PHENYLPYRUVIC OLIGOPHRENIA IN A JEWISH CHILD

被引:37
作者
COHEN, P
KOZINN, PJ
机构
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D O I
10.1016/S0022-3476(49)80202-2
中图分类号
R72 [儿科学];
学科分类号
100202 ;
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页码:76 / 79
页数:4
相关论文
共 10 条
[1]  
Bates RM, 1939, J MENT SCI, V85, P273
[2]  
CLOSS K, 1938, Z PHYSL CHEM, V254, P258
[3]  
Folling A, 1934, HOPPESEYLERS Z PHYSL, V227, P169, DOI [10.1515/bchm2.1934.227.1-4.169, DOI 10.1515/BCHM2.1934.227.1-4.169]
[4]   Phenylpyruvic oligophrenia - Introductory study of fifty cases of mental deficiency associated with excretion of phenylpyruvic acid [J].
Jervis, GA .
ARCHIVES OF NEUROLOGY AND PSYCHIATRY, 1937, 38 (05) :944-963
[5]  
Jervis GA, 1940, J BIOL CHEM, V134, P105
[6]   THE GENETICS OF PHENYLPYRUVIC OLIGOPHRENIA. (A CONTRIBUTION TO THE STUDY OF THE INFLUENCE OF HERDITY ON MENTAL DEFECT) [J].
Jervis, George A. .
JOURNAL OF MENTAL SCIENCE, 1939, 85 (357) :719-762
[7]   A defect in the metabolism of tyrosine and phenylalanine in premature infants. I. Identification and assay of intermediary products [J].
Levine, S. Z. ;
Marples, Eleanor ;
Gordon, Harry H. .
JOURNAL OF CLINICAL INVESTIGATION, 1941, 20 (02) :199-207
[8]   Metabolic studies in phenylketonuria [J].
Penrose, L ;
Quastel, JH .
BIOCHEMICAL JOURNAL, 1937, 31 :266-274
[9]  
Penrose LS, 1935, LANCET, V2, P192
[10]  
PETERS JP, 1946, QUANTITATIVE CLIN CH, V1, P766