Gration, Dylan
9  results:
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2

Congenital anomalies in children with postneonatally acquir..:

Goldsmith, Shona ; McIntyre, Sarah ; Scott, Heather...
Goldsmith , S , McIntyre , S , Scott , H , Himmelmann , K , Smithers-Sheedy , H , Andersen , G L , Blair , E , Badawi , N , Garne , E , The Comprehensive CA-CP Study Group , Barisic , I , Bosnjak Mejaski , V , Uldall , P , Amar , E , Sellier , E , Hollung , S J , Klungsøyr , K , Braz , P , Virella , D , Gibson , C , Källén , K , Reid , S M , Baynam , G , Gration , D , Hansen , M & Watson , L 2021 , ' Congenital anomalies in children with postneonatally acquired cerebral palsy : an international data linkage study ' , Developmental Medicine and Child Neurology , vol. 63 , no. 4 , pp. 421-428 . https://doi.org/10.1111/dmcn.14805.  , 2021
 
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Enabling Global Clinical Collaborations on Identifiable Pat..:

Nellaker, Christoffer ; Alkuraya, Fowzan S ; Baynam, Gareth...
Nellaker , C , Alkuraya , F S , Baynam , G , Bernier , R A , Bernier , F P J , Boulangerw , V , Brudno , M , Brunner , H G , Clayton-Smith , J , Cogne , B , Dawkins , H J S , deVries , B B A , Douzgou , S , Dudding-Byth , T , Eichler , E E , Ferlaino , M , Fieggen , K , Firth , H , FitzPatrick , D R , Gration , D , Groza , T , Haende , M , Hallowel , N , Hamosh , A , Hehir-Kwa , J , Hitz , M-P , Hughes , M , Kini , U , Kleefstra , T , Kooy , R F , Krawitz , P , Kury , S , Lees , M , Lyon , G J , Lyonnet , S , Marcadier , J L , Meyn , S , Moslerova , V , Politei , J M , Poulton , C C , Raymond , F L , Reijnders , M R F , Robinson , P N , Romano , C , Rose , C M , Sainsbury , D C G , Schofield , L , Sutton , V R , Tumovec , M , Van Dijck , A , Van Esch , H , Wilkie , A O M & Minerva Consortium 2019 , ' Enabling Global Clinical Collaborations on Identifiable Patient Data : The Minerva Initiative ' , Frontiers in Genetics , vol. 10 , 611 . https://doi.org/10.3389/fgene.201....  , 2019
 
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Defining and expanding the phenotype of QARS-associated dev..:

Johannesen, Katrine M ; Mitter, Diana ; Janowski, Robert...
Johannesen , K M , Mitter , D , Janowski , R , Roth , C , Toulouse , J , Poulat , A-L , Ville , D M , Chatron , N , Brilstra , E , Geleijns , K , Born , A P , McLean , S , Nugent , K , Baynam , G , Poulton , C , Dreyer , L , Gration , D , Schulz , S , Dieckmann , A , Helbig , K L , Merkenschlager , A , Jamra , R , Finck , A , Gardella , E , Hjalgrim , H , Mirzaa , G , Brancati , F , Bierhals , T , Denecke , J , Hempel , M , Lemke , J R , Rubboli , G , Muschke , P , Guerrini , R , Vetro , A , Niessing , D , Lesca , G & Møller , R S 2019 , ' Defining and expanding the phenotype of QARS-associated developmental epileptic encephalopathy ' , Neurology: Genetics , vol. 5 , no. 6 , pp. e373 . https://doi.org/10.1212/NXG.0000000000000373.  , 2019
 
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Surfacing undiagnosed disease: consideration, counting and ..:

Megan F. Baxter ; Michele Hansen ; Dylan Gration..
https://www.frontiersin.org/articles/10.3389/fped.2023.1283880/full.  , 2023
 
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Digit-all: Rare Diseases:

Gareth Baynam ; Lynsey Chediak ; Gemma Bilkey..
https://www.emjreviews.com/innovations/article/digit-all-rare-diseases/.  , 2020
 
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Enabling Global Clinical Collaborations on Identifiable Pat..:

Christoffer Nellåker ; Fowzan S. Alkuraya ; Gareth Baynam...
https://www.frontiersin.org/article/10.3389/fgene.2019.00611/full.  , 2019
 
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