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5. [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 18; 113(42):1850-3. PubMed ID: 5344645 [No Abstract] [Full Text] [Related]
6. [MAPLE SYRUP DISEASE WITH FAMILIAL INCIDENCE]. DIEZEL PB, MARTIN K. Virchows Arch Pathol Anat Physiol Klin Med; 1964 May 22; 337():425-45. PubMed ID: 14217031 [No Abstract] [Full Text] [Related]
7. [Hereditary amino acid metabolism disorders. Indications for early diagnosis]. Kroll S, Zebisch P, Toussaint W. Fortschr Med; 1972 Apr 13; 90(11):423-8. PubMed ID: 4680607 [No Abstract] [Full Text] [Related]
8. Maple syrup urine disease: report of a case. Rao GP, Ramanamurthy PS, Ghafoorunnisa, Rafeeq MR, Pathak R. Indian Pediatr; 1974 Aug 13; 11(8):585-7. PubMed ID: 4443061 [No Abstract] [Full Text] [Related]
9. [Acute neonatal case of maple syrup urine disease]. Spennati G, Antonozzi I, Giardini O, De Matteis F, Cantani A, Martino F. Minerva Pediatr; 1980 Jan 15; 32(1):65-70. PubMed ID: 7254143 [No Abstract] [Full Text] [Related]
10. [Cerebral findings in aminoaciduria]. Martin JJ, Van Bogaert L, Guazzi GC. Confin Neurol; 1968 Jan 15; 30(2):97-116. PubMed ID: 5698580 [No Abstract] [Full Text] [Related]
11. [Screening newborn infants for phenylketonuria, histadinemia, homocystinuria and maple syrup disease. Results from north rhein-westphalia (1974-1976) (author's transl]. Menne F, Otte HJ, Krüger M, Winterhoff D. MMW Munch Med Wochenschr; 1978 May 05; 120(18):619-22. PubMed ID: 306535 [Abstract] [Full Text] [Related]
15. [Combined forms of metabolic errors detected in newborn infants]. Tănase-Mogoş I, Ciortoloman H, Grigorescu G, Popescu M, Ankăr V. Physiologie; 1978 May 05; 15(4):239-43. PubMed ID: 106407 [No Abstract] [Full Text] [Related]
16. Maple syrup urine disease in Thai infants. Pangkanon S, Charoensiriwatana W, Sangtawesin V. J Med Assoc Thai; 2008 Oct 05; 91 Suppl 3():S41-4. PubMed ID: 19255991 [Abstract] [Full Text] [Related]
18. An approach to the diagnosis of overwhelming metabolic disease in early infancy. Nyhan WL. Curr Probl Pediatr; 1977 Apr 05; ():1-20. PubMed ID: 856539 [Abstract] [Full Text] [Related]
19. Screening for inborn errors of metabolism. Report of a WHO Scientific Group. World Health Organ Tech Rep Ser; 1968 Apr 05; 401():1-57. PubMed ID: 4973455 [No Abstract] [Full Text] [Related]