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2. [Aminoaciduria and ocular pathology]. Ardouin M; Urvoy M; Turquois JP; Chaneac M Bull Soc Ophtalmol Fr; 1980; 80(4-5):409-12. PubMed ID: 7460175 [No Abstract] [Full Text] [Related]
3. AN INBORN ERROR OF METABOLISM ASSOCIATED WITH DEFICIENCY OF ENZYME CYSTATHIONINE SYNTHETASE LEADING TO HOMOCYSTINURIA. WRIGHT LD N Y State J Med; 1965 Feb; 65():559-61. PubMed ID: 14276302 [No Abstract] [Full Text] [Related]
5. HOMOCYSTINURIA: A NEW INBORN ERROR OF METABOLISM ASSOCIATED WITH MENTAL DEFICIENCY. CARSON NA; CUSWORTH DC; DENT CE; FIELD CM; NEILL DW; WESTALL RG Arch Dis Child; 1963 Oct; 38(201):425-36. PubMed ID: 14065982 [No Abstract] [Full Text] [Related]
6. Ocular manifestations in aminoacidopathies. François J Adv Ophthalmol; 1972; 25():28-103. PubMed ID: 4560371 [No Abstract] [Full Text] [Related]
7. Ocular manifestations in aminoacidopathies. François J Monogr Hum Genet; 1972; 6():99-113. PubMed ID: 4541412 [No Abstract] [Full Text] [Related]
8. HOMOCYSTINURIA, AN ERROR IN THE METABOLISM OF METHIONINE. GERRITSEN T; WAISMAN HA Pediatrics; 1964 Mar; 33():413-20. PubMed ID: 14129086 [No Abstract] [Full Text] [Related]
9. HOMOCYSTINURIA DUE TO CYSTATHIONINE SYNTHETASE DEFICIENCY: THE MODE OF INHERITANCE. FINKELSTEIN JD; MUDD SH; IRREVERRE F; LASTER L Science; 1964 Nov; 146(3645):785-7. PubMed ID: 14197572 [TBL] [Abstract][Full Text] [Related]
10. [Involvement of the eye in hereditary metabolic diseases in children]. Bickel H; Jaeger W; Wollensak J; Teller W; Kraus E Ber Zusammenkunft Dtsch Ophthalmol Ges; 1969; 69():13-68. PubMed ID: 4311270 [No Abstract] [Full Text] [Related]
11. [Ocular manifestations of homocystinuria, report of two cases]. Mukuno K; Matsui K; Haraguchi H Nippon Ganka Gakkai Zasshi; 1967 Jan; 71(1):66-73. PubMed ID: 6068744 [No Abstract] [Full Text] [Related]
14. Inborn metabolic disorders with associated ocular lesions in Northern Ireland. Martin VA; Carson NA Trans Ophthalmol Soc U K (1962); 1967; 87():847-70. PubMed ID: 5255262 [No Abstract] [Full Text] [Related]