Search Results - "Goldmann, G"
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Impact of Telemedicine Tools on Record Keeping and Compliance in Haemophilia Care
Published in Hamostaseologie (01-11-2019)“…Record keeping is integral to home treatment for haemophilia. Issues with paper diaries include questionable compliance, data validity and quality…”
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Outcome after total knee arthroplasty in haemophilic patients with stiff knees
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-07-2015)“…Introduction Advanced haemophilic arthropathy of the knee is associated with progressive joint stiffness. Results after total knee arthroplasty (TKA) in stiff…”
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Total ankle replacement in patients with haemophilia and virus infections - a safe alternative to ankle arthrodesis?
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-09-2014)“…Summary Despite reliable results of ankle fusion for advanced haemophilic arthropathy, total ankle replacement (TAR) may be functionally advantageous. There is…”
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QoS aggregation for Web service composition using workflow patterns
Published in Proceedings. Eighth IEEE International Enterprise Distributed Object Computing Conference, 2004. EDOC 2004 (2004)“…Contributions in the field of Web services have identified that (a) finding matches between semantic descriptions of advertised and requested services and (b)…”
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Conference Proceeding -
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Giant haemophilic pseudotumour of the pelvis: case report and literature review
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-11-2015)Get full text
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The relevance of the bleeding severity in the treatment of acquired haemophilia - an update of a single-centre experience with 67 patients
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-05-2010)“…Acquired haemophilia (AH), an autoimmune disorder with clinical features ranging from harmless haematomas to life‐threatening bleedings, still has a mortality…”
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Combined coagulation factor VIII and factor IX deficiency (CDF8F9) in a patient from Lithuania
Published in Hämostaseologie (2016)“…Haemophilia A (FVIII deficiency) and haemophilia B (FIX deficiency) are X-linked inherited bleeding disorders. It is a very rare event to identify both…”
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No increased bleeding risk for oral surgery in patients with severe congenital bleeding disorders due to intense perioperative management
Published in Oral and maxillofacial surgery (01-06-2015)“…Purpose In order to evaluate complication rates of dentoalveolar surgery in patients with congenital bleeding disorders, a retrospective case–control study was…”
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Impact of Preoperative Knee Stiffness on the Postoperative Outcome after Total Knee Arthroplasty in Patients with Haemophilia
Published in Zeitschrift fur Orthopadie und Unfallchirurgie (01-10-2015)“…Total knee arthroplasty (TKA) is an effective treatment option for patients with end-stage haemophilic arthropathy of the knee. However, the procedure is…”
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Elective total knee arthroplasty in haemophilic patients. Proposal for a clinical pathway
Published in Hämostaseologie (2014)“…Total knee arthroplasty (TKA) provides significant pain relief and better function in patients with end-stage haemophilic knee arthropathy. Peri- and…”
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Long-term outcome of liver transplantation in HCV/HIV coinfected haemophilia patients. A single centre study of 10 patients
Published in Hämostaseologie (2015)“…The outcome and clinical features during long term follow-up of 10 haemophilia patients (haemophilia A n = 9, haemophilia B n = 1), who underwent successful…”
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Inhibitor development and management in three non-severe haemophilia A patients with T295A variant
Published in Hämostaseologie (01-01-2014)“…Missense mutations are the most common F8 gene defects among the patients with non-severe haemophilia A. This type of mutation is typically associated with low…”
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Treatment options for haemophilic arthropathy of the elbow after failed conservative therapy. A single centre experience
Published in Hämostaseologie (2014)“…After ankle and knee, the elbow is the most frequent joint affected by haemophilic arthropathy. The objective of this retrospective single centre study is to…”
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Transient elastography discloses identical distribution of liver fibrosis in chronic hepatitis C between HIV-negative and HIV-positive patients on HAART
Published in European journal of medical research (08-04-2010)“…Progressive immunodeficiency associated with HIV-infection leads to a progressive course of liver disease in HIV/HCV-co-infected patients. Highly active…”
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Neoplasm-induced bleeding in inherited, heterozygous FXIII-A deficiency
Published in Hämostaseologie (01-01-2015)“…Inherited mild factor XIII deficiency belongs to one of the most underdiagnosed bleeding disorders so far. This is, because most patients do not develop…”
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Correlation of transient elastography with APRI and FIB-4 in a cohort of patients with congenital bleeding disorders and HCV or HIV/HCV coinfection
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-09-2010)“…Patients with inherited bleeding disorders frequently suffer from chronic hepatitis C virus (HCV) mono‐ or human immunodeficiency virus (HIV)/HCV coinfection…”
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Systemic lupus erythematosus and microchimerism in autoimmunity
Published in Transplantation proceedings (01-11-2002)Get full text
Journal Article Conference Proceeding -
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Muscular compartment syndrome of the forearm in a haemophilia inhibitor patient
Published in Hämostaseologie (01-10-2008)“…Acute compartment syndrome is a complication in which microcirculation is impaired due to increased tissue pressure within a confined (osteo-fibrous) space and…”
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Pseudo tumours in haemophilia patients
Published in Hämostaseologie (01-10-2009)“…Pseudo tumours are amongst the rare yet pathognomonic complications of haemophilia. They are old, encapsulated haematomas which due to their sometimes enormous…”
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Treatment of minor severe acquired haemophilia. Is there a rationale for immunoadsorption?
Published in Atherosclerosis. Supplements (01-05-2015)“…In Acquired Haemophilia (AH) autoantibodies against blood coagulation factors, mainly FVIII, inhibit the blood coagulation cascade. The clinical symptoms can…”
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Journal Article