Výsledky vyhledávání - "Emeli Pontén"

Akademický článek

Stockholm score of lesion detection on computed tomography following mild traumatic brain injury (SELECT-TBI): study protocol for a multicentre, retrospective, observational cohort study

Autor: Li Yang, Therese Djärv, Jiri Bartek, Emeli Pontén, Magnus Boman, Lovisa Strömmer, Alexander Fletcher‑Sandersjöö, Charles Tatter, Philipp Lassarén, Sune Forsberg, Ingrid Grönlund, Viktor Tidehag, Rebecka Rubenson-Wahlin, Karin Westberg, Kristian Ängeby, Olof Lundblad, Eric Peter Thelin

Publikováno v: BMJ Open, Vol 12, Iss 9 (2022)

Introduction Mild traumatic brain injury (mTBI) is one of the most common reasons for emergency department (ED) visits. A portion of patients with mTBI will develop an intracranial lesion that might require medical or surgical intervention. In these

Externí odkaz: https://doaj.org/article/6dba98d7f8d145de8b487f9048601a86

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Stockholm score of lesion detection on computed tomography following mild traumatic brain injury (SELECT-TBI): study protocol for a multicentre, retrospective, observational cohort study

Autor: Alexander Fletcher‑Sandersjöö, Charles Tatter, Li Yang, Emeli Pontén, Magnus Boman, Philipp Lassarén, Sune Forsberg, Ingrid Grönlund, Viktor Tidehag, Rebecka Rubenson-Wahlin, Lovisa Strömmer, Karin Westberg, Kristian Ängeby, Therese Djärv, Olof Lundblad, Jiri Bartek, Eric Peter Thelin

Publikováno v: BMJ open. 12(9)

IntroductionMild traumatic brain injury (mTBI) is one of the most common reasons for emergency department (ED) visits. A portion of patients with mTBI will develop an intracranial lesion that might require medical or surgical intervention. In these p

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcf01a6780f2335d422e63e6b4ce5468
https://pubmed.ncbi.nlm.nih.gov/36581962

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A complex DICER1 syndrome phenotype associated with a germline pathogenic variant affecting the RNase IIIa domain of DICER1

Autor: Emeli, Pontén, Sofia, Frisk, Fulya, Taylan, Raquel, Vaz, Sandra, Wessman, Leanne, de Kock, Niklas, Pal, William D, Foulkes, Kristina, Lagerstedt-Robinson, Ann, Nordgren

Publikováno v: Journal of Medical Genetics

Background Germline pathogenic variants in DICER1 cause DICER1 syndrome, an autosomal dominant, pleiotropic tumour predisposition syndrome with variable expressivity and reduced penetrance for specific dysplastic and neoplastic lesions. Recently, a s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9493501e322d32073d5242392ce260cd
https://pubmed.ncbi.nlm.nih.gov/33208384

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