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 *

105 related articles for article (PubMed ID: 202208)

  • 1. Primary amyloidosis with familial vitreous opacities: an unusual case and family.
    Okayama M; Goto I; Ogata J; Omae T; Yoshida I; Inomata H
    Arch Intern Med; 1978 Jan; 138(1):105-11. PubMed ID: 202208
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Ocular lesions in primary familial amyloidosis (a syndrome associating opacitieis of the vitreous body, vascular lesions of the retina and an amyloid neuropathy)].
    Franceschetti AT; Rabinowicz T
    J Genet Hum; 1969 Oct; 17(3):349-66. PubMed ID: 4319009
    [No Abstract]   [Full Text] [Related]  

  • 3. Treatment of vitreous opacities in a case of familial amyloidotic polyneuropathy by vitreous surgery.
    Giora T; Gad K; Mordechai P
    Metab Pediatr Ophthalmol; 1981; 5(2):105-8. PubMed ID: 6270477
    [No Abstract]   [Full Text] [Related]  

  • 4. [Amyloidosis of the vitreous body. Possibilities of diagnosis].
    Soltau JB; Seiberth V; Knorz MC; Liesenhoff H
    Fortschr Ophthalmol; 1991; 88(4):408-10. PubMed ID: 1786932
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Conference at the Salpêtrière. June 1984. Peripheral neuropathy and vitreous opacities in a 50-year-old man].
    Vallat JM; Wechsler B; Janaud E; Gray F
    Rev Neurol (Paris); 1985; 141(10):672-6. PubMed ID: 3003870
    [No Abstract]   [Full Text] [Related]  

  • 6. A rare transthyretin mutation (Asp18Glu) associated with vitreous amyloid.
    Solano JM; Pulido JS; Salomao DR
    Ophthalmic Genet; 2007 Jun; 28(2):73-5. PubMed ID: 17558848
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Primary familial amyloidosis with vitreous opacities. Report of an autopsy case.
    Ogata J; Okayama M; Goto I; Inomata H; Yoshida I; Omae T
    Acta Neuropathol; 1978 Apr; 42(1):67-70. PubMed ID: 654882
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Familial amyloid polyneuropathy: report of an autopsy case with neuropathy, vitreous opacities and polycystic kidney.
    Scelsi R; Verri AP; Bono G; Marbini A
    Eur Neurol; 1989; 29(1):27-32. PubMed ID: 2540006
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Primary vitreous amyloidosis. Apropos of a case with ultrastructural study].
    Goberville M; Korobelnik JF; D'Hermies F; Cotinat J; Savoldelli M; Chauvaud D; Pouliquen Y
    J Fr Ophtalmol; 1994; 17(6-7):418-22. PubMed ID: 8083492
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [A familial observation of hereditary vitreal amyloidosis associated with glaucoma].
    Limon S; Rousselie F; Joseph E
    Arch Ophtalmol Rev Gen Ophtalmol; 1973; 33(6):525-8. PubMed ID: 4274542
    [No Abstract]   [Full Text] [Related]  

  • 11. Amyloidotic polyneuropathy in a Jewish family. Evidence for the genetic heterogeneity of the lower limb familial amyloidotic neuropathies.
    Gafni J; Fischel B; Reif R; Yaron M; Pras M
    Q J Med; 1985 Apr; 55(216):33-44. PubMed ID: 3859886
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Vitreous amyloidosis without systemic or familial involvement.
    Salvador F; Mateo C; Alegre J; Reventos A; García-Arumi J; Corcostegui B
    Int Ophthalmol; 1993-1994; 17(6):355-7. PubMed ID: 8063479
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Familial amyloid polyneuropathy: report of a family.
    Giangaspero F; Salvi F; Ceccarelli C; Ambrosetto G; Govoni E; Tassinari CA
    Clin Neuropathol; 1985; 4(3):105-10. PubMed ID: 2990786
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Ocular amyloidosis: clinical points learned from one case.
    Bene C; Kranias G
    Ann Ophthalmol; 1990 Mar; 22(3):101-2. PubMed ID: 2331125
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Clinico-pathological observations on familial amyloid neuropathy, with special reference to 2 autopsy cases in 1 family].
    Matsumoto H; Okuzono Y; Yoshida K; Kodama M; Ozaki T
    Naika; 1969 May; 23(5):955-62. PubMed ID: 4309044
    [No Abstract]   [Full Text] [Related]  

  • 16. [Peripheral neuropathy in familial primary amyloidosis, with special reference to 10 cases in one family and a review of the literature].
    Araki S; Mawatari S; Oota M; Iwashita H; Kuroiwa Y
    No To Shinkei; 1968 Jan; 20(1):11-8. PubMed ID: 4298009
    [No Abstract]   [Full Text] [Related]  

  • 17. Vitreous involvement in familial amyloidotic neuropathy: a genealogical and genetic study.
    Sandgren O; Drugge U; Holmgren G; Sousa A
    Clin Genet; 1991 Dec; 40(6):452-60. PubMed ID: 1685700
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Ocular manifestations in systemic amyloidosis].
    Inomata H
    Nihon Rinsho; 1991 Apr; 49(4):896-902. PubMed ID: 2072551
    [No Abstract]   [Full Text] [Related]  

  • 19. Familial oculoleptomeningeal amyloidosis.
    Goren H; Steinberg MC; Farboody GH
    Brain; 1980 Sep; 103(3):473-95. PubMed ID: 7417777
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Oculoleptomeningeal amyloidosis in a patient with a TTR Val30Gly mutation in the transthyretin gene.
    Roe RH; Fisher Y; Eagle RC; Fine HF; Cunningham ET
    Ophthalmology; 2007 Nov; 114(11):e33-7. PubMed ID: 17980738
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.