USE OF 5-HYDROXYTRYPTOPHAN IN A CHILD WITH LESCH-NYHAN SYNDROME

被引：31

作者：

CIARANELLO, RD ^{[1
]}

ANDERS, TF ^{[1
]}

BARCHAS, JD ^{[1
]}

BERGER, PA ^{[1
]}

CANN, HM ^{[1
]}

机构：

[1] STANFORD UNIV,SCH MED,STANFORD,CA 94305

来源：

CHILD PSYCHIATRY & HUMAN DEVELOPMENT | 1976年 / 7卷 / 02期

关键词：

D O I：

10.1007/BF01464036

中图分类号：

B844 [发展心理学（人类心理学）];

学科分类号：

040202 ;

摘要：

引用

收藏

页码：127 / 133

页数：7

相关论文

共 14 条

[1] CIARANELLO RD, IN PRESS
[2] HVA AND 5HIAA CSF MEASUREMENTS AND 5HTP TRIALS IN SOME PATIENTS WITH INVOLUNTARY MOVEMENTS
GUILLEMINAULT, C
THARP, BR
COUSIN, D
[J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1973, 18 (04) : 435 - 441
[3] KALES A, 1973, BENZODIAZEPRINES
[4] URINE URIC ACID TO CREATININE RATIO - A SCREENING TEST FOR INHERITED DISORDERS OF PURINE METABOLISM - PHOSPHORIBOSYLTRANSFERASE (PRT) DEFICIENCY IN X-LINKED CEREBRAL PALSY AND IN A VARIANT OF GOUT
KAUFMAN, JM
GREENE, ML
SEEGMILLER, JE
[J]. JOURNAL OF PEDIATRICS, 1968, 73 (04) : 583 - +
[5] FAMILIAL DISORDER OF URIC ACID METABOLISM + CENTRAL NERVOUS SYSTEM FUNCTION
LESCH, M
NYHAN, WL
[J]. AMERICAN JOURNAL OF MEDICINE, 1964, 36 (04) : 561 - &
[6] X-LINKED HYPOXANTHINE-GUANINE PHOSPHORIBOSYL TRANSFERASE DEFICIENCY - HETEROZYGOTE HAS 2 CLONAL POPULATIONS
MIGEON, BR
DERKALOU.VM
NYHAN, WL
YOUNG, WJ
CHILDS, B
[J]. SCIENCE, 1968, 160 (3826) : 425 - &
[7] MIZUNO T, 1974, LANCET, V1, P761
[8] GENETICS OF AN X-LINKED DISORDER OF URIC ACID METABOLISM AND CEREBRAL FUNCTION
NYHAN, WL
PESEK, J
SWEETMAN, L
CARPENTE.DG
CARTER, CH
[J]. PEDIATRIC RESEARCH, 1967, 1 (01) : 5 - &
[9] PARTINGTON MW, 1971, DEV MED CHILD NEUROL, V13, P362
[10] POTTER WPD, 1969, J PHYSL, V204, P102