Results 151 to 160 of about 2,548 (196)
Some of the next articles are maybe not open access.

OXALOSIS

Pediatrics, 1955
A case is described in which oxalosis occurred in an 11-year-old boy. The patient had experienced the formation of numerous calculi and multiple operations for removal of the calculi. The clinical, pathologic and histochemical findings in the case are presented.
E C, BURKE   +4 more
openaire   +2 more sources

Oxalosis

open access: yesKlinische Wochenschrift, 1957
O. Brož, Z. Šťovíček, I. Štěpán
openaire   +2 more sources

Oxalosis of bone

Pediatric Radiology, 1982
Skeletal survey in an 8-year-old girl with primary hyperoxaluria and in chronic renal failure revealed wide translucent metaphyseal bands and defects at the ends of the long bones. Similar disordered bone growth was seen as rims of rarefaction around the large epiphyses, the patella and the tarsal bones. Bone density was generally increased.
J, Wiggelinkhuizen, R M, Fisher
openaire   +2 more sources

Oxalosis and pregnancy

American Journal of Obstetrics and Gynecology, 1962
0 x A L o s I s is a rare disease characterized by hyperoxaluria and widespread deposits of oxalate crystals throughout the body.‘-’ DoIan* has recently reviewed oxalosis and was unable to find a proved case in pregnancy or the puerperium. His review includes some 39 cases and ascribes the initial description of the disease entity to Lepoutre,” in 1925.
R J, HILDEBRANDT, D R, SHANKLIN
openaire   +2 more sources

OXALOSIS

Pediatrics, 1952
A case is reported of renal failure in a boy subsequent to recurrent calcium oxalate urinary calculi. The post mortem disclosed widespread deposits in the tissues of calcium oxalate crystals. These were particularly prominent in the kidneys and bone marrow. It is suggested that this is the end result of an "inborn error of metabolism" in
L. YING CHOU, W. L. DONOHUE
openaire   +1 more source

Oxalosis

open access: yes, 1974
Paolo Durand
openaire   +2 more sources

Retinal Oxalosis

Archives of Ophthalmology, 1989
A 55-year-old woman with chronic renal failure treated with hemodialysis had severe bilateral visual loss develop due to retinal ischemia. Ophthalmoscopy showed crystals in the distribution of the retinal arteries, but not veins, and this led to a diagnosis of systemic oxalosis.
C G, Wells   +4 more
openaire   +2 more sources

Bone marrow oxalosis

Blood, 2012
![Figure][1] A 28-year-old woman presented with pancytopenia. Her past medical history was significant for primary hyperoxaluria. She had recurrent renal stones and urinary tract infections since the age of 5 years.
Nasir A, Bakshi, Hazzaa, Al-Zahrani
openaire   +2 more sources

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