NEUROPHYSIOLOGICAL INVESTIGATIONS IN 2 CASES OF ALEXANDER DISEASE WITH INFANTILE ONSET

被引：0
|
作者：
BATTAGLIA, A [1 ]
NARDELLI, E [1 ]
PAMPIGLIONE, G [1 ]
HARDEN, A [1 ]
机构：
[1] HOSP SICK CHILDREN,LONDON WC1N 3JH,ENGLAND
来源：
ITALIAN JOURNAL OF NEUROLOGICAL SCIENCES | 1980年 / 1卷 / 03期
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：131 / 138
页数：8
相关论文
共 50 条
  • [21] Infantile Alexander's disease: Serial neuroradiologic findings
    Ni, Q
    Johns, GS
    Manepalli, A
    Martin, DS
    Geller, TJ
    JOURNAL OF CHILD NEUROLOGY, 2002, 17 (06) : 463 - 466
  • [22] Infantile Alexander Disease Presenting with Hydrocephalus and Epileptic Spasms
    Gowda, Vykuntaraju K.
    Srinivasan, Varunvenkat M.
    Bhat, Maya
    Prasad, Chandrajit
    INDIAN JOURNAL OF PEDIATRICS, 2020, 87 (10): : 871 - 872
  • [23] Infantile-Onset Pompe Disease
    Ashrafi, Mahmoud Reza
    Tavasoli, Alireza
    IRANIAN JOURNAL OF CHILD NEUROLOGY, 2012, 6 (04) : 7 - 9
  • [24] INFANTILE CORTICAL HYPEROSTOSIS (CAFFEYS DISEASE), WITH REFERENCE TO 2 CASES
    GILLET, J
    IMANI, E
    BENZAKOUR, M
    GUIGNARD, J
    ANNALES DE RADIOLOGIE, 1974, 17 (07) : 707 - 711
  • [25] Infantile and juvenile presentations of Alexander's disease: a report of two cases (vol 99, pg 158, 1999)
    Deprez, M
    D'Hooghe, M
    Misson, JP
    de Leval, L
    Ceuterick, C
    Reznik, M
    Martin, JJ
    ACTA NEUROLOGICA SCANDINAVICA, 1999, 100 (05): : 354 - 354
  • [26] THE PEROXISOMAL PHENOTYPE - A REPORT OF 2 CASES OF INFANTILE REFSUMS DISEASE
    CLARKE, LA
    APPLEGARTH, DA
    JAN, J
    HARRIS, HM
    HALL, JG
    CLINICAL RESEARCH, 1990, 38 (01): : A185 - A185
  • [27] Infantile Onset Glycogen Storage Disease Type 2: Case Report
    Koca, Serkan Bilge
    Polat, Emine
    Bayram, Bahtisen
    Urel, Gizem
    Senel, Saliha
    Okur, Ilyas
    GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS, 2014, 12 (02): : 131 - 134
  • [28] An unusual GFAP mutation in a Taiwanese child with infantile Alexander disease
    Liang, Jao-Shwann
    Lin, Li-Ju
    Lin, Haung-Chi
    Yang, Ming-Tao
    Wang, Jinn-Shyan
    Lu, Jyh-Feng
    PEDIATRICS AND NEONATOLOGY, 2018, 59 (06): : 624 - 627
  • [29] Cerebral proton magnetic resonance spectroscopy in infantile Alexander disease
    Brockmann, K
    Dechent, P
    Meins, M
    Haupt, M
    Sperner, J
    Stephani, U
    Frahm, J
    Hanefeld, F
    JOURNAL OF NEUROLOGY, 2003, 250 (03) : 300 - 306
  • [30] GFAP mutations in 3 Chinese infantile Alexander disease patients
    Wu, Y.
    Jiang, Y. W.
    Wang, J. M.
    Yang, Y. L.
    Zhang, Y. H.
    Chang, X. Z.
    Qin, J.
    Xiao, J. X.
    Wu, X.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2006, 29 : 66 - 66
12345