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Journal Abstract Search

189 related items for PubMed ID: 12762139

  • 1. A transthyretin mutation (Tyr78Phe) associated with peripheral neuropathy, carpal tunnel syndrome and skin amyloidosis.
    Magy N, Liepnieks JJ, Gil H, Kantelip B, Dupond JL, Kluve-Beckerman B, Benson MD.
    Amyloid; 2003 Mar; 10(1):29-33. PubMed ID: 12762139
    [Abstract] [Full Text] [Related]

  • 2. Transthyretin Tyr69-to-Ile mutation (double-nucleotide substitution in codon 69) in a Japanese familial amyloidosis patient with cardiomyopathy and carpal tunnel syndrome.
    Takei Y, Hattori T, Yazaki M, Tokuda T, Urasawa N, Kanai S, Ikeda S.
    Amyloid; 2003 Mar; 10(1):25-8. PubMed ID: 12762138
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  • 3. A novel transthyretin Lys70Glu (p.Lys90Glu) mutation presenting with vitreous amyloidosis and carpal tunnel syndrome.
    Raivio VE, Jonasson J, Myllykangas L, Ala-Mello S, Kankuri-Tammilehto M, Kiuru-Enari S, Westermark P, Tanskanen M, Kivelä T.
    Amyloid; 2016 Mar; 23(1):46-50. PubMed ID: 26828956
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  • 4. Transthyretin amyloidosis (serine 44) with headache, hearing loss, and peripheral neuropathy.
    Klein CJ, Nakumura M, Jacobson DR, Lacy MQ, Benson MD, Petersen RC.
    Neurology; 1998 Nov; 51(5):1462-4. PubMed ID: 9818883
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  • 5. Familial carpal tunnel syndrome due to amyloidogenic transthyretin His 114 variant.
    Murakami T, Tachibana S, Endo Y, Kawai R, Hara M, Tanase S, Ando M.
    Neurology; 1994 Feb; 44(2):315-8. PubMed ID: 8309582
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  • 13. New transthyretin variants SER 91 and SER 116 associated with familial amyloidotic polyneuropathy. Mutations in brief no. 151. Online.
    Misrahi AM, Plante V, Lalu T, Serre L, Adams D, Lacroix DC, Saïd G.
    Hum Mutat; 1998 Feb; 12(1):71. PubMed ID: 10627135
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  • 14. High prevalence of wild-type transthyretin deposition in patients with idiopathic carpal tunnel syndrome: a common cause of carpal tunnel syndrome in the elderly.
    Sekijima Y, Uchiyama S, Tojo K, Sano K, Shimizu Y, Imaeda T, Hoshii Y, Kato H, Ikeda S.
    Hum Pathol; 2011 Nov; 42(11):1785-91. PubMed ID: 21733562
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  • 15. Heart failure caused by a novel amyloidogenic mutation of the transthyretin gene: ATTR Ala45Ser.
    Janunger T, Anan I, Holmgren G, Lövheim O, Ohlsson PI, Suhr OB, Tashima K.
    Amyloid; 2000 Jun; 7(2):137-40. PubMed ID: 10842718
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  • 17. Transthyretin mutation (TTRGly47Ala) associated with familial amyloid polyneuropathy in a French family.
    Magy N, Valleix S, Grateau G, Algros MP, Guillemain R, Kantelip B, Delpech M, Dupond JL.
    Amyloid; 2002 Dec; 9(4):272-5. PubMed ID: 12557758
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  • 18. A new Arg54Gly transthyretin gene mutation associated with vitreous amyloidosis in Chinese.
    Shi Y, Li J, Hu J, Hu J, Sun L, Li H, Shi R, Yang L, Sun Y, Li C.
    Eye Sci; 2011 Dec; 26(4):230-8. PubMed ID: 22187309
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  • 20. TTR exon scanning in peripheral neuropathies.
    Torres Mde F, Almeida Mdo R, Saraiva MJ.
    Neuromuscul Disord; 1995 May; 5(3):187-91. PubMed ID: 7633183
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