22q11 deletion syndrome as a cause of hypoparathyroidism

被引:0
|
作者
Bagci, Onur [1 ]
Ercan, Oya [1 ]
Kayserili, Hulya [2 ]
机构
[1] Cerrahpasa Med Fac, Istanbul, Turkey
[2] Istanbul Fac Med, Istanbul, Turkey
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
收藏
页码:244 / 244
页数:1
相关论文
共 50 条
  • [41] Networks of attention in children with the 22q11 deletion syndrome
    Sobin, C
    Kiley-Brabeck, K
    Daniels, S
    Blundell, M
    Anyane-Yeboa, K
    Karayiorgou, M
    DEVELOPMENTAL NEUROPSYCHOLOGY, 2004, 26 (02) : 611 - 626
  • [42] Characterization of Endocrinopathies in Patients with 22q11 Deletion Syndrome
    Lasprilla Tovar, Juan
    Zuluaga Espinosa, Nora
    Forero Torres, Adriana
    Sierra Abaunza, Javier
    HORMONE RESEARCH IN PAEDIATRICS, 2018, 90 : 32 - 32
  • [43] Facial features in children with the 22q11 deletion syndrome
    Oskarsdottir, S.
    Holmberg, E.
    Fasth, A.
    Stromland, K.
    ACTA PAEDIATRICA, 2008, 97 (08) : 1113 - 1117
  • [44] Role of Astrocyte Dysfunctions in 22q11 Deletion Syndrome
    Bezzi, Paola
    Zehnder, Tamara
    Laugeray, Anthony
    Rossi, Daniela
    Bagni, Claudia
    Mameli, Manuel
    Polleux, Franck
    BIOLOGICAL PSYCHIATRY, 2020, 87 (09) : S112 - S112
  • [45] Autism phenotype in children with 22Q11 deletion syndrome
    Vorstman, JAS
    Morcus, MEJ
    Swaab-Barneveld, H
    Heineman-de Boer, JA
    Duijff, SN
    Jansen, P
    Beemer, FA
    van Engeland, H
    AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2004, 130B (01): : 73 - 73
  • [46] The 22q11 deletion syndromes
    Scambler, PJ
    HUMAN MOLECULAR GENETICS, 2000, 9 (16) : 2421 - 2426
  • [47] Laryngeal abnormalities are frequent in the 22q11 deletion syndrome
    Leopold, C.
    De Barros, A.
    Cellier, C.
    Drouin-Garraud, V.
    Dehesdin, D.
    Marie, J. -P.
    INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2012, 76 (01) : 36 - 40
  • [48] Chromosome 22q11 deletion syndrome and psychiatric illness
    不详
    NEUROSCIENTIST, 2000, 6 (02): : 73 - 73
  • [49] Disrupted Dopaminergic Neurotransmission in 22q11 Deletion Syndrome
    Erik Boot
    Jan Booij
    Janneke Zinkstok
    Nico Abeling
    Lieuwe de Haan
    Frank Baas
    Don Linszen
    Thérèse van Amelsvoort
    Neuropsychopharmacology, 2008, 33 : 1252 - 1258
  • [50] Neuroanatomical and dopaminergic markers in 22q11 deletion syndrome
    van Amelsvoort, T.
    BEHAVIOR GENETICS, 2007, 37 (06) : 801 - 802