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7. Apparent allelism of the Hurler, Scheie, and Hurler/Scheie syndromes. Mueller OT; Shows TB; Opitz JM Am J Med Genet; 1984 Jul; 18(3):547-56. PubMed ID: 6433708 [TBL] [Abstract][Full Text] [Related]
8. Mucopolysaccharidosis type II in females: case report and review of literature. Tuschl K; Gal A; Paschke E; Kircher S; Bodamer OA Pediatr Neurol; 2005 Apr; 32(4):270-2. PubMed ID: 15797184 [TBL] [Abstract][Full Text] [Related]
10. [Proceedings: Type II mucolipidosis. Discussion of the physiopathol problem apropos of a new case]. Farriaux JP; Dubois O; Blanckaert D; Walbaum R; Richard P; Halle B; Fontaine G; Strecker G; Tondeur M; Leroy J; Martin JJ Arch Fr Pediatr; 1975 Mar; 32(3):294-5. PubMed ID: 131525 [No Abstract] [Full Text] [Related]
11. [Mucolipidosis Type II. STudy of 2 familial cases. Clinical and biochemical aspects]. Joannard A; Bost M; Pont J; Dieterlen M; Frappat P; Beaudoing A Pediatrie; 1974 Dec; 29(8):825-41. PubMed ID: 4218311 [No Abstract] [Full Text] [Related]
14. Inefficacy of fresh frozen plasma therapy of mucopolysaccharidosis II. Erickson RP; Sandman R; Robertson Wv; Epstein CJ Pediatrics; 1972 Nov; 50(5):693-701. PubMed ID: 4343502 [No Abstract] [Full Text] [Related]
15. [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]
16. Clinical presentation and diagnosis of mucopolysaccharidosis type 2 (Hunter syndrome). Patil R; Wasekar N; Jadhav SG; Zore R; Sangoi P; Vishwanathan D J Assoc Physicians India; 2013 Aug; 61(8):574-6. PubMed ID: 24818348 [No Abstract] [Full Text] [Related]
17. What syndrome is this? Hunter Syndrome. Lonergan CL; Payne AR; Wilson WG; Patterson JW; English JC Pediatr Dermatol; 2004; 21(6):679-81. PubMed ID: 15575857 [No Abstract] [Full Text] [Related]
18. [Case of dysostosis multiplex with features of mucolipidosis II (I-cell disease)]. Barylak A Pol Przegl Radiol Med Nukl; 1974; 38(5):617-22. PubMed ID: 4374690 [No Abstract] [Full Text] [Related]
19. [Biochemical differentiation of Hurler's and Hunter's diseases by fracionation of heparitin sulfate]. Maroteaux P Rev Eur Etud Clin Biol; 1970 Feb; 15(2):203-5. PubMed ID: 4245695 [No Abstract] [Full Text] [Related]
20. Recognition and diagnosis of mucopolysaccharidosis II (Hunter syndrome). Martin R; Beck M; Eng C; Giugliani R; Harmatz P; Muñoz V; Muenzer J Pediatrics; 2008 Feb; 121(2):e377-86. PubMed ID: 18245410 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]