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Clinical Spectrum of CADASIL:A Study of 7 Families
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Clinical Genetics in Neurological Disease
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Causal Heterogeneity in Isolated Lissencephaly
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A 6-Year-Old Girl with Progressive Toe Walking
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Huntington Disease: Clinical Features and Diagnosis
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CNS Involvement at the Onset of Primary Hemophagocytic Lymphohistiocytosis
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Neurofibromatosis Type 2
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Neurologic Manifestations of von Hippel-Lindau Disease
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Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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Neuroblastoma -- from Genetic Profiles to Clinical Challenge
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Variable Presentation of Brugada Syndrome: Lessons from Three Generations with Syncope
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Genetic Factors in Alzheimer's Disease:A Review of Recent Advances
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Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
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Autosomal Dominant Migraine with MRI White-Matter Abnormalities Mapping to the CADASIL Locus
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Familial Hemiplegic Migraine and Autosomal Dominant Arteriopathy with Leukoencephalopathy (CADASIL)
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Progress in the Genetics of Cerebrovascular Disease Inherited Subcortical Arteriopathies
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Lissencephaly:A Human Brain Malformation Associated with Deletion of the LIS1 Gene Located at Chromosome 17p13
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New Research in Tuberous Sclerosis, Probably More Common with More Adult Complications
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Detecting Susceptibility to Malignant Hyperthermia
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Unstable DNA Sequence in Myotonic Dystrophy
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