TYROSINEMIA TYPE I: A CASE REPORT

被引:0
|
作者
Lopez, Martinez M.
Fernandez, Perez-Alija A.
Atienza, Martinez M.
Rivera, Garcia M.
机构
关键词
D O I
暂无
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
引用
收藏
页码:S609 / S609
页数:1
相关论文
共 50 条
  • [31] COAGULOPATHY AS CLUE TO THE DIAGNOSIS OF TYROSINEMIA TYPE I
    Di Rocco, M.
    Caruso, U.
    Anna, Allegri E. M.
    Cerone, R.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2005, 28 : 60 - 60
  • [32] Nitisinone for the treatment of hereditary tyrosinemia type I
    McKiernan, Patrick James
    EXPERT OPINION ON ORPHAN DRUGS, 2013, 1 (06): : 491 - 497
  • [33] DIETARY TREATMENT OF TYROSINEMIA TYPE-I
    MICHALS, K
    MATALON, R
    WONG, PWK
    JOURNAL OF THE AMERICAN DIETETIC ASSOCIATION, 1978, 73 (05) : 507 - 514
  • [34] Corneal involvement in tyrosinemia type II mimicking herpetic keratitis: Case report in an adult
    Khochtali, S.
    Daldoul, N.
    Zina, S.
    Kadri, A.
    Ben Yahia, S.
    Khairallah, M.
    JOURNAL FRANCAIS D OPHTALMOLOGIE, 2018, 41 (07): : E315 - E318
  • [35] PERIPHERAL NERVOUS-SYSTEM IN HEREDITARY TYROSINEMIA TYPE-I - A REPORT OF 5 CASES
    MICHAUD, J
    MITCHELL, G
    LAMBERT, M
    LABORATORY INVESTIGATION, 1990, 62 (01) : P6 - P6
  • [36] HEREDITARY ACUTE TYROSINEMIA - CASE-REPORT
    SANJURJO, P
    RODRIGUEZSORIANO, J
    VALLO, A
    BILBAO, F
    LORIDAN, L
    ANALES ESPANOLES DE PEDIATRIA, 1976, 9 (05): : 547 - 552
  • [37] THE ENZYME DEFECTS IN HEREDITARY TYROSINEMIA TYPE-I
    FURUKAWA, N
    HAYANO, T
    SATO, N
    INOUE, F
    MACHIDA, Y
    KINUGASA, A
    IMASHUKU, S
    KUSUNOKI, T
    TAKAMATISU, T
    JOURNAL OF INHERITED METABOLIC DISEASE, 1984, 7 : 137 - 138
  • [38] CHROMOSOMAL INSTABILITY IN HEREDITARY TYROSINEMIA TYPE-I
    WILSON, KS
    TIMMONS, CF
    HILTON, DS
    WEINBERG, AG
    TONK, V
    PEDIATRIC PATHOLOGY, 1994, 14 (06): : 1055 - 1057
  • [39] NEONATAL SCREEN FOR HEREDITARY TYROSINEMIA TYPE-I
    HOLME, E
    LINDSTEDT, S
    LANCET, 1992, 340 (8823): : 850 - 850
  • [40] Neurological and Neuropsychological Problems in Tyrosinemia Type I Patients
    van Ginkel, Willem G.
    Jahja, Rianne
    Huijbregts, Stephan C. J.
    van Spronsen, Francjan J.
    HEREDITARY TYROSINEMIA: PATHOGENESIS, SCREENING AND MANAGEMENT, 2017, 959 : 111 - 122