Results 1 to 10 of about 5,377 (188)
Imbalance of mitochondria and abnormalities in lipid metabolism in Diabetic Tubulopathy [PDF]
Annals of MedicineDiabetic kidney disease (DKD) is a common and serious microvascular complication in patients with diabetes. In recent years, diabetic tubulopathy has emerged as a major research focus, as its prognosis is closely associated with tubular atrophy and ...
Chenchen Sun +5 more
doaj +3 more sources
Apolipoprotein E-associated Lipoprotein Glomerulo-tubulopathy
Internal Medicine, 2023 A 32-year-old man was admitted for the evaluation of proteinuria (5.69 g/day). A light microscopic examination showed markedly dilated glomerular capillary loops with vacuolated areas in many glomeruli, and vacuolated areas were seen on peritubular capillaries in the tubulointerstitium.
Hikaru Tanimizu +16 more
openalex +4 more sources
Exome Sequencing in Saudi Arabian Pediatric Kidney Disease Single-Center Cohort [PDF]
Kidney International ReportsIntroduction: In pediatric patients, monogenic causes are a significant contributor to kidney disease, ranging from approximately 10% in congenital anomalies of the kidney and urinary tract (CAKUT) to about 55% in renal ciliopathies. Exome sequencing has
Katharina Lemberg +23 more
doaj +2 more sources
Kidney Medicine, 2022 Acute kidney injury is a known complication of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection for which many different pathophysiological processes have been reported.
Peter Fahim +3 more
doaj +2 more sources
Light-chain proximal tubulopathy: a retrospective study from a single Chinese nephrology referral center [PDF]
Renal FailureBackground Light-chain proximal tubulopathy (LCPT) is a rare disease characterized by the accumulation of monoclonal light chains within proximal tubular cells.
Xin Wang +4 more
doaj +2 more sources
Amyloid proximal tubulopathy: a novel form of light chain proximal tubulopathy [PDF]
Clinical Kidney Journal, 2012 Light chain proximal tubulopathy is a paraproteinemic-related kidney disease most commonly seen in patients with a plasma cell dyscrasia. The classic description is that of proximal tubules with kappa-restricted intracytoplasmic crystals in a patient with a clinical Fanconi's syndrome.
Christian P. Larsen +2 more
openalex +3 more sources
Gitelman and Bartter Syndrome in a Patient With Morbid Obesity: A Case Report and Literature Review [PDF]
Clinical Case ReportsWe present a case study of a 34‐year‐old man with morbid obesity and a suspected Bartter–Gitelman spectrum tubulopathy (without genetic confirmation), weighing 135 kg, and with a BMI of 42.5 kg/m2, who was referred to the metabolic and bariatric surgery ...
Solmaz Hasani +4 more
doaj +2 more sources
Distal Tubulopathy. Liddle Syndrome
Педиатрическая фармакология, 2019 The clinical recommendations on management of children with Liddle syndrome which is characterized by severe hypertension along with low activity levels of renin and aldosterone in blood plasma, hypokalemia and metabolic alkalosis, were developed by the ...
Alexander A. Baranov +15 more
doaj +3 more sources
Distal Tubulopathy. Gitelman Syndrome
Педиатрическая фармакология, 2019 The clinical recommendations on management of children with Gitelman syndrome developed by the experts of the Union of pediatricians of Russia are presented in this article.
Alexander A. Baranov +15 more
doaj +3 more sources
Bartter Syndrome Presenting with Metabolic Alkalosis: A Case Series [PDF]
Journal of Clinical and Diagnostic Research, 2023 Bartter Syndrome (BS) is a rare, inherited renal tubulopathy characterised by hypokalaemic, hypochloraemic metabolic alkalosis. Children present with the complaint of polyuria, dehydration, failure to thrive and normal blood pressure despite ...
Gulam Mohammed
doaj +1 more source