280 related articles for article (PubMed ID: 4274189)
21. A distinct biochemical deficit in the Maroteaux-Lamy syndrome (mucopolysaccharidosis VI).
Baron RW; Neufeld EF
J Pediatr; 1972 Jan; 80(1):114-6. PubMed ID: 4259536
[No Abstract] [Full Text] [Related]
22. [Clinical variants of hereditary mucopolysaccharidosis].
Geller LI
Klin Med (Mosk); 1970 Jul; 48(7):16-9. PubMed ID: 4250220
[No Abstract] [Full Text] [Related]
23. 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]
24. The detection of carriers and the problem of heterogeneity in genetic counseling.
Porter IH
Birth Defects Orig Artic Ser; 1970 May; 6(1):23-5. PubMed ID: 4257329
[No Abstract] [Full Text] [Related]
25. Lysosomal enzymes in cultured cells from mucopolysaccharidoses.
Keyser AJ; Priest RE; Priest JH
Lab Invest; 1972 Dec; 27(6):600-5. PubMed ID: 4264608
[No Abstract] [Full Text] [Related]
26. [Heritable disorders of the connective tissue].
Friman C; Näntö V
Duodecim; 1969; 85(18):1155-69. PubMed ID: 4244410
[No Abstract] [Full Text] [Related]
27. [Corneal and retinal disorders associated with mucopolysaccharidosis (8 cases)].
Thomas C; Raspiller A; Fall M
Bull Soc Ophtalmol Fr; 1970; 70(9):933-41. PubMed ID: 4262237
[No Abstract] [Full Text] [Related]
28. The genetic mucopolysaccharidoses (GMS).
Haust MD
Int Rev Exp Pathol; 1973; 12():251-314. PubMed ID: 4266979
[No Abstract] [Full Text] [Related]
29. [Mucopolysaccharidosis].
Maroteaux P; Hors-Cayla MC
Ann Biol Clin (Paris); 1972; 30(5):451-8. PubMed ID: 4264383
[No Abstract] [Full Text] [Related]
30. Allelism, non-allelism, and genetic compounds among the mucopolysaccharidoses.
McKusick VA; Howell RR; Hussels IE; Neufeld EF; Stevenson RE
Lancet; 1972 May; 1(7758):993-6. PubMed ID: 4112371
[No Abstract] [Full Text] [Related]
31. Thin layer chromatography of urinary acid glycosaminoglycans as screening procedure for mucopolysaccharidoses.
Teller WM; Ziemann A
Horm Metab Res; 1969 Jan; 1(1):32-5. PubMed ID: 4258873
[No Abstract] [Full Text] [Related]
32. [Clinical and biochemical study of some hereditary metabolic diseases with nervous system lesions].
Gusev EI
Zh Nevropatol Psikhiatr Im S S Korsakova; 1971; 71(10):1475-81. PubMed ID: 4257932
[No Abstract] [Full Text] [Related]
33. Differential diagnosis of mucopolysaccharidosis by means of thin-layer chromatography of urinary acidic glycosaminoglycans.
Humbel R; Marchal C; Fall M
Helv Paediatr Acta; 1969 Dec; 24(6):648-50. PubMed ID: 4244361
[No Abstract] [Full Text] [Related]
34. Urinary hyaluronidase activity in mucopolysaccharidosis.
Józsa L; Szabó L
Acta Paediatr Acad Sci Hung; 1969; 10(1):73-8. PubMed ID: 4240053
[No Abstract] [Full Text] [Related]
35. A new mucopolysaccharidosis.
Horton WA; Schimke RN
J Pediatr; 1970 Aug; 77(2):252-8. PubMed ID: 4988173
[No Abstract] [Full Text] [Related]
36. [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]
37. [Urinary excretion of mucopolysaccarides in normal and pathologic conditions].
Capotorti MA; Ferrara M; Pinto L
Pediatria (Napoli); 1972 Mar; 80(1):43-53. PubMed ID: 4260502
[No Abstract] [Full Text] [Related]
38. [Progress in the diagnosis of congenital metabolic central nervous system diseases. Review].
Nevsímalová S
Cesk Neurol; 1973 Mar; 36(2):120-7. PubMed ID: 4266580
[No Abstract] [Full Text] [Related]
39. [Biochemical differentiation of mucopolysaccharidoses].
Spranger J; Wiedemann HR
Monatsschr Kinderheilkd (1902); 1970 Jun; 118(6):421-3. PubMed ID: 4257110
[No Abstract] [Full Text] [Related]
40. Mucopolysaccharidosis.
Levin B; Jacoby NM
Proc R Soc Med; 1972 Apr; 65(4):339-41. PubMed ID: 4260161
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
