Mesenteric panniculitis presenting with autoimmune haemolytic anaemia
To access publisher full text version of this article. Please click on the hyperlink in Additional Links fieldMesenteric panniculitis is a rare idiopathic inflammatory disorder that can lead to sclerosis.
Matthiasson, Pall +3 more
core +1 more source
Delayed Recognition of Maternal G6PD Heterozygous Status Across Prenatal and Newborn Care Interfaces
ABSTRACT Glucose‐6‐phosphate dehydrogenase (G6PD) deficiency is the most common red blood cell enzymatic disorder worldwide. Although many heterozygotes are asymptomatic, affected neonates have an increased risk for hyperbilirubinemia and related complications.
Mona M. Makhamreh +5 more
wiley +1 more source
Diagnosis and management of newly diagnosed childhood autoimmune haemolytic anaemia. Recommendations from the Red Cell Study Group of the Paediatric Haemato-Oncology Italian Association [PDF]
Autoimmune haemolytic anaemia is an uncommon disorder to which paediatric haematology centres take a variety of diagnostic and therapeutic approaches.
Zanella, Alberto +15 more
core +1 more source
Autoimmune haemolytic anaemia in a patient treated with capecitabine
A 61-year-old female, followed-up for a metastatic breast cancer, was admitted in our institution with conjunctival icterus, asthenia and abdominal crampoid pain.
Sideris, Spyridon +7 more
core +1 more source
Fludarabine induced autoimmune haemolytic anaemia in a patient with chronic lymphocytic leukaemia [PDF]
Autoimmune haemolytic anaemia following fludarabine is an uncommon complication and previously treated patients are at higher risk. We describe a case of 57- year old lady with chronic lymphocytic leukaemia; she received intermittent courses of ...
Khurshid, Mohammad, Syed, Naveen Naz
core
Antifospholipid Syndrome with Autoimun Hemolitic Anemia
: Antiphospholipid syndrome is a part of systemic autoimmune disease (nonspecific organ), characterized by vascular thrombosis (arterial or venous) with a high antibody titter against a plasma protein that binds to phospholipid anions (antiphospholipid ...
Muhammad Huki Zukhrufan, Irza Wahid
doaj +1 more source
Severe delayed autoimmune haemolytic anaemia following artesunate administration in severe malaria: a case report [PDF]
International audienceBackground: Parenteral artesunate is recommended as first-line therapy for severe and complicated malaria. Although its efficacy has been proven, long-term safety profile is still under evaluation.
Mathilde Beguet +11 more
core +1 more source
Systemic lupus erythematosus (SLE) is a chronic autoimmune disorder with a relapsing and remitting course and multi- organ involvement which can present with a wide range of neuropsychiatric manifestations. Acute disseminating encephalomyelitis (ADEM) is
K. D. Ellepola +5 more
doaj +1 more source
ANK1 and EPB41 Variants and The Risk of Glucocorticoid‐Induced Osteonecrosis
Objective Steroid‐induced osteonecrosis of the femoral head (SONFH) is a refractory skeletal disorder influenced by genetic and environmental factors. However, conclusive pathogenic genetic evidence remains elusive due to the limited exploration of rare damaging variants. In this study, we aimed to identify rare variants associated with SONFH.
Shengbao Chen +21 more
wiley +1 more source
Measurement of haemolytic anaemia in a novel treatment response measure for SLE clinical trials
Objectives To define a clinically meaningful treatment response definition for haemolytic anaemia, that will form part of a novel multidomain outcome measure for SLE clinical trials.Methods An international working group comprising 12 clinicians and 4 ...
Ricard Cervera +25 more
doaj +1 more source

