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.
25. Diagnosis of erythropoietic protoporphyria with severe liver injury: A case report. Liu HM; Deng GH; Mao Q; Wang XH World J Gastroenterol; 2019 Feb; 25(7):880-887. PubMed ID: 30809087 [TBL] [Abstract][Full Text] [Related]
34. A family with acute intermittent porphyria. Billoo AG; Lone SW J Coll Physicians Surg Pak; 2008 May; 18(5):316-8. PubMed ID: 18541093 [TBL] [Abstract][Full Text] [Related]
35. Liver transplantation for acute-on-chronic liver failure from erythropoietic protoporphyria. Park PJ; Hwang S; Choi YI; Yu YD; Park GC; Jung SW; Yoon SY; Song GW; Ha TY; Lee SG Clin Mol Hepatol; 2012 Dec; 18(4):411-5. PubMed ID: 23323258 [TBL] [Abstract][Full Text] [Related]
36. Porphyria: What Is It and Who Should Be Evaluated? Edel Y; Mamet R Rambam Maimonides Med J; 2018 Apr; 9(2):. PubMed ID: 29553924 [TBL] [Abstract][Full Text] [Related]
37. Hepatic porphyria: A narrative review. Arora S; Young S; Kodali S; Singal AK Indian J Gastroenterol; 2016 Nov; 35(6):405-418. PubMed ID: 27796941 [TBL] [Abstract][Full Text] [Related]
38. Erythropoietic protoporphyria a clinical and molecular study from Lebanon: Ferrochelatase a potential tumor suppressor gene in colon cancer. Kadara H; Nemer G; Safi R; Rebeiz N; Daou L; Delbani D; Btadini W; Abbas O; Tofaili M; Bitar F; Kibbi AG; Shimomura Y; Kurban M Clin Genet; 2017 Nov; 92(5):495-502. PubMed ID: 28075030 [TBL] [Abstract][Full Text] [Related]
39. Systemic messenger RNA as an etiological treatment for acute intermittent porphyria. Jiang L; Berraondo P; Jericó D; Guey LT; Sampedro A; Frassetto A; Benenato KE; Burke K; Santamaría E; Alegre M; Pejenaute Á; Kalariya M; Butcher W; Park JS; Zhu X; Sabnis S; Kumarasinghe ES; Salerno T; Kenney M; Lukacs CM; Ávila MA; Martini PGV; Fontanellas A Nat Med; 2018 Dec; 24(12):1899-1909. PubMed ID: 30297912 [TBL] [Abstract][Full Text] [Related]
40. Systematic analysis of molecular defects in the ferrochelatase gene from patients with erythropoietic protoporphyria. Rüfenacht UB; Gouya L; Schneider-Yin X; Puy H; Schäfer BW; Aquaron R; Nordmann Y; Minder EI; Deybach JC Am J Hum Genet; 1998 Jun; 62(6):1341-52. PubMed ID: 9585598 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]