Results 121 to 130 of about 7,704 (220)

Crystal-cell interaction inhibition by polysaccharides [PDF]

, 1996
Boeve, E.R., Bruijn, W.C. (Wim) de, Cao, L.C. (Lucheng), Romijn, J.C. (Johannes), Schröder, F.H. (Fritz), Verkoelen, C.F.   +5 more
core   +2 more sources

Novel AAV843 Vector-Mediated Gene Replacement Therapy Rescues Primary Hyperoxaluria Type I in Mice. [PDF]

Cells
Zhang J, Yin Y, Ji B, Sun M, Jiang Y, Wu X, Xiao X, Shen Q, Wu X, Xu H.   +9 more
europepmc   +1 more source

LNP-mediated in vivo base editing corrects Agxt to cure primary hyperoxaluria type 1. [PDF]

Clin Transl Med
Zhang D, Zheng R, Chen Z, Chen X, Yang L, Huo Y, Zhao Y, Huang J, Zhang D, Yin S, Li D, Geng H.   +11 more
europepmc   +1 more source

Surgical Management of Pediatric Primary Hyperoxaluria Type 1: An Eight-Patient Case Series in the Pre-siRNA Era. [PDF]

Pediatr Transplant
Finer G, Darani AN, Switalski MG, Ward SE, Melin-Aldana H, Superina R.   +5 more
europepmc   +1 more source

Vitamin C-induced hyperoxaluria causing reversible tubulointerstitial nephritis and chronic renal failure: a case report [PDF]

Shradha Rathi, William Kern, Kai Lau
core   +1 more source

Biogenesis of Organelles and Membrane Proteins. [PDF]

, 1988
Harmey, Matthew A., Neupert, Walter, Nicholson, Donald W., Stuart, Rosemary A.   +3 more
core   +1 more source

Natural History of Advanced Primary Hyperoxaluria Type 1: A Retrospective Study. [PDF]

Kidney Med
Lieske JC, Groothoff JW, Frishberg Y, Garrelfs SF, Milliner DS, Magen D, Sellier-Leclerc AL, Shasha-Lavsky H, Bakkaloǧlu S, Lemoine S, Fuster DG, Devresse A, Cytter-Kuint R, Kajbaf F, Du W, Gansner JM.   +15 more
europepmc   +1 more source

The Dawn of Precision Medicine in Pediatric Nephrology: Lumasiran and the Era of siRNA Therapies for Primary Hyperoxaluria Type 1. [PDF]

J Pers Med
Dotis J, Fourikou M.
europepmc   +1 more source

Real-world burden of primary hyperoxaluria with chronic kidney disease in the United States: a retrospective administrative claims analysis. [PDF]

BMC Nephrol
Goldfarb DS, Modersitzki F, Skaar JR, Li O, Salem S, Chen JV.   +5 more
europepmc   +1 more source

Primary hyperoxaluria: insights into its clinical presentation, genetic mutations, and transplantation outcomes in a pediatric population in a tertiary care center. [PDF]

Orphanet J Rare Dis
Sayed B, Alhuthil R, Saadeh S, Al-Shareef T, Alhassoun I, Al-Sabban E.   +5 more
europepmc   +1 more source