Screening for Classical Galactosemia in the Newborn: Is It Worth It?

被引：0
|
作者：
Vibhuti Shah
Smadar Friedman
Betty-Ann Platt
Aideen Moore
Annette Feigenbaum
机构：
[1] The Hospital for Sick Children,Division of Neonatology, Division of Laboratory Medicine, Division of Neonatology, Division of Clinical Genetics
[2] University of Toronto,undefined
[3] The Hospital for Sick Children,undefined
[4] The Hospital for Sick Children,undefined
[5] The Hospital for Sick Children,undefined
[6] University of Toronto,undefined
来源：
Pediatric Research | 1999年 / 45卷 / 7期
关键词：
D O I：
10.1203/00006450-199904020-01335
中图分类号：
学科分类号：
摘要：
引用
收藏
页码：224 / 224
相关论文
共 50 条
  • [41] Is it worth screening for congenital structural heart disease in newborn infants?
    Engvall, Jan
    ACTA PAEDIATRICA, 2023, 112 (10) : 2028 - 2029
  • [42] Diet treatment of classical galactosemia
    Kiss Erika
    Balogh Lidia
    Reismann Peter
    ORVOSI HETILAP, 2017, 158 (47) : 1864 - 1867
  • [43] Outcomes of Siblings with Classical Galactosemia
    Hughes, Joanne
    Ryan, Stephanie
    Lambert, Deborah
    Geoghegan, Olivia
    Clark, Anne
    Rogers, Yvonne
    Hendroff, Una
    Monavari, Ahmad
    Twomey, Eilish
    Treacy, Eileen P.
    JOURNAL OF PEDIATRICS, 2009, 154 (05): : 721 - 726
  • [44] Twelve-year review of galactosemia newborn screening in Taiwan: Evolving methods and insights
    Chen, Hui-An
    Hsu, Rai-Hseng
    Chen, Li -Chu
    Lee, Ni-Chung
    Chiu, Pao-Chin
    Hwu, Wuh-Liang
    Chien, Yin-Hsiu
    MOLECULAR GENETICS AND METABOLISM REPORTS, 2024, 38
  • [45] Newborn Screening for Galactosemia: A Review of 5 Years of Data and Audit of a Revised Reporting Approach
    Freer, Dennis E.
    Ficicioglu, Can
    Finegold, David
    CLINICAL CHEMISTRY, 2010, 56 (03) : 437 - 444
  • [46] Erratum to: Newborn screening for congenital hypothyroidism, galactosemia and biotinidase deficiency in Uttar Pradesh, India
    Vignesh Gopalakrishnan
    Kriti Joshi
    Shubha Phadke
    Preeti Dabadghao
    Meenal Agarwal
    Vinita Das
    Suruchi Jain
    Sanjay Gambhir
    Bhaskar Gupta
    Amita Pandey
    Deepa Kapoor
    Mala Kumar
    Vijayalakshmi Bhatia
    Indian Pediatrics, 2015, 52 : 70 - 70
  • [47] Duarte (DG) galactosemia: A study of biochemical and neurodevelopmental assessment in children detected by newborn screening
    Ficicioglu, C.
    Thomas, N.
    Yager, C.
    Gallagher, P. R.
    Hussa, C.
    Forbes, B. J.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2008, 31 : 44 - 44
  • [48] Newborn screening for galactosemia: ultramicro assay for galactose-1-phosphate-uridyltransferase activity
    Rhode, H
    Elei, E
    Taube, I
    Podskarbi, T
    Horn, A
    CLINICA CHIMICA ACTA, 1998, 274 (01) : 71 - 87
  • [49] GALACTOSEMIA - SCREENING AND DIAGNOSIS
    BEUTLER, E
    CLINICAL BIOCHEMISTRY, 1991, 24 (04) : 293 - 300
  • [50] GALACTOSEMIA GENERALLY WITH FULMINATING COURSE - 10 CASES FOUND THROUGH ROUTINE NEWBORN SCREENING
    SCHEIBENREITER, S
    THALHAMMER, O
    WIENER KLINISCHE WOCHENSCHRIFT, 1972, 84 (06) : 93 - +
12345