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 *

155 related articles for article (PubMed ID: 11812437)

  • 21. 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; 124(7):1014-1022. PubMed ID: 28412068
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. 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]  

  • 24. Novel transthyretin missense mutation (Thr34) in an Italian family with hereditary amyloidosis.
    Patrosso MC; Salvi F; De Grandis D; Vezzoni P; Jacobson DR; Ferlini A
    Am J Med Genet; 1998 May; 77(2):135-8. PubMed ID: 9605286
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Vitreous amyloidosis with autonomic neuropathy of the digestive tract associated with a novel transthyretin p.Gly87Arg variant in a Bangladeshi patient: a case report.
    Terrier B; Colombat M; Beugnet C; Quéant A; London J; Daudin JB; Le Jeunne C; Mouthon L; Monnet D; Cauquil C; Lacroix C; Adams D; Brézin A; Valleix S
    J Med Case Rep; 2017 Aug; 11(1):222. PubMed ID: 28802308
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A novel variant of transthyretin (Glu42Asp) associated with sporadic late-onset cardiac amyloidosis.
    Dupuy O; Blétry O; Blanc AS; Droz D; Viémont M; Delpech M; Grateau G
    Amyloid; 1998 Dec; 5(4):285-7. PubMed ID: 10036587
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Oculoleptomeningeal amyloidosis in 3 individuals with the transthyretin variant Tyr69His.
    Schweitzer K; Ehmann D; Garcia R; Alport E
    Can J Ophthalmol; 2009 Jun; 44(3):317-9. PubMed ID: 19491989
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Prenatal detection of a gene for hereditary amyloidosis.
    Nichols WC; Padilla LM; Benson MD
    Am J Med Genet; 1989 Dec; 34(4):520-4. PubMed ID: 2516414
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Solar Eruption in Hereditary Transthyretin Amyloidosis.
    Rousseau A; Bodaghi B; Labetoulle M
    Ophthalmology; 2019 Mar; 126(3):371. PubMed ID: 30803513
    [No Abstract]   [Full Text] [Related]  

  • 30. 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]  

  • 31. Immunostaining images of vitreous transthyretin amyloid.
    Latasiewicz M; Adan A; Solé M
    Can J Ophthalmol; 2015 Oct; 50(5):384-7. PubMed ID: 26455975
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Biochemical characterization of vitreous and cardiac amyloid in Ile84Ser transthyretin amyloidosis.
    Liepnieks JJ; Wilson DL; Benson MD
    Amyloid; 2006 Sep; 13(3):170-7. PubMed ID: 17062384
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A novel mutant (transthyretin Ile-50) related to amyloid polyneuropathy. Single-strand conformation polymorphism as a new genetic marker.
    Saeki Y; Ueno S; Takahashi N; Soga F; Yanagihara T
    FEBS Lett; 1992 Aug; 308(1):35-7. PubMed ID: 1644201
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Vitreal deposits in Val71Ala transthyretin amyloidosis.
    Suan D; Booth DR; Kennedy IH; Downie J; Earls P; Gottlieb D; Stewart GJ; Lin MW
    Intern Med J; 2012 Jan; 42(1):106-8. PubMed ID: 22276564
    [No Abstract]   [Full Text] [Related]  

  • 35. Unusual Vitreous Opacity in a Chinese Patient.
    Yu S; Xu Y; Liang X
    JAMA Ophthalmol; 2019 Dec; 137(12):1454-1455. PubMed ID: 31621813
    [No Abstract]   [Full Text] [Related]  

  • 36. The transthyretin cDNA sequence is normal in transthyretin-derived senile systemic amyloidosis.
    Christmanson L; Betsholtz C; Gustavsson A; Johansson B; Sletten K; Westermark P
    FEBS Lett; 1991 Apr; 281(1-2):177-80. PubMed ID: 2015890
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. The pathologic spectrum of oculoleptomeningeal amyloidosis with Val30Gly transthyretin gene mutation in a postmortem case.
    Martin SE; Benson MD; Hattab EM
    Hum Pathol; 2014 May; 45(5):1105-8. PubMed ID: 24613567
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A second transthyretin mutation at position 33 (Leu/Phe) associated with familial amyloidotic polyneuropathy.
    Harding J; Skare J; Skinner M
    Biochim Biophys Acta; 1991 Oct; 1097(3):183-6. PubMed ID: 1932142
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 8.