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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

215 related articles for article (PubMed ID: 11419842)

  • 21. Hereditary systemic amyloidosis with renal involvement.
    Hawkins PN
    J Nephrol; 2003; 16(3):443-8. PubMed ID: 12832750
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Hereditary nephropathic systemic amyloidosis caused by a novel variant apolipoprotein A-I.
    Persey MR; Booth DR; Booth SE; van Zyl-Smit R; Adams BK; Fattaar AB; Tennent GA; Hawkins PN; Pepys MB
    Kidney Int; 1998 Feb; 53(2):276-81. PubMed ID: 9461086
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The neuromuscular manifestations of amyloidosis.
    Simmons Z; Specht CS
    J Clin Neuromuscul Dis; 2010 Mar; 11(3):145-57. PubMed ID: 20215989
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Primary systemic amyloidosis with giant hepatomegaly and portal hypertension: a case report and a review of the literature.
    Serra L; Poppi MC; Criscuolo M; Zandomeneghi R
    Ital J Gastroenterol; 1993 Oct; 25(8):435-8. PubMed ID: 8286779
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A novel apolipoprotein A-1 variant, Arg173Pro, associated with cardiac and cutaneous amyloidosis.
    Hamidi Asl K; Liepnieks JJ; Nakamura M; Parker F; Benson MD
    Biochem Biophys Res Commun; 1999 Apr; 257(2):584-8. PubMed ID: 10198255
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Low plasma apolipoprotein AII levels in human and mouse amyloidosis with mutant transthyretin (Met-30) gene.
    Ando Y; Tanaka Y; Ueyama H; Sakashita N; Yonehara T; Higuchi K; Araki S
    Ann Neurol; 1993 Jan; 33(1):101-3. PubMed ID: 8494327
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Liver biopsy discloses a new apolipoprotein A-I hereditary amyloidosis in several unrelated Italian families.
    Obici L; Palladini G; Giorgetti S; Bellotti V; Gregorini G; Arbustini E; Verga L; Marciano S; Donadei S; Perfetti V; Calabresi L; Bergonzi C; Scolari F; Merlini G
    Gastroenterology; 2004 May; 126(5):1416-22. PubMed ID: 15131802
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Familial amyloidosis in a large Spanish kindred resulting from a D38V mutation in the transthyretin gene.
    Augustin S; Llige D; Andreu A; González A; Genescà J
    Eur J Clin Invest; 2007 Aug; 37(8):673-8. PubMed ID: 17635579
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Renal involvement in systemic amyloidosis--an Italian retrospective study on epidemiological and clinical data at diagnosis.
    Bergesio F; Ciciani AM; Santostefano M; Brugnano R; Manganaro M; Palladini G; Di Palma AM; Gallo M; Tosi PL; Salvadori M;
    Nephrol Dial Transplant; 2007 Jun; 22(6):1608-18. PubMed ID: 17395661
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Two novel APOA1 gene mutations in a Japanese renal transplant recipient with recurrent apolipoprotein A-I related amyloidosis.
    Horike K; Takeda A; Tsujita M; Goto N; Watarai Y; Uchida K; Katayama A; Nishihira M; Shimizu A; Nozu K; Morozumi K
    Nephrology (Carlton); 2018 Jul; 23 Suppl 2():17-21. PubMed ID: 29968409
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Renal involvement in systemic amyloidosis: an Italian collaborative study on survival and renal outcome.
    Bergesio F; Ciciani AM; Manganaro M; Palladini G; Santostefano M; Brugnano R; Di Palma AM; Gallo M; Rosati A; Tosi PL; Salvadori M;
    Nephrol Dial Transplant; 2008 Mar; 23(3):941-51. PubMed ID: 17951308
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Hereditary apolipoprotein AI-associated renal amyloidosis: A diagnostic challenge.
    Samillán-Sosa Kdel R; Sención-Martínez G; Lopes-Martín V; Martínez-González MA; Solé M; Arostegui JL; Mesa J; García-Díaz Jde D; Rodríguez-Puyol D; Martínez-Miguel P
    Nefrologia; 2015; 35(3):322-7. PubMed ID: 26299174
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Clinical manifestation and patho-typing of biliary cast syndrome in patients after orthotopic liver transplantation].
    Zhu XD; Shen ZY; Chen XG; Zang YJ
    Zhonghua Wai Ke Za Zhi; 2008 May; 46(10):728-32. PubMed ID: 18953924
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Infertility and hypergonadotropic hypogonadism as first evidence of hereditary apolipoprotein A-I amyloidosis.
    Scalvini T; Martini PR; Obici L; Tardanico R; Biasi L; Gregorini G; Scolari F; Merlini G
    J Urol; 2007 Jul; 178(1):344-8. PubMed ID: 17507040
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Hepatic amyloidosis: clinical appraisal in 77 patients.
    Gertz MA; Kyle RA
    Hepatology; 1997 Jan; 25(1):118-21. PubMed ID: 8985276
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Difficulties in the diagnosis of hereditary familial amyloidosis].
    Anokhin IM; Taranova MV; Proskurneva EP; Kozlovskaia LV; Onoprienlo NN
    Ter Arkh; 1995; 67(12):56-7. PubMed ID: 8820061
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Outcome of liver transplantation for familial amyloidotic polyneuropathy.
    Sharma P; Perri RE; Sirven JE; Zeldenrust SR; Brandhagen DJ; Rosen CB; Douglas DD; Mulligan DC; Rakela J; Wiesner RH; Balan V
    Liver Transpl; 2003 Dec; 9(12):1273-80. PubMed ID: 14625827
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Cutis laxa in hereditary gelsolin amyloidosis.
    Kiuru-Enari S; Keski-Oja J; Haltia M
    Br J Dermatol; 2005 Feb; 152(2):250-7. PubMed ID: 15727635
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Familial disseminated amylosis with cutaneous and cardiac predominance by apolipoprotein A1 mutation].
    Moulin G
    Ann Dermatol Venereol; 2000; 127(8-9):748. PubMed ID: 11011171
    [No Abstract]   [Full Text] [Related]  

  • 40. [Hepatic amyloidosis as cause of severe intrahepatic cholestasis].
    Gavilán JC; Bermúdez FJ; Márquez A; Sánchez-Carrillo JJ; González-Santos P
    An Med Interna; 2003 Jan; 20(1):25-7. PubMed ID: 12666305
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.