Published in Eur J Pediatr on April 08, 2014
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Ataxia, intellectual disability, and ocular apraxia with cerebellar cysts: a new disease? Cerebellum (2014) 0.91
Morphological spectrum of prenatal cerebellar disruptions. Eur J Paediatr Neurol (2008) 0.91
Clinical, genetic, and cardiac magnetic resonance imaging findings in primary desminopathies. Neuromuscul Disord (2008) 0.90
Muscle imaging in congenital myopathies. Semin Pediatr Neurol (2011) 0.90
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Disrupted cerebellar development in preterm infants is associated with impaired neurodevelopmental outcome. Eur J Pediatr (2008) 0.90
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Symptomatic SUNCT in an eleven-year-old girl. Neurology (2003) 0.90
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Familial West syndrome and dystonia caused by an Aristaless related homeobox gene mutation. Eur J Pediatr (2005) 0.88
Tradeoffs between hydraulic and mechanical stress responses of mature Norway spruce trunk wood. Tree Physiol (2008) 0.88
Proven startle-provoked epileptic seizures in childhood: semiologic and electrophysiologic variability. Epilepsia (2006) 0.87
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Siblings with infantile cerebral stroke and delayed multivessel involvement--a new hereditary vasculopathy? Eur J Paediatr Neurol (2007) 0.87
Cervical myelomeningocele--follow-up of five patients. Eur J Paediatr Neurol (2003) 0.87
Neonatal neuroimaging findings in inborn errors of metabolism. J Magn Reson Imaging (2012) 0.86
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Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy (PEHO) syndrome in a Swiss child. Eur J Paediatr Neurol (2004) 0.86
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Does diagnostic delay result in decreased survival in paediatric brain tumours? Eur J Pediatr (2008) 0.86
Pituitary duplication and nasopharyngeal teratoma in a newborn: CT, MRI, US and correlative histopathological findings. Neuroradiology (2005) 0.86
Familial X-linked cardiomyopathy (Danon disease): diagnostic confirmation by mutation analysis of the LAMP2gene. Eur J Pediatr (2005) 0.85
Optic nerve sheath meningiomas in patients with neurofibromatosis type 2. Arch Ophthalmol (2006) 0.85
Muscular involvement assessed by MRI correlates to motor function measurement values in oculopharyngeal muscular dystrophy. J Neurol (2011) 0.85