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4. [Biochemical studies on inherited disorders of amino acid metabolism in pediatrics]. Antener I Z Klin Chem Klin Biochem; 1970 Sep; 7(5):427-39. PubMed ID: 5505952 [No Abstract] [Full Text] [Related]
5. A variant form of branched-chain keto aciduria. van der Horst JL; Wadman SK Acta Paediatr Scand; 1971 Sep; 60(5):594-9. PubMed ID: 5125167 [No Abstract] [Full Text] [Related]
6. 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]
7. [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]
8. Investigation of ketoacidurias by two-dimensional paper chromatography. Coward RF; Smith P; Seakins JW J Clin Pathol; 1969 Jul; 22(4):422-6. PubMed ID: 5808092 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. [Systematic detection of hereditary metabolic encephalopathies]. Neimann N; Pierson M; Vidailhet M; Siest G; Badonnel Y; Humbel R; Roos F Ann Pediatr (Paris); 1968 Oct; 15(10):635-41. PubMed ID: 4237831 [No Abstract] [Full Text] [Related]
11. Quantitative measurement of individual free amino acids in urine by means of high voltage paper electrophoresis. Investigations of a group of mentally retarded patients. Juul P Scand J Clin Lab Invest; 1966; 18(6):629-37. PubMed ID: 5959318 [No Abstract] [Full Text] [Related]
12. [Familial glyco-amino-ketoaciduric syndrome (clinical and physiopathological observations)]. CIAMPALINI L; PICCARDO MG; DI LORENZO M; RONCELLA A Rass Fisiopatol Clin Ter; 1962; 34():390-410. PubMed ID: 14021303 [No Abstract] [Full Text] [Related]
13. ["Atypical" metabolic forms of phenylketonuria (PKU) and leucinosis detected in newborn infants]. Tănase I; Ciortoloman H; Popescu M; Grigorescu G; Ankăr V Physiologie; 1977; 14(4):257-61. PubMed ID: 413127 [No Abstract] [Full Text] [Related]
14. Urinary metabolic screening of mentally retarded patients from institutions in the northern part of Sweden. Holmgren G Hum Hered; 1973; 23(6):548-60. PubMed ID: 4276001 [No Abstract] [Full Text] [Related]
15. Urinary amino acid patterns in simple and complicated bilharziasis. Soliman L; Abdel Kader MM; Ata AA; Abdel Wahab F; Emara SH J Trop Med Hyg; 1969 Jul; 72(7):166-70. PubMed ID: 5795955 [No Abstract] [Full Text] [Related]
16. Hereditary vitelliform macular degeneration: variable fundus findings within a single pedigree. Maloney WF; Robertson DM; Duboff SM Arch Ophthalmol; 1977 Jun; 95(6):979-83. PubMed ID: 869756 [TBL] [Abstract][Full Text] [Related]
17. [ON THE PATHOPHYSIOLOGY AND CLINICAL MANIFESTATIONS OF DISORDERS OF RENAL TUBULAR PARTIAL FUNCTION]. GEROK W; PABST K Munch Med Wochenschr; 1965 Jan; 107():73-82. PubMed ID: 14301178 [No Abstract] [Full Text] [Related]