101 related articles for article (PubMed ID: 3123345)
1. [Isolated mucopolysaccharidosis of the cornea].
Witschel H; Hoffmann F
Fortschr Ophthalmol; 1987; 84(5):411-3. PubMed ID: 3123345
[No Abstract] [Full Text] [Related]
2. Histopathology of corneal changes in lecithin-cholesterol acyltransferase deficiency.
Viestenz A; Schlötzer-Schrehardt U; Hofmann-Rummelt C; Seitz B; Küchle M
Cornea; 2002 Nov; 21(8):834-7. PubMed ID: 12410048
[TBL] [Abstract][Full Text] [Related]
3. Lecithin cholesterol acyl transferase deficiency. Light and electron microscopic finding from two corneas.
Bethell W; McCulloch C; Ghosh M
Can J Ophthalmol; 1975 Oct; 10(4):494-501. PubMed ID: 811335
[TBL] [Abstract][Full Text] [Related]
4. Corneal opacity in LCAT disease.
Cogan DG; Kruth HS; Datilis MB; Martin N
Cornea; 1992 Nov; 11(6):595-9. PubMed ID: 1468226
[TBL] [Abstract][Full Text] [Related]
5. Ocular manifestations of the mucopolysaccharidoses.
François J
Ophthalmologica; 1974; 169(5):345-61. PubMed ID: 4370235
[No Abstract] [Full Text] [Related]
6. Familial lecithin:cholesterol acyltransferase deficiency. Biochemistry of the cornea.
Winder AF; Garner A; Sheraidah GA; Barry P
J Lipid Res; 1985 Mar; 26(3):283-7. PubMed ID: 3989388
[TBL] [Abstract][Full Text] [Related]
7. [Type VI-A mucopolysaccharidosis (Maroteaux-Lamy disease). Clinico-pathologic case report].
Stürmer J
Klin Monbl Augenheilkd; 1989 Apr; 194(4):273-81. PubMed ID: 2498570
[TBL] [Abstract][Full Text] [Related]
8. [Corneal opacity as the leading symptom of hereditary lecithin-cholesterol acyltransferase (LCAT) deficiency. Case report and a review of the literature].
Weidle EG; Lisch W
Klin Monbl Augenheilkd; 1987 Mar; 190(3):182-7. PubMed ID: 3586537
[TBL] [Abstract][Full Text] [Related]
9. In vivo imaging of the cornea in a patient with lecithin-cholesterol acyltransferase deficiency.
Lisch W; Saikia P
Cornea; 2010 Oct; 29(10):1207; author reply 1207. PubMed ID: 20628294
[No Abstract] [Full Text] [Related]
10. Ultrastructural and histochemical studies of a newly recognized form of systemic mucopolysaccharidosis. (Maroteaux-Lamy syndrome, mild phenotype).
Quigley HA; Kenyon KR
Am J Ophthalmol; 1974 Jun; 77(6):809-18. PubMed ID: 4365226
[No Abstract] [Full Text] [Related]
11. The Case | Nephrotic syndrome with corneal opacities.
Ozkok A; Onal Y; Kilicaslan I; Solakoglu S; Bayramlar H; Odabas AR
Kidney Int; 2017 Feb; 91(2):515-516. PubMed ID: 28087013
[No Abstract] [Full Text] [Related]
12. In vivo imaging of the cornea in a patient with lecithin-cholesterol acyltransferase deficiency.
Palmiero PM; Sbeity Z; Liebmann J; Ritch R
Cornea; 2009 Oct; 28(9):1061-4. PubMed ID: 19724202
[TBL] [Abstract][Full Text] [Related]
13. Altered corneal stromal matrix organization is associated with mucopolysaccharidosis I, III and VI.
Alroy J; Haskins M; Birk DE
Exp Eye Res; 1999 May; 68(5):523-30. PubMed ID: 10328965
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Clearing of cornea after perforating keratoplasty in mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome).
Naumann G
N Engl J Med; 1985 Apr; 312(15):995. PubMed ID: 3919302
[No Abstract] [Full Text] [Related]
16. Lecithin:cholesterol acyltransferase deficiency.
Bellan L; Mikelberg F; Frohlich J
Can J Ophthalmol; 1988 Oct; 23(6):285-7. PubMed ID: 3203243
[TBL] [Abstract][Full Text] [Related]
17. Ophthalmic observations in lecithin cholesterol acyltransferase deficiency.
Vrabec MP; Shapiro MB; Koller E; Wiebe DA; Henricks J; Albers JJ
Arch Ophthalmol; 1988 Feb; 106(2):225-9. PubMed ID: 3341979
[TBL] [Abstract][Full Text] [Related]
18. [Transparency of the cornea].
Seiler T
Fortschr Ophthalmol; 1987; 84(2):115-7. PubMed ID: 3596408
[No Abstract] [Full Text] [Related]
19. [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]
20. [Histological and ultrastructural study of the cornea in 2 cases of Peter's syndrome].
Pouliquen Y; Graf B; Saraux H
Arch Ophtalmol Rev Gen Ophtalmol; 1971 Oct; 31(10):695-708. PubMed ID: 4256937
[No Abstract] [Full Text] [Related]
[Next] [New Search]
