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Journal Abstract Search

137 related items for PubMed ID: 8345958

  • 41. Cutaneous lymphatic amyloid deposits in "Hungarian-type" familial transthyretin amyloidosis: a case report.
    Harkany T, Garzuly F, Csanaky G, Luiten PG, Nyakas C, Linke RP, Virágh S.
    Br J Dermatol; 2002 Apr; 146(4):674-9. PubMed ID: 11966704
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  • 42. Oculoleptomeningeal amyloidosis in a large kindred with a new transthyretin variant Tyr69His.
    Blevins G, Macaulay R, Harder S, Fladeland D, Yamashita T, Yazaki M, Hamidi Asl K, Benson MD, Donat JR.
    Neurology; 2003 May 27; 60(10):1625-30. PubMed ID: 12771253
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  • 43. Vitreous involvement in familial amyloidotic neuropathy: a genealogical and genetic study.
    Sandgren O, Drugge U, Holmgren G, Sousa A.
    Clin Genet; 1991 Dec 27; 40(6):452-60. PubMed ID: 1685700
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  • 44. Familial amyloid polyneuropathy associated with the transthyretin Cys114 gene in a Japanese kindred.
    Ueno S, Fujimura H, Yorifuji S, Nakamura Y, Takahashi M, Tarui S, Yanagihara T.
    Brain; 1992 Oct 27; 115 ( Pt 5)():1275-89. PubMed ID: 1330202
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  • 45. Ocular Manifestations of Familial Transthyretin Amyloidosis.
    Reynolds MM, Veverka KK, Gertz MA, Dispenzieri A, Zeldenrust SR, Leung N, Pulido JS.
    Am J Ophthalmol; 2017 Nov 27; 183():156-162. PubMed ID: 28911993
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  • 48. Clinical Presentation, Diagnosis and Treatment of TTR Amyloidosis.
    Kapoor M, Rossor AM, Laura M, Reilly MM.
    J Neuromuscul Dis; 2019 Nov 27; 6(2):189-199. PubMed ID: 30829617
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  • 49. Familial amyloidotic polyneuropathy presenting with carpal tunnel syndrome and a new transthyretin mutation, asparagine 70.
    Izumoto S, Younger D, Hays AP, Martone RL, Smith RT, Herbert J.
    Neurology; 1992 Nov 27; 42(11):2094-102. PubMed ID: 1436517
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  • 50. Early skin denervation in hereditary and iatrogenic transthyretin amyloid neuropathy.
    Masuda T, Ueda M, Suenaga G, Misumi Y, Tasaki M, Izaki A, Yanagisawa Y, Inoue Y, Motokawa H, Matsumoto S, Mizukami M, Arimura A, Deguchi T, Nishio Y, Yamashita T, Inomata Y, Obayashi K, Ando Y.
    Neurology; 2017 Jun 06; 88(23):2192-2197. PubMed ID: 28490654
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  • 51. Homozygosity for the transthyretin-met30-gene in two Swedish sibs with familial amyloidotic polyneuropathy.
    Holmgren G, Haettner E, Nordenson I, Sandgren O, Steen L, Lundgren E.
    Clin Genet; 1988 Nov 06; 34(5):333-8. PubMed ID: 3229002
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  • 52. Association between a point mutation at the -743-bp region of the transthyretin (TTR) gene and familial vitreous amyloidosis.
    Nie XM, Cai SJ, Xie B, Chen XW, Jiang M.
    Genet Mol Res; 2016 Mar 31; 15(1):. PubMed ID: 27051017
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  • 53. Vitreous Amyloidosis: Ocular, Systemic, and Genetic Insights.
    Venkatesh P, Selvan H, Singh SB, Gupta D, Kashyap S, Temkar S, Gogia V, Tripathy K, Chawla R, Vohra R.
    Ophthalmology; 2017 Jul 31; 124(7):1014-1022. PubMed ID: 28412068
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  • 60. Oculoleptomeningeal Amyloidosis Secondary to the Rare Transthyretin c.381T>G (p.Ile127Met) Mutation.
    Mathieu F, Morgan E, So J, Munoz DG, Mason W, Kongkham P.
    World Neurosurg; 2018 Mar 31; 111():190-193. PubMed ID: 29277593
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