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 *

139 related articles for article (PubMed ID: 31870669)

  • 21. Coexistence of transthyretin familial amyloid polyneuropathy and hereditary neuropathy with liability to pressure palsy.
    Conceição I; Nzwalo H; de Carvalho M
    Clin Neurol Neurosurg; 2012 Dec; 114(10):1355-7. PubMed ID: 22520972
    [No Abstract]   [Full Text] [Related]  

  • 22. Quality of life outcomes in APOLLO, the phase 3 trial of the RNAi therapeutic patisiran in patients with hereditary transthyretin-mediated amyloidosis.
    Obici L; Berk JL; González-Duarte A; Coelho T; Gillmore J; Schmidt HH; Schilling M; Yamashita T; Labeyrie C; Brannagan TH; Ajroud-Driss S; Gorevic P; Kristen AV; Franklin J; Chen J; Sweetser MT; Wang JJ; Adams D
    Amyloid; 2020 Sep; 27(3):153-162. PubMed ID: 32131641
    [No Abstract]   [Full Text] [Related]  

  • 23. Ocular manifestations in hereditary transthyretin Gly67Glu amyloidosis.
    Leung KCP; Ko TCS
    Amyloid; 2019 Sep; 26(3):171-172. PubMed ID: 31135236
    [No Abstract]   [Full Text] [Related]  

  • 24. Two Spanish sibs with familial amyloidotic polyneuropathy homozygous for the V30M-TTR gene.
    Munar-Qués M; López Domínguez JM; Viader-Farré C; Moreira P; Saraiva MJ
    Amyloid; 2001 Jun; 8(2):121-3. PubMed ID: 11409034
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A case of familial amyloidotic polyneuropathy with a rare Phe33Leu mutation in the TTR gene.
    Chen CH; Huang CW; Lee MJ
    J Formos Med Assoc; 2014 Aug; 113(8):575-6. PubMed ID: 25037766
    [No Abstract]   [Full Text] [Related]  

  • 26. Neurodegeneration in familial amyloidotic polyneuropathy.
    Gasperini RJ; Small DH
    Clin Exp Pharmacol Physiol; 2012 Aug; 39(8):680-3. PubMed ID: 21916933
    [TBL] [Abstract][Full Text] [Related]  

  • 27. TTR-familial amyloid polyneuropathy--neurological aspects.
    Said G; Planté-Bordeneuve V
    Amyloid; 2012 Jun; 19 Suppl 1():25-7. PubMed ID: 22620963
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Familial amyloidotic polyneuropathy without familial occurrence: carrier detection by the radioimmunoassay of variant transthyretin.
    Tanaka M; Hirai S; Matsubara E; Okamoto K; Morimatsu M; Nakazato M
    J Neurol Neurosurg Psychiatry; 1988 Apr; 51(4):576-8. PubMed ID: 3379433
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Familial amyloidotic polyneuropathies].
    Vallat JM; Funalot B; Faugeras F; Magy L
    Bull Acad Natl Med; 2012 Oct; 196(7):1321-9; discussion 1329-31. PubMed ID: 23815017
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Dominant cardiac type of familial amyloidotic polyneuropathy associated with a novel transthyretin variant Thr59Arg.
    Obayashi K; Misumi Y; Watanabe T; Ando T; Akagami T; Tasaki M; Shinriki S; Ueda M; Yamashita T; Hirotani S; Ando Y
    Muscle Nerve; 2013 Nov; 48(5):839-41. PubMed ID: 23836350
    [No Abstract]   [Full Text] [Related]  

  • 31. 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]  

  • 32. Small fibre neuropathy assessments in early stages of hATTR amyloidosis.
    González-Duarte A; Cárdenas-Soto K; Fueyo O; Bañuelos CE; Gibbons C; Freeman R
    Amyloid; 2019; 26(sup1):55-56. PubMed ID: 31343296
    [No Abstract]   [Full Text] [Related]  

  • 33. 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]  

  • 34. Familial amyloidotic polineuropathy and systemic lupus.
    Ferreira AC; Carvalho F; Nolasco F
    Lupus; 2012 Nov; 21(13):1455-8. PubMed ID: 22914816
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Permanent dysphagia in familial amyloid polyneuropathy (ATTRVal30Met).
    Monteiro C; Magalhães M; Correia C; Taipa R
    Amyloid; 2012 Jun; 19(2):110-2. PubMed ID: 22385252
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Bilateral corneal perforation in familial amyloidotic polyneuropathy.
    Dosso AA; Rungger-Brändle E
    Graefes Arch Clin Exp Ophthalmol; 2005 Mar; 243(3):273-7. PubMed ID: 15452724
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Discordant phenotype in monozygotic female twins with Lys35Thr TTR familial amyloidotic polyneuropathy.
    Ruzhansky K; Scoon J; Weimer LH; Maurer MS; Berk JL; Brannagan TH
    J Clin Neuromuscul Dis; 2014 Sep; 16(1):1-6. PubMed ID: 25137508
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Transthyretin Ala97Ser is associated with familial amyloidotic polyneuropathy in a Chinese-Taiwanese family.
    Lachmann HJ; Booth DR; Bybee A; Hawkins PN
    Hum Mutat; 2000 Aug; 16(2):180. PubMed ID: 10923048
    [No Abstract]   [Full Text] [Related]  

  • 39. Clinical variant of familial amyloid polyneuropathy.
    Quan D; Cohen JA
    Muscle Nerve; 2002 Sep; 26(3):417-20. PubMed ID: 12210373
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Carpal tunnel syndrome as an initial manifestation in a case of transthyretin-related familial amyloid polyneuropathy with a novel A120T mutation.
    Koyama S; Kawanami T; Kurokawa K; Tanji H; Iseki C; Arawaka S; Wada M; Kato T
    Clin Neurol Neurosurg; 2012 Jul; 114(6):707-9. PubMed ID: 22209138
    [No Abstract]   [Full Text] [Related]  

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