Re: EIF2AK3 mutations in patients with Wolcott-Rallison syndrome

被引：0
|
作者：
Taha, D [1 ]
机构：
[1] King Faisal Specialist Hosp & Res Ctr, Dept Pediat, Div Pediat Endocrinol, Jeddah 21499, Saudi Arabia
来源：
ANNALS OF SAUDI MEDICINE | 2005年 / 25卷 / 04期
关键词：
D O I：
10.5144/0256-4947.2005.350a
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：350 / 350
页数：1
相关论文
共 50 条
  • [31] Autopsy findings in the Wolcott-Rallison syndrome
    Thornton, CM
    Carson, DJ
    Stewart, FJ
    PEDIATRIC PATHOLOGY & LABORATORY MEDICINE, 1997, 17 (03): : 487 - 496
  • [32] WOLCOTT-RALLISON SYNDROME - A CASE-REPORT
    BARABINO, A
    DIROCCO, M
    COSTANTINO, G
    DELLACQUA, AM
    CAPRINO, D
    MASSOCCO, D
    BORRONE, C
    RIVISTA ITALIANA DI PEDIATRIA-ITALIAN JOURNAL OF PEDIATRICS, 1987, 13 (04): : 443 - 447
  • [33] The Wolcott-Rallison syndrome: two Moroccan observations
    Imane, Z.
    Amhager, S.
    Bennani, N.
    Balafrej, A.
    Ellard, Sian
    DIABETES & METABOLISM, 2010, 36 : A89 - A89
  • [34] Wolcott-Rallison Syndrome: Clinical Case Presentation
    Furdela, Viktoriya
    Pavlishin, Halina
    HORMONE RESEARCH IN PAEDIATRICS, 2016, 86 : 238 - 239
  • [35] Relative hypoaldosteronism in a patient with Wolcott-Rallison syndrome
    Ucar, A.
    Aydemir, Y.
    Dogan, A.
    Tuncez, E.
    DIABETIC MEDICINE, 2016, 33 (03) : E13 - E16
  • [36] Os odontoideum in wolcott-rallison syndrome: a case series of 4 patients
    Dias, R. P.
    Buchanan, C. R.
    Thomas, N.
    Lim, S.
    Solanki, G.
    Connor, S. E. J.
    Barrett, T. G.
    Kapoor, R. R.
    ORPHANET JOURNAL OF RARE DISEASES, 2016, 11
  • [37] Wolcott-Rallison syndrome with 3-hydroxydicarboxylic aciduria and lethal outcome
    Sovik, O.
    Njolstad, P. R.
    Jellum, E.
    Molven, A.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2008, 31 : S293 - S297
  • [38] Os odontoideum in wolcott-rallison syndrome: a case series of 4 patients
    R. P. Dias
    C. R. Buchanan
    N. Thomas
    S. Lim
    G. Solanki
    SEJ Connor
    T. G. Barrett
    R. R. Kapoor
    Orphanet Journal of Rare Diseases, 11
  • [39] Primary hypothyroidism: an unusual manifestation of Wolcott-Rallison syndrome
    Ersoy, Betul
    Ozhan, Bayram
    Kiremitci, Seniha
    Rubio-Cabezas, Oscar
    Ellard, Sian
    EUROPEAN JOURNAL OF PEDIATRICS, 2014, 173 (12) : 1565 - 1568
  • [40] A rare cause of neonatal diabetes mellitus: Wolcott-Rallison syndrome
    Leka, Sofia
    Petropoulou, Theoni
    Kanaka-Gantenbein, Christina
    HORMONE RESEARCH, 2008, 70 : 241 - 241
12345