192 related articles for article (PubMed ID: 4370235)
21. GM1-gangliosidosis. Ocular and pathological manifestations.
Emery JM; Green WR; Wyllie RG; Howell RR
Arch Ophthalmol; 1971 Feb; 85(2):177-87. PubMed ID: 4250987
[No Abstract] [Full Text] [Related]
22. [Anatomo-clinical study of ocular lesions due to gangliosidosis of the GM1 Norman-Landing type].
Seringe P; Dhermy P; Aron JJ
Ann Pediatr (Paris); 1969 Dec; 16(12):748-55. PubMed ID: 5370004
[No Abstract] [Full Text] [Related]
23. The cerebellum in mucopolysaccharidosis. A histological, histochemical, and ultrastructural study.
Doshi R; Sandry SA; Churchill AW; Brownell B
J Neurol Neurosurg Psychiatry; 1974 Oct; 37(10):1133-8. PubMed ID: 4374507
[TBL] [Abstract][Full Text] [Related]
24. [Mucopolysaccharidoses. I. The clinical and radiological aspects of the 6 classical mucopolysaccharidoses].
Bulgarelli R; Romano C
Minerva Pediatr; 1972 Sep; 24(33):1471-578. PubMed ID: 4263584
[No Abstract] [Full Text] [Related]
25. Application of electron microscopy to the study of ocular inborn errors of metabolism.
Tripathi RC; Ashton N
Birth Defects Orig Artic Ser; 1976; 12(3):69-104. PubMed ID: 821566
[No Abstract] [Full Text] [Related]
26. [Crystalline dystrophy of the cornea. Histological and ultrastructural study].
Babel J; Englert U; Ricci A
Arch Ophtalmol Rev Gen Ophtalmol; 1973 Nov; 33(11):721-34. PubMed ID: 4366953
[No Abstract] [Full Text] [Related]
27. Pathology of Terrien's disease. Histochemical and electron microscopic study.
Süveges J; Léval G; Alberth B
Am J Ophthalmol; 1972 Dec; 74(6):1191-200. PubMed ID: 4119040
[No Abstract] [Full Text] [Related]
28. Pre-Descemet's membrane corneal dystrophy.
Curran RE; Kenyon KR; Green WR
Am J Ophthalmol; 1974 May; 77(5):711-6. PubMed ID: 4363036
[No Abstract] [Full Text] [Related]
29. Bietti's tapetoretinal degeneration with marginal corneal dystrophy (crystalline retinopathy): case report.
Harrison RJ; Acheson RR; Dean-Hart JC
Br J Ophthalmol; 1987 Mar; 71(3):220-3. PubMed ID: 3493804
[TBL] [Abstract][Full Text] [Related]
30. Ocular histopathology in Hunter's syndrome. Systemic mucopolysaccharidosis type II.
Goldberg MF; Duke JR
Arch Ophthalmol; 1967 Apr; 77(4):503-12. PubMed ID: 4225692
[No Abstract] [Full Text] [Related]
31. Gargoylism associated with optic atrophy.
Mailer C
Can J Ophthalmol; 1969 Jul; 4(3):266-71. PubMed ID: 4241234
[No Abstract] [Full Text] [Related]
32. Scheie syndrome and macular corneal dystrophy. An ultrastructural comparison of conjunctiva and skin.
Quigley HA; Goldberg MF
Arch Ophthalmol; 1971 May; 85(5):553-64. PubMed ID: 4253322
[No Abstract] [Full Text] [Related]
33. [Ultrastructural aspects and biochemical significance of metachromatic granulations and other inclusions in cultured fibroblasts from lipidosis and mucopolysaccharidosis].
Lyon G; Hors-Cayla MC; Jonsson V; Maroteaux P
J Neurol Sci; 1973 Jun; 19(2):235-53. PubMed ID: 4351452
[No Abstract] [Full Text] [Related]
34. Ocular abnormalities in mucolipidosis IV.
Riedel KG; Zwaan J; Kenyon KR; Kolodny EH; Hanninen L; Albert DM
Am J Ophthalmol; 1985 Feb; 99(2):125-36. PubMed ID: 3918453
[TBL] [Abstract][Full Text] [Related]
35. [Congenital dystrophy of the cornea].
Babel J; Pouliquen Y; Bisson J; Leuenberger P
Arch Ophtalmol Rev Gen Ophtalmol; 1969 Oct; 29(10):683-98. PubMed ID: 4243568
[No Abstract] [Full Text] [Related]
36. [Corneal dystrophy in Morquio's disease].
Negroni L; Tiberio G; Meduri R
Ann Ottalmol Clin Ocul; 1968 Feb; 94(2):140-8. PubMed ID: 4986326
[No Abstract] [Full Text] [Related]
37. Electron microscopy of posterior polymorphous degeneration.
Boruchoff SA; Kuwabara T
Am J Ophthalmol; 1971 Nov; 72(5):879-87. PubMed ID: 4940980
[No Abstract] [Full Text] [Related]
38. Congenital anomalies of the peripheral cornea.
Stanley JA
Int Ophthalmol Clin; 1986; 26(4):15-28. PubMed ID: 3492475
[No Abstract] [Full Text] [Related]
39. The Morquio syndrome--light and electron microscopic findings from two corneas.
Ghosh M; McCulloch C
Can J Ophthalmol; 1974 Oct; 9(4):445-52. PubMed ID: 4279098
[No Abstract] [Full Text] [Related]
40. [Ultrastructure of skin fibroblasts in storage diseases (mucopolysaccharidosis types IV and VI)].
Bruskina VIa; Barer FS; Pavlova MN; Meerson EM
Tsitol Genet; 1980; 14(5):21-6. PubMed ID: 6776669
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
