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44. Inborn errors of metabolism: the need for sugar. Francis DE J Hum Nutr; 1979 Apr; 33(2):146-54. PubMed ID: 438511 [No Abstract] [Full Text] [Related]
46. Diagnosis and mangement of inherited aminoacidopathies in the newborn and the unborn. Rosenberg LE Clin Endocrinol Metab; 1974 Mar; 3(1):145-52. PubMed ID: 4609645 [No Abstract] [Full Text] [Related]
47. Screening programme. Changes in the pipeline. Midwives; 2014; 17(5):10. PubMed ID: 25328969 [No Abstract] [Full Text] [Related]
48. [Detection of hereditary metabolic diseases in Quebec]. Grenier A; Laberge C Union Med Can; 1974 Mar; 103(3):453-6. PubMed ID: 4820873 [No Abstract] [Full Text] [Related]
50. [Detection of metabolic diseases]. Adriaenssens K; Van Sande M Acta Neurol Psychiatr Belg; 1968 Oct; 68(10):719-28. PubMed ID: 4976725 [No Abstract] [Full Text] [Related]
51. [Neonatal diagnosis of hereditary metabolic diseases]. Lambotte C Rev Med Liege; 1973 Dec; 28(24):837-51. PubMed ID: 4769974 [No Abstract] [Full Text] [Related]
52. [Diseases of newborn infants based on inborn anomalies of metabolism. 1. Theoretical principles]. Plöchl E Wien Med Wochenschr; 1970 Oct; 120(41):707-11. PubMed ID: 4918107 [No Abstract] [Full Text] [Related]
55. [Early diagnosis of phenylketonuria, homocystinuria and maple syrup urine disease in the GDR with the aid of Gatri's microbiological inhibitor test]. Makhill G; Knapp A Pediatriia; 1974 Dec; (12):27-30. PubMed ID: 4614217 [No Abstract] [Full Text] [Related]
56. [Methods and results of screening newborn infants for aminoacidopathies]. Bickel H Monatsschr Kinderheilkd (1902); 1976 Sep; 129(9):650-3. PubMed ID: 979984 [No Abstract] [Full Text] [Related]