77 related articles for article (PubMed ID: 4208109)
1. [Histochemical examination of the cornea in a patient with Scheie's disease (presentation of a new family)].
Pinto L; Menna F; Balbi R; Cecio A; Federico A; Carlomagno S; Vitello P; Guazzi GC
Acta Neurol (Napoli); 1974; 29(1):38-57. PubMed ID: 4208109
[No Abstract] [Full Text] [Related]
2. 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]
3. [Scheie's syndrome].
Chistiakov GM; Anisimov MP; D'iachkova AIa; Sharets VG; Nesterenko VN
Vopr Okhr Materin Det; 1973 Oct; 18(10):82-4. PubMed ID: 4274200
[No Abstract] [Full Text] [Related]
4. Heterogeneity of disorders in patients with corneal clouding, normal intellect, and mucopolysaccharidosis.
Constantopoulos G; Dekabian AS; Scheie HG
Am J Ophthalmol; 1971 Dec; 72(6):1106-17. PubMed ID: 4256845
[No 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. Letter: Corneal cloudiness and retinitis pigmentosa in the mucopolysaccharidoses.
Cotlier E
N Engl J Med; 1975 Apr; 292(15):812. PubMed ID: 123035
[No Abstract] [Full Text] [Related]
7. Further electroretinographic studies of patients with mucopolysaccharidoses.
Leung LS; Weinstein GW; Hobson RR
Birth Defects Orig Artic Ser; 1971 Mar; 7(3):32-40. PubMed ID: 5006141
[TBL] [Abstract][Full Text] [Related]
8. [Type 2 mucolipidosis, or inclusion cell disease. Apropos of 3 cases with corneal lesions].
Blanck MF
Bull Soc Ophtalmol Fr; 1973 Jan; 73(1):55-62. PubMed ID: 4207052
[No Abstract] [Full Text] [Related]
9. Scheie's syndrome. An ultrastructural analysis of the cornea.
Zabel RW; MacDonald IM; Mintsioulis G; Addison DJ
Ophthalmology; 1989 Nov; 96(11):1631-8. PubMed ID: 2515507
[TBL] [Abstract][Full Text] [Related]
10. [Type V mucopolysaccharidosis (Ullrich-Scheie syndrome) in children. Description of 2 cases and therapeutic prospects].
Capotorti L; Mancuso G; Iannaccone G
Minerva Pediatr; 1975 Mar; 27(8):490-5. PubMed ID: 804082
[No Abstract] [Full Text] [Related]
11. The genetic mucopolysaccharidoses (GMS).
Haust MD
Int Rev Exp Pathol; 1973; 12():251-314. PubMed ID: 4266979
[No Abstract] [Full Text] [Related]
12. [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]
13. Allelism, non-allelism and genetic compounds among the mucopolysaccharidoses: corrective factors in nosology, genetics and therapy.
McKusick VA; Howell RR; Hussels IE; Neufeld EF; Stevenson RE
Trans Assoc Am Physicians; 1972; 85():151-71. PubMed ID: 4267098
[No Abstract] [Full Text] [Related]
14. Letter: In-vitro confirmation of genetic compound of the Hurler and Scheie syndromes.
Danes BS
Lancet; 1974 Apr; 1(7859):680. PubMed ID: 4132345
[No Abstract] [Full Text] [Related]
15. Myocardial collagen of the fibrous long-spacing type.
Banfield WG; Lee CK; Lee CW
Arch Pathol; 1973 Apr; 95(4):262-6. PubMed ID: 4633115
[No Abstract] [Full Text] [Related]
16. The ultrastructure of the skin in patients with mucopolysaccharidoses.
Spicer SS; Garvin AJ; Wohltmann HJ; Simson JA
Lab Invest; 1974 Nov; 31(5):488-502. PubMed ID: 4214966
[No Abstract] [Full Text] [Related]
17. [Mucopolysaccharidosis type II (Hurler-Hunter) in siblings. Electron microscopic study].
Tichý J; Cihula J; Vortel V
Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove; 1972; 15(2):173-9. PubMed ID: 4209410
[No Abstract] [Full Text] [Related]
18. [Corneal lesions in mucopolysaccharidosis].
Richter S; Kilias M
Padiatr Grenzgeb; 1976; 15(3):129-33. PubMed ID: 824603
[No Abstract] [Full Text] [Related]
19. [Ocular Manifestation of Mucopolysaccharidosis I-S (Scheie's Syndrome)].
Viestenz A; Shin YS; Viestenz A; Naumann GO
Klin Monbl Augenheilkd; 2002 Oct; 219(10):745-8. PubMed ID: 12447720
[TBL] [Abstract][Full Text] [Related]
20. [Heritable disorders of the connective tissue].
Friman C; Näntö V
Duodecim; 1969; 85(18):1155-69. PubMed ID: 4244410
[No Abstract] [Full Text] [Related]
[Next] [New Search]
