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9. [Sanfilippo's disease: clinico-genetic and biological study of 2 families]. Carlomagno S; Federico A; Vitiello F; Pinto L; Vertucci P; Marolda M; Balbi R; Guazzi GC Acta Neurol (Napoli); 1974; 29(3):231-51. PubMed ID: 4213902 [No Abstract] [Full Text] [Related]
10. Kniest syndrome with dominant inheritance and mucopolysacchariduria. Kim HJ; Beratis NG; Brill P; Raab E; Hirschhorn K; Matalon R Am J Hum Genet; 1975 Nov; 27(6):755-64. PubMed ID: 128291 [TBL] [Abstract][Full Text] [Related]
11. [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]
12. [Pfaundler-Huler's gargoylism, forme fruste, and peripheral pigmentary retinal degeneration]. Paufique L; Ravault MP; Manuel Y; Didier-Laurent A Ann Ocul (Paris); 1965 Aug; 198(8):753-66. PubMed ID: 4954979 [No Abstract] [Full Text] [Related]
14. Gargoylism. A report of a case in an African child. Stephens AJ East Afr Med J; 1970 Jul; 47(7):383-8. PubMed ID: 4248337 [No Abstract] [Full Text] [Related]
15. [Case of gargoylism (multiple dysostosis)]. Tanaka H; Katayama T; Suto T; Mori S Seikei Geka; 1970 Apr; 21(4):302-7. PubMed ID: 4988600 [No Abstract] [Full Text] [Related]
16. [Case of gargoylism in a 12-year-old girl]. Lisitsina NF; Chernysheva ZhA; Belousova TK Pediatriia; 1974 Oct; 0(10):86-8. PubMed ID: 4215065 [No Abstract] [Full Text] [Related]
17. [Biochemical diagnosis of hereditary mucopolysaccharidoses in children]. Krasnopol'skaia KD; Lebedeva TV; Odinokova ON; Iakovlev SA Pediatriia; 1985 May; (5):28-32. PubMed ID: 3931048 [No Abstract] [Full Text] [Related]
18. [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]