Results 31 to 40 of about 246,759 (191)

Paroxysmal cold hemoglobinuria in a 7-year-old male child – Was it really cold induced? A diagnostic and management dilemma

Pediatric Hematology Oncology Journal, 2021
Paroxysmal cold haemoglobinuria (PCH) is a rare acquired cause of intravascular haemolysis in children. We are reporting an unusual case of PCH, a 7-year-old boy who presented with acute febrile illness, severe anaemia and passage of red colored urine ...
Akash Kumar, Siyaram Didel, Daisy Khera, Anubhav Gupta, Abhishek Purohit   +4 more
doaj   +1 more source

AUTOIMMUNE HAEMOLYTIC ANAEMIA: A SYSTEMATIC REVIEW [PDF]

, 2021
Autoimmune haemolytic anaemia (AIHA) is a rare and heterogeneous haematological disorder. The diagnostic criteria of AIHA have been debatable and not clearly defined. We performed a systematic review to evaluate the various definitions of AIHA.
Ahmad Adni Ahmad Tajuddin, Kyaw Ko Latt, Wahinuddin Sulaiman, Rizfan Rapidai, Muhammad Arsyad Muhammad Wira   +4 more
core   +1 more source

Myasthenia gravis with thymoma and autoimmune haemolytic anaemia. A case report [PDF]

, 2003
Myasthenia gravis is an autoimmune disorder that affects the neuromuscular junction and leads to weakness of the skeletal muscles. Associated autoimmune diseases such as systemic lupus erythematosus, rheumatoid arthritis and pernicious anaemia are ...
TANRIDAĞ, TÜLİN
core   +1 more source

Evans syndrome in children below 13 years of age - A nationwide population-based cohort study.

PLoS ONE, 2020
Evans syndrome is defined by autoimmune haemolytic anaemia and immune thrombocytopenia occurring in the same patient. Although known to be rare the frequency and prognosis of Evans syndrome in children is unknown, and only few registry-based studies are ...
Nikolaj Mannering, Dennis Lund Hansen, Henrik Frederiksen   +2 more
doaj   +1 more source

Rare Offshoot of a Common Malady Anaemia and Tuberculosis [PDF]

Journal of Clinical and Diagnostic Research, 2016
Haematological manifestations are one of the rarer presentations of tuberculosis and are usually of normocytic normochromic type. An association of Autoimmune Haemolytic Anaemia (AIHA) with active pulmonary tuberculosis is an exceeding rare entity ...
Gautham Kolla, Vishak Acharya, Prashantha Balanthimogru, Arun Mani, Shehzad Ruman   +4 more
doaj   +1 more source

Coombs-Negative Haemolytic Anaemia, Direct Hyperbilirubinaemia and Splenomegaly: A Rare Amalgam

European Journal of Case Reports in Internal Medicine, 2021
Introduction: Epstein-Barr virus (EBV) is notorious for its varied presentation in adults. Reactivation of EBV can occur at any time and is often due to weakened cellular immunity.
Radhika Kulkarni, Amjad Basheer, Aziz Khan   +2 more
doaj   +1 more source

Targeted next-generation sequencing revealed a novel homozygous mutation in the LRBA gene causes severe haemolysis associated with Inborn Errors of Immunity in an Indian family.

Hematology, 2022
Objectives LPS-responsive beige-like anchor protein (LRBA) deficiency abolishes LRBA protein expression due to biallelic mutations in the LRBA gene that lead to autoimmune manifestations, inflammatory bowel disease, hypogammaglobulinemia in early stages,
Prabhakar Kedar, Rashmi Dongerdiye, Shanmukhaiah Chandrakala, Umair Ahmed Bargir, Manisha Madkaikar   +4 more
doaj   +1 more source

Beyond Nature's Blueprint: Macrocyclic Peptides Containing Unnatural Amino Acids in Therapeutic Development

Angewandte Chemie, EarlyView.
Strategic incorporation of unnatural amino acids transforms macrocyclic peptides into drug‐like molecules capable of engaging challenging targets. These building blocks enhance stability, permeability, and bioavailability, accelerating the development of next‐generation peptide therapeutics.
Krishna K. Sharma, Komal Sharma, Anku Sharma, Kamya Rao, Rahul Jain, Brett VanVeller   +5 more
wiley   +2 more sources

Primary autoimmune haemolytic anaemia and coeliac disease

, 2004
Primary autoimmune haemolytic anaemia and coeliac ...
M. Gabrielli, A. Gasbarrini, Santarelli, Luca, GIRELLI, Gabriella, G. Merra, Merra, Giuseppe, Villita, Alessia, P. Pola, M. Candelli, E. C. Nista, A. Villita, L. Santarelli, Gabrielli, Maurizio, Gasbarrini, Antonio, G. Gasbarrini, Gasbarrini, Giovanni Battista, Candelli, Marcello, Pola, Paolo, F. Cremonini, Cremonini, Filippo, F. Franceschi, Franceschi, Francesco   +21 more
core   +1 more source

A Case Report: Autoimmune Haemolytic Anaemia & Paroxysmal Nocturnal Haemoglobinuria Association

Haematology Journal of Bangladesh
Autoimmune haemolytic anaemia (AIHA) and paroxysmal nocturnal haemoglobinuria (PNH) are two distinct causes of haemolytic anaemia. They have different mechanisms that underpin their pathogenesis and, therefore, require different treatment strategies ...
Fatima- Tuz- Zohra, Abu Hasan Rubel, Mohd. Tariqul Islam, Md. Sirazul Islam   +3 more
doaj   +1 more source