Results 61 to 70 of about 2,344 (196)
ABSTRACT Background Alemtuzumab can be an alternative to rabbit anti‐thymocyte globulin (rATG) to treat severe or glucocorticoid‐resistant acute T cell‐mediated kidney transplant rejection (TCMR). Yet, there are few reports in which these two treatments are evaluated let alone, compared.
Lukas K. van Vugt +9 more
wiley +1 more source
Kidney transplantation in primary oxalosis
A 33 yr old patient with primary oxalosis was submitted to cadaver kidney transplantation after 15 mth treatment by hemodialysis. During the dialysis period, he developed complete heart block which immediately followed bilateral nephrectomy.
Toussaint, Charles +2 more
core
Abstract Nephrocalcinosis is a complex disease with a multitude of triggering factors. An association with congenital hypothyroidism has been described in the literature, but the mechanisms leading to its development remain unclear. A 7‐month‐old infant presented with muscular hypotonia and signs of malnutrition was diagnosed with congenital ...
Omar Zgheib +5 more
wiley +1 more source
Primary oxalosis with pan-conduction cardiac disease: electrophysiologic and anatomic correlation.
A 27-year-old man with primary oxalosis and extensive visceral involvement was maintained on long-term chronic hemodialysis. He had an episode of presyncope associated with electrocardiographic findings of an erratic atrial rhythm, atrioventricular ...
B M Massie +6 more
core +1 more source
Oral manifestations of oxalosis: A case report and review of the literature
Primary hyperoxaluria (PH) is a metabolic autosomal recessive disease that causes an error in oxalate metabolism. In 1957, Archer et al(1) introduced the term primary hyperoxaluria. Two types are known.
Oosterhuis, Wolter +3 more
core +1 more source
Bone Marrow Oxalosis: Crystal Flowers in the Bone Marrow Garden
Nabhajit Mallik +1 more
doaj +1 more source
Uremia associated with renal oxalosis in a cat
Renalna oksaloza obilježena je nakupljanjem kristala kalcijeva oksalata u bubrezima što rezultira degeneracijom i nekrozom tubularnih stanica, intersticijskim nefritisom i sklerozom bubrega.
Huber, Doroteja, Doroteja Huber
core
A case of neonatal renal oxalosis in a 7-day-old calf is described. Clinical biochemistry revealed increased blood urea nitrogen. Gross findings included thin renal medulla and dilated renal calyces containing numerous, small, pale yellow and granular ...
Kaya, A, Golen, I, Gulbahar, MY
core
Inborn errors of metabolism cause increase of metabolites in serum and their deposition in various organs including bone marrow. Primary hyperoxaluria (PH) is a rare inborn error in the pathway of glyoxylate metabolism which causes excessive oxalate ...
Pardis Nematollahi +1 more
doaj +1 more source
Extreme intrafamilial variability of Saudi brothers with primary hyperoxaluria type 1
Majid Alfadhel,1 Khalid A Alhasan,2 Mohammed Alotaibi,3 Khalid Al Fakeeh41Division of Genetics, Department of Pediatrics, King Saud bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Riyadh, Saudi Arabia; 2Division of Nephrology ...
Alfadhel M +3 more
doaj

