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Author/Creator Pontén, Emeli

1. A complex DICER1 syndrome phenotype associated with a germline pathogenic variant affecting the RNase IIIa domain of DICER1. Issue 2 (18th November 2020)

Authors:
Pontén, Emeli; Frisk, Sofia; Taylan, Fulya; Vaz, Raquel; Wessman, Sandra; de Kock, Leanne; Pal, Niklas; Foulkes, William D; Lagerstedt-Robinson, Kristina; Nordgren, Ann
Journal:
Journal of medical genetics
Issue:
Volume 59:Issue 2(2022)
Page Start:
141
Record Type:
Journal Article
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2. Stockholm score of lesion detection on computed tomography following mild traumatic brain injury (SELECT-TBI): study protocol for a multicentre, retrospective, observational cohort study. Issue 9 (1st September 2022)

Authors:
Fletcher‑Sandersjöö, Alexander; Tatter, Charles; Yang, Li; Pontén, Emeli; Boman, Magnus; Lassarén, Philipp; Forsberg, Sune; Grönlund, Ingrid; Tidehag, Viktor; Rubenson-Wahlin, Rebecka; Strömmer, Lovisa; Westberg, Karin; Ängeby, Kristian; Djärv, Therese; Lundblad, Olof; Bartek, Jiri; Thelin, Eric ...
Journal:
BMJ open
Issue:
Volume 12:Issue 9(2022)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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