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2022
Mark Merged testing for colorectal cancer syndromes and re-evaluation of genetic variants improve diagnostic yield : Results from a nationwide prospective cohort
Svensson, Sara ^LU ; Zagoras, Theofanis ; Aravidis, Christos ; Askmalm, Marie Stenmark ^LU ; Björck, Erik ; Borg, Åke ^LU ; Kuchinskaya, Ekaterina ; Nilbert, Mef ^LU ; Nordling, Margareta and Rohlin, Anna , et al. (2022) In Genes Chromosomes and Cancer 61(10). p.585-591
- Contribution to journal › Article
Mark Corticotropin releasing hormone as an identifier of bronchiolitis obliterans syndrome
Niroomand, Anna ^LU ; Ghaidan, Haider ^LU ; Hallgren, Oskar ^LU ; Hansson, Lennart ^LU ; Larsson, Hillevi ^LU ; Wagner, Darcy ^LU ; Mackova, Martina ; Halloran, Kieran ; Hyllén, Snejana ^LU and Lindstedt, Sandra ^LU (2022) In Scientific Reports 12. p.1-11
- Contribution to journal › Article
2021
Mark Speech in a consecutive series of children born with cleft lip and palate with and without syndromes and/or additional malformations
Klintö, Kristina ^LU ; Sporre, Maria and Becker, Magnus ^LU (2021) In BMC Pediatrics 21.
- Contribution to journal › Article
2014
Mark Hypertensive encephalopathy and cerebral infarction
Edvardsson, Bengt ^LU (2014) In SpringerPlus 3.
- Contribution to journal › Article
2012
Mark The prevalence and clinical characteristics of Charles Bonnet Syndrome in Danish patients with neovascular age-related macular degeneration
Singh, Amardeep ^LU and Sørensen, Torben L (2012) In Acta Ophthalmologica 90(5). p.80-476
- Contribution to journal › Article
2011
Mark Hallucinationer ved synsnedsaettelse
Singh, Amardeep ^LU and Sørensen, Torben Lykke (2011) In Ugeskrift for Laeger 173(1). p.50-50
- Contribution to journal › Article
Mark Charles Bonnet-syndrom og visuelle hallucinationer
Singh, Amardeep ^LU and Sørensen, Torben Lykke (2011) In Ugeskrift for Laeger 173(1). p.9-47
- Contribution to journal › Article
Mark Charles Bonnet syndrome improves when treatment is effective in age-related macular degeneration
Singh, A ^LU and Sørensen, T L (2011) In British Journal of Ophthalmology 95(2). p.2-291
- Contribution to journal › Letter
2010
Mark 22q11.2 microduplication in two patients with bladder exstrophy and hearing impairment
Lundin, Johanna ; Soderhall, Cilla ; Lunden, Lina ; Hammarsjo, Anna ; White, Irene ; Schoumans, Jacqueline ; Lackgren, Goran ; Clementson Kockum, Christina ^LU and Nordenskjold, Agneta (2010) In European Journal of Medical Genetics 53(2). p.61-65
- Contribution to journal › Article
Mark Molecular Analysis Expands the Spectrum of Phenotypes Associated with GLI3 Mutations
Johnston, Jennifer J. ; Sapp, Julie C. ; Turner, Joyce T. ; Amor, David ; Aftimos, Salim ; Aleck, Kyrieckos A. ; Bocian, Maureen ; Bodurtha, Joann N. ; Cox, Gerald F. and Curry, Cynthia J. , et al. (2010) In Human Mutation 31(10). p.1142-1154
- Contribution to journal › Article

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