinemia Type 1.
    Li L; Zhang Q; Yang H; Zou Q; Lai C; Jiang F; Zhao P; Luo Z; Yang J; Chen Q; Wang Y; Newsome PN; Frampton J; Maxwell PH; Li W; Chen S; Wang D; Siu TS; Tam S; Tse HF; Qin B; Bao X; Esteban MA; Lai L
    J Biol Chem; 2017 Mar; 292(11):4755-4763. PubMed ID: 28053091
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Hereditary tyrosinemia type Ⅰ: newborn screening, diagnosis and treatment.
    Tang Y; Kong Y
    Zhejiang Da Xue Xue Bao Yi Xue Ban; 2021 Aug; 50(4):514-523. PubMed ID: 34704422
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Clinical and genetic characteristics of two patients with tyrosinemia type 1 in Slovenia - A novel fumarylacetoacetate hydrolase (
    Sikonja J; Brecelj J; Zerjav Tansek M; Repic Lampret B; Drole Torkar A; Klemencic S; Lipovec N; Stefanova Kralj V; Bertok S; Kovac J; Faganel Kotnik B; Tesarova M; Remec ZI; Debeljak M; Battelino T; Groselj U
    Mol Genet Metab Rep; 2022 Mar; 30():100836. PubMed ID: 35242570
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Evolution of tyrosinemia type 1 disease in patients treated with nitisinone in Spain.
    Couce ML; Sánchez-Pintos P; Aldámiz-Echevarría L; Vitoria I; Navas V; Martín-Hernández E; García-Volpe C; Pintos G; Peña-Quintana L; Hernández T; Gil D; Sánchez-Valverde F; Bueno M; Roca I; López-Ruzafa E; Díaz-Fernández C
    Medicine (Baltimore); 2019 Sep; 98(39):e17303. PubMed ID: 31574857
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Hepatocellular carcinoma requiring liver transplantation in hereditary tyrosinemia type 1 despite nitisinone therapy and α1-fetoprotein normalization.
    Bhushan S; Noble C; Balouch F; Lewindon P; Lampe G; Hodgkinson P; McGill J; Ee L
    Pediatr Transplant; 2022 Nov; 26(7):e14334. PubMed ID: 35698261
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Hepatic stress in hereditary tyrosinemia type 1 (HT1) activates the AKT survival pathway in the fah-/- knockout mice model.
    Orejuela D; Jorquera R; Bergeron A; Finegold MJ; Tanguay RM
    J Hepatol; 2008 Feb; 48(2):308-17. PubMed ID: 18093685
    [TBL] [Abstract][Full Text] [Related]  

  • 29. HCC prevalence and histopathological findings in liver explants of patients with hereditary tyrosinemia type 1.
    Seda Neto J; Leite KM; Porta A; Fonseca EA; Feier FH; Pugliese R; Miura IK; Chapchap P; Porta G
    Pediatr Blood Cancer; 2014 Sep; 61(9):1584-9. PubMed ID: 24852359
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Long-Term Outcomes and Practical Considerations in the Pharmacological Management of Tyrosinemia Type 1.
    van Ginkel WG; Rodenburg IL; Harding CO; Hollak CEM; Heiner-Fokkema MR; van Spronsen FJ
    Paediatr Drugs; 2019 Dec; 21(6):413-426. PubMed ID: 31667718
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Cross-sectional study of 168 patients with hepatorenal tyrosinaemia and implications for clinical practice.
    Mayorandan S; Meyer U; Gokcay G; Segarra NG; de Baulny HO; van Spronsen F; Zeman J; de Laet C; Spiekerkoetter U; Thimm E; Maiorana A; Dionisi-Vici C; Moeslinger D; Brunner-Krainz M; Lotz-Havla AS; Cocho de Juan JA; Couce Pico ML; Santer R; Scholl-Bürgi S; Mandel H; Bliksrud YT; Freisinger P; Aldamiz-Echevarria LJ; Hochuli M; Gautschi M; Endig J; Jordan J; McKiernan P; Ernst S; Morlot S; Vogel A; Sander J; Das AM
    Orphanet J Rare Dis; 2014 Aug; 9():107. PubMed ID: 25081276
    [TBL] [Abstract][Full Text] [Related]  

  • 32. NTBC Treatment Monitoring in Chilean Patients with Tyrosinemia Type 1 and Its Association with Biochemical Parameters and Liver Biomarkers.
    Fuenzalida K; Leal-Witt MJ; Guerrero P; Hamilton V; Salazar MF; Peñaloza F; Arias C; Cornejo V
    J Clin Med; 2021 Dec; 10(24):. PubMed ID: 34945128
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Liver Cancer in Tyrosinemia Type 1.
    van Ginkel WG; Pennings JP; van Spronsen FJ
    Adv Exp Med Biol; 2017; 959():101-109. PubMed ID: 28755188
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Hypersuccinylacetonaemia and normal liver function in maleylacetoacetate isomerase deficiency.
    Yang H; Al-Hertani W; Cyr D; Laframboise R; Parizeault G; Wang SP; Rossignol F; Berthier MT; Giguère Y; Waters PJ; Mitchell GA;
    J Med Genet; 2017 Apr; 54(4):241-247. PubMed ID: 27876694
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Curative Ex Vivo Hepatocyte-Directed Gene Editing in a Mouse Model of Hereditary Tyrosinemia Type 1.
    VanLith C; Guthman R; Nicolas CT; Allen K; Du Z; Joo DJ; Nyberg SL; Lillegard JB; Hickey RD
    Hum Gene Ther; 2018 Nov; 29(11):1315-1326. PubMed ID: 29764210
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Evaluation of dichloroacetate treatment in a murine model of hereditary tyrosinemia type 1.
    Langlois C; Jorquera R; Finegold M; Shroads AL; Stacpoole PW; Tanguay RM
    Biochem Pharmacol; 2006 May; 71(11):1648-61. PubMed ID: 16581029
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Biochemical and Clinical Aspects of Hereditary Tyrosinemia Type 1.
    Morrow G; Tanguay RM
    Adv Exp Med Biol; 2017; 959():9-21. PubMed ID: 28755181
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Hereditary tyrosinemia type 1 in Turkey: twenty year single-center experience.
    Zeybek AC; Kiykim E; Soyucen E; Cansever S; Altay S; Zubarioglu T; Erkan T; Aydin A
    Pediatr Int; 2015 Apr; 57(2):281-9. PubMed ID: 25223216
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Chronic Phenotype Characterization of a Large-Animal Model of Hereditary Tyrosinemia Type 1.
    Elgilani F; Mao SA; Glorioso JM; Yin M; Iankov ID; Singh A; Amiot B; Rinaldo P; Marler RJ; Ehman RL; Grompe M; Lillegard JB; Hickey RD; Nyberg SL
    Am J Pathol; 2017 Jan; 187(1):33-41. PubMed ID: 27855279
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Pharmacological rescue of the 14CoS/14CoS mouse: hepatocyte apoptosis is likely caused by endogenous oxidative stress.
    Dieter MZ; Freshwater SL; Miller ML; Shertzer HG; Dalton TP; Nebert DW
    Free Radic Biol Med; 2003 Aug; 35(4):351-67. PubMed ID: 12899938
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.