Results 41 to 50 of about 621,963 (341)
Pediatric Liver Transplantation: Then and Now [PDF]
, 2020 This paper reviews the past 50 years of liver transplantation in children from the perspective of patient demographics, perioperative patient management, surgical techniques, immunosuppression and patient ...
Banh, DPT +4 more
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Infections Complicating Orthotopic Liver Transplantation: A Study Emphasizing Graft-Related Septicemia [PDF]
, 1976 In 93 recipients of 102 orthotopic liver homografts, the incidence of bacteremia or fungemia exceeded 70%. The graft itself was usually an entry site for systemic infection after both immunologic and nonimmunologic parenchymal injury, especially if there
Hansbrough, JF +5 more
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Glomerulocystic Kidney Disease and its rare associations: an autopsy report of two unrelated cases
Diagnostic Pathology, 2007 Background Glomerulocystic kidney disease is an uncommon type of cystic renal disease. It is characterized by cortical microsysts, which are represented by cystic dilatation of Bowman's spaces.
Sachdeva Man +2 more
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Modern paradigm in the diagnosis of cystic diseases of the kidneys
PočkiCystic diseases of the kidneys are a fairly common pathology, which has a negative impact on the course of underlying disease affecting the kidneys, or even being the primary renal pathology. The purpose of this review is to analyze the latest literature
I.V. Krasiuk, L.D. Denova, O.V. Karpenko
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Localized renal cystic disease
Indian Journal of Urology, 2015 Localized renal cystic disease (LRCD) is a rare benign non-hereditary, non-progressive condition which must be differentiated from other renal cystic diseases.
Ramakrishna Narayanan +2 more
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Acquired cystic disease and renal cell carcinoma in hemodialysis patients: A case report on three patients [PDF]
Vojnosanitetski Pregled, 2015 Introduction. Renal cell carcinoma (RCC) is derived from renal tubular epithelial cells and represents approximately 3.8% of all malignancies in adults. The incidence of renal cell carcinoma has been growing steadily and ranging from 0.6 to 14.7
Mijušković Mirjana +11 more
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Acquired cystic kidney disease
Kidney International, 1991 A 34-year-old black sales manager was referred for evaluation of azotemia of undetermined duration. He claimed to be in good health except for "borderline" hypertension since age 25. He had no history of urinary tract signs or symptoms. A tumor of unspecified type had been removed from the left anterior chest wall 8 years previously; there had been no ...
openaire +2 more sources
p21 is decreased in polycystic kidney disease and leads to increased epithelial cell cycle progression: roscovitine augments p21 levels. [PDF]
, 2007 BackgroundAutosomal dominant polycystic kidney disease (ADPKD) is a common genetic disease with few treatment options other than renal replacement therapy. p21, a cyclin kinase inhibitor which has pleiotropic effects on the cell cycle, in many cases acts
Anderson, Sharon +6 more
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Nature Genetics, 2013 Although genetic lesions responsible for some mendelian disorders can be rapidly discovered through massively parallel sequencing of whole genomes or exomes, not all diseases readily yield to such efforts.
Andrew W. Kirby +42 more
semanticscholar +1 more source
Cystic fibrosis and renal disease: a case report
Journal of Medical Case Reports, 2007 Background Cystic fibrosis (CF) is an autosomal recessive disease that is predominantly seen in the Caucasian population and involves multiple organs. Traditionally it has been thought that the kidney is the only organ which does not seem to be generally
Al-Shawwa Baha A, Rao Aparna R
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