Results 71 to 80 of about 4,323 (173)

Primary Hyperoxaluria

Annals of the Academy of Medicine, Singapore, 2010
Niranjan, Khandelwal, Kushaljit Singh, Sodhi, Vivek, Virmani, Navneet, Sharma   +3 more
openaire   +3 more sources

The Aetiology of Primary Hyperoxaluria [PDF]

BMJ, 1958
H E, ARCHER, A E, DORMER, E F, SCOWEN, R W, WATTS   +3 more
openaire   +2 more sources

Navigating the Evolving Landscape of Primary Hyperoxaluria: Traditional Management Defied by the Rise of Novel Molecular Drugs

Biomolecules
Primary hyperoxalurias (PHs) are inherited metabolic disorders marked by enzymatic cascade disruption, leading to excessive oxalate production that is subsequently excreted in the urine.
Yueqi Huang, Wei Zhu, Jia Zhou, Qiulin Huang, Guohua Zeng   +4 more
doaj   +1 more source

CHRONIC RENAL FAILURE DUE TO HYPER OXALURIA IN PEDIATRIC PATIENTS

Turkish Journal of Nephrology, 2019
Primary hyperoxaluria is a rarely encountered disease characterised by recurrent urolithiasis, nephrocalcinosis, and oxalate deposition in almost all tissues, generally inherited in autosomal recessive fashion and the important complications of which can
Ali DELİBAŞ, Özlem ERDOĞAN, Mehmet BÜLBÜL, Kenan BEK, Gülay DEMİRCİN, Ayşe ÖNER   +5 more
doaj  

PRIMARY HYPEROXALURIA

Medicine, 1964
T D, HOCKADAY, J E, CLAYTON, E W, FREDERICK, L H, SMITH   +3 more
openaire   +2 more sources

Primary hyperoxaluria and systemic oxalosis

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

Primary hyperoxaluria

Indian Journal of Pathology and Microbiology, 2021
Sudip Roy, Uttara Chatterjee, Moumita Sengupta, Suchandra Ray   +3 more
openaire   +1 more source

A case of oxalate nephropathy presenting with acute kidney injury [PDF]

Journal of Krishna Institute of Medical Sciences University
Oxalate Nephropathy (ON) represents a serious condition characterized by a decline in renal function associated with calcium oxalate crystal deposition within renal tubules. It can arise from Primary Hyperoxaluria (PH) due to genetic defects or secondary
Pradnya Mukund Diggikar, Mayank Mundada, Raju Hansini Reddy, Tushar Pancholi   +3 more
doaj  

Current status of primary hyperoxaluria type 1 in Japan. [PDF]

Urolithiasis
Ogawa T, Okamoto K, Yamamoto M, Sato Y, Ushijima K, Numahata D, Takeshita H, Inai H, Onozawa M, Miyazaki J, Takayama T.   +10 more
europepmc   +1 more source

Clinical Approaches and Emerging Therapeutic Horizons in Primary Hyperoxaluria. [PDF]

J Clin Med
Martínez-Galindo R, Campuzano-Pérez M, Konstantouli A, Aguilar-Ramírez MDP, Rodríguez JAM, Abad-López P, Shabaka A, Cansino R.   +7 more
europepmc   +1 more source