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2021
Mark Healthcare utilisation patterns among older people with intellectual disability and with affective and anxiety diagnoses in comparison with the general population
El Mrayyan, Nadia ^LU ; Bökberg, Christina ^LU ; Eberhard, Jonas ^LU and Ahlström, Gerd ^LU (2021) In Aging and Mental Health 25(8). p.1525-1534
- Contribution to journal › Article
2020
Mark Incidents resulting in health care among older people with intellectual disability in comparison with the general population : A national register study
Axmon, Anna ^LU ; Ekwall, Anna ^LU and Ahlström, Gerd ^LU (2020) In Journal of Intellectual and Developmental Disability 45(2). p.139-143
- Contribution to journal › Article
Mark Health care utilisation among older people with Down syndrome compared to specific medical guidelines for health surveillance : a Swedish national register study
Ahlström, G. ^LU ; Axmon, A. ^LU ; Sandberg, M. ^LU and Flygare Wallén, E. (2020) In BMC Health Services Research 20(1).
- Contribution to journal › Article
2019
Mark Pharmacotherapy for mood and anxiety disorders in older people with intellectual disability in comparison with the general population
Axmon, Anna ^LU ; El Mrayyan, Nadia ^LU ; Eberhard, Jonas ^LU and Ahlström, Gerd ^LU (2019) In BMC Psychiatry 19(1).
- Contribution to journal › Article
Mark Prescription of pain medication among older cancer patients with and without an intellectual disability : A national register study
Segerlantz, Mikael ^LU ; Axmon, Anna ^LU ; Gagnemo Persson, Rebecca ^LU ; Brun, Eva ^LU and Ahlström, Gerd ^LU (2019) In BMC Cancer 19(1).
- Contribution to journal › Article
2018
Mark Psychiatric diagnoses in older people with intellectual disability in comparison with the general population a register study
Axmon, A ^LU ; Björne, P ; Nylander, L ^LU and Ahlström, G ^LU (2018) In Epidemiology and Psychiatric Sciences 27(5). p.479-491
- Contribution to journal › Article
2011
Mark Biparental inheritance of chromosomal abnormalities in male twins with non-syndromic mental retardation
Gilling, Mette ; Lind-Thomsen, Allan ; Mang, Yuan ; Bak, Mads ; Moller, Morten ; Ullmann, Reinhard ; Kristoffersson, Ulf ^LU ; Kalscheuer, Vera M. ; Henriksen, Karen Friis and Bugge, Merete , et al. (2011) In European Journal of Medical Genetics 54(4). p.383-388
- Contribution to journal › Article
2009
Mark Novel pathogenic mechanism suggested by ex vivo analysis of MCT8 (SLC16A2) mutations
Visser, W Edward ; Jansen, Jurgen ; Frieserna, Edith C ; Kester, Monique H. A. ; Mancilla, Edna ; Lundgren, Johan ^LU ; van der Knaap, Marjo S. ; Lunsing, Roelineke J. ; Brouwar, Oebele F. and Visser, Theo J. (2009) In Human Mutation 30(1). p.29-38
- Contribution to journal › Article
2008
Mark Autism spectrum conditons in myotonic dystrophy type 1: A study on 57 individuals with congenital and childhood forms
Ekstrom, Anne-Berit ; Hakenas-Plate, Louise ; Samuelsson, Lena ; Tulinius, Mar and Wentz, Elisabet ^LU (2008) In American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B(6). p.918-926
- Contribution to journal › Article
Mark Analysis of genes encoding laminin beta 2 and related proteins in patients with Galloway-Mowat syndrome
Dietrich, Andreas ; Matejas, Verena ; Bitzan, Martin ; Hashmi, Seema ; Kiraly-Borri, Cathy ; Lin, Shuan-Pei ; Mildenberger, Eva ; Hoppe, Bernd ; Palm, Lars ^LU and Shiihara, Takashi , et al. (2008) In Pediatric Nephrology 23(10). p.1779-1786
- Contribution to journal › Article

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