Search Results - "Fager, Marcus"
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Proton beam radiation induces DNA damage and cell apoptosis in glioma stem cells through reactive oxygen species
Published in Scientific reports (10-09-2015)“…Glioblastoma multiforme (GBM) is among the most lethal of human malignancies. Most GBM tumors are refractory to cytotoxic therapies. Glioma stem cells (GSCs)…”
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Linear Energy Transfer Painting With Proton Therapy: A Means of Reducing Radiation Doses With Equivalent Clinical Effectiveness
Published in International journal of radiation oncology, biology, physics (01-04-2015)“…Purpose The purpose of this study was to propose a proton treatment planning method that trades physical dose (D) for dose-averaged linear energy transfer…”
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Germline heterozygous variants in genes associated with familial hemophagocytic lymphohistiocytosis as a cause of increased bleeding
Published in Platelets (Edinburgh) (01-01-2018)“…Familial hemophagocytic lymphohistiocytosis (FHL) is caused by biallelic variants in genes regulating granule secretion in cytotoxic lymphocytes. In FHL3-5,…”
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A rare case of IgE kappa monoclonal gammopathy of undetermined significance identified in a Swedish female
Published in Scandinavian journal of clinical and laboratory investigation (01-09-2021)“…Monoclonal gammopathies involving immunoglobulin E (IgE) is a very rare phenomenon, with less than 70 cases being previously described in the literature. The…”
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A rare heterozygous variant in FGB (Fibrinogen Merivale) causing hypofibrinogenemia in a Swedish family
Published in Blood coagulation & fibrinolysis (01-10-2020)“…Fibrinogen is essential for normal hemostasis. Congenital fibrinogen disorders (afibrinogenemia, hypofibrinogenemia, dysfibrinogenemia and…”
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Collagen remodelling and plasma ascorbic acid levels in patients suspected of inherited bleeding disorders harbouring germline variants in collagen‐related genes
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-01-2021)“…Introduction Variants in collagen‐related genes COL1A1, COL3A1, COL5A1 and COL5A2 are associated with Ehlers‐Danlos syndrome (EDS), a heterogeneous group of…”
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Genetic screening of children with suspected inherited bleeding disorders
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-03-2020)“…Introduction Genetic screening using high‐throughput DNA sequencing has become a tool in diagnosing patients with suspected inherited bleeding disorders (IBD)…”
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Severe Congenital Thrombocytopenia Characterized by Decreased Platelet Sialylation and Moderate Complement Activation Caused by Novel Compound Heterozygous Variants in GNE
Published in Frontiers in immunology (09-11-2021)“…Hereditary thrombocytopenias constitute a genetically heterogeneous cause of increased bleeding. We report a case of a 17-year-old boy suffering from severe…”
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On the stability of Leksell Vantage stereotactic head frame fixation in Gamma Knife radiosurgery: a study based on cone-beam computed tomography imaging and the High Definition Motion Management system
Published in Journal of neurosurgery (01-09-2023)“…The authors' objective was to investigate the stability of the newly introduced Vantage stereotactic frame fixation in single-fraction Gamma Knife…”
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Range optimization for mono- and bi-energetic proton modulated arc therapy with pencil beam scanning
Published in Physics in medicine & biology (07-11-2016)“…The development of rotational proton therapy plans based on a pencil-beam-scanning (PBS) system has been limited, among several other factors, by the…”
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Proposed linear energy transfer areal detector for protons using radiochromic film
Published in Review of scientific instruments (01-04-2015)“…Radiation therapy depends on predictably and reliably delivering dose to tumors and sparing normal tissues. Protons with kinetic energy of a few hundred MeV…”
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Sickle cell disease - common and dangerous complications
Published in Läkartidningen (12-07-2024)“…Sickle cell disease is a genetic disorder affecting hundreds of thousands of people worldwide. This article will focus on the most common and dangerous acute…”
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Evaluation of the Sialidase Inhibitor Oseltamivir in GNE-associated Thrombocytopenia
Published in The XXIX Congress of the International Society on Thrombosis and Haemostasis (ISTH),2021-07-17 - 2021-07-21 (2021)“…Background: GNE encodes UDP-N-acetyl-glucosamine-2-epimerase/N-acetylmannosamine kinase, the rate limiting enzyme of sialic acid biosynthesis. Biallelic…”
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Conference Proceeding -
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Collagen Turnover and Plasma Ascorbic Acid Levels in Patients Suspected of Inherited Bleeding Disorders Harboring Variants in Collagen-related Genes
Published in The XXVIII Congress of the International Society on Thrombosis and Haemostasis (ISTH),2020-07-12 - 2020-07-14 (2020)Get full text
Conference Proceeding