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62. [Progressive encephalopathy after a symptom-free period in the newborn infant, due to disorders of amino acid metabolism. Illustrated with case histories of patients with hyperglycinemia and maple syrup urine disease]. Raven EJ Ned Tijdschr Geneeskd; 1969 Oct; 113(42):1850-3. PubMed ID: 5344645 [No Abstract] [Full Text] [Related]
63. Diagnosis and therapy of organic acidurias. Sperl W Padiatr Padol; 1993; 28(1):3-8. PubMed ID: 8446425 [TBL] [Abstract][Full Text] [Related]
64. Clinical diagnosis of the inborn errors of metabolism in the neonatal period. Burton BK; Nadler HL Pediatrics; 1978 Mar; 61(3):398-405. PubMed ID: 643414 [No Abstract] [Full Text] [Related]
65. [Diagnosis and acute treatment of inborn metabolic diseases in infants]. Lund AM; Christensen E; Skovby F Ugeskr Laeger; 2002 Nov; 164(48):5613-9. PubMed ID: 12523004 [TBL] [Abstract][Full Text] [Related]
66. Screening for metabolic disorders among high risk infants and children. Berry HK Health Lab Sci; 1977 Jul; 14(3):183-93. PubMed ID: 141435 [TBL] [Abstract][Full Text] [Related]
67. [Expanded newborn screening in the Region of Murcia, Spain. Three-years experience]. Juan-Fita MJ; Egea-Mellado JM; González-Gallego I; Moya-Quiles MR; Fernández-Sánchez A Med Clin (Barc); 2012 Dec; 139(13):566-71. PubMed ID: 22137990 [TBL] [Abstract][Full Text] [Related]
68. [Current problems in the detection of inborn errors of metabolism using screening tests in newborns]. Hübschmann K Padiatr Grenzgeb; 1971; 10(2):115-25. PubMed ID: 5148734 [No Abstract] [Full Text] [Related]
69. Screening tests and chromatography for the detection of inborn errors of metabolism. Stuber A Clin Chim Acta; 1972 Feb; 36(2):309-13. PubMed ID: 5008795 [No Abstract] [Full Text] [Related]
70. Inborn errors of metabolism in infancy: a guide to diagnosis. Burton BK Pediatrics; 1998 Dec; 102(6):E69. PubMed ID: 9832597 [TBL] [Abstract][Full Text] [Related]
71. Screening programme. Changes in the pipeline. Midwives; 2014; 17(5):10. PubMed ID: 25328969 [No Abstract] [Full Text] [Related]
72. [MAPLE SYRUP DISEASE WITH FAMILIAL INCIDENCE]. DIEZEL PB; MARTIN K Virchows Arch Pathol Anat Physiol Klin Med; 1964 May; 337():425-45. PubMed ID: 14217031 [No Abstract] [Full Text] [Related]
73. Genetic-metabolic considerations in the sick neonate. Aleck KA; Shapiro LJ Pediatr Clin North Am; 1978 Aug; 25(3):431-51. PubMed ID: 358106 [No Abstract] [Full Text] [Related]
75. [Diagnosis of inborn amino acid metabolism errors. Important symptoms and laboratory methods]. Kroll S; Zebisch P; Toussaint W Fortschr Med; 1972 Apr; 90(11):430-1. PubMed ID: 4681731 [No Abstract] [Full Text] [Related]
76. [Test program for the earlydetection of inborn errors of metabolism]. Thlhamer O Monatsschr Kinderheilkd (1902); 1969 Jan; 117(1):37-8. PubMed ID: 5398916 [No Abstract] [Full Text] [Related]
77. [Early diagnosis of hereditary metabolic diseases in the newborn by means of microbiological Guthrie tests]. Schmid-Rüter E Fortschr Med; 1978 Jun; 96(24):1289-93. PubMed ID: 96002 [TBL] [Abstract][Full Text] [Related]
79. Detection of inborn errors of metabolism using GC-MS: over 3 years of experience in southern China. Jiang M; Liu L; Mei H; Li X; Cheng J; Cai Y J Pediatr Endocrinol Metab; 2015 Mar; 28(3-4):375-80. PubMed ID: 25781538 [TBL] [Abstract][Full Text] [Related]
80. Transient hyperammonemias in infants with and without organic acidemia. Nyhan WL; Rubio V; Jordá A; Grisolia S; Gutierez F; Canosa C Adv Exp Med Biol; 1982; 153():331-8. PubMed ID: 7164908 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]