BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

240 related articles for article (PubMed ID: 4319009)

  • 1. [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]  

  • 2. 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]  

  • 3. [Genetic considerations on a series of cases of peripheral neuropathy of the hereditary paramyloidosis type].
    Fariello R; Curtoni ES; Delsedime M; Mutani R; Quattrocolo G; Fariello R; Furlan PM
    Arch Sci Med (Torino); 1971; 128(4):181-5. PubMed ID: 4342668
    [No Abstract]   [Full Text] [Related]  

  • 4. [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]  

  • 5. 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]  

  • 6. [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]  

  • 7. [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]  

  • 8. [Familial cerebral hemorrhage as a result of cerebral amyloid angiopathy].
    Luyendijk W; Bots GT; Vegter-van der Vlis M; Went LN
    Ned Tijdschr Geneeskd; 1986 Oct; 130(43):1935-40. PubMed ID: 3774041
    [No Abstract]   [Full Text] [Related]  

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

  • 10. [Perforating cutaneous amyloidosis].
    Bacharach-Buhles M; Schultz-Ehrenburg U; Altmeyer P
    Hautarzt; 1992 Jun; 43(6):364-8. PubMed ID: 1628970
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. [Familial amyloid neuropathies in 3 families of French origin].
    Julien J; Vital C; Vallat JM; Lagueny A; Ferrer X
    Rev Neurol (Paris); 1983; 139(4):259-67. PubMed ID: 6310716
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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]  

  • 14. Amyloid polyneuropathy, type II (Indiana, or Rukavina type).
    Mahloudji M; Nissim J
    Birth Defects Orig Artic Ser; 1971 Feb; 7(2):100-1. PubMed ID: 4375502
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. An unusual case of ocular involvement in primary systemic nonfamilial amyloidosis.
    Schwartz MF; Green WR; Michels RG; Kincaid MC; Fogle J
    Ophthalmology; 1982 Apr; 89(4):394-401. PubMed ID: 7099557
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hereditary amyloid neuropathy.
    Mahloudji M; Teasdall RD; Adamkiewicz JJ; McKusick VA
    Trans Am Neurol Assoc; 1967; 92():46-9. PubMed ID: 4329416
    [No Abstract]   [Full Text] [Related]  

  • 18. 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]  

  • 19. Primary familial amyloidosis.
    Wong VG; McFarlin DE
    Arch Ophthalmol; 1967 Aug; 78(2):208-13. PubMed ID: 4952599
    [No Abstract]   [Full Text] [Related]  

  • 20. Primary amyloidosis with polyneuropathy. Some aspects on the histopathological diagnosis ante mortem based on studies of biopsy specimens from 30 familial and non-familial cases.
    Andersson R; Hofer PA
    Acta Med Scand; 1974; 196(1-2):115-20. PubMed ID: 4138132
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 12.