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Leventer, Richard J.
313
results:
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Online (313)
Mediatypes
Articles (Online) (148)
OpenAccess-fulltext (164)
Video (Online) (1)
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1
Why did my seizures start now? Influences of lesion connect..:
Macdonald‐Laurs, Emma
;
Warren, Aaron E. L.
;
Leventer, Richard J.
.
Epilepsia. 65 (2024) 6 - p. 1644-1657 , 2024
Link:
https://doi.org/10.1111/..
?
2
Solving the Etiology of Developmental and Epileptic Encepha..:
Viswanathan, Sindhu
;
Oliver, Karen L.
;
Regan, Brigid M.
...
Annals of Neurology. , 2024
Link:
https://doi.org/10.1002/..
?
3
Language and communication functioning in children and adol..:
Moser, Charlene
;
Spencer-Smith, Megan M.
;
Anderson, Peter J.
...
Brain and Language. 255 (2024) - p. 105448 , 2024
Link:
https://doi.org/10.1016/..
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4
Diagnostic utility of exome sequencing followed by research..:
Kooshavar, Daniz
;
Amor, David J
;
Boggs, Kirsten
...
Brain Communications. 6 (2024) 2 - p. , 2024
Link:
https://doi.org/10.1093/..
?
5
The clinical, imaging, pathological and genetic landscape o..:
Macdonald-Laurs, Emma
;
Warren, Aaron E L
;
Francis, Peter
...
Brain. 147 (2023) 4 - p. 1264-1277 , 2023
Link:
https://doi.org/10.1093/..
?
6
PathogenicRHEBSomatic Variant in a Child With Tuberous Scle..:
Lee, Wei Shern
;
Macdonald-Laurs, Emma
;
Stephenson, Sarah
...
Neurology. 101 (2023) 2 - p. 78-82 , 2023
Link:
https://doi.org/10.1212/..
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7
Aicardi Syndrome Is a Genetically Heterogeneous Disorder:
Ha, Thuong T.
;
Burgess, Rosemary
;
Newman, Morgan
...
Genes. 14 (2023) 8 - p. 1565 , 2023
Link:
https://doi.org/10.3390/..
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8
Inhibitory control in children with agenesis of the corpus ..:
Soon, Emilyn
;
Siffredi, Vanessa
;
Anderson, Peter J.
...
Journal of the International Neuropsychological Society. 30 (2023) 1 - p. 18-26 , 2023
Link:
https://doi.org/10.1017/..
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9
WWOX developmental and epileptic encephalopathy: Understand..:
Oliver, Karen L.
;
Trivisano, Marina
;
Mandelstam, Simone A.
...
Epilepsia. 64 (2023) 5 - p. 1351-1367 , 2023
Link:
https://doi.org/10.1111/..
?
10
Cortical Dysplasia and the mTOR Pathway: How the Study of H..:
Lee, Wei Shern
;
Baldassari, Sara
;
Stephenson, Sarah E. M.
...
International Journal of Molecular Sciences. 23 (2022) 3 - p. 1344 , 2022
Link:
https://doi.org/10.3390/..
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11
Heterozygous PNPT1 Variants Cause Spinocerebellar Ataxia Ty..:
Barbier, Mathieu
;
Bahlo, Melanie
;
Pennisi, Alessandra
...
Annals of Neurology. 92 (2022) 1 - p. 122-137 , 2022
Link:
https://doi.org/10.1002/..
?
12
Droplet digital PCR as a first-tier molecular diagnostic to..:
Lee, Wei Shern
;
Leventer, Richard J
;
Lockhart, Paul J
Brain. 145 (2022) 12 - p. e119-e121 , 2022
Link:
https://doi.org/10.1093/..
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13
Basal ganglia dysplasia and mTORopathy: A potential cause o..:
Lee, Wei Shern
;
Macdonald‐Laurs, Emma
;
Stephenson, Sarah E M
...
Epilepsia Open. 8 (2022) 1 - p. 205-210 , 2022
Link:
https://doi.org/10.1002/..
?
14
Intrinsic and secondary epileptogenicity in focal cortical ..:
Macdonald‐Laurs, Emma
;
Warren, Aaron E. L.
;
Lee, Wei Shern
...
Epilepsia. 64 (2022) 2 - p. 348-363 , 2022
Link:
https://doi.org/10.1111/..
?
15
Sporadic hypothalamic hamartoma is a ciliopathy with somati..:
Green, Timothy E
;
Motelow, Joshua E
;
Bennett, Mark F
...
Human Molecular Genetics. 31 (2022) 14 - p. 2307-2316 , 2022
Link:
https://doi.org/10.1093/..
1-15