Petit, Hayley J.
13  Ergebnisse:
Personensuche X
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Biallelic inherited SCN8A variants, a rare cause of SCN8A-r..:

Wengert, Eric R ; Tronhjem, Cathrine E ; Wagnon, Jacy L...
Wengert , E R , Tronhjem , C E , Wagnon , J L , Johannesen , K M , Petit , H , Krey , I , Saga , A U , Panchal , P S , Strohm , S M , Lange , J , Kamphausen , S B , Rubboli , G , Lemke , J R , Gardella , E , Patel , M K , Meisler , M H & Møller , R S 2019 , ' Biallelic inherited SCN8A variants, a rare cause of SCN8A-related developmental and epileptic encephalopathy ' , Epilepsia , vol. 60 , no. 11 , pp. 2277-2285 . https://doi.org/10.1111/epi.16371.  , 2019
 
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Cohort study of congenital complete heart block among prete..:

Hernstadt, Hayley ; Regan, William ; Bhatt, Hitarth..
European Journal of Pediatrics.  181 (2021)  3 - p. 1047-1054 , 2021
 
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