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Research ArticlePediatrics
Open Access

Neuroradiologic Features in X-linked α-Thalassemia/Mental Retardation Syndrome

T. Wada, H. Ban, M. Matsufuji, N. Okamoto, K. Enomoto, K. Kurosawa and N. Aida
American Journal of Neuroradiology October 2013, 34 (10) 2034-2038; DOI: https://doi.org/10.3174/ajnr.A3560
T. Wada
aFrom the Divisions of Neurology (T.W.)
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H. Ban
dDepartment of Pediatrics (H.B.), Himeji Red Cross Hospital, Himeji, Japan
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M. Matsufuji
eDepartment of Pediatrics (M.M.), Yanagawa Institute for Developmental Disabilities, Yanagawa, Japan
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N. Okamoto
fDepartment of Molecular Medicine (N.O.), Osaka Medical Center and Research Institute for Maternal and Child Health, Osaka, Japan.
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K. Enomoto
bGenetics (K.E., K.K.)
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K. Kurosawa
bGenetics (K.E., K.K.)
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N. Aida
cRadiology (N.A.), Kanagawa Children's Medical Center, Yokohama, Japan
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Article Information

vol. 34 no. 10 2034-2038
DOI 
https://doi.org/10.3174/ajnr.A3560
PubMed 
23681356

Published By 
American Journal of Neuroradiology
Print ISSN 
0195-6108
Online ISSN 
1936-959X
History 
  • Received September 28, 2012
  • Accepted after revision December 17, 2012
  • Published online October 8, 2013.

Copyright & Usage 
© 2013 by American Journal of Neuroradiology Indicates open access to non-subscribers at www.ajnr.org

Author Information

  1. T. Wadaa,
  2. H. Band,
  3. M. Matsufujie,
  4. N. Okamotof,
  5. K. Enomotob,
  6. K. Kurosawab and
  7. N. Aidac
  1. aFrom the Divisions of Neurology (T.W.)
  2. bGenetics (K.E., K.K.)
  3. cRadiology (N.A.), Kanagawa Children's Medical Center, Yokohama, Japan
  4. dDepartment of Pediatrics (H.B.), Himeji Red Cross Hospital, Himeji, Japan
  5. eDepartment of Pediatrics (M.M.), Yanagawa Institute for Developmental Disabilities, Yanagawa, Japan
  6. fDepartment of Molecular Medicine (N.O.), Osaka Medical Center and Research Institute for Maternal and Child Health, Osaka, Japan.
  1. Please address correspondence to Takahito Wada, MD, PhD, 2-138-4 Mutsukawa, Minami-ku, Yokohama, Kanagawa 232-8555, Japan; e-mail: takahito.wada0001{at}me.com
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Cite this article
T. Wada, H. Ban, M. Matsufuji, N. Okamoto, K. Enomoto, K. Kurosawa, N. Aida
Neuroradiologic Features in X-linked α-Thalassemia/Mental Retardation Syndrome
American Journal of Neuroradiology Oct 2013, 34 (10) 2034-2038; DOI: 10.3174/ajnr.A3560

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Neuroradiologic Features in X-linked α-Thalassemia/Mental Retardation Syndrome
T. Wada, H. Ban, M. Matsufuji, N. Okamoto, K. Enomoto, K. Kurosawa, N. Aida
American Journal of Neuroradiology Oct 2013, 34 (10) 2034-2038; DOI: 10.3174/ajnr.A3560
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Cited By...

  • A new mouse model of ATR-X syndrome carrying a common patient mutation exhibits neurological and morphological defects
  • Systemic and intrinsic functions of ATRX in glial cell fate and CNS myelination
  • Glial ensheathment of the somatodendritic compartment regulates sensory neuron structure and activity
  • Crossref (22)
  • Google Scholar

This article has been cited by the following articles in journals that are participating in Crossref Cited-by Linking.

  • The Role of ATRX in Glioma Biology
    Pravanya Nandakumar, Alireza Mansouri, Sunit Das
    Frontiers in Oncology 2017 7
  • Glial ensheathment of the somatodendritic compartment regulates sensory neuron structure and activity
    Smita Yadav, Susan H. Younger, Linghua Zhang, Katherine L. Thompson-Peer, Tun Li, Lily Y. Jan, Yuh Nung Jan
    Proceedings of the National Academy of Sciences 2019 116 11
  • Effect of ATRX and G‐Quadruplex Formation by the VNTR Sequence on α‐Globin Gene Expression
    Yue Li, Junetha Syed, Yuki Suzuki, Sefan Asamitsu, Norifumi Shioda, Takahito Wada, Hiroshi Sugiyama
    ChemBioChem 2016 17 10
  • Alpha-thalassemia X-linked intellectual disability syndrome identified by whole exome sequencing in two boys with white matter changes and developmental retardation
    Jin Sook Lee, Sangmoon Lee, Byung Chan Lim, Ki Joong Kim, Yong Seung Hwang, Murim Choi, Jong-Hee Chae
    Gene 2015 569 2
  • Neurodevelopmental Disorders Caused by Defective Chromatin Remodeling: Phenotypic Complexity Is Highlighted by a Review of ATRX Function
    Sara Timpano, David J. Picketts
    Frontiers in Genetics 2020 11
  • Genetic interaction screen for severe neurodevelopmental disorders reveals a functional link between Ube3a and Mef2 in Drosophila melanogaster
    Jonas Straub, Anne Gregor, Tatjana Sauerer, Anna Fliedner, Laila Distel, Christine Suchy, Arif B. Ekici, Fulvia Ferrazzi, Christiane Zweier
    Scientific Reports 2020 10 1
  • Thalassemia and risk of dementia: A nationwide population-based retrospective cohort study
    Yu-Guang Chen, Te-Yu Lin, Hsuan-Ju Chen, Ming-Shen Dai, Ching-Liang Ho, Chia-Hung Kao
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  • Neuroimaging Findings in Pediatric Genetic Skeletal Disorders: A Review
    Matthias W. Wagner, Andrea Poretti, Jane E. Benson, Thierry A. G. M. Huisman
    Journal of Neuroimaging 2017 27 2
  • Genetics behind Cerebral Disease with Ocular Comorbidity: Finding Parallels between the Brain and Eye Molecular Pathology
    Kao-Jung Chang, Hsin-Yu Wu, Aliaksandr Yarmishyn, Cheng-Yi Li, Yu-Jer Hsiao, Yi-Chun Chi, Tzu-Chen Lo, He-Jhen Dai, Yi-Chiang Yang, Ding-Hao Liu, De-Kuang Hwang, Shih-Jen Chen, Chih-Chien Hsu, Chung-Lan Kao
    International Journal of Molecular Sciences 2022 23 17
  • The value of genome-wide analysis in craniosynostosis
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