Search Results - "Gehrisch, S"
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Application of Time-Resolved 3D Digital Subtraction Angiography to Plan Cerebral Arteriovenous Malformation Radiosurgery
Published in American journal of neuroradiology : AJNR (01-04-2017)“…Time-resolved 3D-DSA (4D-DSA) enables viewing vasculature from any desired angle and time frame. We investigated whether these advantages may facilitate…”
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Phamacokinetics of rivaroxaban in adolescents
Published in Hämostaseologie (2014)“…The direct factor Xa inhibitor rivaroxaban is approved for venous thromboembolism (VTE) treatment in adults. However, in all phase-III trials children or…”
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Optimization of the Surgical Approach in AVMs Using MRI and 4D DSA Fusion Technique
Published in Clinical neuroradiology (Munich) (01-12-2017)“…Purpose Previously published data demonstrated the possibility of displaying the angioarchitecture of intracranial vascular malformations using time-resolved…”
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Optimization of the Surgical Approach in AVMs Using MRI and 4D DSA Fusion Technique: A technical note
Published in Clinical neuroradiology (Munich) (01-12-2017)“…Purpose Previously published data demonstrated the possibility of displaying the angioarchitecture of intracranial vascular malformations using time-resolved…”
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Utility of dual-phase cone-beam CT: Can it predict tumor response after super-selective TACE for HCC?
Published in Journal of vascular and interventional radiology (01-03-2016)Get full text
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Therapy refractory menorrhagia as first manifestation of Hermansky-Pudlak syndrome
Published in Hämostaseologie (01-11-2011)“…Oculocutaneous albinism (OCA) in combination with a platelet function defect caused by a disturbed release reaction from platelet δ-granules (storage pool…”
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Therapy of inherited diseases of platelet function. Interdisciplinary S2K guideline of the Permanent Paediatric Committee of the Society of Thrombosis and Haemostasis Research (GTH e. V.)
Published in Hämostaseologie (2014)“…Inherited disorders of platelet function are a heterogeneous group. For optimal prevention and management of bleeding, classification and diagnosis of the…”
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Evaluation of haemostasis in children treated with valproic acid
Published in Hämostaseologie (01-11-2010)“…Coagulation parameters were determined in children with valproic acid mono- and valproic acid-lamotrigin combination therapy. Monotherapy group (n = 22; mean…”
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Clinical and laboratory aspects of the Aspirin-like defect as hereditary thrombocytopathy
Published in Hämostaseologie (01-05-2009)“…The Aspirin-like defect (ALD) is caused by defects in the intraplatelet arachidonic acid (AA)-metabolism. We here present the characteristics of a larger…”
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Clinical importance of prothrombotic risk factors in pediatric patients with malignancy--impact of central venous lines
Published in European journal of pediatrics (01-12-1999)“…To evaluate the role of inherited thrombophilia in the development of central venous line (CVL)-related thrombosis, the following parameters were determined in…”
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Venous thrombosis after long-haul flights
Published in Archives of internal medicine (1960) (08-12-2003)“…The risk for venous thromboembolism after long-haul flights represents a controversial issue. The aim of our study was to assess the incidence of venous…”
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Deep vein and isolated calf muscle vein thrombosis following long-haul flights: pilot study
Published in Blood coagulation & fibrinolysis (01-12-2002)“…The risk of venous thromboembolism associated with long-haul flights is the subject of controversy. In a prospective, controlled study, we examined 160…”
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Eight novel LDL receptor gene mutations among patients under LDL apheresis in Dresden and Leipzig
Published in Human mutation (2001)“…LDL apheresis is highly efficient in reducing elevated plasma cholesterol. Due to strict indications only patients with severe, refractory hypercholesterolemia…”
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Increased clearance of low density lipoprotein precursors in patients with heterozygous familial defective apolipoprotein B-100: a stable isotope approach
Published in Journal of lipid research (01-10-1996)“…In familial defective apolipoprotein B-100 (FDB) the presence of a mutant apolipoprotein (apo) B-100 (FDB3500Q/W) in LDL markedly reduces their affinity for…”
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New missense mutation in exon 13 (N789T) of the coagulation factor V gene
Published in Human mutation (01-10-1999)Get full text
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Method-dependent influence of certain polymorphisms in the factor V B-domain on the response to activated protein C
Published in Blood coagulation & fibrinolysis (01-09-2000)“…The factor V (FV) B-domain is extremely important to the cofactor function of native FV for activated protein C (APC) in the inactivation of factor VIII…”
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Mutations of the human hepatic lipase gene in patients with combined hypertriglyceridemia/hyperalphalipoproteinemia and in patients with familial combined hyperlipidemia
Published in Journal of molecular medicine (Berlin, Germany) (01-10-1999)“…Hepatic lipase is an enzyme which hydrolyzes triglycerides from plasma lipoproteins and thus takes part in the metabolism of intermediate density lipoproteins…”
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18 bp insertion/duplication with internal missense mutation in human hepatic lipase gene exon 3. Mutations in brief no. 181. Online
Published in Human mutation (1998)“…Human hepatic lipase (hHL) plays an important role in hydrolysis of triglycerides from plasma lipoproteins. The enzyme also hydrolyzes HDL2 lipids resulting in…”
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Time-Resolved 3D-Rotational Angiography of Intracranial Vascular Malformations
Published in Clinical neuroradiology (Munich) (01-09-2016)“…Purpose: The purpose of this pilot study was to demonstrate the applicability of time-resolved 4D reconstructions from 3D DSA rotational angiography data sets…”
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