Results 71 to 80 of about 2,548 (196)
Bone Marrow Oxalosis: Crystal Flowers in the Bone Marrow Garden
Nabhajit Mallik +1 more
doaj +1 more source
Bone health in children with primary hyperoxaluria type 1 following liver and kidney transplantation
BackgroundPrimary hyperoxaluria type 1 is characterized by hepatic oxalate overproduction, leading to nephrocalcinosis, kidney stones, kidney failure and systemic oxalosis, including oxalate osteopathy.
Rainer Büscher +2 more
doaj +1 more source
Background!#!Infantile oxalosis, the most devastating form of primary hyperoxaluria type 1 (PH1), often leads to end-stage renal disease (ESRD) during the first weeks to months of life.!##!Case-diagnosis!#!Here, we report the outcome of the therapeutic ...
Krohne, Tim U. +4 more
core +1 more source
Biogenesis of l-glyceric aciduria, oxalosis and renal injury in rats simulating type II primary hyperoxaluria [PDF]
Tracer experiments in rats mimicking type II primary hyperoxaluria, with an expanded intracellular pool of hydroxypyruvate, showed that the excess formation of oxalate did not originate from its immediate precursor glyoxylate.
M. Lathika, Kunnathattu +6 more
core +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
Objectives Calcium oxalate (CaOx) crystal deposition in acute kidney injury (AKI) patients is under recognized but impacts renal outcomes. This study investigates its determinants and effects.Methods We studied 814 AKI patients with native kidney ...
Weiwei Yang +5 more
doaj +1 more source
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
A 27-year-old man presented with influenza-like symptoms and rapidly progressing respiratory failure requiring mechanical ventilation and venovenous extracorporeal membrane oxygenation on the day of admission.
Salmina J. Guivala +8 more
doaj +1 more source
Kidney Transplantation in Primary Oxalosis: Data From the EDTA Registry [PDF]
This paper reports the results of 98 first kidney transplantations in patients with oxalosis as the primary renal disease as recorded by the EDTA Registry.
Geerlings, W. +10 more
core
Hematological and serum biochemical reference values and cohort analysis in the Gilbert's potoroo (Potorous gilbertii) [PDF]
Hematology and serum biochemistry blood values are tabulated for Australia's most critically endangered mammal, the Gilbert's potoroo (Potorous gilbertii).
Antony J. Friend +13 more
core +1 more source

