Results 41 to 50 of about 246,759 (191)

Autoimmune Haemolytic Anaemia-A Spectrum of Presentation in Children [PDF]

Journal of Clinical and Diagnostic Research, 2017
Autoimmune Haemolytic Anaemias (AIHAs) are rare in children. They can be either a primary disease or secondary to/triggered by a host of other clinical conditions.
Amitabh Singh, Anirban Mandal, Ankita Patel, Sataroopa Mishra   +3 more
doaj   +1 more source

Prevalence of HIV-related autoimmune haemolytic anaemia in Lagos, Nigeria

, 2014
Background: Despite a high frequency of anaemia, a positive direct antiglobulin test (DAT) and bone marrow hyperplasia HIV-infected patients, lack of reticulocytosis may cause underdiagnosis autoimmune haemolytic anaemia (AIHA) in them.
Adewumi, A A, Sulaimon, A A, Vincent, O O, Osamuedemen, V A, Titilope, A A, Akinsegun, A A, Dapus, O D   +6 more
core   +1 more source

Autoimmune Haemolytic Anaemia: An Unusual Manifestation of Kawasaki Disease [PDF]

Journal of Clinical and Diagnostic Research, 2018
Intravenous Immunoglobulin (IVIg) can cause Autoimmune Haemolytic Anaemia (AIHA) in some patients. There are many reports of AIHA developing in children with Kawasaki Disease (KD) after they were treated with IVIg. However, AIHA is seldom reported at the
Aashish Gupta, Rahi Raza, Ayush Manchanda, Jacob Puliyel   +3 more
doaj   +1 more source

Haemolytic anaemia in an HIV-infected patient with severe falciparum malaria after treatment with oral artemether-lumefantrine

Malaria Journal, 2012
Intravenous (i.v.) artesunate is now the recommended first-line treatment of severe falciparum malaria in adults and children by WHO guidelines. Nevertheless, several cases of haemolytic anaemia due to i.v. artesunate treatment have been reported.
Corpolongo Angela, De Nardo Pasquale, Ghirga Piero, Gentilotti Elisa, Bellagamba Rita, Tommasi Chiara, Paglia Maria, Nicastri Emanuele, Narciso Pasquale   +8 more
doaj   +1 more source

Severe Haemolytic Anaemia Resulting from a Malpositioned Haemodialysis Catheter [PDF]

, 2021
Severe haemolytic anaemia is a rare complication of haemodialysis that is often difficult to recognize, especially when there are other potential differential diagnoses.
Gill, Prabhsimrat S, Liaqat, Hania, Prabhsimrat Gill, Ammad Ud Din, Mohammad, Low, Soon Khai, Soon Khai Low, Hania Liaqat, Mohammad Ammad Ud Din   +7 more
core   +1 more source

GAD65 Antibody ELISA With Extended Reportable Range: Validation and Guidance for Neurological Practice

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To (1) validate GAD65‐ELISA detection and quantification for type 1 diabetes mellitus and autoimmune neurological diagnoses, (2) correlate ELISA results (reference range < 5 IU/mL) with established radioimmunoprecipitation assay (RIA; ≤ 0.02 nmol/L), and (3) define ELISA clinical utility and pitfalls.
Andrew McKeon, Dana Olofson, Diana Anissian, Divyanshu Dubey, Eoin P. Flanagan, Max C. Herman, Sarosh R. Irani, Daniel H. Lachance, Maria A. Willrich, Sean Pittock, John R. Mills, Anastasia Zekeridou   +11 more
wiley   +1 more source

Common presentation of an uncommon anaemia in a resource-limited setting: A diagnostic challenge

Journal of Family Medicine and Primary Care, 2019
A 38-year-old female in the reproductive age group presented with anaemia in a resource-poor setting. The patient was given multiple transfusions during the course of her treatment.
Shankar Roy, Monika Pathania, Ravi Kant, Minakshi Dhar, Amisha, Paras Malik, Vyas Kumar Rathaur   +6 more
doaj   +1 more source

Characteristics and Outcomes of Male Participants in a Multicenter Longitudinal Australian Study Cohort

Arthritis Care &Research, EarlyView.
Objective The aim of this study was to determine the differences in demographic, serologic, and clinical characteristics between male and female patients with systemic sclerosis (SSc) in an Australian cohort. Methods This was a retrospective observational study using data from the Australian Scleroderma Cohort Study.
Emily Lin, Dylan Hansen, Laura Ross, Gene‐Siew Ngian, Susanna Proudman, Gabor Major, Maryam Tabesh, Mandana Nikpour, Jennifer Walker, Lauren Host, Nava Ferdowsi, Alannah Quinlivan, Wendy Stevens, Joanne Sahhar, Diane Apostolopoulos   +14 more
wiley   +1 more source

The sting in the tail of severe falciparum malaria: Post-artesunate delayed haemolysis

Southern African Journal of Infectious Diseases, 2022
Post-artesunate delayed haemolysis (PADH) is thought to occur because of delayed clearance of previously malarial infected erythrocytes spared by ‘pitting’ during treatment.
Yael Benjamin, David Stead
doaj   +1 more source

Targeting B‐Cell‐Activating Factor and Its Receptor in Immune Thrombocytopenia and Warm Autoimmune Hemolytic Anemia

American Journal of Hematology, EarlyView.
ABSTRACT Current treatments for immune thrombocytopenia (ITP) and warm autoimmune hemolytic anemia (wAIHA), rare autoimmune diseases in which autoreactive B cells play a major role, can lead to high response rates; however, for many patients these responses are not durable or maintained after treatment discontinuation.
Matthieu Mahévas, Nichola Cooper, Vickie McDonald, Karina Yazdanbakhsh, Wilma Barcellini   +4 more
wiley   +1 more source