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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

126 related items for PubMed ID: 7951260

  • 1. A new mutation (TTR Ala-47) in the transthyretin gene associated with hereditary amyloidosis.
    Ferlini A, Patrosso MC, Repetto M, Frattini A, Villa A, Fini S, Salvi F, Vezzoni P, Forabosco A.
    Hum Mutat; 1994; 4(1):61-4. PubMed ID: 7951260
    [No Abstract] [Full Text] [Related]

  • 2. Two transthyretin variants (TTR Ala-49 and TTR Gln-89) in two Sicilian kindreds with hereditary amyloidosis.
    Almeida MR, Ferlini A, Forabosco A, Gawinowicz M, Costa PP, Salvi F, Plasmati R, Tassinari CA, Altland K, Saraiva MJ.
    Hum Mutat; 1992; 1(3):211-5. PubMed ID: 1301926
    [Abstract] [Full Text] [Related]

  • 3. A novel variant of transthyretin, 59Thr-->Lys, associated with autosomal dominant cardiac amyloidosis in an Italian family.
    Booth DR, Tan SY, Hawkins PN, Pepys MB, Frustaci A.
    Circulation; 1995 Feb 15; 91(4):962-7. PubMed ID: 7850982
    [Abstract] [Full Text] [Related]

  • 4. A new transthyretin mutation associated with amyloid cardiomyopathy.
    Saraiva MJ, Almeida Mdo R, Sherman W, Gawinowicz M, Costa P, Costa PP, Goodman DS.
    Am J Hum Genet; 1992 May 15; 50(5):1027-30. PubMed ID: 1570831
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. A novel transthyretin mutation at position 30 (Leu for Val) associated with familial amyloidotic polyneuropathy.
    Murakami T, Atsumi T, Maeda S, Tanase S, Ishikawa K, Mita S, Kumamoto T, Araki S, Ando M.
    Biochem Biophys Res Commun; 1992 Aug 31; 187(1):397-403. PubMed ID: 1520326
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Cardiac Amyloidosis Phenotype Associated With a Glu89Lys Transthyretin Mutation.
    Bourque PR, McCurdy AR, Mielniczuk LM, Dennie C, Veinot JP, Warman Chardon J.
    Can J Cardiol; 2017 Jun 31; 33(6):830.e5-830.e7. PubMed ID: 28395866
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. 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 31; 42(11):2094-102. PubMed ID: 1436517
    [Abstract] [Full Text] [Related]

  • 16. 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 31; 26(4):230-8. PubMed ID: 22187309
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. [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 31; 29(1):13-5. PubMed ID: 22311483
    [Abstract] [Full Text] [Related]

  • 19. Transthyretin-related hereditary amyloidosis in a Chinese family with TTR Y114C mutation.
    Zhang Y, Deng YL, Ma JF, Zheng L, Hong Z, Wang ZQ, Sheng CY, Xiao Q, Cao L, Chen SD.
    Neurodegener Dis; 2011 Feb 31; 8(4):187-93. PubMed ID: 21135536
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.