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22. [Chief clinical syndromes in children with tryptophan metabolism disorders (literature survey)]. Tabolin VA; Kruglov BV; Lebedev VP; Levitina NO Vopr Okhr Materin Det; 1972 Jun; 17(6):45-8. PubMed ID: 4560708 [No Abstract] [Full Text] [Related]
23. BIOCHEMICAL ASPECTS OF THE HARTNUP DISEASE. III. GENERAL DISCUSSION AND CONCLUSIONS. DELAEY P; HOOFT C; TIMMERMANS J; SNOECK J Ann Paediatr; 1964; 202():321-31. PubMed ID: 14168315 [No Abstract] [Full Text] [Related]
24. [Idiopathic renal acidosis of the infant; Lightwood syndrome]. JEUNE M; CHARRAT A Pediatrie; 1956; 11(2):205-26. PubMed ID: 13335371 [No Abstract] [Full Text] [Related]
26. [Inborn errors of metabolism (as seen by the pediatrist]. Schreier K Z Gesamte Inn Med; 1967 Feb; 22(4):Suppl:61-4 c. PubMed ID: 4869798 [No Abstract] [Full Text] [Related]
27. ACUTE CEREBELLAR ATAXIA ASSOCIATED WITH SOME FEATURES OF THE HARTNUP SYNDROME. PRESENTATION OF A CASE. FOIS A; LECCHINI L Helv Paediatr Acta; 1964 Jun; 19():42-9. PubMed ID: 14189842 [No Abstract] [Full Text] [Related]
28. Inborn errors of metabolism: the essentials of clinical diagnosis. Roth KS Clin Pediatr (Phila); 1991 Mar; 30(3):183-90. PubMed ID: 2009725 [No Abstract] [Full Text] [Related]
29. [Biochemical and analytical bases of exploration of metabolism of tryptophan]. Lemonnier A; Charpentier C; Leluc R Ann Pediatr (Paris); 1964 Mar; 11(3):147-55. PubMed ID: 5878703 [No Abstract] [Full Text] [Related]
31. [Chronic hypercalcemia, renal function disorder and cardiac and ocular anomalies in a young child]. DURAND P Minerva Pediatr; 1955 Dec; 7(48):1541-7. PubMed ID: 13288212 [No Abstract] [Full Text] [Related]
32. [Inborn errors of metabolism, associated with ocular symptoms]. Oura T Nihon Ganka Kiyo; 1969 Aug; 20(8):749-58. PubMed ID: 5391478 [No Abstract] [Full Text] [Related]
33. Hypertryptophanemia and indoleketonuria in two mentally subnormal siblings. Snedden W; Mellor CS; Martin JR N Engl J Med; 1982 Nov; 307(22):1405. PubMed ID: 7133092 [No Abstract] [Full Text] [Related]
34. Digestion and absorption of protein. Freeman HJ; Kim YS Annu Rev Med; 1978; 29():99-116. PubMed ID: 348054 [No Abstract] [Full Text] [Related]
35. [LATE AORTIC LESIONS FOLLOWING SEVERE INFANTILE HYPERCALCEMIA?]. NEWMAN CG Dtsch Med Wochenschr; 1964 Dec; 89():2389. PubMed ID: 14225045 [No Abstract] [Full Text] [Related]
37. High performance liquid chromatography (HPLC) method for confirming thin layer chromatography (TLC) findings in inborn errors of metabolism children in Malaysia. Yahya NA; Ismail Z; Embong KH; Mohamad SA Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():130-3. PubMed ID: 8629091 [TBL] [Abstract][Full Text] [Related]
38. [Screening of newborn infants for inborn errors of metabolism]. Halvorsen S; Skjelkvåle L Tidsskr Nor Laegeforen; 1970 Jan; 90(2):233-5. PubMed ID: 5430194 [No Abstract] [Full Text] [Related]
39. [Amino acid transfer systems and their importance in pathology. II. Specific abnormalities in renal and intestinal amino acid transfer]. Boisse J; Moatti N Ann Biol Clin (Paris); 1973; 31(4):249-55. PubMed ID: 4579284 [No Abstract] [Full Text] [Related]