128 related articles for article (PubMed ID: 35359044)
1. [Clinicopathological features of hepatic fibrinogen storage disease in children].
Fang Y; Wang YZ; Chen L; Yin JS; Wang X; Wei SM; Li XM; Wu X
Zhonghua Bing Li Xue Za Zhi; 2022 Apr; 51(4):326-331. PubMed ID: 35359044
[No Abstract] [Full Text] [Related]
2. Fibrinogen Gamma Chain Mutations Provoke Fibrinogen and Apolipoprotein B Plasma Deficiency and Liver Storage.
Callea F; Giovannoni I; Sari S; Guldal E; Dalgic B; Akyol G; Sogo T; Al-Hussaini A; Maggiore G; Bartuli A; Boldrini R; Francalanci P; Bellacchio E
Int J Mol Sci; 2017 Dec; 18(12):. PubMed ID: 29244742
[TBL] [Abstract][Full Text] [Related]
3. Novel fibrinogen mutation γ314Thr→Pro (fibrinogen AI duPont) associated with hepatic fibrinogen storage disease and hypofibrinogenaemia.
Brennan SO; Davis RL; Conard K; Savo A; Furuya KN
Liver Int; 2010 Nov; 30(10):1541-7. PubMed ID: 20666993
[TBL] [Abstract][Full Text] [Related]
4. Fibrinogen angers with a new deletion (gamma GVYYQ 346-350) causes hypofibrinogenemia with hepatic storage.
Dib N; Quelin F; Ternisien C; Hanss M; Michalak S; De Mazancourt P; Rousselet MC; Calès P
J Thromb Haemost; 2007 Oct; 5(10):1999-2005. PubMed ID: 17883696
[TBL] [Abstract][Full Text] [Related]
5. Hepatic Fibrinogen Storage Disease in a Patient with Hypofibrinogenemia: Report of a Case with a Missense Mutation of the FGA Gene.
Lee MJ; Venick R; Bhuta S; Li X; Wang HL
Semin Liver Dis; 2015 Nov; 35(4):439-43. PubMed ID: 26676819
[TBL] [Abstract][Full Text] [Related]
6. Fibrinogen storage disease in a Chinese boy with de novo fibrinogen Aguadilla mutation: Incomplete response to carbamazepine and ursodeoxycholic acid.
Zhang MH; Knisely AS; Wang NL; Gong JY; Wang JS
BMC Gastroenterol; 2016 Aug; 16(1):92. PubMed ID: 27520927
[TBL] [Abstract][Full Text] [Related]
7. [Infant glycogen storage disease type Ⅳ: a clinicopathological and genetic characteristics analysis of five cases].
Wang QY; Wang JS; Chen L
Zhonghua Bing Li Xue Za Zhi; 2023 Dec; 52(12):1255-1260. PubMed ID: 38058043
[No Abstract] [Full Text] [Related]
8. Hypofibrinogenemia and liver disease: a new case of Aguadilla fibrinogen and review of the literature.
Casini A; Sokollik C; Lukowski SW; Lurz E; Rieubland C; de Moerloose P; Neerman-Arbez M
Haemophilia; 2015 Nov; 21(6):820-7. PubMed ID: 25990487
[TBL] [Abstract][Full Text] [Related]
9. Novel fibrinogen gamma375 Arg-->Trp mutation (fibrinogen aguadilla) causes hepatic endoplasmic reticulum storage and hypofibrinogenemia.
Brennan SO; Maghzal G; Shneider BL; Gordon R; Magid MS; George PM
Hepatology; 2002 Sep; 36(3):652-8. PubMed ID: 12198657
[TBL] [Abstract][Full Text] [Related]
10. The fibrous form of intracellular inclusion bodies in recombinant variant fibrinogen-producing cells is specific to the hepatic fibrinogen storage disease-inducible variant fibrinogen.
Arai S; Ogiwara N; Mukai S; Takezawa Y; Sugano M; Honda T; Okumura N
Int J Hematol; 2017 Jun; 105(6):758-768. PubMed ID: 28161763
[TBL] [Abstract][Full Text] [Related]
11. Fibrinogen storage disease without hypofibrinogenemia associated with estrogen therapy.
Simsek Z; Ekinci O; Cindoruk M; Karakan T; Degertekin B; Akyol G; Unal S
BMC Gastroenterol; 2005 Nov; 5():36. PubMed ID: 16287505
[TBL] [Abstract][Full Text] [Related]
12. Fibrinogen gamma375 arg-->trp mutation (fibrinogen aguadilla) causes hereditary hypofibrinogenemia, hepatic endoplasmic reticulum storage disease and cirrhosis.
Rubbia-Brandt L; Neerman-Arbez M; Rougemont AL; Malé PJ; Spahr L
Am J Surg Pathol; 2006 Jul; 30(7):906-11. PubMed ID: 16819336
[TBL] [Abstract][Full Text] [Related]
13. Rethinking fibrinogen storage disease of the liver: ground glass and globular inclusions do not represent a congenital metabolic disorder but acquired collective retention of proteins.
Zen Y; Nishigami T
Hum Pathol; 2020 Jun; 100():1-9. PubMed ID: 32330484
[TBL] [Abstract][Full Text] [Related]
14. Endoplasmic storage disease of liver: characterization of intracytoplasmic hyaline inclusions.
Ng IO; Ng M; Lai EC; Wu PC
Histopathology; 1989 Nov; 15(5):473-81. PubMed ID: 2480934
[TBL] [Abstract][Full Text] [Related]
15. Autophagy-enhancing drug carbamazepine diminishes hepatocellular death in fibrinogen storage disease.
Puls F; Goldschmidt I; Bantel H; Agne C; Bröcker V; Dämmrich M; Lehmann U; Berrang J; Pfister ED; Kreipe HH; Baumann U
J Hepatol; 2013 Sep; 59(3):626-30. PubMed ID: 23707368
[TBL] [Abstract][Full Text] [Related]
16. Hepatic fibrinogen storage disease and hypofibrinogenemia caused by fibrinogen Aguadilla mutation: a case report.
Gu L; Wang B; Liu L; Gan Q; Liu X; Chen L; Chen L
J Int Med Res; 2020 Jan; 48(1):300060519898033. PubMed ID: 31965886
[TBL] [Abstract][Full Text] [Related]
17. Hereditary Hypofibrinogenemia with Hepatic Storage.
Asselta R; Paraboschi EM; Duga S
Int J Mol Sci; 2020 Oct; 21(21):. PubMed ID: 33105716
[TBL] [Abstract][Full Text] [Related]
18. Fibrinogen storage disease without hypofibrinogenaemia associated with acute infection.
Marucci G; Morandi L; Macchia S; Betts CM; Tardio ML; Dal Monte PR; Pession A; Foschini MP
Histopathology; 2003 Jan; 42(1):22-5. PubMed ID: 12493021
[TBL] [Abstract][Full Text] [Related]
19. Pathology teach and tell: fibrinogen storage disease in a child with hypofibrinogenemia and decreased ceruloplasmin.
Bruzzi C; Bader A; Luban NL; Przygodzki R; Ahmed AA
Fetal Pediatr Pathol; 2007; 26(2):101-5. PubMed ID: 17701692
[TBL] [Abstract][Full Text] [Related]
20. Pediatric non-alcoholic steatohepatitis: the first report on the ultrastructure of hepatocyte mitochondria.
Lotowska JM; Sobaniec-Lotowska ME; Bockowska SB; Lebensztejn DM
World J Gastroenterol; 2014 Apr; 20(15):4335-40. PubMed ID: 24764670
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]