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.
45. 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]
46. Evidence for delayed histidine transamination in neonates with histidinemia. Levy HL; Madigan PM; Peneva P Pediatrics; 1971 Jan; 47(1):128-32. PubMed ID: 5547620 [No Abstract] [Full Text] [Related]
47. [Contribution to the knowledge of qualitative and quantitative aminoaciduria in cystinosis and in cystinuria (Study with ionic exchange resins)]. MAGGIONI G; BOTTINI E; BIAGI G Minerva Pediatr; 1960 Aug; 12():914-7. PubMed ID: 13765231 [No Abstract] [Full Text] [Related]
48. [Physiopathological considerations on the limits of detection of certain metabolic syndromes of the cystinuria-cystinosis type. Possibilities of rapid diagnosis]. Pâtea P; Tănase-Mogos I; Ciortoloman H; Petrescu L; Ciucă C; Orăşeanu D; Jemna M; Meila P Physiologie; 1980; 17(2):113-20. PubMed ID: 6770383 [No Abstract] [Full Text] [Related]
49. [Disturbance of the Histidine Reabsorption of the Renal Tubes in Patient with Cystine Lysinuria in Conjunction with Severe Cerebral Damage (author's transl)]. Ludescher E; jarosch E; berger H Padiatr Padol; 1975; 10(1):66-73. PubMed ID: 1124211 [TBL] [Abstract][Full Text] [Related]
50. [Cystinuria in children in the light of our observations]. Hanicka M; Bernasowska-Knapczykowa K; Kos S Przegl Lek; 1966; 22(11):700-2. PubMed ID: 5959614 [No Abstract] [Full Text] [Related]
51. A case of hyperlysinemia: biochemical and clinical observations. Armstrong MD; Robinow M Pediatrics; 1967 Apr; 39(4):546-54. PubMed ID: 6022933 [No Abstract] [Full Text] [Related]
52. [Thin layer chromatography separation of keto acids in the urine of patients with phenylketonuria and cystinosis]. Lutz P; von Reutern GM Z Klin Chem Klin Biochem; 1969 Nov; 7(6):586-9. PubMed ID: 5365463 [No Abstract] [Full Text] [Related]
53. [Hyperargininemia with arginase deficiency. A new familial metabolic disease. II. Biochemical studies]. Terheggen HG; Schwenk A; Lowenthal A; van Sande M; Colombo JP Z Kinderheilkd; 1970; 107(4):313-23. PubMed ID: 5438972 [No Abstract] [Full Text] [Related]
54. [Biochemical studies in a patient with maple syrup urine disease (author's transl)]. Vaca G; Rivas F; Sánchez-Corona J; Olivares N; Aguirre-Negrete MG; González-Quiroga G; Medina C; Hernández A; Cantú JM Rev Invest Clin; 1981; 33(4):379-82. PubMed ID: 7330511 [No Abstract] [Full Text] [Related]
55. Simple biochemical methods for the study of lipidoses and aminoacidopathies. Adriaenssens K; Karcher D Riv Patol Nerv Ment; 1970 Oct; 91(5):274-6. PubMed ID: 5525772 [No Abstract] [Full Text] [Related]