Results 111 to 120 of about 6,612,749 (247)

Delayed hemolytic anemia after artemether-lumefantrine in Plasmodium falciparum malaria: A case report

open access: yesInternational Journal of Infectious Diseases
Delayed hemolytic anemia (DHA) is a rare, severe complication of artemisinin-based therapies. We report a case of DHA following an extended course of oral artemether–lumefantrine (AL) in a 50-year-old male with follicular lymphoma treated with rituximab ...
Oğuz Usta   +3 more
doaj   +1 more source

From Undifferentiated Connective Tissue Disease to Common Variable Immunodeficiency: A Novel NFKB1 Mutation in a Pediatric Case

open access: yesClinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT Common variable immunodeficiency (CVID) may initially manifest as undifferentiated connective tissue disease (UCTD) in the absence of recurrent infections or hypogammaglobulinemia. In patients presenting with warning signs, neither older age nor normal immunoglobulin levels should preclude consideration of CVID; early genetic testing is ...
Yu‐Jie Hu   +4 more
wiley   +1 more source

Pancreatitis and Myocardial Infarction as Complications of Thrombotic Thrombocytopenic Purpura: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT Thrombotic thrombocytopenic purpura (TTP) is a rare disease with a mortality rate of 90% if not treated promptly. Due to limited clinical experience and sometimes atypical presentation, early detection of TTP is not always easy. The pathophysiological mechanisms underlying TTP can accelerate thrombus formation and vascular occlusion ...
Farid Poursadegh   +3 more
wiley   +1 more source

Family Sculpture with Playmobil Pieces

open access: yes
Mit dem FSPlay werden innere "Arbeitsmodelle" (Schemata) von Bindungs-/Familien-/Partnerschafts-/Freundschaftsbeziehungen erhoben. Anhand mehrerer Spielfiguren sollen eine oder mehrere Skulpturen gestaltet werden, z. B.
Sydow, K. v.
core   +1 more source

TTP‐Like Syndrome and Subsequent Non‐Aneurysmal Subarachnoid Hemorrhage in HbSC Disease: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT Sickle cell disease (SCD) with hemoglobin‐ (Hb‐) SC genotype is often considered a milder SCD variant, yet life‐threatening complications can occur. A 26‐year‐old man with HbSC disease presented with an infection triggered vaso‐occlusive crisis (VOC), acute chest syndrome (ACS), severe thrombocytopenia, Coombs‐negative hemolysis with ...
Benjamin Vieten   +9 more
wiley   +1 more source

Introducing Microcells into Macrocellular Networks: A Case Study

open access: yes, 1999
?The performance in terms of signal-to-interference ratio (SIR), teletraffic, and spectral efficiency of a combined macrocellular and microcellular network is investigated when either both types of cells share the same channel set, or when the channel ...
Steele, R, Coombs, R
core   +1 more source

Correlation between maternal parity and ABO hemolytic disease of the fetus and newborn

open access: yesZhongguo shuxue zazhi
[Objective] To investigate the correlation between maternal parity and ABO hemolytic disease of the fetus and newborn (ABO-HDFN). [Methods] A total of 244 neonates diagnosed with ABO-HDFN who were admitted to the neonatology department of of our hospital
YANG Li, LIU Wei, ZHAO Yuan, LI Daihong
doaj   +1 more source

ECR-G-10. Experiences in Close Relationships Scale - German 10-Item Short Form

open access: yes
Der ECR-G-10, die Kurzform des Bochumer Bindungsfragebogens (BoBi), erfasst mit 10 Items das Erleben und Verhalten in der partnerschaftlichen Bindung im Erwachsenenalter und wurde auf der Grundlage des zweidimensionalen Modells von Bindung, das zwischen ...
Rohmann, E., Sattel, H., Neumann, E.
core   +1 more source

Severe Macrocytic Anemia Associated With a Novel ALAS2 Mutation: A Case Report and Literature Review

open access: yesClinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT X‐linked sideroblastic anemia (XLSA), caused by pathogenic variants in ALAS2, typically presents as microcytic anemia in males. However, heterozygous females occasionally exhibit an atypical macrocytic phenotype, often leading to diagnostic ambiguity and confusion with nutritional anemias or myelodysplastic syndromes.
Haodong Cai   +5 more
wiley   +1 more source

The prevalence of erythrocyte alloimmunization in clinical practice: A hospital-based study

open access: yesIraqi Journal of Hematology
BACKGROUND: One of the complications of blood transfusion is the development of red cell alloimmunization. Little published literature on the prevalence and actual significance of red cell alloantibodies among nonregularly transfused patients and the ...
Inas Bashar Faisal   +4 more
doaj   +1 more source

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