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 *

123 related articles for article (PubMed ID: 31343317)

  • 41. Significant reduction in proteinuria after treatment with tafamidis.
    Ferrer-Nadal A; Ripoll T; Uson M; Figuerola A; Andreu H; Losada I; Gonzalez J; Cisneros-Barroso E; Buades J
    Amyloid; 2019; 26(sup1):67-68. PubMed ID: 31343359
    [No Abstract]   [Full Text] [Related]  

  • 42. Teaching NeuroImages: Neuromyopathy in a patient with hereditary transthyretin Thr60Ala amyloidosis.
    Pinto MV; Tracy JA; Grogan M; Mauermann ML
    Neurology; 2019 Mar; 92(12):e1403-e1404. PubMed ID: 30886082
    [No Abstract]   [Full Text] [Related]  

  • 43. Systemic angiopathy and axonopathy in hereditary transthyretin amyloidosis with Ala97Gly (p. Ala117Gly) mutation: a post-mortem analysis.
    Koike H; Yasuda T; Nishi R; Ikeda S; Kawagashira Y; Iijima M; Sobue G; Katsuno M
    Amyloid; 2018 Jun; 25(2):141-142. PubMed ID: 29855203
    [No Abstract]   [Full Text] [Related]  

  • 44. Curcumin could reduce the monomer of TTR with Tyr114Cys mutation via autophagy in cell model of familial amyloid polyneuropathy.
    Li H; Zhang Y; Cao L; Xiong R; Zhang B; Wu L; Zhao Z; Chen SD
    Drug Des Devel Ther; 2014; 8():2121-8. PubMed ID: 25382970
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Myopathic phenotype of familial amyloid polyneuropathy with a rare transthyretin variant: ATTR Ala45Asp.
    Misumi Y; Doki T; Ueda M; Obayashi K; Tasaki M; Tamura A; Ando Y
    Amyloid; 2014 Sep; 21(3):216-7. PubMed ID: 24953234
    [No Abstract]   [Full Text] [Related]  

  • 46. Familial amyloid polyneuropathy due to p.ALA140 SER mutation.
    Gürsoy AE; Yeşil G; Ergun SS; Tosuner Z
    Neurol India; 2018; 66(1):238-241. PubMed ID: 29322995
    [No Abstract]   [Full Text] [Related]  

  • 47. Diflunisal stabilizes familial amyloid polyneuropathy-associated transthyretin variant tetramers in serum against dissociation required for amyloidogenesis.
    Tojo K; Sekijima Y; Kelly JW; Ikeda S
    Neurosci Res; 2006 Dec; 56(4):441-9. PubMed ID: 17028027
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Monoclonal gammopathy of undetermined significance in systemic transthyretin amyloidosis (ATTR).
    Phull P; Sanchorawala V; Connors LH; Doros G; Ruberg FL; Berk JL; Sarosiek S
    Amyloid; 2018 Mar; 25(1):62-67. PubMed ID: 29424556
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Dual AApoAIV amyloidosis and ATTR amyloidosis arising in the same patient: a report of three cases.
    Dalland JC; Dao LN; Dasari S; Theis JD; Chiu A; Rech KL; Howard MT; Grogan M; Hagen C; Bois MC; McPhail ED
    Amyloid; 2024 Jun; 31(2):153-155. PubMed ID: 38099717
    [No Abstract]   [Full Text] [Related]  

  • 50. Neurofilament light chain as a biomarker for monitoring response to change in treatment in hereditary ATTR amyloidosis.
    Sato M; Mochizuki Y; Takahashi Y; Takasone K; Aldinc E; Ticau S; Jia G; Sekijima Y
    Amyloid; 2023 Sep; 30(3):351-352. PubMed ID: 36908191
    [No Abstract]   [Full Text] [Related]  

  • 51. Ala97Ser mutation is common among ethnic Chinese Malaysians with transthyretin familial amyloid polyneuropathy.
    Low SC; Tan CY; Md Sari NA; Ahmad-Annuar A; Wong KT; Lin KP; Shahrizaila N; Tan CT; Goh KJ
    Amyloid; 2019; 26(sup1):7-8. PubMed ID: 31343308
    [No Abstract]   [Full Text] [Related]  

  • 52. [Familial amyloid neuropathy associated with the Cys114 mutation of the transthyretin gene in a Russian family].
    Strokov IA; Diukova GM; Pogromov AP; Generozov EV; Zhadin PM; Kovalchuk MO
    Zh Nevrol Psikhiatr Im S S Korsakova; 2007; 107(9):67-72. PubMed ID: 18688962
    [No Abstract]   [Full Text] [Related]  

  • 53. Transthyretin amyloidosis: a little history of hereditary amyloidosis.
    Benson MD
    Amyloid; 2017 Mar; 24(sup1):76-77. PubMed ID: 28434305
    [No Abstract]   [Full Text] [Related]  

  • 54. Doxycycline-tauroursodeoxycholic acid treatment: effects in the heart of a transthyretin V30M transgenic mouse model.
    Teixeira C; Costelha S; Martins HS; Teixeira A; Saraiva MJ
    Amyloid; 2017 Mar; 24(sup1):80. PubMed ID: 28434372
    [No Abstract]   [Full Text] [Related]  

  • 55. Genetic testing improves identification of transthyretin amyloid (ATTR) subtype in cardiac amyloidosis.
    Brown EE; Lee YZJ; Halushka MK; Steenbergen C; Johnson NM; Almansa J; Tedford RJ; Cingolani O; Russell SD; Sharma K; Judge DP
    Amyloid; 2017 Jun; 24(2):92-95. PubMed ID: 28494620
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Is it better than it seems or just good enough? The tafamidis saga.
    de Carvalho M
    Muscle Nerve; 2012 Dec; 46(6):839-40. PubMed ID: 23042137
    [No Abstract]   [Full Text] [Related]  

  • 57. [Clinical diversity, diagnosis and treatment of hereditary amyloid neuropathy].
    Sekijima Y
    Rinsho Shinkeigaku; 2014; 54(12):953-6. PubMed ID: 25672679
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Effects of liver transplantation and tafamidis in hereditary transthyretin amyloidosis caused by transthyretin Leu55Pro mutation: a case report.
    Kon T; Misumi Y; Nishijima H; Honda M; Suzuki C; Baba M; Inomata Y; Obayashi K; Ando Y; Tomiyama M
    Amyloid; 2015; 22(3):203-4. PubMed ID: 26123280
    [No Abstract]   [Full Text] [Related]  

  • 59. Diflunisal tolerability in transthyretin cardiac amyloidosis: a single center's experience.
    Ikram A; Donnelly JP; Sperry BW; Samaras C; Valent J; Hanna M
    Amyloid; 2018 Sep; 25(3):197-202. PubMed ID: 30388377
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Coronary ectasia in amyloid cardiomyopathy and neuropathy due to the transthyretin mutation c.323A>G.
    Finsterer J; Stöllberger C; Rauschka H; Gatterer E
    Heart Lung; 2018; 47(2):127-129. PubMed ID: 29246775
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.