These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
4. The prenatal diagnosis of inborn errors of metabolism. Milunsky A; Littlefield JW Annu Rev Med; 1972; 23():57-76. PubMed ID: 4264784 [No Abstract] [Full Text] [Related]
5. Improved high-resolution high-voltage paper electrophoresis system for use in screening for aminoacidopathies. Spiekerman AM; Hetherly ME; Hall FF Clin Chem; 1975 Dec; 21(13):1981-2. PubMed ID: 162 [TBL] [Abstract][Full Text] [Related]
6. [1H-NMR urinalysis: simultaneous screening of inborn errors of metabolism of amino acid and organic acid disorders]. Yamamoto H; Yamaguchi S Rinsho Byori; 1988 Feb; 36(2):182-90. PubMed ID: 3379790 [No Abstract] [Full Text] [Related]
7. Urinary metabolic screening in children with psycho-neurological diseases. Evaluation of different screening tests. Hambraeus L; Holmgren G Ups J Med Sci Suppl; 1974; 15():1-23. PubMed ID: 4274307 [No Abstract] [Full Text] [Related]
9. Amino acid screening of mentally defective patients by high voltage electrophoresis. Meyer JS; Wood MJ Mo Med; 1972 Feb; 69(2):112-6. PubMed ID: 5058792 [No Abstract] [Full Text] [Related]
10. Rapid single column analysis of amino acids related to some aminoacidopathies. Benson JV; Cormick J; Patterson JA Clin Chem; 1969 Jul; 15(7):621-30. PubMed ID: 5794155 [No Abstract] [Full Text] [Related]
11. Rapid screening of aminoacidurias. Ganger C Am J Med Technol; 1971 Nov; 37(11):434-9. PubMed ID: 5154330 [No Abstract] [Full Text] [Related]
12. Aminoacidopathies in mental retardation. Brante G; Börjesson M; Rayner S Monogr Hum Genet; 1972; 6():146-7. PubMed ID: 4663889 [No Abstract] [Full Text] [Related]
13. Screening for disorders of amino acid metabolism by thin-layer high voltage electrophoresis. Farrelly RO; Watkins WB Clin Chim Acta; 1968 May; 20(2):291-4. PubMed ID: 4297715 [No Abstract] [Full Text] [Related]
14. [Study of aminoaciduria and aminoacidemia by chromato-ion-ophoresis. Technic and application to the dynamic study of various amino acid metabolic disorders]. Vovan L; Perrimond H; Pierron H; Orsini A Pediatrie; 1967 Sep; 22(6):732-3. PubMed ID: 5621096 [No Abstract] [Full Text] [Related]
15. Fructose-1,6-diphosphatase deficiency: another enzyme defect which can present itself with the clinical features of "tyrosinosis". Bakker HD; de Bree PK; van Sprang FJ; Wadman SK Clin Chim Acta; 1974 Aug; 55(1):41-7. PubMed ID: 4370029 [No Abstract] [Full Text] [Related]
16. Rapid short-column chromatography of amino acids. A method for blood and urine specimens in the diagnosis and treatment of metabolic disease. Shih VE; Efron ML; Mechanic GL Anal Biochem; 1967 Aug; 20(2):299-311. PubMed ID: 6048171 [No Abstract] [Full Text] [Related]
17. [A case of combined lysinuric protein intolerance and hypoactivity of argininosuccinate synthetase (citrullinemia)]. Shioya K; Yamamura Y; Kurihara T; Matsukura S Nihon Naika Gakkai Zasshi; 1988 May; 77(5):667-73. PubMed ID: 3145960 [No Abstract] [Full Text] [Related]
18. Membrane transport in disorders of imino-acid metabolism. Scriver CR Am J Dis Child; 1967 Jan; 113(1):170-4. PubMed ID: 6015898 [No Abstract] [Full Text] [Related]
19. A new look at the inborn errors of metabolism. Sinclair L Ann Clin Biochem; 1982 Jul; 19 (Pt 4)():314-21. PubMed ID: 6812485 [No Abstract] [Full Text] [Related]
20. Routine investigation of amino acid patterns in blood serum and urine by thin-layer electrophoresis. Fahie-Wilson MN J Med Lab Technol; 1969 Oct; 26(4):363-70. PubMed ID: 5355354 [No Abstract] [Full Text] [Related] [Next] [New Search]