Kayla M D Cornett
11PUBLICATIONS
41CO-AUTHORS

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Publications (11)
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|Jun 09, 2025
Charcot-Marie-Tooth disease type 1E: clinical natural history and molecular impact of PMP22 variants.Kailee S Ward, Christopher P Ptak, Natalya Pashkova
|May 09, 2025
Charcot-Marie-Tooth disease type 1E: Clinical Natural History and Molecular Impact of PMP22 Variants.Kailee S Ward, Christopher P Ptak, Natalya Pashkova
|Oct 25, 2024
RNA mis-splicing in children with congenital myotonic dystrophy is associated with physical function.Julia M Hartman, Kobe Ikegami, Marina Provenzano
|Sep 10, 2024
Long-term outcomes in children with riboflavin transporter deficiency and surveillance recommendations.Jack R Fennessy, Kayla M D Cornett, Gabrielle A Donlevy
|Mar 06, 2024
Development of a functional outcome measure for riboflavin transporter deficiency.Jack R Fennessy, Gabrielle A Donlevy, Marnee J McKay
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Frequent Collaborators
5 joint publications
Manoj P Menezes
4 joint publications
Davide Pareyson
3 joint publications
Jack R Fennessy
3 joint publications
Marnee J McKay
3 joint publications
Michael E Shy
2 joint publications
Jacqueline Montes
2 joint publications
Robert C Piper
2 joint publications
David N Herrmann
2 joint publications
Chiara Pisciotta
2 joint publications
Richard Finkel