Peter Crino

University of Pennsylvania School of Medicine, Philadelphia, PA, United States 
Epilepsy (Tuberous Sclerosis)
"Peter Crino"
Mean distance: 18.18 (cluster 17)
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Iffland PH, Baybis M, Barnes AE, et al. (2018) DEPDC5 and NPRL3 modulate cell size, filopodial outgrowth, and localization of mTOR in neural progenitor cells and neurons. Neurobiology of Disease
Mills JD, Iyer AM, van Scheppingen J, et al. (2017) Coding and small non-coding transcriptional landscape of tuberous sclerosis complex cortical tubers: implications for pathophysiology and treatment. Scientific Reports. 7: 8089
Mühlebner A, van Scheppingen J, Hulshof HM, et al. (2016) Novel Histopathological Patterns in Cortical Tubers of Epilepsy Surgery Patients with Tuberous Sclerosis Complex. Plos One. 11: e0157396
Bhoj EJ, Li D, Harr M, et al. (2016) Mutations in TBCK, Encoding TBC1-Domain-Containing Kinase, Lead to a Recognizable Syndrome of Intellectual Disability and Hypotonia. American Journal of Human Genetics
Srivastava IN, Shperdheja J, Baybis M, et al. (2015) mTOR pathway inhibition prevents neuroinflammation and neuronal death in a mouse model of cerebral palsy. Neurobiology of Disease. 85: 144-154
Sim JC, Scerri T, Fanjul-Fernández M, et al. (2015) Familial cortical dysplasia caused by mutation in the mTOR regulator NPRL3. Annals of Neurology
Moon UY, Park JY, Park R, et al. (2015) Impaired Reelin-Dab1 Signaling Contributes to Neuronal Migration Deficits of Tuberous Sclerosis Complex. Cell Reports
Jinks RN, Puffenberger EG, Baple E, et al. (2015) Recessive nephrocerebellar syndrome on the Galloway-Mowat syndrome spectrum is caused by homozygous protein-truncating mutations of WDR73. Brain : a Journal of Neurology. 138: 2173-90
Crino PB. (2015) Focal Cortical Dysplasia. Seminars in Neurology. 35: 201-8
Crino PB. (2015) The enlarging spectrum of focal cortical dysplasias. Brain : a Journal of Neurology. 138: 1446-8
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