Results 61 to 70 of about 2,138 (167)

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

Oxalosis

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

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

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

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

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  

Bronchopulmonary oxalosis revealing pulmonary aspergillosis in an immunocompetent patient: a case report. [PDF]

Oxf Med Case Reports
Abdouh S, Gourti M, Sellam I, Makloul M, Maidi EM.   +4 more
europepmc   +1 more source

Primary hyperoxaluria and systemic oxalosis

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