Mitochondrial disease caused by the m.3243A>G mutation

被引：0
|
作者：
Varhaug, Kristin N. [1 ]
Hikmat, Omar [2 ]
Bindoff, Laurence A. [1 ]
机构：
[1] Univ Bergen, Klin Inst 1, Haukeland Univ Sjukehus, Nevrol Avdeling, Bergen, Norway
[2] Univ Bergen, Klin Inst 1, Haukeland Univ Sjukehus, Barne & Ungdomsklinikken, Bergen, Norway
来源：
TIDSSKRIFT FOR DEN NORSKE LAEGEFORENING | 2022年 / 142卷 / 10期
关键词：
DYSFUNCTION; NUCLEAR;
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：871 / 874
页数：4
相关论文
共 50 条
  • [31] Optimal Estimate for Energy Requirements in Adult Patients With the m.3243A>G Mutation in Mitochondrial DNA
    Zweers, Heidi E. E.
    Janssen, Mirian C. H.
    Wanten, Geert J. A.
    JOURNAL OF PARENTERAL AND ENTERAL NUTRITION, 2021, 45 (01) : 158 - 164
  • [32] Mitochondrial mutation m.3243A>G associates with insulin resistance in non-diabetic carriers
    Langdahl, Jakob Hogild
    Frederiksen, Anja Lisbeth
    Vissing, John
    Frost, Morten
    Yderstraede, Knud Bonnet
    Andersen, Per Heden
    ENDOCRINE CONNECTIONS, 2019, 8 (07): : 829 - 837
  • [33] Glucose metabolism derangements in adults with the MELAS m.3243A>G mutation
    El-Hattab, Ayman W.
    Emrick, Lisa T.
    Hsu, Jean W.
    Chanprasert, Sirisak
    Jahoor, Farook
    Scaglia, Fernando
    Craigen, William J.
    MITOCHONDRION, 2014, 18 : 63 - 69
  • [34] Mitochondrial cardiomyopathy due to m.3243A>G mitochondrial DNA mutation presenting in late adulthood: a case report
    Chau, Elaine M. C.
    Ma, Edmond S. K.
    Chan, Annie O. O.
    Tsio, T. H.
    Law, W. L.
    HONG KONG MEDICAL JOURNAL, 2020, 26 (03) : 240 - 242
  • [35] Cardiac involvement in adults with m.3243A>G MELAS gene mutation
    Vydt, Tom C. G.
    de Coo, Ren F. M.
    Soliman, Osama I. I.
    ten Cate, Folkert J.
    van Geuns, Robert-Jan M.
    Vletter, Wim B.
    Schoonderwoerd, Kees
    van den Bosch, Bianca J. C.
    Smeets, Hubert J. M.
    Geleijnse, Marcel L.
    AMERICAN JOURNAL OF CARDIOLOGY, 2007, 99 (02): : 264 - 269
  • [36] Evidence of early cardiac impairment in m.3243A>G mutation carriers
    Bates, M. G.
    Hollingsworth, K. G.
    Newman, J.
    Jakovljevic, D.
    Dixon, B. J.
    Blamire, A. M.
    MacGowan, G. A.
    Keavney, B. D.
    Chinnery, P. F.
    Turnbull, D. M.
    Taylor, R. W.
    Trenell, M. I.
    Gorman, G. S.
    NEUROMUSCULAR DISORDERS, 2012, 22 : S22 - S23
  • [37] GLUCOSE METABOLISM DERANGEMENTS IN ADULTS WITH THE MELAS MUTATION M.3243A>G
    El-Hattab, Ayman W.
    Emrick, Lisa T.
    Chanprasert, Sirisak
    Hsu, Jean W.
    Jahoor, Farook
    Scaglia, Fernando
    Craigen, William J.
    MOLECULAR GENETICS AND METABOLISM, 2014, 111 (03) : 262 - 262
  • [38] The first concurrent detection of mitochondrial DNA m.3243A>G mutation, deletion, and depletion in a family with mitochondrial diabetes
    Tabebi, Mouna
    Safi, Wajdi
    Felhi, Rahma
    Alila Fersi, Olfa
    Keskes, Leila
    Abid, Mohamed
    Mnif, Mouna
    Fakhfakh, Faiza
    MOLECULAR GENETICS & GENOMIC MEDICINE, 2020, 8 (07):
  • [39] Frequencies of myohistological mitochondrial changes in patients with mitochondrial DNA deletions and the common m.3243A>G point mutation
    Zierz, Charlotte Maria
    Joshi, Pushpa Raj
    Zierz, Stephan
    NEUROPATHOLOGY, 2015, 35 (02) : 130 - 136
  • [40] m.3243A>G: Many faces of one single point mutation
    Lederer, Stephan R.
    Klopstock, Thomas
    Schiffl, Helmut
    WIENER KLINISCHE WOCHENSCHRIFT, 2010, 122 (19-20) : 601 - 602
12345