Clinical picture of a case of diabetes with mitochondrial tRNA mutation at position (vol 19, pg 1304, 1996)

被引:0
|
作者
Suzuki, Y
Tsukuda, K
Atsumi, Y
Goto, Y
Hosokawa, K
Asahina, T
Nonaka, I
Matsuoka, K
Oka, Y
机构
关键词
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
下载
收藏
页码:1458 / 1458
页数:1
相关论文
共 50 条
  • [31] The clinical characteristics of patients with mitochondrial tRNA Leu(UUR)m.3243A > G mutation: Compared with type 1 diabetes and early onset type 2 diabetes
    Zhu, Jie
    Yang, Peng
    Liu, Xiang
    Yan, Li
    Rampersad, Sharvan
    Li, Feng
    Li, Hong
    Sheng, Chunjun
    Cheng, Xiaoyun
    Zhang, Manna
    Qu, Shen
    JOURNAL OF DIABETES AND ITS COMPLICATIONS, 2017, 31 (08) : 1354 - 1359
  • [32] Pyrosequencing Is an Accurate and Reliable Method for the Analysis of Heteroplasmy of the A32430 Mutation in Patients with Mitochondrial Diabetes (vol 16, pg 431, 2014)
    Yan, Jing-bin
    Zhang, Rong
    Xiong, Can
    Hu, Cheng
    Lv, Yao
    Wang, Cong-rong
    Jia, Wei-ping
    Zeng, Fanyi
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2014, 16 (05): : 591 - 591
  • [34] Clinical considerations for patients with diabetes in times of COVID-19 epidemic (vol 14, pg 211, 2020)
    Gupta, Ritesh
    Ghosh, Amerta
    Singh, Awadhesh Kumar
    Misra, Anoop
    DIABETES & METABOLIC SYNDROME-CLINICAL RESEARCH & REVIEWS, 2021, 15 (01) : 467 - 467
  • [35] A NEW MITOCHONDRIAL-DNA MUTATION ASSOCIATED WITH NON-INSULIN-DEPENDENT DIABETES-MELLITUS (VOL 209, PG 664, 1995)
    NAKAGAWA, Y
    IKEGAMI, H
    YAMATO, E
    TAKEKAWA, K
    FUJISAWA, T
    HAMADA, Y
    UEDA, H
    UCHIGATA, Y
    MIKI, T
    KUMAHARA, Y
    OGIHARA, T
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 212 (02) : 718 - 718
  • [36] Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case–control study
    P. Massin
    D. Dubois-Laforgue
    T. Meas
    M. Laloi-Michelin
    H. Gin
    B. Bauduceau
    C. Bellanné-Chantelot
    E. Bertin
    J.-F. Blickle
    B. Bouhanick
    J. Cahen-Varsaux
    S. Casanova
    G. Charpentier
    P. Chedin
    O. Dupuy
    A. Grimaldi
    B. Guerci
    E. Kaloustian
    A. Lecleire-Collet
    F. Lorenzini
    A. Murat
    H. Narbonne
    F. Olivier
    V. Paquis-Flucklinger
    M. Virally
    M. Vincenot
    B. Vialettes
    J. Timsit
    P. J. Guillausseau
    Diabetologia, 2008, 51 : 1664 - 1670
  • [37] Clinical Characteristics of 28 Patients with Diabetes and COVID-19 in Wuhan, China (vol 26, pg 668, 2020)
    Wang, Fen
    Yang, Yan
    Dong, Kun
    Yan, Yongli
    Zhang, Shujun
    Ren, Huihui
    Yu, Xuefeng
    Shi, Xiaoli
    ENDOCRINE PRACTICE, 2024, 30 (03)
  • [38] Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case-control study
    Massin, P.
    Dubois-Laforgue, D.
    Meas, T.
    Laloi-Michelin, M.
    Gin, H.
    Bauduceau, B.
    Bellanne-Chantelot, C.
    Bertin, E.
    Blickle, J. -F.
    Bouhanick, B.
    Cahen-Varsaux, J.
    Casanova, S.
    Charpentier, G.
    Chedin, P.
    Dupuy, O.
    Grimaldi, A.
    Guerci, B.
    Kaloustian, E.
    Lecleire-Collet, A.
    Lorenzini, F.
    Murat, A.
    Narbonne, H.
    Olivier, F.
    Paquis-Flucklinger, V.
    Virally, M.
    Vincenot, M.
    Vialettes, B.
    Timsit, J.
    Guillausseau, P. J.
    DIABETOLOGIA, 2008, 51 (09) : 1664 - 1670
  • [39] A case of perinatal hypophosphatasia with a novel mutation in the ALPL gene: clinical course and review of the literature (vol 27, pg 179, 2018)
    Oyachi, Maki
    Harada, Daisuke
    Sakamoto, Natsuko
    Ueyama, Kaoru
    Kondo, Kawai
    Kishimoto, Kanako
    Izui, Masafumi
    Nagamatsu, Yuiko
    Kashiwagi, Hiroko
    Yamamuro, Miho
    Tamura, Makoto
    Kikuchi, Shin
    Akiyama, Tomoyuki
    Michigami, Toshimi
    Seino, Yoshiki
    Namba, Noriyuki
    CLINICAL PEDIATRIC ENDOCRINOLOGY, 2019, 28 (01) : 23 - 23
  • [40] Clinical and biochemical heterogeneity in females of a large pedigree with ornithine transcarbamylase deficiency due to the R141Q mutation (vol 66, pg 311, 1996)
    Ahrens, MJ
    Berry, SA
    Whitley, CB
    Markowitz, DJ
    Plante, RJ
    Tuchman, M
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1997, 71 (01): : 125 - 125