12 YEARS AUSTRIAN NEWBORN SCREENING FOR INBORN-ERRORS OF METABOLISM

被引：9

作者：

THALHAMMER, O

SCHEIBENREITER, S

KNOLL, E

WEHLE, E

SCHON, R

机构：

来源：

KLINISCHE PADIATRIE | 1980年 / 192卷 / 06期

关键词：

D O I：

10.1055/s-2008-1035649

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：589 / 598

页数：10

共 25 条

[11]

SCHEIBEN.S, 1973, MONATSSCHR KINDERH, V121, P163

[12] HYPERPHENYLALANINEMIA OR PHENYLKETONURIA (PKU) - PROBLEMS OF EARLY DISTINCTION IN 15 AND 34 CASES RESPECTIVELY [J].

SCHEIBENREITER, S ;

THALHAMMER, O .

ZEITSCHRIFT FUR KINDERHEILKUNDE, 1972, 112 (02) :153-+

[13]

SCHON R, 1976, PADIATR PADOL, V11, P319

[14]

SCHON R, 1977, LANCET, V1, P43

[15]

SCHON R, 1976, Z KLIN CHEM KLIN BIO, V14, P159

[16]

SCHON R, 1976, KLIN CHEM, V15, P109

[17] INTELLECTUAL LEVEL (IQ) IN HETEROZYGOTES FOR PHENYLKETONURIA (PKU) - IS PKU GENE ALSO ACTING BY MEANS OTHER THAN PHENYLALANINE-BLOOD LEVEL ELEVATION [J].

THALHAMMER, O ;

HAVELEC, L ;

KNOLL, E ;

WEHLE, E .

HUMAN GENETICS, 1977, 38 (03) :285-288

[18] GENETIC DIFFERENCE BETWEEN HYPERPHENYLALANNINEMIA AND PHENYLKETONURIA [J].

THALHAMMER, O ;

SCHEIBER, V .

NEUROPADIATRIE, 1972, 3 (04) :358-+

[19]

THALHAMMER O, 1977, WIEN KLIN WOCHENSCHR, V89, P684

[20]

THALHAMMER O, 1973, MONATSSCHR KINDERH, V121, P201

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