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Atypical benign partial epilepsy of childhood with acquired neurocognitive, lexical semantic, and autistic spectrum disorder. [electronic resource] by
- Allen, Nicholas M
- Conroy, Judith
- Deonna, Thierry
- McCreary, Dara
- McGettigan, Paul
- Madigan, Cathy
- Carter, Imogen
- Ennis, Sean
- Lynch, Sally A
- Shahwan, Amre
- King, Mary D
Producer: 20160809
In:
Epilepsy & behavior case reports vol. 6
Availability: No items available.
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36.
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Unexplained early onset epileptic encephalopathy: Exome screening and phenotype expansion. [electronic resource] by
- Allen, Nicholas M
- Conroy, Judith
- Shahwan, Amre
- Lynch, Bryan
- Correa, Raony G
- Pena, Sergio D J
- McCreary, Dara
- Magalhães, Tiago R
- Ennis, Sean
- Lynch, Sally A
- King, Mary D
Producer: 20160728
In:
Epilepsia vol. 57
Availability: No items available.
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37.
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Derivation of two iPSC lines from a sporadic ASD patient (NUIGi033-A) and a paternal control (NUIGi034-A). [electronic resource] by
- de la Cruz, Berta Marcó
- Ding, Yicheng
- McInerney, Veronica
- Krawczyk, Janusz
- Lu, Yin
- Yang, Guangming
- Qian, Xiaohong
- Li, Weidong
- Howard, Linda
- Allen, Nicholas M
- O'Brien, Timothy
- Gallagher, Louise
- Shen, Sanbing
Producer: 20210621
In:
Stem cell research vol. 44
Availability: No items available.
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38.
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A comparison of genomic diagnostics in adults and children with epilepsy and comorbid intellectual disability. [electronic resource] by
- Benson, Katherine A
- White, Maire
- Allen, Nicholas M
- Byrne, Susan
- Carton, Robert
- Comerford, Elizabeth
- Costello, Daniel
- Doherty, Colin
- Dunleavey, Brendan
- El-Naggar, Hany
- Gangadharan, Nisha
- Heavin, Sinéad
- Kearney, Hugh
- Lench, Nicholas J
- Lynch, John
- McCormack, Mark
- Regan, Mary O'
- Podesta, Karl
- Power, Kevin
- Rogers, Anthony S
- Steward, Charles A
- Sweeney, Brian
- Webb, David
- Fitzsimons, Mary
- Greally, Marie
- Delanty, Norman
- Cavalleri, Gianpiero L
Producer: 20210601
In:
European journal of human genetics : EJHG vol. 28
Availability: No items available.
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39.
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Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies. [electronic resource] by
- Masnada, Silvia
- Hedrich, Ulrike B S
- Gardella, Elena
- Schubert, Julian
- Kaiwar, Charu
- Klee, Eric W
- Lanpher, Brendan C
- Gavrilova, Ralitza H
- Synofzik, Matthis
- Bast, Thomas
- Gorman, Kathleen
- King, Mary D
- Allen, Nicholas M
- Conroy, Judith
- Ben Zeev, Bruria
- Tzadok, Michal
- Korff, Christian
- Dubois, Fanny
- Ramsey, Keri
- Narayanan, Vinodh
- Serratosa, Jose M
- Giraldez, Beatriz G
- Helbig, Ingo
- Marsh, Eric
- O'Brien, Margaret
- Bergqvist, Christina A
- Binelli, Adrian
- Porter, Brenda
- Zaeyen, Eduardo
- Horovitz, Dafne D
- Wolff, Markus
- Marjanovic, Dragan
- Caglayan, Hande S
- Arslan, Mutluay
- Pena, Sergio D J
- Sisodiya, Sanjay M
- Balestrini, Simona
- Syrbe, Steffen
- Veggiotti, Pierangelo
- Lemke, Johannes R
- Møller, Rikke S
- Lerche, Holger
- Rubboli, Guido
Producer: 20171030
In:
Brain : a journal of neurology vol. 140
Availability: No items available.
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