Abstracts
Conference of Commission on Child Neurology and Commission on Neuropathology and Neurooncology of the Committee on Neurological Sciences, Polish Academy of Sciences

Conference of Commission on Child Neurology and Commission on Neuropathology and Neurooncology of the Committee on Neurological Sciences,

Polish Academy of Sciences

"Abnormal development of the cortex and white matter – clinical, neuroradiological and neuropathological studies" organized in memory of Professor Maria Dąmbska

Warsaw, October 20, 2006



The Conference was sponsored by Minister of Science and Higher Education through Committee on Neurological Sciences, of the Division VI Medical Sciences, Polish Academy of Sciences





[A1]

Malformations of cortical development in children: clinical manifestation, neuroimaging and neuropathology

in selected cases



[A2]

Familial Westphal variant of Huntington’s disease. Report of the clinical abnormalities



[A3]

Encephalopathy with vanishing white matter



[A4]

Histopathologic features of hemimegalencephaly – a case report



[A5]

Is focal cortical dysplasia type IIB the focal form of tuberous sclerosis complex?



[A6]

Faulty position of cerebellar cortical neurons as sequel of disturbed neuronal migration



[A7]

Clinical aspects of agenesis of corpus callosum and associated brain abnormalities



[A8]

Cortical dysplasias – common neuropathological changes in intractable temporal epilepsy



[A9]

Ectopic cerebellum in anterior cranial fossa. Report of a unique case associated with skull congenital malformations and epilepsy



[A10]

Correlation of neuroradiological, electroencephalographic and clinical findings in cortical dysplasias in children



[A11]

Disturbances in central nervous system development in a rat model of familial amyotrophic lateral sclerosis



[A12]

Surgical treatment of children with refractory epilepsy due to malformations of cortical development



[A13]

Brain and cerebellar hemidysplasia in a case with ipsilateral body dysplasia (suspicion of CHILD syndrome)



[A14]

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