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Author/Creator Jenkinson, Emma M.

1. Clinical, radiological and possible pathological overlap of cystic leukoencephalopathy without megalencephaly and Aicardi-Goutières syndrome. (July 2016)

Authors:
Tonduti, Davide; Orcesi, Simona; Jenkinson, Emma M.; Dorboz, Imen; Renaldo, Florence; Panteghini, Celeste; Rice, Gillian I.; Henneke, Marco; Livingston, John H.; Elmaleh, Monique; Burglen, Lydie; Willemsen, Michèl A.A.P.; Chiapparini, Luisa; Garavaglia, Barbara; Rodriguez, Diana; Boespflug-Tanguy...
Journal:
European journal of paediatric neurology
Issue:
Volume 20:Number 4(2016:Jul.)
Page Start:
604
Record Type:
Journal Article
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2. Genome sequencing in persistently unsolved white matter disorders. Issue 1 (7th January 2020)

Authors:
Helman, Guy; Lajoie, Bryan R.; Crawford, Joanna; Takanohashi, Asako; Walkiewicz, Marzena; Dolzhenko, Egor; Gross, Andrew M.; Gainullin, Vladimir G.; Bent, Stephen J.; Jenkinson, Emma M.; Ferdinandusse, Sacha; Waterham, Hans R.; Dorboz, Imen; Bertini, Enrico; Miyake, Noriko; Wolf, Nicole I.; Abbin...
Journal:
Annals of clinical and translational neurology
Issue:
Volume 7:Issue 1(2020)
Page Start:
144
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Update and Mutational Analysis of SLC20A2: A Major Cause of Primary Familial Brain Calcification. Issue 5 (6th April 2015)

Authors:
Lemos, Roberta R.; Ramos, Eliana M.; Legati, Andrea; Nicolas, Gaël; Jenkinson, Emma M.; Livingston, John H.; Crow, Yanick J.; Campion, Dominique; Coppola, Giovanni; Oliveira, João R. M.
Journal:
Human mutation
Issue:
Volume 36:Issue 5(2015:May)
Page Start:
489
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗