DIAGNOSIS IN RELATIONSHIP TO TREATMENT OF HYPERPHENYLALANINEMIA

被引：8

作者：

BLASKOVICS, ME ^{[1
]}

机构：

[1] CHILDRENS HOSP,LOS ANGELES,CA 90027

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 1986年 / 9卷

关键词：

D O I：

10.1007/BF01799702

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：178 / 182

页数：5

共 8 条

[1]

Bickel H, 1980, J Inherit Metab Dis, V3, P123, DOI 10.1007/BF02312546

[2] PHENYLALANINAEMIA - DIFFERENTIAL DIAGNOSIS [J].

BLASKOVICS, ME ;

SCHAEFFLER, GE ;

HACK, S .

ARCHIVES OF DISEASE IN CHILDHOOD, 1974, 49 (11) :835-843

[3]

BLASKOVICS ME, 1971, INT S PHENYLKETONURI, P218

[4]

BLASKOVICS ME, 1971, PHENYLKETONURIA SOME, P98

[5] HEPATIC PHENYLALANINE-HYDROXYLASE ACTIVITY IN HYPERPHENYLALANINEMIA [J].

DHONDT, JL ;

FARRIAUX, JP .

JOURNAL OF INHERITED METABOLIC DISEASE, 1981, 4 (02) :59-60

[6] DETECTION BY PHENYLALANINE TOLERANCE TESTS OF HETEROZYGOUS CARRIERS OF PHENYLKETONURIA [J].

HSIA, DYY ;

DRISCOLL, KW ;

TROLL, W ;

KNOX, WE .

NATURE, 1956, 178 (4544) :1239-1240

[7] STANDARDIZED LOADING TEST WITH PROTEIN FOR THE DIFFERENTIATION OF PHENYLKETONURIA FROM HYPERPHENYLALANINEMIA [J].

LUTZ, P ;

SCHMIDT, H ;

FREY, G ;

BICKEL, H .

JOURNAL OF INHERITED METABOLIC DISEASE, 1982, 5 (01) :29-35

[8] THE DIAGNOSIS OF PHENYLKETONURIA - A REPORT FROM THE COLLABORATIVE STUDY OF CHILDREN TREATED FOR PHENYLKETONURIA [J].

OFLYNN, ME ;

HOLTZMAN, NA ;

BLASKOVICS, M ;

AZEN, C ;

WILLIAMSON, ML .

AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1980, 134 (08) :769-774

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