1 – 56 of 56
- show: 250
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2021
-
Mark
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
(
- Contribution to journal › Article
- 2020
-
Mark
Repositioning of the global epicentre of non-optimal cholesterol
(
- Contribution to journal › Article
- 2019
-
Mark
Sicca/Sjögren's syndrome triggered by PD-1/PD-L1 checkpoint inhibitors. Data from the International Immunocancer Registry (ICIR)
(
- Contribution to journal › Article
-
Mark
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
(
- Contribution to journal › Article
-
Mark
Primary fatty amides in plasma associated with brain amyloid burden, hippocampal volume, and memory in the European Medical Information Framework for Alzheimer's Disease biomarker discovery cohort
(
- Contribution to journal › Article
- 2018
-
Mark
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes article
(
- Contribution to journal › Article
-
Mark
Timing of onset affects arthritis presentation pattern in antisynthetase syndrome
(
- Contribution to journal › Article
-
Mark
Ultrasonography in psoriatic arthritis: Which sites should we scan?
(
- Contribution to journal › Letter
- 2017
-
Mark
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease
(
- Contribution to journal › Article
-
Mark
A low-frequency inactivating AKT2 variant enriched in the finnish population is associated with fasting insulin levels and type 2 diabetes risk
(
- Contribution to journal › Article
- 2016
-
Mark
Indications for cataract surgery in a changing world.
(
- Contribution to journal › Letter
-
Mark
Living unnoticed: Cognitive impairment in older people with multimorbidity
(
- Contribution to journal › Article
-
Mark
Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies
(
- Contribution to journal › Article
-
Mark
The genetic architecture of type 2 diabetes
(
- Contribution to journal › Article
-
Mark
Loci associated with ischaemic stroke and its subtypes (SiGN): A genome-wide association study
(
- Contribution to journal › Article
- 2015
-
Mark
Frailty and comprehensive geriatric assessment organized as CGA-ward or CGA-consult for older adult patients in the acute care setting: A systematic review and meta-analysis
(
- Contribution to journal › Scientific review
-
Mark
A mutation in caspase-9 decreases the expression of BAFFR and ICOS in patients with immunodeficiency and lymphoproliferation
(
- Contribution to journal › Article
-
Mark
Global, regional, and national comparative risk assessment of 79 behavioural, environmental and occupational, and metabolic risks or clusters of risks in 188 countries, 1990-2013: A systematic analysis for the Global Burden of Disease Study 2013
(
- Contribution to journal › Article
- 2014
-
Mark
IL-17 protects T cells from apoptosis and contributes to development of ALPS-like phenotypes
(
- Contribution to journal › Article
- 2012
-
Mark
Age-dependent variation of genotypes in MHC II transactivator gene (CIITA) in controls and association to type 1 diabetes
(
- Contribution to journal › Article
-
Mark
Health-Related Quality of Life among Patients with Coronary Artery Disease: A Post-Treatment Follow-Up Study in Iran
(
- Contribution to journal › Article
- 2007
-
Mark
Tracking the neurodegeneration of parkinsonian disorders - A pilot study
(
- Contribution to journal › Article
- 2005
-
Mark
The Children’s Revised Impact of Event Scale (CRIES): Validity as a screening instrument for PTSD.
(
- Contribution to journal › Article
-
Mark
Festschrift for William Yule
(
- Contribution to journal › Article
- 2002
-
Mark
On-line automated sample preparation for liquid chromatography using parallel supported liquid membrane extraction and microporous membrane liquid-liquid extraction
(
- Contribution to journal › Article
- 2001
-
Mark
Somatic mosaicism in hemophilia A: A fairly common event
(
- Contribution to journal › Article
- 2000
-
Mark
Treatment of children with haemophilia in Europe: A survey of 20 centres in 16 countries
(
- Contribution to journal › Article
-
Mark
Determination of thiophanate-methyl and its metabolites at trace level in spiked natural water using the supported liquid membrane extraction and the microporous membrane liquid-liquid extraction techniques combined on-line with high-performance liquid chromatography
(
- Contribution to journal › Article
-
Mark
Automated determination of Vinclozolin at the ppb level in aqueous samples by a combination of microporous membrane liquid-liquid extraction and adsorption chromatography
(
- Contribution to journal › Article
- 1999
-
Mark
Prenatal diagnosis of haemophilia
(
- Contribution to journal › Scientific review
-
Mark
Long-term psychological effects of carrier testing and prenatal diagnosis of haemophilia: Comparison with a control group
(
- Contribution to journal › Article
-
Mark
The Ala25-Thr mutation in the thrombomodulin gene is not frequent in Swedish patients suffering from ischemic heart disease [9]
(
- Contribution to journal › Letter
-
Mark
Prevalence of IgA-antiendomysium and IgA-antigliadin autoantibodies at diagnosis of insulin-dependent diabetes mellitus in Swedish children and adolescents
(
- Contribution to journal › Article
-
Mark
Prevalence of coeliac disease in Turner syndrome
(
- Contribution to journal › Article
- 1998
-
Mark
Prophylactic treatment in Sweden - Overtreatment or optimal model?
(
- Contribution to journal › Article
-
Mark
Can haemophilic arthropathy be prevented?
(
- Contribution to journal › Special issue (editor)
-
Mark
A common 4G allele in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene as a risk factor for pulmonary embolism and arterial thrombosis in hereditary protein S deficiency
(
- Contribution to journal › Article
-
Mark
The A20210 allele of the prothrombin gene is frequently associated with the factor V Arg 506 to Gln mutation but not with protein S deficiency in thrombophilic families [3]
(
- Contribution to journal › Letter
- 1997
-
Mark
Identifying carriers at high risk for negative reactions when performing prenatal diagnosis of haemophilia
(
- Contribution to journal › Article
-
Mark
The factor VR5O6Q mutation causing APC resistance is highly prevalent amongst unselected outpatients with clinically suspected deep venous thrombosis
(
- Contribution to journal › Article
-
Mark
Genetic and phenotypic analysis of a large (122-member) protein S-deficient kindred provides an explanation for the familial coexistence of type I and type III plasma phenotypes
(
- Contribution to journal › Article
-
Mark
Evaluation of original and modified APC-resistance tests in unselected outpatients with clinically suspected thrombosis and in healthy controls
(
- Contribution to journal › Article
- 1996
-
Mark
Detection of virus in vertically exposed HIV-antibody-negative children
(
- Contribution to journal › Article
-
Mark
Four novel mutations in deficiency of coagulation factor XIII: Consequences to expression and structure of the A-subunit
(
- Contribution to journal › Article
-
Mark
Noise colour and the risk of population extinctions
(
- Contribution to journal › Article
-
Mark
Familial thrombophilia : clinical and molecular analysis of Swedish families with inherited resistance to activated protein C or protein S deficiency
1996) In Scandinavian journal of clinical and laboratory investigation. Supplementum 56(226). p.19-46(
- Contribution to journal › Scientific review
-
Mark
Resistance to activated protein C, the FV:Q506 allele, and venous thrombosis
(
- Contribution to journal › Scientific review
-
Mark
Inherited resistance to activated protein C caused by presence of the FV:Q506 allele as a basis of venous thrombosis
(
- Contribution to journal › Article
- 1995
-
Mark
Activated protein C resistance : from phenotype to genotype and clinical practice
(
- Contribution to journal › Article
-
Mark
Evaluation of the relationship between protein S and C4b-binding protein isoforms in hereditary protein S deficiency demonstrating type I and type III deficiencies to be phenotypic variants of the same genetic disease
(
- Contribution to journal › Article
-
Mark
Homozygous APC-resistance combined with inherited type I protein S deficiency in a young boy with severe thrombotic disease
(
- Contribution to journal › Article
- 1994
-
Mark
High titer inhibitors in severe haemophilia A. A meta-analysis based on eight long-term follow-up studies concerning inhibitors associated with crude or intermediate purity factor VIII products [4]
(
- Contribution to journal › Letter
-
Mark
Identification of the same factor V gene mutation in 47 out of 50 thrombosis-prone families with inherited resistance to activated protein C
(
- Contribution to journal › Article
-
Mark
Differential regulation of α and β chains of C4b-binding protein during acute-phase response resulting in stable plasma levels of free anticoagulant protein S
(
- Contribution to journal › Article
- 1993
-
Mark
HIV infection in haemophilia - A European cohort
(
- Contribution to journal › Article
- 1992
-
Mark
Symptoms following mild head injury: Expectation as aetiology
(
- Contribution to journal › Article