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The Fault in Their Stars-Accumulating Astrocytic Inclusions Associated With Clusters of Epileptic Spasms in Children With Global Developmental Delay. [electronic resource] by
- Whitney, Robyn
- AlMehmadi, Sameer
- McCoy, Bláthnaid
- Yau, Ivanna
- Ochi, Ayako
- Otsubo, Hiroshi
- Weiss, Shelly K
- Rutka, James
- Hazrati, Lili-Naz
- Snead, O Carter
- Go, Cristina
Producer: 20180413
In:
Pediatric neurology vol. 73
Availability: No items available.
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A prospective open-label trial of a CBD/THC cannabis oil in dravet syndrome. [electronic resource] by
- McCoy, Bláthnaid
- Wang, Laura
- Zak, Maria
- Al-Mehmadi, Sameer
- Kabir, Nadia
- Alhadid, Kenda
- McDonald, Kyla
- Zhang, Grace
- Sharma, Rohit
- Whitney, Robyn
- Sinopoli, Katia
- Snead, O Carter
Publication details: Annals of clinical and translational neurology Sep 2018
In:
Annals of clinical and translational neurology vol. 5
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24.
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Misleading Focal Clinical, Neurophysiologic, and Imaging Features in 2 Children With Generalized Epilepsy Who Underwent Invasive Electroencephalographic (EEG) Monitoring. [electronic resource] by
- Ba-Armah, Duaa
- Jain, Puneet
- Whitney, Robyn
- Donner, Elizabeth
- Drake, James
- Go, Cristina
- Nair, Rajesh Ramachandran
- Snead, O Carter
- Weiss, Shelly
- Widjaja, Elysa
- Yamamoto, Eriko
- Ye, Annette
- Yamasaki, Haruka
- Ochi, Ayako
Producer: 20211013
In:
Journal of child neurology vol. 35
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Intra-operative cortical motor mapping using subdural grid electrodes in children undergoing epilepsy surgery evaluation and comparison with the conventional extra-operative motor mapping. [electronic resource] by
- Jain, Puneet
- Whitney, Robyn
- Strantzas, Samuel
- McCoy, Blathnaid
- Ochi, Ayako
- Otsubo, Hiroshi
- Snead, O Carter
- Weiss, Shelly
- Donner, Elizabeth
- Pang, Elizabeth
- Sharma, Rohit
- Viljoen, Amrita
- Keller, Anne
- Drake, James M
- Rutka, James T
- Go, Cristina
Producer: 20190910
In:
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology vol. 129
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The role of surgery in refractory epilepsy secondary to polymicrogyria in the pediatric population. [electronic resource] by
- Jalloh, Ibrahim
- Cho, Newton
- Nga, Vincent D W
- Whitney, Robyn
- Jain, Puneet
- Al-Mehmadi, Sameer
- Yau, Ivanna
- Okura, Hidehiro
- Widjaja, Elysa
- Otsubo, Hiroshi
- Ochi, Ayako
- Donner, Elizabeth
- McCoy, Blathnaid
- Drake, James
- Go, Cristina
- Rutka, James T
Producer: 20190314
In:
Epilepsia vol. 59
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27.
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Advanced dynamic statistical parametric mapping with MEG in localizing epileptogenicity of the bottom of sulcus dysplasia. [electronic resource] by
- Nakajima, Midori
- Wong, Simeon
- Widjaja, Elysa
- Baba, Shiro
- Okanishi, Tohru
- Takada, Lynne
- Sato, Yosuke
- Iwata, Hiroki
- Sogabe, Maya
- Morooka, Hikaru
- Whitney, Robyn
- Ueda, Yuki
- Ito, Tomoshiro
- Yagyu, Kazuyori
- Ochi, Ayako
- Carter Snead, O
- Rutka, James T
- Drake, James M
- Doesburg, Sam
- Takeuchi, Fumiya
- Shiraishi, Hideaki
- Otsubo, Hiroshi
Producer: 20190520
In:
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology vol. 129
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KCNT1-related epilepsy: An international multicenter cohort of 27 pediatric cases. [electronic resource] by
- Borlot, Felippe
- Abushama, Ahmed
- Morrison-Levy, Nadine
- Jain, Puneet
- Puthenveettil Vinayan, Kollencheri
- Abukhalid, Musaad
- Aldhalaan, Hesham M
- Almuzaini, Hanin S
- Gulati, Sheffali
- Hershkovitz, Tova
- Konanki, Ramesh
- Lingappa, Lokesh
- Luat, Aimee F
- Shafi, Shatha
- Tabarki, Brahim
- Thomas, Maya
- Yoganathan, Sangeetha
- Alfadhel, Majid
- Arya, Ravindra
- Donner, Elizabeth J
- Ehaideb, Salleh N
- Gowda, Vykuntaraju K
- Jain, Vivek
- Madaan, Priyanka
- Myers, Kenneth A
- Otsubo, Hiroshi
- Panda, Prateek
- Sahu, Jitendra K
- Sampaio, Letícia P B
- Sharma, Suvasini
- Simard-Tremblay, Elisabeth
- Zak, Maria
- Whitney, Robyn
Producer: 20201016
In:
Epilepsia vol. 61
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Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling. [electronic resource] by
- Rice, Gillian I
- Del Toro Duany, Yoandris
- Jenkinson, Emma M
- Forte, Gabriella Ma
- Anderson, Beverley H
- Ariaudo, Giada
- Bader-Meunier, Brigitte
- Baildam, Eileen M
- Battini, Roberta
- Beresford, Michael W
- Casarano, Manuela
- Chouchane, Mondher
- Cimaz, Rolando
- Collins, Abigail E
- Cordeiro, Nuno Jv
- Dale, Russell C
- Davidson, Joyce E
- De Waele, Liesbeth
- Desguerre, Isabelle
- Faivre, Laurence
- Fazzi, Elisa
- Isidor, Bertrand
- Lagae, Lieven
- Latchman, Andrew R
- Lebon, Pierre
- Li, Chumei
- Livingston, John H
- Lourenço, Charles M
- Mancardi, Maria Margherita
- Masurel-Paulet, Alice
- McInnes, Iain B
- Menezes, Manoj P
- Mignot, Cyril
- O'Sullivan, James
- Orcesi, Simona
- Picco, Paolo P
- Riva, Enrica
- Robinson, Robert A
- Rodriguez, Diana
- Salvatici, Elisabetta
- Scott, Christiaan
- Szybowska, Marta
- Tolmie, John L
- Vanderver, Adeline
- Vanhulle, Catherine
- Vieira, Jose Pedro
- Webb, Kate
- Whitney, Robyn N
- Williams, Simon G
- Wolfe, Lynne A
- Zuberi, Sameer M
- Hur, Sun
- Crow, Yanick J
Producer: 20140616
In:
Nature genetics vol. 46
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Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1. [electronic resource] by
- Crow, Yanick J
- Chase, Diana S
- Lowenstein Schmidt, Johanna
- Szynkiewicz, Marcin
- Forte, Gabriella M A
- Gornall, Hannah L
- Oojageer, Anthony
- Anderson, Beverley
- Pizzino, Amy
- Helman, Guy
- Abdel-Hamid, Mohamed S
- Abdel-Salam, Ghada M
- Ackroyd, Sam
- Aeby, Alec
- Agosta, Guillermo
- Albin, Catherine
- Allon-Shalev, Stavit
- Arellano, Montse
- Ariaudo, Giada
- Aswani, Vijay
- Babul-Hirji, Riyana
- Baildam, Eileen M
- Bahi-Buisson, Nadia
- Bailey, Kathryn M
- Barnerias, Christine
- Barth, Magalie
- Battini, Roberta
- Beresford, Michael W
- Bernard, Geneviève
- Bianchi, Marika
- Billette de Villemeur, Thierry
- Blair, Edward M
- Bloom, Miriam
- Burlina, Alberto B
- Carpanelli, Maria Luisa
- Carvalho, Daniel R
- Castro-Gago, Manuel
- Cavallini, Anna
- Cereda, Cristina
- Chandler, Kate E
- Chitayat, David A
- Collins, Abigail E
- Sierra Corcoles, Concepcion
- Cordeiro, Nuno J V
- Crichiutti, Giovanni
- Dabydeen, Lyvia
- Dale, Russell C
- D'Arrigo, Stefano
- De Goede, Christian G E L
- De Laet, Corinne
- De Waele, Liesbeth M H
- Denzler, Ines
- Desguerre, Isabelle
- Devriendt, Koenraad
- Di Rocco, Maja
- Fahey, Michael C
- Fazzi, Elisa
- Ferrie, Colin D
- Figueiredo, António
- Gener, Blanca
- Goizet, Cyril
- Gowrinathan, Nirmala R
- Gowrishankar, Kalpana
- Hanrahan, Donncha
- Isidor, Bertrand
- Kara, Bülent
- Khan, Nasaim
- King, Mary D
- Kirk, Edwin P
- Kumar, Ram
- Lagae, Lieven
- Landrieu, Pierre
- Lauffer, Heinz
- Laugel, Vincent
- La Piana, Roberta
- Lim, Ming J
- Lin, Jean-Pierre S-M
- Linnankivi, Tarja
- Mackay, Mark T
- Marom, Daphna R
- Marques Lourenço, Charles
- McKee, Shane A
- Moroni, Isabella
- Morton, Jenny E V
- Moutard, Marie-Laure
- Murray, Kevin
- Nabbout, Rima
- Nampoothiri, Sheela
- Nunez-Enamorado, Noemi
- Oades, Patrick J
- Olivieri, Ivana
- Ostergaard, John R
- Pérez-Dueñas, Belén
- Prendiville, Julie S
- Ramesh, Venkateswaran
- Rasmussen, Magnhild
- Régal, Luc
- Ricci, Federica
- Rio, Marlène
- Rodriguez, Diana
- Roubertie, Agathe
- Salvatici, Elisabetta
- Segers, Karin A
- Sinha, Gyanranjan P
- Soler, Doriette
- Spiegel, Ronen
- Stödberg, Tommy I
- Straussberg, Rachel
- Swoboda, Kathryn J
- Suri, Mohnish
- Tacke, Uta
- Tan, Tiong Y
- te Water Naude, Johann
- Wee Teik, Keng
- Thomas, Maya Mary
- Till, Marianne
- Tonduti, Davide
- Valente, Enza Maria
- Van Coster, Rudy Noel
- van der Knaap, Marjo S
- Vassallo, Grace
- Vijzelaar, Raymon
- Vogt, Julie
- Wallace, Geoffrey B
- Wassmer, Evangeline
- Webb, Hannah J
- Whitehouse, William P
- Whitney, Robyn N
- Zaki, Maha S
- Zuberi, Sameer M
- Livingston, John H
- Rozenberg, Flore
- Lebon, Pierre
- Vanderver, Adeline
- Orcesi, Simona
- Rice, Gillian I
Producer: 20150916
In:
American journal of medical genetics. Part A vol. 167A
Availability: No items available.
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