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2. Diagnosis of disorders in amino acid methabolism by chemical ionization mass spectrometry. Issachar D; Yinon J Clin Chim Acta; 1976 Dec; 73(2):307-14. PubMed ID: 1000850 [TBL] [Abstract][Full Text] [Related]
3. Aminoaciduria and hyperaminoaciduria in childhood. Brodehl J; Bickel H Clin Nephrol; 1973; 1(3):149-68. PubMed ID: 4593448 [No Abstract] [Full Text] [Related]
4. Year-long validation study and reference values for urinary amino acids using a reversed-phase HPLC method. Venta R Clin Chem; 2001 Mar; 47(3):575-83. PubMed ID: 11238314 [TBL] [Abstract][Full Text] [Related]
5. Determination of creatinine and ultraviolet-absorbing amino acids and organic acids in urine by reversed-phase high-performance liquid chromatography. Yokoyama Y; Tsuchiya M; Sato H; Kakinuma H J Chromatogr; 1992 Nov; 583(1):1-10. PubMed ID: 1484080 [TBL] [Abstract][Full Text] [Related]
6. [Primary and secondary hyperaminoaciduria in children (review of the literature)]. Lebedev VP; Iur'eva EA; Mukhina IuG; Buravina TA; Koroleva IA Vopr Okhr Materin Det; 1970 Nov; 15(11):64-8. PubMed ID: 4928437 [No Abstract] [Full Text] [Related]
7. Aminoacidopathies: a review of 3 years experience of investigations in a Kuwait hospital. Yadav GC; Reavey PC J Inherit Metab Dis; 1988; 11(3):277-84. PubMed ID: 3148069 [TBL] [Abstract][Full Text] [Related]
8. Early cystinuria, a risk factor for metabolic urolithiasis. Mogoş T; Tănase I; Mogoş C; Pănuş C; Mincu I Rom J Intern Med; 1994; 32(4):299-303. PubMed ID: 7613503 [TBL] [Abstract][Full Text] [Related]
13. Amino acid excretion in infancy and early childhood. A survey of 200,000 infants. Turner B; Brown DA Med J Aust; 1972 Jan; 1(2):62-5. PubMed ID: 5025157 [No Abstract] [Full Text] [Related]
14. Simultaneous retention index analysis of urinary amino acids and carboxylic acids for graphic recognition of abnormal state. Paik MJ; Lee HJ; Kim KR J Chromatogr B Analyt Technol Biomed Life Sci; 2005 Jul; 821(1):94-104. PubMed ID: 15894518 [TBL] [Abstract][Full Text] [Related]
15. Mellituria screening in some metabolic diseases. Piccardo MG; Rosa M; Russo L Enzyme; 1983; 29(2):138-41. PubMed ID: 6851989 [TBL] [Abstract][Full Text] [Related]
16. A patient with nonketotic hyperglycinemia: biochemical findings and therapeutic approaches. Trijbels JM; Monnens LA; van der Zee SP; Vrenken JA; Sengers RC; Schretlen ED Pediatr Res; 1974 May; 8(5):598-605. PubMed ID: 4545188 [No Abstract] [Full Text] [Related]
17. Simultaneous determination of urinary creatinine and UV-absorbing amino acids using a novel low-capacity cation-exchange chromatography for the screening of inborn errors of metabolism. Yokoyama Y; Yamasaki K; Sato H J Chromatogr B Analyt Technol Biomed Life Sci; 2005 Feb; 816(1-2):333-8. PubMed ID: 15664367 [TBL] [Abstract][Full Text] [Related]
18. 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]
20. Screening for biochemical abnormalities in the urine of the mentally handicapped in Dublin. Moore PT; Martin MC; Coffey VP J Ment Defic Res; 1972 Jun; 16(2):128-38. PubMed ID: 4277644 [No Abstract] [Full Text] [Related] [Next] [New Search]