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5. Familial oxalosis. Report of three cases and review of the literature. Takahashi A; Saito K; Kondo Y; Kurosawa T Acta Pathol Jpn; 1973 Aug; 23(3):559-75. PubMed ID: 4800726 [No Abstract] [Full Text] [Related]
6. [Alpha-1-antitrypsin deficiency, fatty liver and ulcerative colitis. A hitherto unknown symptom complex with account of familial predisposition]. Pedersen JK Ugeskr Laeger; 1974 Dec; 136(49):2741-4. PubMed ID: 4548588 [No Abstract] [Full Text] [Related]
7. An overview of renal oxalosis. Lueck FM Nephrol Nurse; 1980; 2(3):13-4. PubMed ID: 6991966 [No Abstract] [Full Text] [Related]
8. [Primary congenital glaucoma and heredity]. Daghfous MT; Ayed S; Ben Nejma L; Kamoun S; Boussen S Tunis Med; 1986 Oct; 64(10):831-5. PubMed ID: 3824540 [No Abstract] [Full Text] [Related]
9. Uridine diphosphate galactose 4-epimerase deficiency. II. Clinical follow-up, biochemical studies and family investigation. Gitzelmann R; Steinmann B Helv Paediatr Acta; 1973 Dec; 28(6):497-510. PubMed ID: 4785150 [No Abstract] [Full Text] [Related]
10. Estimation of the frequency of the recessive gene of acatalasemia in Japan. Ogata M; Hayashi S; Takahara S Acta Med Okayama (1952); 1971 Jun; 25(3):193-8. PubMed ID: 4263520 [No Abstract] [Full Text] [Related]
11. [Familial urolithiasis due to primary hyperoxaluria type I]. Cos Welsh J; Salgado Cabrera QF; Matus Sequeira A Bol Med Hosp Infant Mex; 1976; 33(4):887-902. PubMed ID: 952662 [No Abstract] [Full Text] [Related]
13. [Oxalosis--a hereditary metabolic disease as a cause of terminal renal insufficiency]. Francisković V; Matić-Glazar D; Sabolić J; Strizić V; Cohar F; Zuza B; Orlić P Acta Chir Iugosl; 1984 Mar; 31(2):235-44. PubMed ID: 6516661 [No Abstract] [Full Text] [Related]
14. [Oxalosis: two family studies in Tunisia (author's transl)]. Ramadhane MS; Khrouf N; Brauner R; Ben Jilani S; Hamza M; Hamza B Ann Pediatr (Paris); 1982 Feb; 29(2):148-51. PubMed ID: 7059122 [No Abstract] [Full Text] [Related]
15. The fate of a child with primary hyperoxaluria (oxalosis). Berger H Acta Paediatr Hung; 1984; 25(1-2):11-22. PubMed ID: 6477762 [TBL] [Abstract][Full Text] [Related]
16. Renal homotransplantation in a patient with primary familial oxalosis. Deodhar SD; Tung KS; Zühlke V; Nakamoto S Arch Pathol; 1969 Jan; 87(1):118-24. PubMed ID: 4881324 [No Abstract] [Full Text] [Related]
17. The field investigation for acatalasemic gene carriers. Wakisaka G; Yamamoto T; Yamamoto Y; Sakamoto K; Sawada M Naika Hokan; 1967 May; 14(5):151-7. PubMed ID: 5624288 [No Abstract] [Full Text] [Related]
18. Familial dysautonomia. A report of genetic and clinical studies, with a review of the literature. Brunt PW; McKusick VA Medicine (Baltimore); 1970 Sep; 49(5):343-74. PubMed ID: 4322121 [No Abstract] [Full Text] [Related]
19. Hereditary diseases in Finland; rare flora in rare soul. Norio R; Nevanlinna HR; Perheentupa J Ann Clin Res; 1973 Jun; 5(3):109-41. PubMed ID: 4584134 [No Abstract] [Full Text] [Related]
20. [Case report on the clinical picture of oxalosis]. Orf G Med Welt; 1965 Nov; 46():2603-4. PubMed ID: 5885124 [No Abstract] [Full Text] [Related] [Next] [New Search]