Cerebellar hypoplasias
Author:
Publisher
Elsevier
Reference83 articles.
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3. Oligophrenin‐1 (OPHN1) gene mutation causes syndromic X‐linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia;Bergmann;Brain,2003
4. A syndrome of primary combined immunodeficiency with microcephaly, cerebellar hypoplasia, growth failure and progressive pancytopenia;Berthet;Eur J Pediatr,1994
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Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. When one is Enough: Impaired Multisensory Integration in Cerebellar Agenesis;Cerebral Cortex;2016-03-05
2. Diffusion Tractography Biomarkers of Pediatric Cerebellar Hypoplasia/Atrophy: Preliminary Results Using Constrained Spherical Deconvolution;American Journal of Neuroradiology;2015-12-10
3. Synaptogenesis in the Foetal and Neonatal Cerebellar System. 2. Pontine Nuclei and Cerebellar Cortex;Developmental Neuroscience;2013
4. The use of muscle biopsy in the diagnosis of undefined ataxia with cerebellar atrophy in children;European Journal of Paediatric Neurology;2012-05
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