Results 91 to 100 of about 2,548 (196)

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

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

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

Granulomatous Inflammation and Hypercalcemia in Patients With Severe Systemic Oxalosis

Kidney International Reports, 2022
Peggy Perrin, Jérome Olagne, Arnaud Delbello, Stanislas Bataille, Laurent Mesnard, Claire Borni, Bruno Moulin, Sophie Caillard   +7 more
doaj   +1 more source

Oxalosis [PDF]

American Journal of Kidney Diseases, 2000
openaire   +2 more sources

Autopsy Findings of a Case with Oxalosis

Oxalosis, deposition of calcium oxalate in tissues, is the final stage of hyperoxaluric syndromes. Being a rare entity, it is often missed, or the diagnosis is delayed, since the definitive diagnosis requires special laboratory tests.
Doganavsargil, B, Sen, S, Mir, S, Akil, I, Basdemir, G   +4 more
core  

Bicytopenia secondary to systemic oxalosis

Indian Journal of Pathology and Microbiology, 2015
Mansoor C Abdulla, Jemshad Alungal, Asiq Siddik, Mohthash Musambil   +3 more
doaj   +1 more source

Oxalate Nephropathy Secondary to Chronic Pancreatitis: Case Report

Turkish Journal of Nephrology, 2019
Chronic pancreatitis is a rare cause of oxalate nephropathy. The aim of this case report was to present a patient hospitalized with acute kidney injury who was diagnosed with oxalate nephropathy and concurrent chronic pancreatitis on further ...
Nergiz BAYRAKCI, Nihal ÖZKAYAR, Aysel ÇOLAK, Müge EREK ERSÖZEN, Ebru GÖK OĞUZ, Fatih DEDE   +5 more
doaj  

Primary hyperoxaluria and systemic oxalosis

Indian Journal of Urology, 2007
K Sriram, Nitin S Kekre, Ganesh Gopalakrishnan   +2 more
doaj   +1 more source

Optical coherence tomography: Angiography visualization of retinal oxalosis in primary hyperoxaluria, a case report

Indian Journal of Ophthalmology, 2022
A Barigali, P R Aswin, S M Abdul Khadar
doaj   +1 more source