BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

287 related articles for article (PubMed ID: 26243339)

  • 1. A study of the neuropathy associated with transthyretin amyloidosis (ATTR) in the UK.
    Carr AS; Pelayo-Negro AL; Evans MR; Laurà M; Blake J; Stancanelli C; Iodice V; Wechalekar AD; Whelan CJ; Gillmore JD; Hawkins PN; Reilly MM
    J Neurol Neurosurg Psychiatry; 2016 Jun; 87(6):620-7. PubMed ID: 26243339
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Ala97Ser transthyretin amyloidosis-associated polyneuropathy, clinical and neurophysiological profiles in a Thai cohort.
    Pasutharnchat N; Taychargumpoo C; Vorasettakarnkij Y; Amornvit J
    BMC Neurol; 2021 May; 21(1):206. PubMed ID: 34022837
    [TBL] [Abstract][Full Text] [Related]  

  • 3. CNS involvement in V30M transthyretin amyloidosis: clinical, neuropathological and biochemical findings.
    Maia LF; Magalhães R; Freitas J; Taipa R; Pires MM; Osório H; Dias D; Pessegueiro H; Correia M; Coelho T
    J Neurol Neurosurg Psychiatry; 2015 Feb; 86(2):159-67. PubMed ID: 25091367
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hereditary Transthyretin Amyloidosis- Clinical and Genetic Characteristics of a Multiracial South-East Asian Cohort in Singapore.
    Chen Z; Koh JS; Saini M; Tay KSS; Jayne Tan Y; Chai JYH; Fam SR; Juraidah AR; Lim PK; Ng ASL; Prasad K; Tan CB; Umapathi T; Verma KK; Yong MH; Yu C; Ng PS
    J Neuromuscul Dis; 2021; 8(4):723-733. PubMed ID: 34024775
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Expert consensus recommendations to improve diagnosis of ATTR amyloidosis with polyneuropathy.
    Adams D; Ando Y; Beirão JM; Coelho T; Gertz MA; Gillmore JD; Hawkins PN; Lousada I; Suhr OB; Merlini G
    J Neurol; 2021 Jun; 268(6):2109-2122. PubMed ID: 31907599
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cardiac phenotype and clinical outcome of familial amyloid polyneuropathy associated with transthyretin alanine 60 variant.
    Sattianayagam PT; Hahn AF; Whelan CJ; Gibbs SD; Pinney JH; Stangou AJ; Rowczenio D; Pflugfelder PW; Fox Z; Lachmann HJ; Wechalekar AD; Hawkins PN; Gillmore JD
    Eur Heart J; 2012 May; 33(9):1120-7. PubMed ID: 21992998
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic and clinical characteristics of hereditary transthyretin amyloidosis in endemic and non-endemic areas: experience from a single-referral center in Japan.
    Yamashita T; Ueda M; Misumi Y; Masuda T; Nomura T; Tasaki M; Takamatsu K; Sasada K; Obayashi K; Matsui H; Ando Y
    J Neurol; 2018 Jan; 265(1):134-140. PubMed ID: 29177547
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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]  

  • 9. Hereditary transthyretin amyloidosis in mainland China: a unicentric retrospective study.
    Du K; Li F; Wang H; Miao Y; Lv H; Zhang W; Wang Z; Yuan Y; Meng L
    Ann Clin Transl Neurol; 2021 Apr; 8(4):831-841. PubMed ID: 33739616
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Carpal tunnel syndrome and spinal canal stenosis: harbingers of transthyretin amyloid cardiomyopathy?
    Aus dem Siepen F; Hein S; Prestel S; Baumgärtner C; Schönland S; Hegenbart U; Röcken C; Katus HA; Kristen AV
    Clin Res Cardiol; 2019 Dec; 108(12):1324-1330. PubMed ID: 30953182
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hereditary ATTR Amyloidosis with Cardiomyopathy Caused by the Novel Variant Transthyretin Y114S (p.Y134S).
    Nakase T; Yamashita T; Matsuo Y; Nomura T; Sasada K; Masuda T; Misumi Y; Takamatsu K; Oda S; Furukawa Y; Obayashi K; Matsui H; Ando Y; Ueda M
    Intern Med; 2019 Sep; 58(18):2695-2698. PubMed ID: 31178489
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Same same, but different? The neurological presentation of wildtype transthyretin (ATTRwt) amyloidosis.
    Kleefeld F; Scherret E; Knebel F; Messroghli D; Heidecker B; Wetz C; Schatka I; Barzen G; Tschöpe C; Amthauer H; Hahn K
    Amyloid; 2022 Jun; 29(2):92-101. PubMed ID: 34994254
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Transthyretin-related familial amyloidotic polyneuropathy: description of a cohort of patients with Leu64 mutation and late onset.
    Russo M; Mazzeo A; Stancanelli C; Di Leo R; Gentile L; Di Bella G; Minutoli F; Baldari S; Vita G
    J Peripher Nerv Syst; 2012 Dec; 17(4):385-90. PubMed ID: 23279339
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical and genetic profiles of hereditary transthyretin amyloidosis in Taiwan.
    Chao HC; Liao YC; Liu YT; Guo YC; Chang FP; Lee YC; Lin KP
    Ann Clin Transl Neurol; 2019 May; 6(5):913-922. PubMed ID: 31139689
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Variable presentations of TTR-related familial amyloid polyneuropathy in seventeen patients.
    Cappellari M; Cavallaro T; Ferrarini M; Cabrini I; Taioli F; Ferrari S; Merlini G; Obici L; Briani C; Fabrizi GM
    J Peripher Nerv Syst; 2011 Jun; 16(2):119-29. PubMed ID: 21692911
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hereditary cardiac amyloidosis associated with Pro24Ser transthyretin mutation: a case report.
    Yamamoto H; Hashimoto T; Kawamura S; Hiroe M; Yamashita T; Ando Y; Yokochi T
    J Med Case Rep; 2018 Dec; 12(1):370. PubMed ID: 30553273
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Phenotypes Associated With the Val122Ile, Leu58His, and Late-Onset Val30Met Variants in Patients With Hereditary Transthyretin Amyloidosis.
    Zampino S; Sheikh FH; Vaishnav J; Judge D; Pan B; Daniel A; Brown E; Ebenezer G; Polydefkis M
    Neurology; 2023 May; 100(19):e2036-e2044. PubMed ID: 36941075
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Changes in nerve conduction studies predate clinical symptoms onset in early onset Val30Met hereditary ATTR amyloidosis.
    Castro J; Miranda B; de Castro I; Conceição I
    Eur J Neurol; 2022 Mar; 29(3):826-832. PubMed ID: 34751997
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Phenotype of a second Irish variant causing hereditary amyloidogenic transthyretin amyloidosis.
    Asad M; Bermingham N; McNamara B; Kearney P; Ryan AM
    J Neurol; 2022 Sep; 269(9):4802-4807. PubMed ID: 35428899
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Frequencies and geographic distributions of genetic mutations in transthyretin- and non-transthyretin-related familial amyloidosis.
    Zhen DB; Swiecicki PL; Zeldenrust SR; Dispenzieri A; Mauermann ML; Gertz MA
    Clin Genet; 2015 Oct; 88(4):396-400. PubMed ID: 25211232
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.