The multiple faces of urinary glucose tetrasaccharide as biomarker for patients with hepatic glycogen storage diseases

被引：17
|
作者：
Heiner-Fokkema, M. Rebecca [1 ]
van der Krogt, Jennifer [1 ]
de Boer, Foekje [2 ]
Fokkert-Wilts, Marieke J. [2 ]
Maatman, Ronald G. H. J. [1 ]
Hoogeveen, Irene J. [2 ]
Derks, Terry G. J. [2 ]
机构：
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Lab Med, Groningen, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, Beatrix Childrens Hosp, Div Metab Dis, Groningen, Netherlands
来源：
GENETICS IN MEDICINE | 2020年 / 22卷 / 11期
关键词：
POMPE DISEASE; EXCRETION;
D O I：
10.1038/s41436-020-0878-2
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：1915 / 1916
页数：2
相关论文
共 50 条
  • [1] Glucose tetrasaccharide as a biomarker in Pompe disease and other glycogen storage diseases
    Harvey, Katie
    Manwearing, Vicki
    Lukovic, Biljana
    Prunty, Helen
    Burke, Derek
    Heales, Simon
    MOLECULAR GENETICS AND METABOLISM, 2013, 108 (02) : S47 - S47
  • [2] UTILITY OF A URINARY TETRASACCHARIDE AS A BIOMARKER FOR GLYCOGEN STORAGE DISEASE TYPE III
    Tolun, A. A.
    Boyd, K. F.
    Austin, S. L.
    Vertilus, S. M.
    Case, L. E.
    Wechsler, S. B.
    Millington, D. S.
    Bali, D.
    Young, S. P.
    Kishnani, P. S.
    MOLECULAR GENETICS AND METABOLISM, 2009, 98 (1-2) : 39 - 39
  • [3] Urine analysis of glucose tetrasaccharide by HPLC; a useful marker for the investigation of patients with Pompe and other glycogen storage diseases
    Manwaring, Victoria
    Prunty, Helen
    Bainbridge, Katie
    Burke, Derek
    Finnegan, Niamh
    Franses, Rebecca
    Lam, Amanda
    Vellodi, Ashok
    Heales, Simon
    JOURNAL OF INHERITED METABOLIC DISEASE, 2012, 35 (02) : 311 - 316
  • [4] Body composition in patients with hepatic glycogen storage diseases
    dos Santos, Bruna B.
    Colonetti, Karina
    Nalin, Tatiele
    de Oliveira, Bibiana M.
    de Souza, Carolina F. M.
    Spritzer, Poli Mara
    V.d. Schwartz, Ida
    NUTRITION, 2022, 104
  • [5] Urinary glucose tetrasaccharide, a useful prognostic biomarker for Pompe disease?
    Heales, Simon
    Harvey, Katie
    Cleary, Maureen
    Prunty, Helen
    Davison, James
    Burke, Derek
    Guilder, Laura
    MOLECULAR GENETICS AND METABOLISM, 2019, 126 (02) : S70 - S70
  • [6] Bone Mineral Density in Patients with Hepatic Glycogen Storage Diseases
    Jacoby, Jesica Tamara
    dos Santos, Bruna Bento
    Nalin, Tatiele
    Colonetti, Karina
    Refosco, Lilia Farret
    de Souza, Carolina F. M.
    Spritzer, Poli Mara
    Poloni, Soraia
    Hack-Mendes, Roberta
    Doederlein Schwartz, Ida Vanessa
    NUTRIENTS, 2021, 13 (09)
  • [7] Assessment of auditory functions in patients with hepatic glycogen storage diseases
    Sanli, Merve Emecen
    Gokay, Nuriye Yildirim
    Tutar, Hakan
    Gunduz, Bulent
    Ozsaydi, Ekin
    Kilic, Ayse
    Inci, Asli
    Okur, Ilyas
    Ezgu, Fatih
    Tumer, Leyla
    TURKISH JOURNAL OF PEDIATRICS, 2022, 64 (04) : 658 - 670
  • [8] Glucose continuous monitoring in hepatic glycogen storage diseases -: What dietectic benefits
    Patricio, Z.
    Figueiredo, C.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2008, 31 : 142 - 142
  • [9] Hepatic Resection and Transplant in Glycogen Storage Diseases
    Singh, Navdeep
    El-Hinnawi, Ashraf
    Hill, Bryan
    Elkhammas, Elmahdi
    Eze, Ogechukwu
    Alebrahim, Musab
    Michaels, Anthony
    Schenk, Austin
    Washburn, Kenneth
    Black, Sylvester
    EXPERIMENTAL AND CLINICAL TRANSPLANTATION, 2022, 20 (06) : 609 - 612
  • [10] Natural history of hepatic glycogen storage diseases
    Labrune, Philippe
    Eberschweiler, Pascale Trioche
    Boudjemline, Alix Mollet
    Hubert-Buron, Aurelie
    Petit, Francois
    Gajdos, Vincent
    PRESSE MEDICALE, 2008, 37 (7-8): : 1172 - 1177
12345