Clinical and genetic characterisation in a cohort of 80 Italian patients affected by spinocerebellar ataxia

被引：0
|
作者：
Masciullo, M. [1 ]
Modoni, A. [1 ]
Pomponi, M. G. [1 ]
Neri, G. [1 ]
Tonali, P. A. [1 ]
Silvestri, G. [1 ]
机构：
[1] Catholic Univ, Rome, Italy
来源：
JOURNAL OF NEUROLOGY | 2007年 / 254卷
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：68 / 69
页数：2
相关论文
共 50 条
  • [21] Clinical and genetic analysis of spinocerebellar ataxia type 11
    Johnson, Janel
    Wood, Nicholas
    Giunti, Paola
    Houlden, Henry
    CEREBELLUM, 2008, 7 (02): : 159 - 164
  • [22] Spinocerebellar ataxia type 28 (SCA28): clinical and genetic characterisation of a novel form of autosomal dominant cerebellar ataxia
    DiBella, D.
    Mariotti, C.
    Gellera, C.
    Plumari, M.
    Fracasso, V.
    Fancellu, R.
    Cagnoli, C.
    Brusco, A.
    Lazzaro, F.
    Muzi-Falconi, M.
    DiDonato, S.
    Taroni, F.
    JOURNAL OF NEUROLOGY, 2007, 254 : 28 - 28
  • [23] Clinical, Radiological, and Genetic Profile of Spinocerebellar Ataxia 12: A Hospital-Based Cohort Analysis
    Ganaraja, Valakunja Harikrishna
    Holla, Vikram V.
    Stezin, Albert
    Kamble, Nitish
    Yadav, Ravi
    Purushottam, Meera
    Jain, Sanjeev
    Pal, Pramod Kumar
    TREMOR AND OTHER HYPERKINETIC MOVEMENTS, 2022, 12
  • [24] Genetic study of patients affected by eating disorders in an Italian cohort
    Ceccarini, M.
    Tasegian, A.
    Franzago, M.
    Stuppia, L.
    Patria, F.
    Codini, M.
    Conte, C.
    Albi, E.
    Bertelli, M.
    Dalla Ragione, L.
    Beccari, T.
    JOURNAL OF BIOTECHNOLOGY, 2019, 305 : S7 - S8
  • [25] 'Costa da Morte' ataxia is spinocerebellar ataxia 36: clinical and genetic characterization
    Garcia-Murias, Maria
    Quintans, Beatriz
    Arias, Manuel
    Seixas, Ana I.
    Cacheiro, Pilar
    Tarrio, Rosa
    Pardo, Julio
    Millan, Maria J.
    Arias-Rivas, Susana
    Blanco-Arias, Patricia
    Dapena, Dolores
    Moreira, Ramon
    Rodriguez-Trelles, Francisco
    Sequeiros, Jorge
    Carracedo, Angel
    Silveira, Isabel
    Sobrido, Maria J.
    BRAIN, 2012, 135 : 1423 - 1435
  • [26] Screening for FMRI gene permutations in Italian patients with spinocerebellar ataxia
    Cellini, E
    Nacmias, B
    Forleo, P
    Piacentini, S
    Tedde, A
    Bagnoli, S
    Sorbi, S
    NEUROLOGY, 2006, 66 (05) : 277 - 277
  • [27] Clinical and genetic heterogeneity in Indian subcontinent patients with Autosomal Dominant Spinocerebellar Ataxia 42
    Mehta, A.
    Javali, M.
    Haskar, K.
    Gupta, D.
    Acharya, P.
    Srinivasa, S.
    MOVEMENT DISORDERS, 2019, 34 : S109 - S114
  • [28] Clinical features and genetic analysis of a new form of spinocerebellar ataxia
    Devos, D
    Schraen-Maschke, S
    Vuillaume, I
    Dujardin, K
    Nazé, P
    Willoteaux, C
    Destée, A
    Sablonnière, B
    NEUROLOGY, 2001, 56 (02) : 234 - 238
  • [29] Clinical features and genetic diagnosis of hereditary spinocerebellar ataxia 3
    Wang, Yaoguang
    Yang, Xiaokai
    Ma, Weide
    Li, Jinxin
    Zhang, Qingyuan
    Xia, Shuqi
    Wang, Hai
    Zhang, Chenghui
    Xu, Xiaomin
    Zheng, Jiayong
    MOLECULAR MEDICINE REPORTS, 2016, 14 (04) : 3731 - 3734
  • [30] Clinical and Genetic Characterization of a Cohort of Brazilian Patients With Congenital Ataxia
    Raslan, Ivana R.
    Silva, Thiago Yoshinaga Tonholo
    Kok, Fernando
    Rodrigues, Marcelo M.
    Aragao, Marcelo M.
    Pinho, Ricardo S.
    Franca, Marcondes C.
    Barsottini, Orlando G.
    Pedroso, Jose Luiz
    NEUROLOGY-GENETICS, 2024, 10 (03)
12345