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2. [Histochemical investigations in a case of Hurler-Pfaundler disease]. HORVATH E; BILICZKI F Acta Histochem; 1959 Oct; 8():371-80. PubMed ID: 14403245 [No Abstract] [Full Text] [Related]
3. [On the clinical aspects and pathological anatomy of Pfaundler-Hurler disease (gargoylism)]. POTACS W; SKALA O Neue Osterr Z Kinderheilkd; 1959; 4():269-80. PubMed ID: 14434432 [No Abstract] [Full Text] [Related]
4. [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]
5. Oral manifestations of the Fitzgerald-Gardner, Pringle-Bourneville, Robin. adrenogenital, and Hurler-Pfaundler syndromes. GORLIN RJ; CHAUDHARY AP; KELLN EE Oral Surg Oral Med Oral Pathol; 1960 Oct; 13():1233-44. PubMed ID: 13707263 [No Abstract] [Full Text] [Related]
6. [Histopathology & histochemistry of the Hurler-Pfaundier disease (gargoylism)]. MATTYUS A; JOBST C Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr; 1959; 198(3):317-30. PubMed ID: 13628197 [No Abstract] [Full Text] [Related]
7. Chemical nature of the storage substance in gargoylism, Hurler-Pfaundler's disease. UZMAN LL AMA Arch Pathol; 1955 Sep; 60(3):308-18. PubMed ID: 13248343 [No Abstract] [Full Text] [Related]
8. [On unusually marked skin changes in Pfaundler-Hurler disease (gargoylism, dysostotic idiocy)]. CATEL W Frankf Z Pathol; 1960; 70():324-36. PubMed ID: 13808399 [No Abstract] [Full Text] [Related]
9. The oral signs of Hurler-Hunter syndrome: report of four cases. Liu KL ASDC J Dent Child; 1980; 47(2):122-7. PubMed ID: 6767763 [No Abstract] [Full Text] [Related]
10. [Hunter-Hurler syndrome (gargolismo), presentation of a case with electrophoretic studies]. LEFEVRE AB; VALENTE MI; MATTOS CA Arq Neuropsiquiatr; 1956 Mar; 14(1):46-60. PubMed ID: 13315058 [No Abstract] [Full Text] [Related]
11. Gargoylism (Hunter-Hurler disease, dysostosis multiplex, lipochondrodystrophy) prenatal and neonatal bone lesions and their early postnatal evolution. CAFFEY J Am J Roentgenol Radium Ther Nucl Med; 1952 May; 67(5):715-31. PubMed ID: 14914945 [No Abstract] [Full Text] [Related]
12. Gargoylism (Hunter-Hurler disease, dysostosis multiplex, lipochondrodystrophy); prenatal and neonatal bone lesions and their early postnatal evolution. CAFFEY J Bull Hosp Joint Dis; 1951 Oct; 12(2):38-66. PubMed ID: 14905097 [No Abstract] [Full Text] [Related]
13. Clear cells in the atrioventricular valves of infants with severe human mucopolysaccharidosis (Hurler syndrome) are activated valvular interstitial cells. Braunlin E; Tolar J; Mackey-Bojack S; Masinde T; Krivit W; Schoen FJ Cardiovasc Pathol; 2011; 20(5):315-21. PubMed ID: 20619689 [TBL] [Abstract][Full Text] [Related]
14. The Hurler and Hunter syndromes. Dorfman A; Matalon R Am J Med; 1969 Nov; 47(5):691-707. PubMed ID: 4243120 [No Abstract] [Full Text] [Related]
15. The pathology and biochemistry of gargoylism; a report of three cases with a review of the literature. HENDERSON JL; MacGREGOR AR; THANNHAUSER SJ; HOLDEN R Arch Dis Child; 1952 Jun; 27(133):230-53. PubMed ID: 14934278 [No Abstract] [Full Text] [Related]
19. Pulmonary disability in the Hurler syndrome (lipochondrodystrophy): a study of two cases. MURRAY JF N Engl J Med; 1959 Aug; 261():378-82. PubMed ID: 14425432 [No Abstract] [Full Text] [Related]