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Author/Creator Lacroix, Amy

3. Genetic convergence of developmental and epileptic encephalopathies and intellectual disability. (11th July 2021)

Authors:
Carvill, Gemma L; Jansen, Sandra; Lacroix, Amy; Zemel, Matthew; Mehaffey, Michele; De Vries, Petra; Brunner, Han G; Scheffer, Ingrid E; De Vries, Bert B A; Vissers, Lisenka E L M; Mefford, Heather C
Journal:
Developmental medicine & child neurology
Issue:
Volume 63:Number 12(2021)
Page Start:
1441
Record Type:
Journal Article
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4. Severe infantile onset developmental and epileptic encephalopathy caused by mutations in autophagy gene WDR45. (24th November 2017)

Authors:
Carvill, Gemma L.; Liu, Aijie; Mandelstam, Simone; Schneider, Amy; Lacroix, Amy; Zemel, Matthew; McMahon, Jacinta M.; Bello‐Espinosa, Luis; Mackay, Mark; Wallace, Geoffrey; Waak, Michaela; Zhang, Jing; Yang, Xiaoling; Malone, Stephen; Zhang, Yue‐Hua; Mefford, Heather C.; Scheffer, Ingrid E.
Journal:
Epilepsia
Issue:
Volume 59:issue 1(2018)
Page Start:
e5
Record Type:
Journal Article
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5. The epilepsy phenotypic spectrum associated with a recurrent CUX2 variant. Issue 5 (30th April 2018)

Authors:
Chatron, Nicolas; Møller, Rikke S.; Champaigne, Neena L.; Schneider, Amy L.; Kuechler, Alma; Labalme, Audrey; Simonet, Thomas; Baggett, Lauren; Bardel, Claire; Kamsteeg, Erik‐Jan; Pfundt, Rolph; Romano, Corrado; Aronsson, Johan; Alberti, Antonino; Vinci, Mirella; Miranda, Maria J.; Lacroix, Amy; ...
Journal:
Annals of neurology
Issue:
Volume 83:Issue 5(2018)
Page Start:
926
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗