Results 181 to 190 of about 33,878 (223)
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Oncology Nursing Forum, 2008
A.P., a 42-year-old woman, presented with rectal bleeding to her primary care physician. Endoscopic examination revealed a mass in the anal canal. Biopsy was positive for squamous cell carcinoma. A.P. underwent local excision and was established as stage ii (T2n0m0).
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A.P., a 42-year-old woman, presented with rectal bleeding to her primary care physician. Endoscopic examination revealed a mass in the anal canal. Biopsy was positive for squamous cell carcinoma. A.P. underwent local excision and was established as stage ii (T2n0m0).
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Nephron, 1973
The clinical and pathological characteristics of the acute stage of the HUS are described on the basis of 678 patients and the study of 52 autopsies and 3 kidney biopsies.
C A, Gianantonio +4 more
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The clinical and pathological characteristics of the acute stage of the HUS are described on the basis of 678 patients and the study of 52 autopsies and 3 kidney biopsies.
C A, Gianantonio +4 more
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Pediatric Clinics of North America, 1976
It is becoming increasingly apparent that the hemolytic uremic syndrome is a heterogenic and heterogeneous syndrome. There has been a dramatic reduction in the number of patients who die in the acute phase of the illness. Any claims for the use of heparin and streptokinase must be measured against the improved results which are now being obtained with ...
B S, Kaplan +2 more
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It is becoming increasingly apparent that the hemolytic uremic syndrome is a heterogenic and heterogeneous syndrome. There has been a dramatic reduction in the number of patients who die in the acute phase of the illness. Any claims for the use of heparin and streptokinase must be measured against the improved results which are now being obtained with ...
B S, Kaplan +2 more
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Hemolytic-Uremic Syndrome Colitis
Journal of Clinical Gastroenterology, 1980The hemolytic-uremic syndrome has varied prodromal symptoms. In a few patients the dominant initial gastrointestinal symptoms have led to a presumptive diagnosis of ulcerative colitis. The colitis tends to be self-limited, to have minimal lesions detected by proctoscopic or roentgenographic studies, and usually to resolve spontaneous without specific ...
R S, Yates, R K, Osterholm
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Atypical Hemolytic–Uremic Syndrome
New England Journal of Medicine, 2009The hemolytic–uremic syndrome, which is characterized by nonimmune hemolytic anemia, thrombocytopenia, and renal impairment, occurs most frequently in young children. Most cases are secondary to infection with Escherichia coli O157:H7 and other Shiga-toxin–producing strains.
Marina Noris, Giuseppe Remuzzi
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The Journal of Pediatrics, 1972
IN 1955 Gasser and his associates1 introduced the term hemolytie-uremic syndrome to describe 5 children with a fatal disease characterized by acute renal failure, hemolytic anemia and thrombocytopenia. They considered that the severe renal disease distinguished the disorder in their patients from the disorder called thrombotic thrombocytopenic purpura ...
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IN 1955 Gasser and his associates1 introduced the term hemolytie-uremic syndrome to describe 5 children with a fatal disease characterized by acute renal failure, hemolytic anemia and thrombocytopenia. They considered that the severe renal disease distinguished the disorder in their patients from the disorder called thrombotic thrombocytopenic purpura ...
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Pediatric Blood & Cancer, 2011
AbstractWe describe three children who developed isolated but severe microangiopathic hemolytic anemia without other manifestations of hemolytic uremic syndrome (HUS) or thrombotic thrombocytopenic purpura (TTP). All three recovered without specific treatment.
Kenneth S, Chen +3 more
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AbstractWe describe three children who developed isolated but severe microangiopathic hemolytic anemia without other manifestations of hemolytic uremic syndrome (HUS) or thrombotic thrombocytopenic purpura (TTP). All three recovered without specific treatment.
Kenneth S, Chen +3 more
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The hemolytic uremic syndromes
Current Opinion in Critical Care, 2005Recent studies have provided a better understanding of the molecular mechanisms responsible for hemolytic uremic syndromes. In this review, we summarize biochemical and genetic data that may lead to new clinical approaches.The structures and modes of action of Shiga toxins have been deciphered.
Jessica, Caprioli +2 more
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Atypical hemolytic uremic syndrome
Current Opinion in Hematology, 2010The last few years revealed a molecular distinction between thrombotic thrombocytopenic purpura, a disease characterized by a lack of ADAMTS13 activity, and atypical hemolytic uremic syndrome (aHUS), a disease of complement overactivation. Many different predisposing genetic factors resulting in complement overactivation have been described in aHUS ...
Kavanagh D, Goodship THJ
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Recurrent Hemolytic Uremic Syndrome
Clinical Pediatrics, 2002Hemolytic uremic syndrome (HUS) in children follows a diarrheal prodrome (D+) approximately 90% of the time, and recurrence due to enteric reinfection with Shiga toxin producing E. coli (e.g., 0157:H7) can occur but is rare. It is not well recognized that nondiarrheal (D-) recurrences can also follow an episode of D+ HUS; we report 2 unrelated females
Richard L, Siegler +2 more
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