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Sarah Aylett

Showing results (11-20 of 13) with videos related to

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The Journal of Investigative Dermatology|December 16, 2019
GNA11 Mutation as a Cause of Sturge-Weber Syndrome: Expansion of the Phenotypic Spectrum of G<sub>α/11</sub> Mosaicism and the Associated Clinical DiagnosesSatyamaanasa Polubothu, Lara Al-Olabi, Maria Carmen Del Boente, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|September 16, 2005
Nonconvulsive status epilepticus: Epilepsy Research Foundation workshop reportsMatthew Walker, Helen Cross, Shelagh Smith, et al.
Brain : a Journal of Neurology|June 18, 2010
Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency)Philippa B Mills, Emma J Footitt, Kevin A Mills, et al.
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Showing results (11-20 of 13) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 13 results.
The Journal of Investigative Dermatology|December 16, 2019
GNA11 Mutation as a Cause of Sturge-Weber Syndrome: Expansion of the Phenotypic Spectrum of G<sub>α/11</sub> Mosaicism and the Associated Clinical DiagnosesSatyamaanasa Polubothu, Lara Al-Olabi, Maria Carmen Del Boente, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|September 16, 2005
Nonconvulsive status epilepticus: Epilepsy Research Foundation workshop reportsMatthew Walker, Helen Cross, Shelagh Smith, et al.
Brain : a Journal of Neurology|June 18, 2010
Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency)Philippa B Mills, Emma J Footitt, Kevin A Mills, et al.
Pageof 2