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23. Corneal erosions in tyrosinosis. Zaleski WA; Hill A; Murray RG Can J Ophthalmol; 1973 Oct; 8(4):556-9. PubMed ID: 4148055 [No Abstract] [Full Text] [Related]
24. Urinary aminoacids in mental retardation. Dhatt PS; Gupta HL; Saini AS Indian J Pediatr; 1968 Oct; 35(249):469-75. PubMed ID: 5719650 [No Abstract] [Full Text] [Related]
25. Enzyme defect in saccharopinuria. Simell O; Johansson T; Aula P J Pediatr; 1973 Jan; 82(1):54-7. PubMed ID: 4404606 [No Abstract] [Full Text] [Related]
26. Hyperprolinaemia in two successive generations of a North American Indian family. Perry TL; Hardwick DF; Lowry RB; Hansen S Ann Hum Genet; 1968 May; 31(4):401-7. PubMed ID: 4299764 [No Abstract] [Full Text] [Related]
28. Alaninuria, associated with microcephaly, dwarfism, enamel hypoplasia, and diabetes mellitus in two sisters. Stimmler L; Jensen N; Toseland P Arch Dis Child; 1970 Oct; 45(243):682-5. PubMed ID: 5477682 [TBL] [Abstract][Full Text] [Related]
29. [Aminoacidpathies of neurological interest]. Diament AJ Arq Neuropsiquiatr; 1974 Jun; 32(2):93-103. PubMed ID: 4848013 [No Abstract] [Full Text] [Related]
30. [Chorio-retinal degenerations and aminoaciduria. III. Atrophia gyrata]. Rodriguez Caballero ML Arch Ophtalmol Rev Gen Ophtalmol; 1975 Dec; 35(12):973-4. PubMed ID: 132162 [No Abstract] [Full Text] [Related]
31. [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]
32. Hereditary hematuria associated with mental retardation, convulsions, abnormal EEG and ocular abnormalities. Hirooka M; Ono T; Kubota N; Yoshioka K; Ikeda S Tohoku J Exp Med; 1969 Jun; 98(2):199-211. PubMed ID: 5811104 [No Abstract] [Full Text] [Related]
33. Aminoaciduria in bone diseases in children. Opieńska-Blauth J; Gebala A; Sanecka-Obacz M; Kozlowska T; Stryjecka M Ann Paediatr; 1966; 207(2):115-24. PubMed ID: 5953604 [No Abstract] [Full Text] [Related]
35. [Chromatographic study of aminoaciduria in subjects with progressive muscular dystrophy and in healthy carriers of such a defect]. Brunelli B; Falorni A; Cao A; Lungarotti MS; Tangheroni W Pediatria (Napoli); 1971; 79(2):168-80. PubMed ID: 5095771 [No Abstract] [Full Text] [Related]
37. Incidence of phenylketonuria and other inborn errors of the amino acid metabolism in the normal and mentally retarded population. Hyánek J; Homolka J; Seemanová E Rev Czech Med; 1974; 20(1):18-22. PubMed ID: 4815837 [No Abstract] [Full Text] [Related]
38. The clinical and biochemical findings in three cases of hypersarcosinemia and one case of transient hypersarcosinuria associated with folic acid deficiency. Tippett P; Danks DM Helv Paediatr Acta; 1974 Aug; 29(3):261-7. PubMed ID: 4854684 [No Abstract] [Full Text] [Related]
39. Mental retardation due to inborn errors of amino acid metabolism in Puerto Rico. Results of a screening test and a review of other documented cases. Crosby PF Bol Asoc Med P R; 1971 Jul; 63(7):184-6. PubMed ID: 5286510 [No Abstract] [Full Text] [Related]