Anaphylaxis in an urban Belgian emergency department: epidemiology and aetiology [0.03%]
比利时城市急诊科过敏急救的流行病学和病因学
Y Mostmans,M Blykers,P Mols et al.
Y Mostmans et al.
Objectives: Anaphylaxis is an emergency condition of which reliable epidemiological data are lacking. This study focusses on epidemiology and aetiology of anaphylactic reactions in an urban Belgian emergency department (E...
Philip R A Vanbrabant,Bruno J G De Turck,Marjan Petrick
Philip R A Vanbrabant
Corrigendum [0.03%]
勘误表
Published Erratum
Acta clinica Belgica. 2015 Feb;70(1):79. DOI:10.1179/0001551215Z.000000000164 2015
V Wiwanitkit
V Wiwanitkit
Koenraad R P Veys,Martine T P Besouw,Anne-Marie Pinxten et al.
Koenraad R P Veys et al.
Cystinosis is a rare, autosomal recessive inherited lysosomal storage disease. It is the most frequent and potentially treatable cause of the inherited renal Fanconi syndrome. If left untreated, renal function rapidly deteriorates towards e...
Rachid Attou,Pascal Reper
Rachid Attou
Congenital cystic adenomatoid malformation, also named congenital pulmonary airway malformation (CPAM), is a congenital lung abnormality which is uncommon in adults. The usual radiological appearance of CPAM is a cystic space-occupying lesi...
Phenotype variability and therapeutic response to Patisiran in patients with hereditary transthyretin amyloidosis: a Belgian real-world experience [0.03%]
帕拉米坦治疗遗传性甲状腺素运载蛋白淀粉样变患者的表型可变性和治疗反应：比利时真实世界体验
Introduction: Hereditary transthyretin amyloidosis (hATTRv) is a rare, genetic, adult-onset, multisystemic disorder which can affect diverse organs, including peripheral nerves, heart, kidneys, gastrointestinal tract, liv...