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R Guerrini

Showing results (211-220 of 276) with videos related to

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Brain : a Journal of Neurology|November 10, 2001
Autosomal dominant cortical myoclonus and epilepsy (ADCME) with complex partial and generalized seizures: A newly recognized epilepsy syndrome with linkage to chromosome 2p11.1-q12.2R Guerrini, P Bonanni, A Patrignani, et al.
Journal of Medical Genetics|December 20, 2003
Patient with bilateral periventricular nodular heterotopia and polymicrogyria with apparently balanced reciprocal translocation t(1;6)(p12;p12.2) that interrupts the mannosidase alpha, class 1A, and glutathione S-transferase A2 genesE P Leeflang, S E Marsh, E Parrini, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 20, 2008
GALNS gene expression profiling in Morquio A patients' fibroblastsL Carraresi, R Parini, C Filoni, et al.
Neurology|August 23, 2006
Periventricular heterotopia in fragile X syndromeF Moro, T Pisano, B Dalla Bernardina, et al.
AJNR. American Journal of Neuroradiology|April 20, 2013
Bilateral cavitations of ganglionic eminence: a fetal MR imaging sign of halted brain developmentA Righini, C Frassoni, F Inverardi, et al.
European Journal of Pharmacology|September 30, 2000
Inverse agonism by Dmt-Tic analogues and HS 378, a naltrindole analogueM Labarre, J Butterworth, S St-Onge, et al.
AJNR. American Journal of Neuroradiology|September 27, 2014
Ultra-high-field MR imaging in polymicrogyria and epilepsyA De Ciantis, A J Barkovich, M Cosottini, et al.
British Journal of Pharmacology|June 16, 1999
Comparison of the effects of [Phe1psi(CH2-NH)Gly2]nociceptin(1-13)NH2 in rat brain, rat vas deferens and CHO cells expressing recombinant human nociceptin receptorsH Okawa, B Nicol, R Bigoni, et al.
Neurology|August 18, 2010
Protocadherin 19 mutations in girls with infantile-onset epilepsyC Marini, D Mei, L Parmeggiani, et al.
Experimental Neurology|June 2, 2016
Dynamic changes of depolarizing GABA in a computational model of epileptogenic brain: Insight for Dravet syndromeP Kurbatova, F Wendling, A Kaminska, et al.
Pageof 28

Showing results (211-220 of 276) with videos related to

Sort By:
Pageof 28
Brain : a Journal of Neurology|November 10, 2001
Autosomal dominant cortical myoclonus and epilepsy (ADCME) with complex partial and generalized seizures: A newly recognized epilepsy syndrome with linkage to chromosome 2p11.1-q12.2R Guerrini, P Bonanni, A Patrignani, et al.
Journal of Medical Genetics|December 20, 2003
Patient with bilateral periventricular nodular heterotopia and polymicrogyria with apparently balanced reciprocal translocation t(1;6)(p12;p12.2) that interrupts the mannosidase alpha, class 1A, and glutathione S-transferase A2 genesE P Leeflang, S E Marsh, E Parrini, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 20, 2008
GALNS gene expression profiling in Morquio A patients' fibroblastsL Carraresi, R Parini, C Filoni, et al.
Neurology|August 23, 2006
Periventricular heterotopia in fragile X syndromeF Moro, T Pisano, B Dalla Bernardina, et al.
AJNR. American Journal of Neuroradiology|April 20, 2013
Bilateral cavitations of ganglionic eminence: a fetal MR imaging sign of halted brain developmentA Righini, C Frassoni, F Inverardi, et al.
European Journal of Pharmacology|September 30, 2000
Inverse agonism by Dmt-Tic analogues and HS 378, a naltrindole analogueM Labarre, J Butterworth, S St-Onge, et al.
AJNR. American Journal of Neuroradiology|September 27, 2014
Ultra-high-field MR imaging in polymicrogyria and epilepsyA De Ciantis, A J Barkovich, M Cosottini, et al.
British Journal of Pharmacology|June 16, 1999
Comparison of the effects of [Phe1psi(CH2-NH)Gly2]nociceptin(1-13)NH2 in rat brain, rat vas deferens and CHO cells expressing recombinant human nociceptin receptorsH Okawa, B Nicol, R Bigoni, et al.
Neurology|August 18, 2010
Protocadherin 19 mutations in girls with infantile-onset epilepsyC Marini, D Mei, L Parmeggiani, et al.
Experimental Neurology|June 2, 2016
Dynamic changes of depolarizing GABA in a computational model of epileptogenic brain: Insight for Dravet syndromeP Kurbatova, F Wendling, A Kaminska, et al.
Pageof 28