CONGENITAL EXPRESSION OF PROLIDASE DEFECT IN PROLIDASE DEFICIENCY

被引：11

作者：

NAUGHTEN, ER

PROCTOR, SP

LEVY, HL

COULOMBE, JT

AMPOLA, MG

机构：

[1] MASSACHUSETTS GEN HOSP, NEUROL SERV, JOSEPH P KENNEDY JR LABS, BOSTON, MA 02114 USA

[2] HARVARD UNIV, SCH MED, DEPT NEUROL, BOSTON, MA 02115 USA

[3] MASSACHUSETTS DEPT PUBL HLTH, INST STATE LAB, BOSTON, MA 02130 USA

[4] TUFTS UNIV, NEW ENGLAND MED CTR, AMINO ACID LAB, BOSTON, MA 02111 USA

来源：

PEDIATRIC RESEARCH | 1984年 / 18卷 / 03期

关键词：

D O I：

10.1203/00006450-198403000-00008

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：259 / 261

页数：3

共 23 条

[1] PROLIDASE DEFICIENCY - DERMATOLOGICAL MANIFESTATIONS AND SOME ADDITIONAL BIOCHEMICAL STUDIES [J].

ARATA, J ;

UMEMURA, S ;

YAMAMOTO, Y ;

HAGIYAMA, M ;

NOHARA, N .

ARCHIVES OF DERMATOLOGY, 1979, 115 (01) :62-67

[2] CHEMICAL PATHOLOGY OF HUNTINGTONS-DISEASE [J].

BIRD, ED .

ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1980, 20 :533-551

[3] FURTHER STUDIES ON A PATIENT WITH IMINODIPEPTIDURIA - PROBABLE CASE OF PROLIDASE DEFICIENCY [J].

BUIST, NRM ;

BELLINGE.JF ;

KENNAWAY, NG ;

STRANDHO.JJ .

METABOLISM-CLINICAL AND EXPERIMENTAL, 1972, 21 (12) :1113-&

[4] GENETIC EXPRESSION OF WILSONS-DISEASE IN CELL-CULTURE - A DIAGNOSTIC MARKER [J].

CHAN, WY ;

CUSHING, W ;

COFFMAN, MA ;

RENNERT, OM .

SCIENCE, 1980, 208 (4441) :299-300

[5] PROLIDASE DEFICIENCY WITH IMINODIPEPTIDURIA - BIOCHEMICAL INVESTIGATIONS AND 1ST RESULTS OF ATTEMPTED THERAPY [J].

CHARPENTIER, C ;

DAGBOVIE, K ;

LEMONNIER, A ;

LARREGUE, M ;

JOHNSTONE, RAW .

JOURNAL OF INHERITED METABOLIC DISEASE, 1981, 4 (02) :77-78

[6] SIMPLE CHROMATOGRAPHIC SCREENING TEST FOR DETECTION OF DISORDERS OF AMINO ACID METABOLISM [J].

EFRON, ML ;

MACCREADY, RA ;

YOUNG, D ;

MOSER, HW .

NEW ENGLAND JOURNAL OF MEDICINE, 1964, 270 (26) :1378-+

[7] SCREENING METHOD FOR PROLIDASE DEFICIENCY [J].

ENDO, F ;

MATSUDA, I .

HUMAN GENETICS, 1981, 56 (03) :349-351

[8] HUMAN-ERYTHROCYTE PROLIDASE AND PROLIDASE DEFICIENCY [J].

ENDO, F ;

MATSUDA, I ;

OGATA, A ;

TANAKA, S .

PEDIATRIC RESEARCH, 1982, 16 (03) :227-231

[9] A SYNDROME RESEMBLING LATHYRISM ASSOCIATED WITH IMINODIPEPTIDURIA [J].

GOODMAN, SI ;

SOLOMONS, CC ;

MUSCHENHEIM, F ;

MCINTYRE, CA ;

MILES, B ;

OBRIEN, D .

AMERICAN JOURNAL OF MEDICINE, 1968, 45 (01) :152-+

[10] PROLIDASE DEFICIENCY WITH IMIDODIPEPTIDURIA - FAMILIAL CASE WITH AND WITHOUT CLINICAL SYMPTOMS [J].

ISEMURA, M ;

HANYU, T ;

GEJYO, F ;

NAKAZAWA, R ;

IGARASHI, R ;

MATSUO, S ;

IKEDA, K ;

SATO, Y .

CLINICA CHIMICA ACTA, 1979, 93 (03) :401-407

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