ACUTE HEREDITARY TYROSINEMIA TYPE-I - CLINICAL, BIOCHEMICAL AND HEMATOLOGICAL STUDIES IN TWINS

被引：16
|
作者：
GRAY, RGF
PATRICK, AD
PRESTON, FE
WHITFIELD, MF
机构：
[1] UNIV SHEFFIELD,SUBDEPT MED GENET,SHEFFIELD S10 5DN,ENGLAND
[2] UNIV LONDON,INST CHILD HLTH,LONDON WC1N 1EH,ENGLAND
[3] CHILDRENS HOSP,DEPT PAEDIAT,SHEFFIELD S10 2TH,S YORKSHIRE,ENGLAND
[4] ROYAL HALLAMSHIRE HOSP,DEPT HAEMATOL,SHEFFIELD S10 2JF,ENGLAND
来源：
JOURNAL OF INHERITED METABOLIC DISEASE | 1981年 / 4卷 / 01期
关键词：
D O I：
10.1007/BF02263580
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：37 / 40
页数：4
相关论文
共 50 条
  • [21] IDENTIFICATION OF A PREDOMINANT MUTATION IN HEREDITARY TYROSINEMIA TYPE-I PATIENTS FROM QUEBEC
    TANGUAY, RM
    STLOUIS, M
    DEMERS, SI
    LECLERC, B
    ALDHALIMY, M
    GROMPE, M
    AMERICAN JOURNAL OF HUMAN GENETICS, 1993, 53 (03) : 954 - 954
  • [22] FUMARYLACETOACETASE MEASUREMENT AS A MASS-SCREENING PROCEDURE FOR HEREDITARY TYROSINEMIA TYPE-I
    LABERGE, C
    GRENIER, A
    VALET, JP
    MORISSETTE, J
    AMERICAN JOURNAL OF HUMAN GENETICS, 1990, 47 (02) : 325 - 328
  • [23] TREATMENT OF HEREDITARY TYROSINEMIA TYPE-I BY INHIBITION OF 4-HYDROXYPHENYLPYRUVATE DIOXYGENASE
    LINDSTEDT, S
    HOLME, E
    LOCK, EA
    HJALMARSON, O
    STRANDVIK, B
    LANCET, 1992, 340 (8823): : 813 - 817
  • [24] HEREDITARY TYROSINEMIA TYPE-I - SELF-INDUCED CORRECTION OF THE FUMARYLACETOACETASE DEFECT
    KVITTINGEN, EA
    ROOTWELT, H
    BRANDTZAEG, P
    BERGAN, A
    BERGER, R
    JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (04): : 1816 - 1821
  • [25] DIFFERENT MOLECULAR-BASIS FOR FUMARYLACETOACETATE HYDROLASE DEFICIENCY IN THE 2 CLINICAL FORMS OF HEREDITARY TYROSINEMIA (TYPE-I)
    TANGUAY, RM
    VALET, JP
    LESCAULT, A
    DUBAND, JL
    LABERGE, C
    LETTRE, F
    PLANTE, M
    AMERICAN JOURNAL OF HUMAN GENETICS, 1990, 47 (02) : 308 - 316
  • [26] LIVER-TRANSPLANTATION IN 2 CHILDREN WITH TYROSINEMIA TYPE-I - BIOCHEMICAL ASPECTS
    RIUDOR, E
    RIBES, A
    LLORET, J
    FRIDEN, J
    HOLME, E
    JAKOBS, C
    IBANEZ, VM
    JOURNAL OF INHERITED METABOLIC DISEASE, 1991, 14 (03) : 281 - 284
  • [27] DIETARY TREATMENT OF TYROSINEMIA TYPE-I
    MICHALS, K
    MATALON, R
    WONG, PWK
    JOURNAL OF THE AMERICAN DIETETIC ASSOCIATION, 1978, 73 (05) : 507 - 514
  • [28] Clinical, biochemical, and genetic analysis of a Korean neonate with hereditary tyrosinemia type 1
    Park, Hyung-Doo
    Lee, Dong Hwan
    Choi, Tae-Youn
    Lee, You Kyoung
    Kim, Jong-Won
    Ki, Chang-Seok
    Lee, Yong-Wha
    CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2009, 47 (08) : 930 - 933
  • [29] Tyrosinemia type I -: clinical and biochemical symptoms of three infants
    Crone, J
    Huber, WD
    Möslinger, D
    Felberbauer, F
    Utermann, K
    Gratzl, R
    Stöckler-Ipsiroglu, S
    MONATSSCHRIFT KINDERHEILKUNDE, 2000, 148 (11) : 1001 - 1005
  • [30] Tyrosinemia type I: clinical and biochemical analysis of patients in Mexico
    Fernandez-Lainez, Cynthia
    Ibarra-Gonzalez, Isabel
    Belmont-Martinez, Leticia
    Monroy-Santoyo, Susana
    Guillen-Lopez, Sara
    Vela-Amieva, Marcela
    ANNALS OF HEPATOLOGY, 2014, 13 (02) : 265 - 272
12345