Results 31 to 40 of about 65,987 (236)

Combined Hereditary Spherocytosis and β-thalassemia trait: A Rare Co-existence [PDF]

Journal of Clinical and Diagnostic Research, 2018
Haemoglobinopathies are the commonest haemolytic disorders, prevalent in India and form a major bulk of patients in most of the haematology outpatient clinics.
Hanaganahalli Basavaiah Sridevi, Saraswathy Sreeram, Anupama Hegde, Prashantha Balanthimogru, Shrijeet Chakraborti   +4 more
doaj   +1 more source

RETICULOCYTE COUNT TO ASSESS REGENERATIVE RESPONSE IN DOGS WITH IMMUNE MEDIATED HAEMOLYTIC ANAEMIA [PDF]

Journal of Veterinary and Animal Sciences, 2016
Twenty five immune mediated haemolytic anaemia cases confirmed by saline agglutination test and Coombs’ test werevstudied for bone marrow response on the dayvof presentation.
M. Ashwini, N.P. Usha, S. Ajithkumar, P.V. Tresamol, C. Deepa   +4 more
doaj  

Case Report: Haemolytic anaemia with ceftazidime use in a patient with cystic fibrosis [version 1; referees: 2 approved]

F1000Research, 2018
Drug-induced Immune Haemolytic Anaemia (DIIHA) is a rare but serious complication of cephalosporin use. Ceftazidime is recognized to be a rare cause of DIIHA.
Jun Yong, Freddy Frost, Dilip Nazareth, Martin Walshaw   +3 more
doaj   +1 more source

Clinico-Haematological Profile of Hereditary Haemolytic Anaemias in a Tertiary Health Care Hospital in South India [PDF]

Journal of Clinical and Diagnostic Research, 2017
Introduction: Hereditary haemolytic anaemia is a common inherited disorder causing varying degree of morbidity and mortality. This includes disorders due to haemoglobin defect, membrane defect, and enzyme defect.
Chaitra Venkataswamy, AM Shanthala Devi
doaj   +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

Development Of Haemolytic Uremic Syndrome İn Renal Transplant Recipient: Typhoid Fever; A Case Report And Brief Summary Of The Literature.

Southern Clinics of Istanbul Eurasia, 2019
Haemolytic Uremic Syndrome (HUS) is characterized by microangiopathic haemolytic anaemia, thrombocytopenia and acute renal failure. Typhoid fever caused by salmonella typhi, a systemic infectious disease which affects many organs, is rarely encountered ...
Yasemin Özgür, Seher Tanrıkulu, Zeynep Ece Demirbaş, Yasemin Kaldırım, Murat Gücün, Gülizar Şahin   +5 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 after valvuloplasty and annuloplasty

, 2010
Haemolytic anaemia is a well-recognised but rare complication of heart-valve prostheses. The authors report a case of an 80-year-old woman with severe haemolytic anaemia previously treated with valvuloplasty and annuloplasty without rings.
P. Delva, L. Pozzani, S. Al Zeer, DELVA, Pietro, A. Lechi, DALBENI, Andrea, A. Dalbeni   +6 more
core   +1 more source

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

Vitamin B12 deficiency: an unusual presentation. Case report

Portuguese Journal of Pediatrics, 2023
Vitamin B12 or cobalamin is a water-soluble vitamin absorbed in the terminal ileum after binding to intrinsic factor and has important physiologic roles in haematopoiesis, intermediary metabolism, growth, and early brain development.
Inês Martins, Joana Faustino, Lígia Paulos, Ana S. Nicolau, Sofia Fernandes   +4 more
doaj   +1 more source