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22. [Urinary acid mucopolysaccharide-peptide complexes in children. 2. Urinary acid mucopolysaccharide-peptide complexes in Hunter's syndrome]. Ri T Nihon Shonika Gakkai Zasshi; 1970 Jan; 74(1):137-47. PubMed ID: 4245240 [No Abstract] [Full Text] [Related]
23. [Familial cases of Hunter's syndrome]. Kawamura N; Narikawa J; Takahira T; Ito K; Kato M Nihon Rinsho; 1973 Aug; 31(8):2606-9. PubMed ID: 4203266 [No Abstract] [Full Text] [Related]
24. The defect in Hurler's and Hunter's syndromes: faulty degradation of mucopolysaccharide. Fratantoni JC; Hall CW; Neufeld EF Proc Natl Acad Sci U S A; 1968 Jun; 60(2):699-706. PubMed ID: 4236091 [No Abstract] [Full Text] [Related]
25. An early case of Hurler's syndrome (Hunter-Hurler-Pfaundler syndrome, mucopolysaccharidosis I, dysostosis multiplex): report of a case. Fay JT J Oral Med; 1972; 27(3):64-6. PubMed ID: 4625583 [No Abstract] [Full Text] [Related]
26. [Hunter's syndrome (type II) in a 4-year-old child]. Zoch-Zwierz W; Zadrozna B; Kilczewska D Wiad Lek; 1976 Apr; 29(7):641-4. PubMed ID: 131419 [No Abstract] [Full Text] [Related]
27. Hunter's syndrome: beta-galactosidase deficiency in skin. Gerich JE N Engl J Med; 1969 Apr; 280(15):799-802. PubMed ID: 4975290 [No Abstract] [Full Text] [Related]
28. The linkage relation of the loci for the Xm serum system and the X-linked form of Hurler's syndrome (Hunter's syndrome). Berg K; Danes BS; Bearn AG Am J Hum Genet; 1968 Jul; 20(4):398-401. PubMed ID: 4969416 [No Abstract] [Full Text] [Related]
29. [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]
30. Mild form of the Hunter syndrome, indentity of the biochemical defect with the severe type. Wiesmann UN; Rampini S Helv Paediatr Acta; 1974 Apr; 29(1):73-8. PubMed ID: 4275601 [No Abstract] [Full Text] [Related]
31. Retinitis pigmentosa and nanophthalmos in a patient with attenuated Hunter's syndrome. Dos Santos Martins TG; de Azevedo Costa ALF; Pimentel SLG; Oyamada MK; Finzi S Doc Ophthalmol; 2023 Jun; 146(3):273-279. PubMed ID: 36807032 [TBL] [Abstract][Full Text] [Related]
32. [Prenatal diagnosis of Hunter's disease]. Bolodár A; Török O; Horváth K; Németi M; Szabó M; Papp Z Orv Hetil; 1990 May; 131(19):1025-7. PubMed ID: 2111903 [TBL] [Abstract][Full Text] [Related]
33. [Comments on a case of Hurler's syndrome (gargoylism)]. Martínez de Letona J; Alvárez Manzanero J; López Varela J; Peláez Cueto JL; Perianes Carro J Rev Clin Esp; 1965 Apr; 97(2):115-8. PubMed ID: 4953451 [No Abstract] [Full Text] [Related]
34. On urinary acid mucopolysaccharides in a case of gargoylism (Hurler's syndrome). A preliminary note. Kamikubo K; Mori J; Shimada K Fukushima J Med Sci; 1965 Dec; 12(3):131-6. PubMed ID: 4223890 [No Abstract] [Full Text] [Related]
35. Letter: Question raised regarding diagnosis of Hunter syndrome. Kelly TE Pediatrics; 1974 Oct; 54(4):522-3. PubMed ID: 4213222 [No Abstract] [Full Text] [Related]
36. Demonstration of the heterozygous state in Hunter's syndrome. Booth CW; Nadler HL Pediatrics; 1974 Mar; 53(3):396-9. PubMed ID: 4273646 [No Abstract] [Full Text] [Related]
37. [Mitral insuffiency and Hurler's disease. Apropos of 2 cases of 2 half brothers]. Neimann N; Pernot C; Marchal C; Fall M Ann Pediatr (Paris); 1968 Oct; 15(10):612-8. PubMed ID: 4237828 [No Abstract] [Full Text] [Related]
39. Electroretinography and fundus oculi findings in Hurler's disease and allied mucopolysaccharidoses. Gills JP; Hobson R; Hanley WB; McKusick VA Arch Ophthalmol; 1965 Nov; 74(5):596-603. PubMed ID: 4954407 [No Abstract] [Full Text] [Related]
40. Clinical and probable genetic heterogeneity within mucopolysaccharidosis. II. Report of a family with a mild form. Lichtenstein JR; Bilbrey GL; McKusick VA Johns Hopkins Med J; 1972 Dec; 131(6):425-35. PubMed ID: 4629084 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]