Results 71 to 80 of about 59,391 (246)

Acute ketone monoester ingestion lowers resting cerebral blood flow: a randomized cross‐over trial

The Journal of Physiology, EarlyView.
Abstract figure legend This double‐blind, placebo‐controlled, randomized cross‐over trial investigated the effects of ketone monoester (KME) ingestion on resting cerebral blood flow (CBF) in young adults. We demonstrate that KME supplementation lowers CBF in a dose‐dependent manner over 2‐houra post‐ingestion, whereas CBF remained unchanged following ...
Aedan J. Rourke, Claudia M.S. Yong, Geoff B. Coombs, Addriana R. Odisho, Jenna A. Nash, Jack Bone, Baraa K. Al‐Khazraji, Jeremy J. Walsh   +7 more
wiley   +1 more source

Autoimmune hemolytic anemia with negative Coombs test

Revista de Ciencias Médicas de Pinar del Río, 2017
Introduction: autoimmune hemolytic anemia is a type of low-grade acquired hemolytic anemia, produced by antibodies against the patient's own erythrocytes leading to their destruction.   Case report: a 12 year-old female patient arrived in the emergency
Juan Manuel Acosta Piloto, César Valdés Sojo   +1 more
doaj  

Iptacopan for Immune Thrombocytopenia and Cold Agglutinin Disease: A Global Phase 2 Basket Clinical Trial

American Journal of Hematology, Volume 101, Issue 2, Page 242-254, February 2026.
ABSTRACT Iptacopan is a first‐in‐class, oral, selective inhibitor of complement factor B that has demonstrated positive efficacy across several complement‐driven diseases. Here we evaluate the efficacy and safety of iptacopan monotherapy in adult patients with primary immune thrombocytopenia (ITP) and primary cold agglutinin disease (CAD). We performed
Alexander Röth, Wilma Barcellini, Christine Ademokun, Junho Jang, Maria Luisa Lozano, David Valcarcel Ferreiras, Cristina Pascual‐Izquierdo, Shripad Chitnis, Sofiya Matviykiv, Alessandra Vitaliti, Chi Chen, Vasiliki Katsanou, Raghav Chawla, Hanny Al‐Samkari   +13 more
wiley   +1 more source

Primary Sjogren’s syndrome presenting as autoimmune cytopenia

Clinics and Practice, 2019
Sjogren’s syndrome (SS) is a chronic systemic autoimmune disease, characterized by lymphocytic infiltration of lacrimal and salivary glands. Although extra glandular manifestations are uncommon, they can occur with the musculoskeletal, renal, pulmonary ...
Durga Shankar Meena, Gopal Krishana Bohra   +1 more
doaj   +1 more source

Miliary Tuberculosis With Immune Thrombocytopenia in 50‐Year‐Old Ethiopian Woman: A Case Report and Brief Review of Literature

Clinical Case Reports, Volume 14, Issue 2, February 2026.
Diffuse petechiae and non‐palpable purpura (lower extremities below knee, admission photo). ABSTRACT Immune thrombocytopenia (ITP) is a rare but recognized hematologic complication of tuberculosis (TB), particularly miliary TB. We present a case of a 50‐year‐old female with severe thrombocytopenia and hemorrhagic manifestations secondary to miliary TB.
Hayatu Awel Abdela, Tamirat Godebo Woyimo, Ragasa Getachew Bayisa, Sisay Tagese Tafese   +3 more
wiley   +1 more source

HEREDITARYSPHEROCYTOSIS DIAGNOSED IN 16 YEAR FEMALE- ACASE REPORT [PDF]

Perspectives In Medical Research, 2019
Hereditary Spherocytosis (HS) is relatively common haemolytic anemia in which basic abnormality is an intrinsic defect of red cell membrane. Clinically patients may asymptomatic to intermittent jaundice,anemia, abdominal pain and splenomegaly.
Majed B Momin1 , Anamika Aluri2
doaj  

Letter regarding “Effect of dilution of canine blood samples on the specificity of saline agglutination tests for immune‐mediated hemolysis,” original and modified saline agglutination tests vs direct Coombs’ tests [PDF]

, 2021
Urs Giger
openalex   +1 more source

Concurrent Scrub Typhus, Dengue, and Leptospirosis: A Rare Triple Co‐Infection: A Case Report and Comprehensive Literature Review

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT In endemic areas, acute undifferentiated febrile illness has a wide differential with overlapping features that can lead to misdiagnosis. Although triple co‐infection with scrub typhus, dengue, and leptospirosis is extremely rare, high clinical suspicion and early detection are vital to avoid delayed treatment, multi‐organ dysfunction, and ...
Sulav Kumar Jha, Bistrit Dahal, Anamika Adhikari, Kushal Singh Basnet, Shivaditya Singh, Manaswi Acharya   +5 more
wiley   +1 more source

Maternal-fetal isoimmunization – a risk for the development of hemolytic disease of the newborn [PDF]

Pharmacia
Hemolytic disease of the newborn is a condition caused by maternal alloimmunization against fetal red blood cell antigens. Transplacental hemorrhage, for example, can provoke an immune response in the mother.
Maria Hristova Savcheva, Angelina Georgieva Kirkova-Bogdanova, Maria Stamova Vakrilova Becheva, Yozlem Ali Kobakova, Maria Georgieva Moneva-Sakelarieva, Stefka Achkova Ivanova, Maria Sevdelinova Chaneva, Ventseslava Petrova Atanasova, Yonko Tsvetanov Yonchev, Radoslav Fedeev Todorov, Nikolay Zarkov Bashev, Ismail Elhanov Bashov, Diana Nikolaeva Teneva, Silviya Milchova Pavlova, Konstantin Ivanov Kostov, Kiril Todorov Atliev, Petar Yordanov Atanasov, Adel Habib Ibrahim, Pavel Bogdanov Pavlov   +18 more
doaj   +3 more sources

A rare case of immune hydrops in an “Elevated D” pregnancy

Global Journal of Transfusion Medicine, 2020
The D-/-phenotype is a rare variant of the Rh system, in which red blood cells express only D antigen. Sensitized D-/-women carry a risk of hemolytic disease of fetus and newborn (HDFN) and pose a challenge in management due to nonavailability of antigen
Amit Kumar Biswas, Anantpreet Kaur Bajaj, Joseph Philip, Neerja Kushwaha   +3 more
doaj   +1 more source