The A3243G mitochondrial DNA mutation in cerebral artery dissections

被引：0
|
作者：
Kalashnikova, L. A. [1 ]
Dobrynina, L. A.
Sakharova, A. V.
Chaykovskaya, R. P.
Nazarova, M. A.
Mir-Kasimov, M. F.
Patrusheva, N. L.
Patrushev, L. I.
Konovalov, R. N.
Protskiy, S. V.
机构：
[1] Russian Acad Med Sci, Res Ctr Neurol, Moscow 109801, Russia
来源：
ZHURNAL NEVROLOGII I PSIKHIATRII IMENI S S KORSAKOVA | 2012年 / 112卷 / 01期
关键词：
cerebral artery dissection; mitochondrial cytopathy; mitochondrial disease; A3243G mtDNA mutation; mitochondrial DNA; STROKE-LIKE EPISODES; LACTIC-ACIDOSIS; CLINICAL PHENOTYPE; MELAS; ENCEPHALOPATHY; ENCEPHALOMYOPATHY; MANAGEMENT; DISORDERS; DIAGNOSIS; MYOPATHY;
D O I：
暂无
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
引用
收藏
页码：84 / +
页数：6
相关论文
共 50 条
  • [41] Mitochondrial A3243G mutation results in corneal endothelial polymegathism
    Bakhoum, Mathieu F.
    Wu, Wei-Pu
    White, Eugenia C.
    Sengillo, Jesse D.
    Sanfilippo, Christian
    Morcos, Marcelle M.
    Freund, K. Bailey
    Perry, Henry D.
    Sarraf, David
    Tsang, Stephen H.
    GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 2018, 256 (03) : 583 - 588
  • [42] Mitochondrial A3243G Mutation With Manifestation of Acute Dilated Cardiomyopathy
    Stalder, Nicolas
    Yarol, Nuray
    Tozzi, Piergiorgio
    Rotman, Samuel
    Morris, Michael
    Fellmann, Florence
    Schwitter, Juerg
    Hullin, Roger
    CIRCULATION-HEART FAILURE, 2012, 5 (01) : E1 - E3
  • [43] Eye movement and vestibular dysfunction in mitochondrial A3243G mutation
    Sung-Hee Kim
    Ziyoda Abdulkhaevna Akbarkhodjaeva
    Ileok Jung
    Ji-Soo Kim
    Neurological Sciences, 2016, 37 : 1159 - 1162
  • [44] An infant with a mitochondrial A3243G mutation demonstrating the MELAS phenotype
    Kanaumi, T
    Hirose, S
    Goto, Y
    Naitou, E
    Mitsudome, A
    PEDIATRIC NEUROLOGY, 2006, 34 (03) : 235 - 238
  • [45] Screening for the mitochondrial DNA A3243G mutation in children with insulin-dependent diabetes mellitus
    Abad, MM
    Cotter, PD
    Fodor, FH
    Larson, S
    GinsbergFellner, F
    Desnick, RJ
    Abdenur, JE
    METABOLISM-CLINICAL AND EXPERIMENTAL, 1997, 46 (04): : 445 - 449
  • [46] Maternally inherited deafness and unusual phenotypic manifestations associated with A3243G mitochondrial DNA mutation
    Komlósi, K
    Kellermayer, R
    Maász, A
    Havasi, V
    Hollódy, K
    Vincze, O
    Merkli, H
    Pál, E
    Melegh, B
    PATHOLOGY & ONCOLOGY RESEARCH, 2005, 11 (02) : 82 - 86
  • [47] Mitochondrial DNA haplogroups do not play a role in the variable phenotypic presentation of the A3243G mutation
    Torroni, A
    Campos, Y
    Rengo, C
    Sellitto, D
    Achilli, A
    Magri, C
    Semino, O
    García, A
    Jara, P
    Arenas, J
    Scozzari, R
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 72 (04) : 1005 - 1012
  • [48] Cochlear implantation In patients with mitochondria! DNA A3243G mutation
    Yamasoba, T.
    Suzuki, M.
    Kaga, K.
    Ogata, E.
    Akamatsu, Y.
    7TH ASIA PACIFIC SYMPOSIUM ON COCHLEAR IMPLANTS AND RELATED SCIENCES - APSCI, 2009, : 196 - +
  • [49] The Mitochondrial A3243G Mutation Involves the Peripheral Vestibule As Well As the Cochlea
    Iwasaki, Shinichi
    Egami, Naoya
    Fujimoto, Chisato
    Chihara, Yasuhiro
    Ushio, Munetaka
    Kashio, Akinori
    Yamasoba, Tatsuya
    LARYNGOSCOPE, 2011, 121 (08): : 1821 - 1824
  • [50] Single-cell A3243G mitochondrial DNA mutation load assays for segregation analysis
    Tafrechi, Roshan S. Jahangir
    van de Rijke, Frans M.
    Allallou, Amin
    Larsson, Chatarina
    Sloos, Willem C. R.
    van de Sande, Marchien
    Wahlby, Carolina
    Janssen, George M. C.
    Raap, Anton K.
    JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2007, 55 (11) : 1159 - 1166
12345