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 *

131 related articles for article (PubMed ID: 1520336)

  • 61. Laboratory assessment of transthyretin amyloidosis.
    Benson MD; Yazaki M; Magy N
    Clin Chem Lab Med; 2002 Dec; 40(12):1262-5. PubMed ID: 12553428
    [TBL] [Abstract][Full Text] [Related]  

  • 62. A new mutation causing familial amyloidotic polyneuropathy.
    Skare JC; Saraiva MJ; Alves IL; Skare IB; Milunsky A; Cohen AS; Skinner M
    Biochem Biophys Res Commun; 1989 Nov; 164(3):1240-6. PubMed ID: 2590199
    [TBL] [Abstract][Full Text] [Related]  

  • 63. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Retrospective molecular detection of Transthyretin Met 111 mutation in a Danish kindred with familial amyloid cardiomyopathy, using DNA from formalin-fixed and paraffin-embedded tissues.
    Nordvåg BY; Ranløv I; Riise HM; Husby G; el-Gewely MR
    Hum Genet; 1993 Oct; 92(3):265-8. PubMed ID: 8406434
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Cardiac amyloidosis associated with the transthyretin Ile122 mutation in a Caucasian family.
    Hamidi Asl K; Nakamura M; Yamashita T; Benson MD
    Amyloid; 2001 Dec; 8(4):263-9. PubMed ID: 11791619
    [TBL] [Abstract][Full Text] [Related]  

  • 66. A new transthyretin variant Leu55Gln in a patient with systemic amyloidosis.
    Yazaki M; Varga J; Dyck PJ; Benson MD
    Amyloid; 2002 Dec; 9(4):268-71. PubMed ID: 12557757
    [TBL] [Abstract][Full Text] [Related]  

  • 67. A new transthyretin variant from a patient with familial amyloidotic polyneuropathy has asparagine substituted for histidine at position 90.
    Skare JC; Milunsky JM; Milunsky A; Skare IB; Cohen AS; Skinner M
    Clin Genet; 1991 Jan; 39(1):6-12. PubMed ID: 1997217
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Transthyretin Ser-44 mutation in a case with vitreous amyloidosis.
    Murakami A; Fujiki K; Hasegawa S; Imamura S; Kawano H; Kanai A; Matsumoto T
    Am J Ophthalmol; 2002 Feb; 133(2):272-3. PubMed ID: 11812437
    [TBL] [Abstract][Full Text] [Related]  

  • 69. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 70. A new transthyretin variant (Ser23Asn) associated with familial amyloidosis in a Portuguese patient.
    Connors LH; Théberge R; Skare J; Costello CE; Falk RH; Skinner M
    Amyloid; 1999 Jun; 6(2):114-8. PubMed ID: 10439117
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Two siblings diagnosed to have transthyretin-related familial amyloid cardiomyopathy around the same time at different hospitals.
    Miyamura M; Terasaki F; Ishibashi K; Shimazaki C; Kimura F; Kuwabara H; Tsuji M; Shibayama Y; Sekijima Y; Tojo K; Ishizaka N
    Intern Med; 2012; 51(5):465-9. PubMed ID: 22382560
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Late-onset familial amyloid polyneuropathy with the TTR Met 30 mutation in France.
    Grateau G; Adams D; Malapert D; Viemont M; Delpech M; Said G
    Clin Genet; 1993 Mar; 43(3):143-5. PubMed ID: 8500260
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Oculoleptomeningeal amyloidosis associated with a new transthyretin variant Ser64.
    Uemichi T; Uitti RJ; Koeppen AH; Donat JR; Benson MD
    Arch Neurol; 1999 Sep; 56(9):1152-5. PubMed ID: 10488818
    [TBL] [Abstract][Full Text] [Related]  

  • 74. A DNA test for Indiana/Swiss hereditary amyloidosis (FAP II).
    Wallace MR; Conneally PM; Benson MD
    Am J Hum Genet; 1988 Aug; 43(2):182-7. PubMed ID: 2840822
    [TBL] [Abstract][Full Text] [Related]  

  • 75. 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; 15(1):. PubMed ID: 27051017
    [TBL] [Abstract][Full Text] [Related]  

  • 76. 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]  

  • 77. [Identification of a TTR gene mutation in a family with hereditary vitreous amyloidosis].
    Xie Y; Zhao Y; Zhou JJ; Wang X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Feb; 29(1):13-5. PubMed ID: 22311483
    [TBL] [Abstract][Full Text] [Related]  

  • 78. A novel transthyretin mutation associated with familial amyloidotic polyneuropathy.
    Murakami T; Maeda S; Yi S; Ikegawa S; Kawashima E; Onodera S; Shimada K; Araki S
    Biochem Biophys Res Commun; 1992 Jan; 182(2):520-6. PubMed ID: 1734866
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Late onset cardiomyopathy as presenting sign of ATTR A45G amyloidosis caused by a novel TTR mutation (p.A65G).
    Klaassen SHC; Lemmink HH; Bijzet J; Glaudemans AWJM; Bos R; Plattel W; van den Berg MP; Slart RHJA; Nienhuis HLA; van Veldhuisen DJ; Hazenberg BPC
    Cardiovasc Pathol; 2017; 29():19-22. PubMed ID: 28460244
    [TBL] [Abstract][Full Text] [Related]  

  • 80. [A sporadic case of late onset familial amyloidotic polyneuropathy preceded by cardiac involvement].
    Aoki K; Koike R; Yuasa T; Ikeda S; Tsuji S
    Rinsho Shinkeigaku; 1993 Aug; 33(8):905-8. PubMed ID: 8261706
    [TBL] [Abstract][Full Text] [Related]  

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