Results 161 to 170 of about 2,548 (196)
Some of the next articles are maybe not open access.

Bone Scintigraphy in Oxalosis

Clinical Nuclear Medicine, 1993
Several physiologic and pathologic conditions demonstrating extraosseous localization of bone scanning agents have been described, including metastatic calcification of the soft tissues secondary to metabolic disorders, malignancies, and chronic renal failure.
S, Murthy   +4 more
openaire   +2 more sources

Hand manifestations of oxalosis

The Journal of Hand Surgery, 1993
Oxalosis is an unusual metabolic disease that results either from an inherited hepatic enzyme deficiency or as the result of poor oxalate clearance during chronic hemodialysis. We present two cases of oxalosis and describe the hand manifestations of this condition and their treatment.
A A, Freiberg, D N, Fish, D S, Louis
openaire   +2 more sources

Primary oxalosis

The American Journal of Medicine, 1973
L, Boquist   +3 more
openaire   +3 more sources

Oxalosis with nephrocalcinosis

Nephrology Dialysis Transplantation, 2000
D R, Singh   +4 more
openaire   +2 more sources

Oxalosis

Acta Medica Scandinavica, 1965
E, ENGER, A, SERCK-HANSSEN, T, ROKKONES
openaire   +2 more sources

[Oxalosis].

Die Medizinische Welt, 1983
E. Meerhoff   +3 more
openaire   +3 more sources

Oxalosis in infancy.

Clinical nephrology, 1984
Two cases of oxalosis in infancy are reported, the diagnosis and therapy are discussed and the world literature reviewed. Oxalosis in infancy is a rare condition, probably most frequently caused by a fulminant form of the autosomal recessive type I primary hyperoxaluria. It presents symptoms of renal failure in early infancy.
F E, de Zegher   +3 more
openaire   +1 more source

Management of oxalosis.

Kidney international. Supplement, 1996
Oxalosis is the final stage of primary hyperoxaluria type I (PHI) when reduction of GFR produces oxalate accumulation. It involves bones, arteries, eyes, heart, nerves, etc. The management of oxalosis starts with prevention of nephrocalcinosis and renal failure by diluting urine and by inhibiting oxalate crystal formation either by increasing the ...
M, Broyer   +4 more
openaire   +1 more source

Bone marrow oxalosis with pancytopenia in a patient with short bowel syndrome: Report of a case and review of the literature

Journal of Parenteral and Enteral Nutrition, 2023
Jamie Bering   +2 more
exaly  

Home - About - Disclaimer - Privacy