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Journal Abstract Search

130 related items for PubMed ID: 25913657

  • 1. [Meretoja syndrome: Identification of a family and description of the corneal involvement by confocal microscopy].
    Bonnin N, Borel A, Daniel E, Tiple A, Joubert R, Heng AE, Chiambaretta F.
    J Fr Ophtalmol; 2015 Jun; 38(6):e111-5. PubMed ID: 25913657
    [No Abstract] [Full Text] [Related]

  • 2. Heavy-chain amyloidosis in TGFBI-negative and gelsolin-negative atypical lattice corneal dystrophy.
    Pradhan MA, Henderson RA, Patel D, McGhee CN, Vincent AL.
    Cornea; 2011 Oct; 30(10):1163-6. PubMed ID: 21743312
    [Abstract] [Full Text] [Related]

  • 3. [Lattice dystrophy. Primary and familial localized corneal amyloidosis].
    Dhermy P, Brégeat P, Hamard H, Rizman P, Offret H.
    Arch Ophtalmol Rev Gen Ophtalmol; 1973 Oct; 33(6):477-84. PubMed ID: 4132515
    [No Abstract] [Full Text] [Related]

  • 4. Meretoja syndrome. Lattice dystrophy of the cornea with hereditary generalized amyloidosis.
    Donders PC, Blanksma LJ.
    Ophthalmologica; 1979 Oct; 178(3):173-80. PubMed ID: 314081
    [Abstract] [Full Text] [Related]

  • 5. [Reticular dystrophy of the cornea. A form of hereditary-familial amyloidosis].
    Garrido C, Malbran E, Stefani C.
    Arch Oftalmol B Aires; 1968 Jun; 43(6):139-45. PubMed ID: 4181889
    [No Abstract] [Full Text] [Related]

  • 6. Corneal dystrophies: a clinical, pathological, and surgical approach. 28 Edward Jackson Memorial Lecture.
    Malbran ES.
    Am J Ophthalmol; 1972 Nov; 74(5):771-809. PubMed ID: 4118882
    [No Abstract] [Full Text] [Related]

  • 7. [Electron microscopic study of a Haab-Dimmer lattice dystrophy].
    Pouliquen Y, Dhermy P, Taillebourg O.
    Arch Ophtalmol Rev Gen Ophtalmol; 1973 Nov; 33(6):485-99. PubMed ID: 4132516
    [No Abstract] [Full Text] [Related]

  • 8. Corneal morphology and sensitivity in lattice dystrophy type II (familial amyloidosis, Finnish type).
    Rosenberg ME, Tervo TM, Gallar J, Acosta MC, Müller LJ, Moilanen JA, Tarkkanen AH, Vesaluoma MH.
    Invest Ophthalmol Vis Sci; 2001 Mar; 42(3):634-41. PubMed ID: 11222521
    [Abstract] [Full Text] [Related]

  • 9. [General amyloidosis with lattice dystrophy of the cornea].
    Meretoja J.
    Duodecim; 1971 Mar; 87(21):1412-9. PubMed ID: 5315643
    [No Abstract] [Full Text] [Related]

  • 10. Late onset lattice corneal dystrophy with systemic familial amyloidosis, amyloidosis V, in an English family.
    Stewart HS, Parveen R, Ridgway AE, Bonshek R, Black GC.
    Br J Ophthalmol; 2000 Apr; 84(4):390-4. PubMed ID: 10729296
    [Abstract] [Full Text] [Related]

  • 11. A possibly new familial superficial corneal dystrophy.
    Smith EL, Wilson WM, Williams DK.
    Can J Ophthalmol; 1971 Jan; 6(1):30-7. PubMed ID: 5313312
    [No Abstract] [Full Text] [Related]

  • 12. Lattice corneal dystrophy type II: clinical, pathologic, and molecular study in a Spanish family.
    Huerva V, Velasco A, Sánchez MC, Mateo AJ, Matías-Guiu X.
    Eur J Ophthalmol; 2007 Jan; 17(3):424-9. PubMed ID: 17534828
    [Abstract] [Full Text] [Related]

  • 13. A case of one eye with gelatinous drop-like corneal dystrophy and the other eye with band-shaped spheroidal corneal degeneration.
    Akiya S, Takahashi H, Furukawa H, Hamada T, Sugahara S, Suzuki T, Ninomiya H, Yoshimura M, Shimazaki J, Tsubota K.
    Ophthalmologica; 1995 Jan; 209(2):96-100. PubMed ID: 7746654
    [Abstract] [Full Text] [Related]

  • 14. Clinical and genetical diagnosis of a case of Meretoja syndrome and frontotemporal lifting procedure.
    Galindo-Bocero J, García-Martínez I, Portillo M, Hernando Acero I, García-González N.
    Arch Soc Esp Oftalmol (Engl Ed); 2022 Oct; 97(10):583-586. PubMed ID: 36114141
    [Abstract] [Full Text] [Related]

  • 15. Natural course of Finnish gelsolin amyloidosis.
    Nikoskinen T, Schmidt EK, Strbian D, Kiuru-Enari S, Atula S.
    Ann Med; 2015 Oct; 47(6):506-11. PubMed ID: 26339870
    [Abstract] [Full Text] [Related]

  • 16. Danish type gelsolin-related amyloidosis in a Brazilian family: case reports.
    Solari HP, Ventura MP, Antecka E, Belfort Junior R, Burnier MN.
    Arq Bras Oftalmol; 2011 Oct; 74(4):286-8. PubMed ID: 22068858
    [Abstract] [Full Text] [Related]

  • 17. [Histopathological study of familial systemic amyloidosis with latticed corneal dystrophy].
    Wang SJ.
    Zhonghua Yi Xue Za Zhi; 1985 Feb; 65(2):78-9. PubMed ID: 3921213
    [No Abstract] [Full Text] [Related]

  • 18. [Bilateral hereditary corneal dermoid (author's transl)].
    Pouliquen Y, Dhermy P, Cotinat J, Giraud JP, Savoldelli M.
    J Fr Ophtalmol; 1978 Feb; 1(6-7):443-50. PubMed ID: 151704
    [Abstract] [Full Text] [Related]

  • 19. Lattice corneal dystrophy. An inherited variety of amyloidosis restricted to the cornea.
    Klintworth GK.
    Am J Pathol; 1967 Mar; 50(3):371-99. PubMed ID: 4163628
    [No Abstract] [Full Text] [Related]

  • 20. [Hereditary gelsolin amyloidosis--40 years of Meretoja disease].
    Kiuru-Enari S, Haltia M.
    Duodecim; 2010 Mar; 126(10):1162-71. PubMed ID: 20597346
    [Abstract] [Full Text] [Related]

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