Publications
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Frontal sinus stenting: indications and long term follow-up. Vrije Universiteit Brussel
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Stage determination and follow-up Institute of Tropical Medicine
EPICOR (long-term follow-up of antithrombotic management patterns in acute CORonary syndrome patients) study : rationale, design, and baseline characteristics Vrije Universiteit Brussel
High loss to follow-up following obstetric fistula repair surgery in rural Burundi: is there a way forward? Institute of Tropical Medicine
Long-term follow-up results of multimodal treatment with initial surgical approach for acromegaly in a single center Vrije Universiteit Brussel
The purpose of this study is to evaluate long-term results in acromegaly patients who received surgery as first-line treatment. Repeated surgery, radiation therapy and medical treatment were considered in patients showing no postoperative remission or who suffered a relapse. Thirty-five patients suffering from acromegaly were operated on between 1993 and 2009. The patients with persistent hypersecretion received a new surgery when ...
Quality of Life and Patient Satisfaction After Video-Assisted Thoracic Sympathicolysis for Essential Hyperhidrosis: A Follow-Up of 138 Patients Vrije Universiteit Brussel
Objectives: Essential hyperhidrosis (EH) is defined as excessive functioning of the sudomotor sweat system. Definitive treatment of choice is video-assisted thoracoscopic sympathetic interruption. Success rates are high, but compensatory hyperhidrosis (CH) remains a troublesome side effect. The aim of this study was to document patient satisfaction and side effects at least 6 months after thoracoscopic sympathicolysis.
Methods: ...
Methods: ...
Arrhythmogenic right ventricular dysplasia/cardiomyopathy pathogenic desmosome mutations in index-patients predict outcome of family screening: Dutch arrhythmogenic right ventricular dysplasia/cardiomyopathy genotype-phenotype follow-up study Ghent University
Background: Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is an autosomal dominant inherited disease with incomplete penetrance and variable expression. Causative mutations in genes encoding 5 desmosomal proteins are found in approximate to 50% of ARVD/C index patients. Previous genotype-phenotype relation studies involved mainly overt ARVD/C index patients, so follow-up data on relatives are scarce. Methods and Results: ...