Results 71 to 80 of about 319,257 (287)
To determine the approximate incidence and clinical features of pernicious anemia in a Korean population, we retrospectively analyzed clinical data for patients with pernicious anemia who were diagnosed between 1995 and 2010 at five hospitals in Chungnam
I. Song+10 more
semanticscholar +1 more source
ABSTRACT Malabsorption is a complex and multifaceted condition characterised by the defective passage of nutrients into the blood and lymphatic streams. Several congenital or acquired disorders may cause either selective or global malabsorption in both children and adults, such as cystic fibrosis, exocrine pancreatic insufficiency (EPI), coeliac ...
Marco Vincenzo Lenti+29 more
wiley +1 more source
Genetic migraine disorders and the response to calcitonin gene‐related peptide antagonist treatment
Abstract Calcitonin gene‐related peptide (CGRP) is a potent cerebral vasodilator and part of the trigeminal migraine cascade. Newer migraine therapies target CGRP signaling for both acute and preventative management of headache. In this series, we present two cases of genetic conditions, of which migraine is a key feature, responsive to CGRP antagonist
Andrea M. Kuczynski, William S. Kingston
wiley +1 more source
The Treatment of Pernicious Anemia [PDF]
n ...
openaire +2 more sources
Clonal hematopoiesis of indeterminate potential and the risk of autoimmune diseases
Abstract Background Clonal hematopoiesis of indeterminate potential (CHIP), characterized by the age‐related expansion of blood cells carrying preleukemic mutations, is associated with immune aging. This study aimed to investigate the association between CHIP and established autoimmune diseases. Methods We analyzed baseline data from 456,692 UK Biobank
Hanzhang Wu+4 more
wiley +1 more source
Acquired Thrombotic Thrombocytopenic Purpura in a Patient with Pernicious Anemia
Introduction. Acquired thrombotic thrombocytopenic purpura (TTP) has been associated with different autoimmune disorders. However, its association with pernicious anemia is rarely reported. Case Report.
Ramesh Kumar Pandey+4 more
doaj +1 more source
ABSTRACT Background Supposed ‘spontaneous’ remissions in chronic lymphocytic leukaemia (CLL) are extremely rare. By the most stringent immunophenotypic criteria, there are only seven cases to date of unexplained, immune system effected cures. A historic review of this phenomenon is presented as context for this eighth case of CLL immunophenotypic ...
Carmen Wheatley
wiley +1 more source
A long-standing undiagnosed case of vitamin B12 deficiency: a case report
Background Pernicious anemia, an autoimmune disease, presents with gradual, nonspecific symptoms, often leading to delayed diagnosis owing to its overlap with other conditions and variability in laboratory findings, such as neurological symptoms without ...
Amirhossein Mesgarankarimi+2 more
doaj +1 more source
Severe Megaloblastic Anaemia in an Infant [PDF]
Vitamin B 12 or cobalamin deficiency, a rare clinical entity in pediatric age, is found most exclusively in breastfed infants, whose mothers are strictly vegetarian non-supplemented or with pernicious anaemia.
Brito, MJ+4 more
core +2 more sources
Abstract The clinical and immunophenotypic attributes of reactive γδ T‐cell expansions are less well characterized than their malignant counterparts, which can pose diagnostic challenges. This study aims to investigate the characteristics and long‐term clinical outcomes of reactive γδ T‐cell expansions.
Hamza Tariq+6 more
wiley +1 more source