Results 111 to 120 of about 33,878 (223)

Adult hemolytic-uremic syndrome

Kidney International, 1980
A 17-year-old male was transferred to the New England Medical Center Hospital (NEMCH) for evaluation of acute renal failure following a 5-day episode of nausea and vomiting. During a routine examination 3 months earlier, his blood pressure had been 98/64 mm Hg and laboratory findings included a hematocrit of 40% and a white blood cell count of 8700 mm3
openaire   +2 more sources

Frequency and Significance of HIV Infection among Patients Diagnosed with Thrombotic Thrombocytopenic Purpura [PDF]

, 2017
Background. Case series of patients with a diagnosis of thrombotic thrombocytopenic purpura (TTP) have reported different frequencies of human immunodeficiency virus (HIV) infection; some series suggest that HIV infection may cause TTP. Methods.
Benjamin, Melody, Dezube, Bruce J., George, James N., Kremer Hovinga, Johanna A., Lämmle, Bernhard, Terrell, Deirdra R., Vesely, Sara K., Voskuhl, Gene W.   +7 more
core  

Vitamin B12 Deficiency with Pseudothrombotic Microangiopathy and Thrombotic Thrombocytopenic Purpura: Similarities and Differences [PDF]

, 2020
Buess, Charles, Germann, Alexander, Maloney, Eamon, Mohammed, Alaeldin   +3 more
core   +2 more sources

Hemolytic Uremic Syndrome Associated with Pneumococcal Pneumonia. A Case Report

Medisur, 2013
Hemolytic uremic syndrome is a condition characterized by hemolytic microangiopathic anemia, thrombocytopenia and acute renal failure. In its classic form it is associated with diarrhea and it has a good prognosis.
Ariel Efrén Uriarte Méndez, Andrés Prieto Apesteguía, Jesús Vila Díaz, Jorge Luis Capote Padrón, Kendrie Villavicencio Cardoso, Alnilam Fernández González   +5 more
doaj   +2 more sources

Atypical hemolytic-uremic syndrome, manifesting without thrombocytopenia (clinical case)

Известия высших учебных заведений. Поволжский регион: Медицинские науки
Background. Atypical hemolytic uremic syndrome is an ultra-rare (orphan) disease from the group of thrombotic microangiopathies of progressive course, which is caused by uncontrolled activation of the alternative complement pathway of hereditary or ...
A.A. Dyachkova, A.N. Anokhin, M.A. Shlykova, I.S. Kiseleva   +3 more
doaj   +1 more source

Administração profiláctica de plasma no síndrome hemolítico urémico atípico recorrente [PDF]

, 2006
O síndrome hemolítico urémico (SHU) define- se pela ocorrência simultânea de anemia hemolítica microangiopática, trombocitopenia e insuficiência renal aguda.
Almeida, Marta Pinto de, Barbot, José, Costa, Elísio, Costa, Elísio, Costa, Teresa, Faria, Maria Sameiro, Mota, Conceição, Pereira, Elói   +7 more
core  

Concurrent Atypical Hemolytic Uremic Syndrome and Autoimmune Hemolytic Anemia: a case report

Caspian Journal of Pediatrics, 2018
Background: Atypical hemolytic uremic syndrome (aHUS) is a life-threatening and scarce disorder characterized by acute renal failure and disease, non-immune microangiopathic hemolytic anemia and thrombocytopenia, leading to end-stage renal failure or ...
Sayed Yousef Mojtahedi, Mohammad Kaji Yazdi   +1 more
doaj  

A Case of Carfilzomib-Induced Atypical Hemolytic Uremic Syndrome

Annals of Internal Medicine: Clinical Cases
Atypical hemolytic uremic syndrome (aHUS) is a rare non-Shiga toxin thrombotic microangiopathy caused by uncontrolled activation of the alternative complement pathway.
Kwasi Opare-Addo, Sammudeen Ibrahim, Basilio Addo, Jorge Chancay Rodriguez   +3 more
doaj   +1 more source

Evaluation of Hypertension in Pediatric Hemolytic Uremic Syndrome (A Cross-Sectional Study). [PDF]

Health Sci Rep
Nourmohammadi MB, Askarian F, Abbasi A, Bazargani B, Fahimi D, Moghtaderi M.   +5 more
europepmc   +1 more source

Importance of case age in the purported association between phylogenetics and hemolytic uremic syndrome in Escherichia coli O157:H7 infections [PDF]

, 2018
Besser, T.E., Mayer, J., Oltean, H.N., Phipps, A.I., Rabinowitz, P., Shringi, S., Tarr, G.A.M., Tarr, P.I., Wakefield, J.   +8 more
core   +1 more source