ATYPICAL PHENYLKETONURIA WITH NORMAL DIHYDROPTERIDINE REDUCTASE-ACTIVITY

被引：0

|

作者：

REY, F

BLANDINSAVOJA, F

REY, J

机构：

来源：

NEW ENGLAND JOURNAL OF MEDICINE | 1976年 / 295卷 / 20期

关键词：

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

收藏

页码：1138 / 1138

页数：1

相关论文

共 50 条

[21] DIHYDROPTERIDINE REDUCTASE DEFICIENT PHENYLKETONURIA DETECTED BY NEONATAL SCREENING IN TAIWAN
HSIAO, KJ
CHIANG, SH
WU, SJ
LIU, TT
CHIU, PC
CLINICAL CHEMISTRY, 1990, 36 (06) : 979 - 979
[22] PHENYLKETONURIA DUE TO DIHYDROPTERIDINE REDUCTASE DEFICIENCY - PRESENTATION OF 2 CASES
LONGHI, R
RIVA, E
VALSASINA, R
PACCANELLI, S
GIOVANNINI, M
JOURNAL OF INHERITED METABOLIC DISEASE, 1985, 8 : 97 - 98
[23] DIHYDROPTERIDINE REDUCTASE-ACTIVITY IN DRIED BLOOD SPOTS - EFFECTS OF AGING AND SENILE DEMENTIA OF THE ALZHEIMER TYPE
JEEPS, CM
SILCOX, A
LLOYD, B
CLAYTON, BE
JOURNAL OF CLINICAL PATHOLOGY, 1986, 39 (02) : 199 - 203
[24] THE OXIDATION OF APOMORPHINE AND OTHER CATECHOL COMPOUNDS BY HORSERADISH-PEROXIDASE - RELEVANCE TO THE MEASUREMENT OF DIHYDROPTERIDINE REDUCTASE-ACTIVITY
MILSTIEN, S
KAUFMAN, S
BIOCHIMICA ET BIOPHYSICA ACTA, 1987, 923 (03) : 333 - 338
[25] DIHYDROPTERIDINE REDUCTASE-ACTIVITY IN ELUATES FROM DRIED BLOOD SPOTS - AUTOMATION OF AN ASSAY FOR A NATIONAL SCREENING SERVICE
SURPLICE, IM
GRIFFITHS, PD
GREEN, A
LEEMING, RJ
JOURNAL OF INHERITED METABOLIC DISEASE, 1990, 13 (02) : 169 - 177
[26] ACTIVITY OF DIHYDROPTERIDINE REDUCTASE IN LEUKOCYTES AND CULTURED FIBROBLASTS OF HEALTHY-PERSONS AND OF PATIENTS WITH TYPICAL FORM OF PHENYLKETONURIA
GROMOV, PS
VALYANO, NM
AKHUNOV, VS
ANNENKOV, GA
VOPROSY MEDITSINSKOI KHIMII, 1983, 29 (05): : 66 - 69
[27] Effects of the metals on dihydropteridine reductase activity
Altindag, ZZ
Baydar, T
Engin, AB
Sahin, G
TOXICOLOGY IN VITRO, 2003, 17 (5-6) : 533 - 537
[28] RECOGNITION OF TETRAHYDROBIOPTERIN DEFICIENCY IN NEWBORN BABIES WITH PHENYLKETONURIA AND DIAGNOSIS OF DIHYDROPTERIDINE REDUCTASE DEFICIENCY
DANKS, DM
COTTON, RGH
FIRGAIRA, F
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 1980, 22 (02): : 252 - 253
[29] ATYPICAL PKU, SEIZURES, AND DEVELOPMENTAL DELAY WITH DIHYDROPTERIDINE REDUCTASE DEFICIENCY
BREWSTER, TG
ABROMS, IF
KAUFMAN, S
BRESLOW, JL
MOSKOWITZ, MA
VILLEE, DB
SNODGRASS, RS
PEDIATRIC RESEARCH, 1976, 10 (04) : 446 - 446
[30] HYPERPHENYLALANINEMIA WITH NORMAL PHENYLALANINE-HYDROXYLASE ACTIVITY - DEFICIENCY OF TETRAHYDROBIOPTERIN AND DIHYDROPTERIDINE-REDUCTASE
REY, F
HARPEY, JP
LEEMING, RJ
BLAIR, JA
AICARDI, J
REY, J
ARCHIVES FRANCAISES DE PEDIATRIE, 1977, 34 : 109 - 120

← 1 2 3 4 5 →