نتایج جستجو برای: antibody deficiency

تعداد نتایج: 299696  

Journal: :Health and Quality of Life Outcomes 2005
Hanne Marie Høybråten Sigstad Asbjørg Stray-Pedersen Stig S Frøland

BACKGROUND Living with a chronic disease, such as primary antibody deficiency, will often have consequences for quality of life. Previous quality-of-life studies in primary antibody deficiency patients have been limited to different treatment methods. We wanted to study how adults with primary antibody deficiencies manage their conditions and to identify factors that are conducive to coping, go...

Journal: :Annals of psychiatry and treatment 2021

Evidence is emerging that clozapine can adversely affect immunoglobulin levels. We present a case series of 17 clozapine-treated patients referred to clinical immunology centres in the north west England with otherwise-unexplained hypogammaglobulinaemia. This adds existing evidence and suggests cause clinically significant antibody deficiency will sometimes require specialist intervention. We...

Journal: :The European respiratory journal 2005
A H Morice S Mulrennan A Clark

therapy to control lung damage in patients with common variable immunodeficiency. Int Immunopharmacol 2004; 6: 745–753. 4 de Gracia J, Morell F, Bofill JM, Rodrigo MJ, Cosculluela C. Impaired lung function in patients with IgA deficiency and low levels of IgG2 or IgG3. N Engl J Med 1986; 314: 925–926. 5 de Gracia J, Miravitlles M, Vendrell M, Rodrigo MJ, Codina R, Morell F. Study of the IgG sub...

Journal: :The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology 2013
Vildan Ertekin Mahya Sultan Tozun Nuran Küçük

BACKGROUND/AIMS Celiac disease is an immune-mediated enteropathy caused by a permanent sensitivity to gluten in genetically susceptible individuals. Iron-deficiency anemia is the most commonly encountered anemia in humans. Iron-deficiency anemia also is a common extraintestinal manifestation of celiac disease. To determine the celiac disease prevalence in children with iron-deficiency anemia an...

Journal: :Journal of diagnostic pathology and oncology 2023

Gaucher's disease is a rare, inherited autosomal recessive metabolic disorder due to deficiency of enzyme Glucocerebrosidase resulting in deposition glucosylceramide. Deposition glucosylceramide different organs causes dysfunction and responsible for specific systemic symptoms signs. In the present cases, first case was 24-year-old female who presented with severe weakness abdominal fullness ma...

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