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141.
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Open-label use of highly purified CBD (Epidiolex®) in patients with CDKL5 deficiency disorder and Aicardi, Dup15q, and Doose syndromes. [electronic resource] by
- Devinsky, Orrin
- Verducci, Chloe
- Thiele, Elizabeth A
- Laux, Linda C
- Patel, Anup D
- Filloux, Francis
- Szaflarski, Jerzy P
- Wilfong, Angus
- Clark, Gary D
- Park, Yong D
- Seltzer, Laurie E
- Bebin, E Martina
- Flamini, Robert
- Wechsler, Robert T
- Friedman, Daniel
Producer: 20190325
In:
Epilepsy & behavior : E&B vol. 86
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142.
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143.
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144.
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145.
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Severity Assessment in CDKL5 Deficiency Disorder. [electronic resource] by
- Demarest, Scott
- Pestana-Knight, Elia M
- Olson, Heather E
- Downs, Jenny
- Marsh, Eric D
- Kaufmann, Walter E
- Partridge, Carol-Anne
- Leonard, Helen
- Gwadry-Sridhar, Femida
- Frame, Katheryn Elibri
- Cross, J Helen
- Chin, Richard F M
- Parikh, Sumit
- Panzer, Axel
- Weisenberg, Judith
- Utley, Karen
- Jaksha, Amanda
- Amin, Sam
- Khwaja, Omar
- Devinsky, Orrin
- Neul, Jeffery L
- Percy, Alan K
- Benke, Tim A
Producer: 20200601
In:
Pediatric neurology vol. 97
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146.
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147.
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148.
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De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females. [electronic resource] by
- Palmer, E E
- Stuhlmann, T
- Weinert, S
- Haan, E
- Van Esch, H
- Holvoet, M
- Boyle, J
- Leffler, M
- Raynaud, M
- Moraine, C
- van Bokhoven, H
- Kleefstra, T
- Kahrizi, K
- Najmabadi, H
- Ropers, H-H
- Delgado, M R
- Sirsi, D
- Golla, S
- Sommer, A
- Pietryga, M P
- Chung, W K
- Wynn, J
- Rohena, L
- Bernardo, E
- Hamlin, D
- Faux, B M
- Grange, D K
- Manwaring, L
- Tolmie, J
- Joss, S
- Cobben, J M
- Duijkers, F A M
- Goehringer, J M
- Challman, T D
- Hennig, F
- Fischer, U
- Grimme, A
- Suckow, V
- Musante, L
- Nicholl, J
- Shaw, M
- Lodh, S P
- Niu, Z
- Rosenfeld, J A
- Stankiewicz, P
- Jentsch, T J
- Gecz, J
- Field, M
- Kalscheuer, V M
Producer: 20190215
In:
Molecular psychiatry vol. 23
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149.
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Apolipoprotein E isoforms and susceptibility to genetic generalized epilepsies. [electronic resource] by
- Chaves, João
- Martins-Ferreira, Ricardo
- Carvalho, Cláudia
- Bettencourt, Andreia
- Brás, Sandra
- Chorão, Rui
- Freitas, Joel
- Samões, Raquel
- Lopes, João
- Ramalheira, João
- Silva, Berta M
- Pinho E Costa, Paulo
- da Silva, António Martins
- Leal, Bárbara
Producer: 20210607
In:
The International journal of neuroscience vol. 130
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150.
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The antidepressant tianeptine reverts synaptic AMPA receptor defects caused by deficiency of CDKL5. [electronic resource] by
- Tramarin, Marco
- Rusconi, Laura
- Pizzamiglio, Lara
- Barbiero, Isabella
- Peroni, Diana
- Scaramuzza, Linda
- Guilliams, Tim
- Cavalla, David
- Antonucci, Flavia
- Kilstrup-Nielsen, Charlotte
Producer: 20190225
In:
Human molecular genetics vol. 27
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151.
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152.
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Cyclin-Dependent Kinase-Like 5 Deficiency Disorder: Clinical Review. [electronic resource] by
- Olson, Heather E
- Demarest, Scott T
- Pestana-Knight, Elia M
- Swanson, Lindsay C
- Iqbal, Sumaiya
- Lal, Dennis
- Leonard, Helen
- Cross, J Helen
- Devinsky, Orrin
- Benke, Tim A
Producer: 20200601
In:
Pediatric neurology vol. 97
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153.
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154.
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Rescue of prepulse inhibition deficit and brain mitochondrial dysfunction by pharmacological stimulation of the central serotonin receptor 7 in a mouse model of CDKL5 Deficiency Disorder. [electronic resource] by
- Vigli, Daniele
- Rusconi, Laura
- Valenti, Daniela
- La Montanara, Paolo
- Cosentino, Livia
- Lacivita, Enza
- Leopoldo, Marcello
- Amendola, Elena
- Gross, Cornelius
- Landsberger, Nicoletta
- Laviola, Giovanni
- Kilstrup-Nielsen, Charlotte
- Vacca, Rosa A
- De Filippis, Bianca
Producer: 20190304
In:
Neuropharmacology vol. 144
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155.
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156.
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157.
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HDAC4: a key factor underlying brain developmental alterations in CDKL5 disorder. [electronic resource] by
- Trazzi, Stefania
- Fuchs, Claudia
- Viggiano, Rocchina
- De Franceschi, Marianna
- Valli, Emanuele
- Jedynak, Paulina
- Hansen, Finn K
- Perini, Giovanni
- Rimondini, Roberto
- Kurz, Thomas
- Bartesaghi, Renata
- Ciani, Elisabetta
Producer: 20170720
In:
Human molecular genetics vol. 25
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158.
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Outcomes and comorbidities of SCN1A-related seizure disorders. [electronic resource] by
- de Lange, Iris M
- Gunning, Boudewijn
- Sonsma, Anja C M
- van Gemert, Lisette
- van Kempen, Marjan
- Verbeek, Nienke E
- Sinoo, Claudia
- Nicolai, Joost
- Knoers, Nine V A M
- Koeleman, Bobby P C
- Brilstra, Eva H
Producer: 20190709
In:
Epilepsy & behavior : E&B vol. 90
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159.
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Alteration of serum lipid profile, SRB1 loss, and impaired Nrf2 activation in CDKL5 disorder. [electronic resource] by
- Pecorelli, Alessandra
- Belmonte, Giuseppe
- Meloni, Ilaria
- Cervellati, Franco
- Gardi, Concetta
- Sticozzi, Claudia
- De Felice, Claudio
- Signorini, Cinzia
- Cortelazzo, Alessio
- Leoncini, Silvia
- Ciccoli, Lucia
- Renieri, Alessandra
- Jay Forman, Henry
- Hayek, Joussef
- Valacchi, Giuseppe
Producer: 20160603
In:
Free radical biology & medicine vol. 86
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160.
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