Results 81 to 90 of about 2,344 (196)

Acute Renal Failure, Microangiopathic Haemolytic Anemia, and Secondary Oxalosis in a Young Female Patient

International Journal of Nephrology, 2011
A 29-year old female presented with a one-week history of vomiting, diarrhoea, abdominal pain, and headache. On admission, she had acute renal failure requiring dialysis. Tests revealed a hemolytic anemia with thrombocytopenia.
Karolina M. Stepien, Peter Prinsloo, Tony Hitch, Thomas A. McCulloch, Rebecca Sims   +4 more
doaj   +1 more source

Combined liver-kidney transplantation for primary hyperoxaluria type I in children

, 2001
BACKGROUND: Primary hyperoxaluria type 1 (PH1) is a rare condition in which deficiency of the liver enzyme alanine:glyoxylate aminotransferase leads to renal failure and systemic oxalosis.
Ellis, SR, Hulton, Sally-Anne, De Ville de Goyet, J, Kelly, Deirdre, McKiernan, Patrick   +4 more
core   +1 more source

Skeletal features of primary hyperoxaluria type 1, revisited

Journal of Children's Orthopaedics, 2008
Purpose The purpose of this study was to describe the skeletal manifestations of primary hyperoxaluria type 1 (PH1), the most common of the primary hyperoxalurias. Methods We clinically and radiographically reviewed 12 consecutive patients diagnosed with
Samer El Hage, Ismat Ghanem, André Baradhi, Chebel Mourani, Samir Mallat, Fernand Dagher, Khalil Kharrat   +6 more
doaj   +1 more source

Success of kidney transplantation in oxalosis is unrelated to residual hepatic enzyme activity

, 1992
Success of kidney transplantation in oxalosis is unrelated to residual hepatic enzyme activity. We evaluated hepatic alanine glyoxylate aminotransferase (AGT) activity in percutaneous hepatic biopsy material obtained from four children with long-term ...
Scheinman, Jonathan I., Katz, Avi, Freese, Deborah, Danpure, Christopher J., Mauer, S. Michael   +4 more
core   +1 more source

Oxalosis

Journal of British Surgery, 1962
G D, CHISHOLM, B E, HEARD
openaire   +2 more sources

Kidney Transplantation in Primary Oxalosis: Data From the EDTA Registry

, 2017
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., Brynger, H., Fassbinder, W., Tufveson, G., Wing, A. J., Selwood, N. H., Dykes, S. R., Ehrich, J. H. H., Broyer, M., Brunner, F. P., Rizzoni, G.   +10 more
core  

Liver-Kidney Transplantation in Primary Hyperoxaluria Type-1: Case Report and Literature Review

International Journal of Organ Transplantation Medicine, 2011
Primary hyperoxaluria type-1 (PH1) is a rare inherited autosomal recessive disorder in which a deficiency of the hepatic enzyme alanine-glyoxylate aminotransferase leads to endogenous oxalate overproduction, renal failure, systemic oxalate deposition and
D Siegal, WS Su, D DaBreo, M Puglia, L Gregor, AS Gangji   +5 more
doaj  

Histopathologic Perspective of Combined Liver–kidney Transplant: In Primary Hyperoxaluria Type 1 Patient

Indian Journal of Transplantation
Primary hyperoxaluria (PH) type 1 is a rare autosomal recessive disorder of glyoxylate metabolism. Its prevalence is 1–3 cases/million people. Glyoxylate is the precursor of oxalate which is believed to be produced by oxidation in liver peroxisomes ...
Charusheela Rajesh Gore, Banyameen Iqbal, Nikita Ghanshamdas Chhablani   +2 more
doaj   +1 more source

Hematological and serum biochemical reference values and cohort analysis in the Gilbert's potoroo (Potorous gilbertii)

, 2009
Hematology and serum biochemistry blood values are tabulated for Australia's most critically endangered mammal, the Gilbert's potoroo (Potorous gilbertii).
Antony J. Friend, Palmer, C., Carly Palmer, Mills, J., Cree L. Monaghan, Jennifer S. Mills, Friend, A.J., Fenwick, S., Warren, K.S., Kristin S. Warren, Rebecca J. Vaughan, Stan Fenwick, Vaughan, R.J., Monaghan, C.   +13 more
core   +1 more source

Mutation characteristics of primary hyperoxaluria in the Chinese population and current international diagnosis and treatment status

Kidney Diseases
Background: Primary hyperoxaluria (PH) is a rare autosomal recessive disorder, mainly due to the increase in endogenous oxalate production, causing a series of clinical features such as kidney stones, nephrocalcinosis, progressive impairment of renal ...
Xingying Zhu, Wai W. Cheung, Aihua Zhang, Guixia Ding   +3 more
doaj   +1 more source