The mitochondrial A3243G mutation in maternally inherited migraine without aura.

被引:0
|
作者
Casali, C
Di Gennaro, G
Costa, A
Santorelli, FM
Buzzi, MG
Ciccarelli, O
Fortini, D
Fiermonte, G
D'Onofrio, M
Nappi, G
Pierelli, F
Amabile
机构
[1] Univ Rome La Sapienza, Nervous & Mental Dis Inst, Rome, Italy
[2] IRCCS, Pozzilli, IS, Italy
[3] IRCCS, Pavia, Italy
[4] Univ Rome La Sapienza, Dept Neurol Sci, I-00185 Rome, Italy
关键词
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:424 / 425
页数:2
相关论文
共 50 条
  • [1] Demonstration of the A3243G mitochondrial mutation in families with maternally inherited diabetes and deafness
    Thorns, C
    Widjaja, A
    Boeck, N
    Skamira, C
    Zühlke, H
    [J]. DIABETOLOGIA, 1998, 41 : A109 - A109
  • [2] Heteroplasmy of the mitochondrial A3243G mutation and the phenotype of maternally inherited diabetes and deafness.
    van Essen, EHR
    't Hart, LM
    Jansen, JJ
    van den Ouweland, JMW
    Maassen, JA
    Lemkes, HHPJ
    [J]. DIABETOLOGIA, 1998, 41 : A111 - A111
  • [3] 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
    [J]. PATHOLOGY & ONCOLOGY RESEARCH, 2005, 11 (02) : 82 - 86
  • [4] A3243G melas mutation in migraine with aura (MwoA) and in three-generation female migraine without aura (MwoA).
    Buzzi, MG
    Di Gennaro, G
    D'Onofrio, M
    Ciccarelli, O
    Santorelli, FM
    Fortini, D
    Pierelli, F
    Nicoletti, F
    Nappi, G
    Morocutti, C
    Casali, C
    [J]. CEPHALALGIA, 1999, 19 (04) : 425 - 425
  • [5] Assessing the relative incidence of mitochondrial DNA A3243G in migraine without aura with maternal inheritance
    Di Gennaro, G
    Buzzi, MG
    Ciccarelli, O
    Santorelli, FM
    Pierelli, F
    Fortini, D
    D'Onofrio, M
    Costa, A
    Nappi, G
    Casali, C
    [J]. HEADACHE, 2000, 40 (07): : 568 - 571
  • [6] Involvement of nervous system in maternally inherited diabetes and deafness (MIDD) with the A3243G mutation of mitochondrial DNA
    Lien, LM
    Lee, HC
    Wang, KL
    Chiu, JC
    Chiu, HC
    Wei, YH
    [J]. ACTA NEUROLOGICA SCANDINAVICA, 2001, 103 (03): : 159 - 165
  • [7] Diagnosis of maternally inherited diabetes and deafness (mitochondrial A3243G mutation) based on funduscopic appearance in an asymptomatic patient
    Strauss, Danielle Savitsky
    Freund, K. Bailey
    [J]. BRITISH JOURNAL OF OPHTHALMOLOGY, 2012, 96 (04) : 604 - 609
  • [8] Heterogeneous phenotypic manifestations of maternally inherited deafness associated with the mitochondrial A3243G mutation. Case report
    Hoptasz, Magdalena
    Szczucinski, Adam
    Losy, Jacek
    [J]. NEUROLOGIA I NEUROCHIRURGIA POLSKA, 2014, 48 (02) : 150 - 153
  • [9] Manifestations of the mitochondrial A3243G mutation
    Finsterer, Josef
    [J]. INTERNATIONAL JOURNAL OF CARDIOLOGY, 2009, 137 (01) : 60 - 62
  • [10] HLA-DQ polymorphism and degree of heteroplasmy of the A3243G mitochondrial DNA mutation in maternally inherited diabetes and deafness
    van Essen, EHR
    Roep, BO
    't Hart, LM
    Jansen, JJ
    Van den Ouweland, JMW
    Lemkes, HHPJ
    Maassen, JA
    [J]. DIABETIC MEDICINE, 2000, 17 (12) : 841 - 847