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METABOLIC DISORDERS
Author(s) -
Taciane Alegra
Publication year - 1970
Publication title -
developmental medicine and child neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.658
H-Index - 143
eISSN - 1469-8749
pISSN - 0012-1622
DOI - 10.1111/j.1469-8749.1970.tb02409.x
Subject(s) - citation , computer science , medicine , information retrieval , library science
1685. ADRIAENSSENS, K., VAN SANDE, M. (1968) ‘The detection of metabolic diseases.’ (French.) Acta neurol. psychiat. belg., 68, 71 9-728. 1686. AMPOLA, M .G., EFRON, M. L., BIXBY, E. M., MESHORER, E. (1969) ‘Mental deficiency and a new aminoacidemia.’ Amer. J. Dis. Child., 117, 66-70. 1687. BARBER, G. W., SPAETH, G. L. (1969) ‘The successful treatment of homocystinuria with pyridoxine.’ J. Pediat., 75, 463-478. 1688. BERMAN, J. L., CUNNINGHAM, G. C., DAY, R. W., FORD, R., HSIA, D. Y.-Y. (1969) ‘Causes for high phenylalanine with normal tyrosine.’ Amer. J. Dis. Child., 117, 54-67. 1689. BERMAN, P. H., BALIS, M. F., DANCIS, J. (1969) ‘Congenital hyperuricemia. An inborn error of purine metabolism associated with psychomotor retardation, athetosis and selfmutilation.’ Arch. Neurol. (Chic.), 20, 44-53. 1690. BICKEL, H. (1969) ‘Recent advances in the early detection and treatment of inborn errors with brain damage.’ Neuropadiat., 1, 1-1 1 . 1691. BICKEL, H., FEIST, D., MULLER, H., QUADBECK, G. (1969) ‘Ornithinemia: a new amino acid metabolic disease causing brain damage.’ (German.) Mschr. Kinderheilk., 117, 369. (Abstract.) 1692. BICKEL, H., FEIST, D., MULLER, H., QUADBECK, G. (1968) ‘Ornithinaemia: another disorder of amino-acid metabolism causing brain damage.’ (German.) Rtsch. med. Wschr., 93, 2247-225 1, 1693. BLATTNER, . J. (1969) ‘Iminoaciduria.’J. Pediut., 74, 144-146. 1694. BRENTON, D. P. (1969) ‘Treatment of homocystinuria.’ Develop. Med. Child Neurol., 11, 519-521. (Annotation.) 1695. BRITISH MEDICAL JOURNAL (1969) ‘Screening for inborn errors of metabolism.’ Brit. med. J., i, 266-267. (Leading Article.) 1696. BROWN, D. F. (1968) ‘Home placement of a PKU child with severe mental retardation.’ Develop. Med. Child Neurol., 10, 776-780. 1697. BROWN, D. F., TAYLOR, A. J. W. (1968) ‘Some children with phenylketonuria.’ N.Z. med. J., 68, 304307. 1698. CANADIAN MEDICAL ASSOCIATION JOURNAL (1969) ‘The search for phenylketonuria.’ Canad. med. Ass. J., 101, 235-237. (Editorial). 1699. CAREY, M. C., DONOVAN, D. E., FITZGERALD, O. MCAULEY, F. D. (1968) ‘Homocystinuria. I. A clinical and pathological study of nine subjects in six families.’ Amer. J. Med., 45,