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Isabell Kasesalu

Isabell Kasesalu | Aleris Rehab Station Aleris Rehab Station Hoppa till huvudinnehåll Öppna sökruta Öppna Huvudmeny Sök på saco.se Om oss Mer information för dig som medlem Medlemsförmåner Medlemsavgift Hitta ditt förbund inom Saco Lön Lönesättning Löneprocess Nyheter Webinarium om fysioterapins roll i en hållbar neurosjukvård/rehabilitering Kalender Kontaktuppgifter Medlemsmöten Fika med facket S

https://www.saco.se/fortroendevald/lokalt-fackligt-arbete/lokala-akademikerforeningar/privat/aleris-rehab-station/kontaktuppgifter/styrelsen/isabell-kasesalu/ - 2026-10-13

Linnéa Söderström

Linnéa Söderström | Aleris Rehab Station Aleris Rehab Station Hoppa till huvudinnehåll Öppna sökruta Öppna Huvudmeny Sök på saco.se Om oss Mer information för dig som medlem Medlemsförmåner Medlemsavgift Hitta ditt förbund inom Saco Lön Lönesättning Löneprocess Nyheter Webinarium om fysioterapins roll i en hållbar neurosjukvård/rehabilitering Kalender Kontaktuppgifter Medlemsmöten Fika med facket

https://www.saco.se/fortroendevald/lokalt-fackligt-arbete/lokala-akademikerforeningar/privat/aleris-rehab-station/kontaktuppgifter/styrelsen/linnea-soderstrom/ - 2026-10-13

Rose-Marie Jungeby

Rose-Marie Jungeby | Aleris Rehab Station Aleris Rehab Station Hoppa till huvudinnehåll Öppna sökruta Öppna Huvudmeny Sök på saco.se Om oss Mer information för dig som medlem Medlemsförmåner Medlemsavgift Hitta ditt förbund inom Saco Lön Lönesättning Löneprocess Nyheter Webinarium om fysioterapins roll i en hållbar neurosjukvård/rehabilitering Kalender Kontaktuppgifter Medlemsmöten Fika med facket

https://www.saco.se/fortroendevald/lokalt-fackligt-arbete/lokala-akademikerforeningar/privat/aleris-rehab-station/kontaktuppgifter/styrelsen/rosemarie-jungeby/ - 2026-10-13

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Introduction: Harboring two copies of the apolipoprotein E (APOE) ε2 allele strongly protects against Alzheimer's disease (AD). However, the effect of this genotype on gray matter (GM) volume in cognitively unimpaired individuals has not yet been described. Methods: Multicenter brain magnetic resonance images (MRIs) from cognitively unimpaired ε2 homozygotes were matched (1:1) against all other AP

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Spina bifida (SB) is a debilitating birth defect caused by multiple gene and environment interactions. Though SB shows non-Mendelian inheritance, genetic factors contribute to an estimated 70% of cases. Nevertheless, identifying human mutations conferring SB risk is challenging due to its relative rarity, genetic heterogeneity, incomplete penetrance, and environmental influences that hamper genome

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BACKGROUND: In the Netherlands, surgery for peritoneal metastases of colorectal cancer (PMCRC) is centralised, whereas PMCRC is diagnosed in all hospitals. This study assessed whether hospital of diagnosis affects treatment selection and overall survival (OS).METHODS: Between 2005 and 2015, all patients with synchronous PMCRC without systemic metastases were selected from the Netherlands Cancer Re

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INTRODUCTION: Cytoreductive surgery and hyperthermic intraperitoneal chemotherapy (CRS + HIPEC) is currently considered the standard of care for pseudomyxoma peritonei, mesothelioma and peritoneal metastases (PM) from colorectal cancer. CRS + HIPEC has also been suggested as a potential treatment option in PM of the much rarer small bowel cancer. Therefore, the current study was undertaken to inve

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BACKGROUND: The purpose of the present study was to evaluate the value of discussing rectal cancer patients in a multidisciplinary team (MDT).METHODS: All treated rectal cancer patients (>T1M0) diagnosed in 2006-2008 were included. According to the national guidelines, neoadjuvant (chemo)radiotherapy should be given to all rectal cancer patients. Patients were scored as "discussed" (MDT+) only if

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The ability of lentiviral vectors to transfer genes into human hematopoietic stem cells was studied, using a human immunodeficiency virus 1 (HIV-1)-derived vector expressing the green fluorescence protein (GFP) downstream of the phosphoglycerate kinase (PGK) promoter and pseudotyped with the G protein of vesicular stomatitis virus (VSV). High-efficiency transduction of human cord blood CD34(+) cel

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We describe a new Type II congenital disorder of glycosylation (CDG-II) caused by mutations in the conserved oligomeric Golgi (COG) complex gene, COG8. The patient has severe psychomotor retardation, seizures, failure to thrive and intolerance to wheat and dairy products. Analysis of serum transferrin and total serum N-glycans showed normal addition of one sialic acid, but severe deficiency in sub

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Growing evidence demonstrates that human mesenchymal stromal cells (MSCs) modify their in vivo anti-inflammatory actions depending on the specific inflammatory environment encountered. Understanding this better is crucial to refine MSC-based cell therapies for lung and other diseases. Using acute exacerbations of cystic fibrosis (CF) lung disease as a model, the effects of ex vivo MSC exposure to

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Background and aimsElevated body weight in adolescence is associated with early cardiovascular disease, but whether this association is traceable to weight in early adulthood, weight in midlife or to weight gain is not known. The aim of this study is to assess the risk of midlife coronary atherosclerosis being associated with body weight at age 20, body weight in midlife and body weight change.Met

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BACKGROUND: It is not clear if the European Systematic Coronary Risk Evaluation algorithm is useful for identifying prevalent subclinical atherosclerosis in a population of apparently healthy individuals. Our aim was to explore the association between the risk estimates from Systematic Coronary Risk Evaluation and prevalent subclinical atherosclerosis.DESIGN: The design of this study was as a cros

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Type 1 diabetes is a complex disease characterized by the lack of endogenous insulin secreted from the pancreatic β-cells. Although β-cell targeted autoimmune processes and β-cell dysfunction are known to occur in type 1 diabetes, a complete understanding of the cell-to-cell interactions that support pancreatic function is still lacking. To characterize the pancreatic endocrine compartment, we stu

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In a large multicentre sample of cognitively normal subjects, as a function of age, gender and APOE genotype, we studied the frequency of abnormal cerebrospinal fluid levels of Alzheimer's disease biomarkers including: total tau, phosphorylated tau and amyloid-β1-42. Fifteen cohorts from 12 different centres with either enzyme-linked immunosorbent assays or Luminex® measurements were selected for

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The majority of genetic risk variants for type 2 diabetes (T2D) affect insulin secretion, but the mechanisms through which they influence pancreatic islet function remain largely unknown. We functionally characterized human islets to determine secretory, biophysical, and ultrastructural features in relation to genetic risk profiles in diabetic and nondiabetic donors. Islets from donors with T2D ex

Hagelstedt 2015

5003 Dynamisk  simulering  för   att  förbättra  hanteringen   av  järnvägsstörningar     Ove  Hagelstedt       Division  of  Risk  Management  and  Societal  Safety   Lund  University,  Sweden     Riskhantering  och  samhällssäkerhet   Lunds  tekniska  högskola   Lunds  universitet     Report  5003,  Lund  2015       II III Dynamisk  simulering  för  att  förbättra  hanteringen  av   järnvägsstör

https://www.cencip.lu.se/sites/cencip.lu.se/files/hagelstedt_2015.pdf - 2026-10-14

Lunds-universitets-magasin-1-2017

Oärliga handledare lurar doktorander Centrumbildningar flyttar till fakulteter Eksem speglar trender Sverige idag LUNDS UNIVERSITETS MAGASIN | NR 1 | 2017 FÖREDÖME ELLER SKRÄCKEXEMPEL? 2 LUM NR 1 | 2017 LUM NR 1 | 2017 3 Med fulla hus på samtliga arrange­ mang finns det anledning för en ordförande i universitetets jubi­ leumskommitté att vara nöjd. – Det har varit en enastående start på jubileet m

https://www.lu.se/sites/www.lu.se/files/lunds-universitets-magasin-1-2017.pdf - 2026-10-14

Workreport2015complete

workreport SASNET Work Report (Verksamhetsberättelse) 1 januari – 31 december 2015 Swedish South Asian Studies Network (SASNET) at Lund University (Nätverket för Sydasienstudier i Sverige) Box 114, 221 00 Lund http://www.sasnet.lu.se Administrativ rapport No. 16 Lund 29 Februari 2016 Sammanställd av: Anna Lindberg, föreståndare/koordinator Lars Eklund, bitr. föreståndare/forskningskommunikatör Inn

https://www.sasnet.lu.se/sites/sasnet.lu.se/files/workreport2015complete.pdf - 2026-10-14

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Blood concentrations of lipoproteins and lipids are heritable risk factors for cardiovascular disease. Using genome-wide association data from three studies (n = 8,816 that included 2,758 individuals from the Diabetes Genetics Initiative specific to the current paper as well as 1,874 individuals from the FUSION study of type 2 diabetes and 4,184 individuals from the SardiNIA study of aging-associa