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 *

136 related articles for article (PubMed ID: 10842698)

  • 1. Hereditary amyloidosis: some words on the history and present status of our eminent subject.
    Benson MD
    Amyloid; 2000 Mar; 7(1):15-6. PubMed ID: 10842698
    [No Abstract]   [Full Text] [Related]  

  • 2. [Hereditary amyloid neuropathies].
    Adams D; Said G
    Ann Med Interne (Paris); 1995; 146(3):157-65. PubMed ID: 7653916
    [No Abstract]   [Full Text] [Related]  

  • 3. Amyloid polyneuropathy caused by wild-type transthyretin.
    Lam L; Margeta M; Layzer R
    Muscle Nerve; 2015 Jul; 52(1):146-9. PubMed ID: 25557530
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A case of transthyretin amyloidosis with myopathy, neuropathy, and cardiomyopathy resulting from an exceedingly rare mutation transthyretin Ala120Ser (c.418G > T, p.Ala140Ser).
    Patel K; Tagoe C; Bieri P; Weidenheim K; Tauras JM
    Amyloid; 2018 Sep; 25(3):211-212. PubMed ID: 30039724
    [No Abstract]   [Full Text] [Related]  

  • 5. Transthyretin-related hereditary amyloid polyneuropathy presenting with large fibre involvement and cardiomyopathy.
    Cruz S; Cortes-Vicente E; Illa I; Rojas-Garcia R
    Amyloid; 2016; 23(1):64-5. PubMed ID: 26806028
    [No Abstract]   [Full Text] [Related]  

  • 6. A case of hereditary amyloidosis transthyretin variant Met 30 with amyloid cardiomyopathy, less polyneuropathy, and the presence of giant cells.
    Nakamura Y; Yutani C; Nakazato M; Date Y; Baba T; Goto Y
    Pathol Int; 1999 Oct; 49(10):898-902. PubMed ID: 10571824
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cardiac amyloid in patients with familial amyloid polyneuropathy consists of abundant wild-type transthyretin.
    Yazaki M; Tokuda T; Nakamura A; Higashikata T; Koyama J; Higuchi K; Harihara Y; Baba S; Kametani F; Ikeda S
    Biochem Biophys Res Commun; 2000 Aug; 274(3):702-6. PubMed ID: 10924339
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The molecular biology and clinical features of amyloid neuropathy.
    Benson MD; Kincaid JC
    Muscle Nerve; 2007 Oct; 36(4):411-23. PubMed ID: 17554795
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Amyloid neuropathy resulting from an unknown protein].
    Younsi R; Birouk N; Kissani N
    Rev Med Interne; 2009 Mar; 30(3):277-8. PubMed ID: 18584922
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Vitreous amyloidosis in familial amyloidotic polyneuropathy. Report of a case with the Val30Met transthyretin mutation.
    Ciulla TA; Tolentino F; Morrow JF; Dryja TP
    Surv Ophthalmol; 1995; 40(3):197-206. PubMed ID: 8599155
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Epidemiological and clinical characteristics of persons with transthyretin hereditary amyloid polyneuropathy: a global synthesis of 532 cases.
    Cruz MW; Schmidt H; Botteman MF; Carter JA; Chopra AS; Stewart M; Hopps M; Fallet S; Amass L
    Amyloid; 2017 Mar; 24(sup1):109-110. PubMed ID: 28434345
    [No Abstract]   [Full Text] [Related]  

  • 12. New structural information and update on liver transplantation in transthyretin-associated amyloidosis. Report from the 4th International Symposium on Familial Amyloidotic Polyneuropathy and Other Transthyretin Related Disorders & the 3rd International Workshop on Liver Transplantation in Familial Amyloid Polyneuropathy, Umeå Sweden, June 1999.
    Ericzon BG; Holmgren G; Lundgren E; Suhr OB
    Amyloid; 2000 Jun; 7(2):145-7. PubMed ID: 10842720
    [No Abstract]   [Full Text] [Related]  

  • 13. 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; 88(23):2192-2197. PubMed ID: 28490654
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A case of biopsy-proven leptomeningeal amyloidosis and intravenous Ig-responsive polyneuropathy associated with the Ala25Thr transthyretin gene mutation.
    Shimizu Y; Takeuchi M; Matsumura M; Tokuda T; Iwata M
    Amyloid; 2006 Mar; 13(1):37-41. PubMed ID: 16690499
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular genetics of familial amyloidotic polyneuropathy.
    Saraiva MJ
    J Peripher Nerv Syst; 1996; 1(3):179-88. PubMed ID: 10970108
    [No Abstract]   [Full Text] [Related]  

  • 16. [Hereditary amyloidosis].
    Schmidt HH; Pröpsting MJ; Manns MP
    Internist (Berl); 1999 May; 40(5):493-501. PubMed ID: 10407759
    [No Abstract]   [Full Text] [Related]  

  • 17. [Hereditary amyloidosis].
    Grateau G
    Rev Med Interne; 1994 Apr; 15(4):250-6. PubMed ID: 8059145
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Ocular amyloidosis, with special reference to the hereditary forms with vitreous involvement.
    Sandgren O
    Surv Ophthalmol; 1995; 40(3):173-96. PubMed ID: 8599154
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Transthyretin Val71Ala mutation in a Dutch family with familial amyloidotic polyneuropathy.
    Haagsma EB; Scheffer H; Altland K; De Jager AE; Hazenberg BP
    Amyloid; 2000 Sep; 7(3):218-21. PubMed ID: 11019863
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Transgenic mouse model of familial amyloidotic polyneuropathy type I: its production, biological features, and usefulness.
    Yi S; Takahashi K; Araki S; Yamamura K
    Lab Anim Sci; 1995 Apr; 45(2):173-5. PubMed ID: 7603019
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.