Results 121 to 130 of about 25,762 (279)
Pediatric nephrology (Berlin, West), 2020 Atypical hemolytic uremic syndrome (aHUS) is a rare, complement-mediated disease associated with poor outcomes if untreated. Ravulizumab, a long-acting C5 inhibitor developed through minimal, targeted modifications to eculizumab was recently approved for
Kazuki Tanaka +7 more
semanticscholar +1 more source
Evaluation of Hypertension in Pediatric Hemolytic Uremic Syndrome (A Cross‐Sectional Study)
Health Science Reports, Volume 8, Issue 11, November 2025.ABSTRACT Background Hemolytic uremic syndrome (HUS), particularly the Shiga toxin‐producing Escherichia coli (STEC)‐associated subtype, is a major cause of acute kidney injury [AKI] in children. Although hypertension (HTN) is a recognized complication of HUS, its prevalence and related risk factors in these children are particularly poorly studied ...
Mahdi Banaei Nourmohammadi +5 more
wiley +1 more source
Atypical Hemolytic Uremic Syndrome
Advances in Pediatrics, 2014 Kaan GÜLLEROĞLU +2 more
+8 more sources
Intravascular Large B-Cell Lymphoma Presenting as Dementia and Hemolytic Anemia [PDF]
, 2010 Background: Intravascular lymphoma (IVL) is an uncommon disease characterized by atypical lymphoid cells growing inside the lumina of small vessels. The diversity of clinical presentation due to possible involvement of multiple organs often complicates ...
Ahle, Guido +6 more
core +1 more source
Veterinary Medicine and Science, Volume 11, Issue 6, November 2025.GRAPHICAL ABSTRACT Camel milk exhibited Staphylococcus aureus and Escherichia coli contamination with associated antibiotic resistance and virulence genes. Concurrently, heavy metal levels (Pb, As and Cd) in these samples were low and below safety limits, providing a comprehensive assessment of dual hazards in this vital food source.
Elahe Yazdanian Ghahfarokhi +3 more
wiley +1 more source
Clinical case of thrombotic microangiopathy in obstetric practice
Сеченовский вестник, 2017 Trombotic microangiopathy is heterogeneous group of the diseases united by a community of a histological and clinical implications at difference of pathogenetic mechanisms, presents clinical-morphological syndrome characterizing a lesion of vessels of a ...
M. N. Mochalova +5 more
doaj
Hemolytic uremic syndrome and IgA nephropathy in a child: Coincidence or not?
The Turkish Journal of Pediatrics, 2018 A previously healthy 18-month old boy, presenting with diarrhea, anemia, thrombocytopenia and acute renal failure was admitted to our hospital. Hemolytic uremic syndrome (HUS) was diagnosed with his clinical and laboratory findings.
Serra Sürmeli-Döven +7 more
doaj +1 more source
The global aHUS registry: methodology and initial patient characteristics [PDF]
, 2015 Background: Atypical hemolytic uremic syndrome (aHUS) is a rare, genetically-mediated systemic disease most often caused by chronic, uncontrolled complement activation that leads to systemic thrombotic microangiopathy (TMA) and renal and other end-organ ...
Ardissino, Gianluigi +11 more
core +2 more sources
Immunology, Volume 176, Issue 3, Page 363-372, November 2025.The membrane attack complex (MAC) is formed by the stepwise assembly of five proteins: C5b, C6, C7, C8 and C9. MAC plays a key role in driving inflammation in numerous diseases. This study compares the inhibitory mechanisms of MAC assembly by soluble CD59 (sCD59), a disulphide‐locked C9 mutant (C9lock) and horse C9 (HoC9).
Rebekah S. Cooke +5 more
wiley +1 more source
A Case of Carfilzomib-Induced Atypical Hemolytic Uremic Syndrome
Annals of Internal Medicine: Clinical CasesAtypical hemolytic uremic syndrome (aHUS) is a rare non-Shiga toxin thrombotic microangiopathy caused by uncontrolled activation of the alternative complement pathway.
Kwasi Opare-Addo +3 more
doaj +1 more source