Results 111 to 120 of about 2,138 (167)

Molecular and Genetic Determinants of Nephrocalcinosis: Mechanisms, Genotype-Phenotype Correlations, and Precision Medicine. [PDF]

Int J Mol Sci
Popa S, Grădinaru AC, Braha EE, Grămescu M, Babici R, Ailenei C, Butnariu LI.   +6 more
europepmc   +1 more source

Spinal Cord Compression as the First Presentation of Primary Hyperoxaluria in a Patient With Kidney Failure: A Case Report and Literature Review. [PDF]

Kidney Med
Kliea M, Alsultan M, Qatleesh S, Haroun Y, Aziz OA, Basha K.   +5 more
europepmc   +1 more source

Population Pharmacokinetic and Pharmacodynamic Modelling and Simulation for Nedosiran Clinical Development and Dose Guidance in Pediatric Patients with Primary Hyperoxaluria Type 1. [PDF]

Clin Pharmacokinet
Zhang S, Gamallo P, Rawson V.
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

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Calcium Oxalosis

Radiology, 1974
G M, Carsen, M A, Radkowski
exaly   +3 more sources

OXALOSIS

Pediatrics, 1955
A case is described in which oxalosis occurred in an 11-year-old boy. The patient had experienced the formation of numerous calculi and multiple operations for removal of the calculi. The clinical, pathologic and histochemical findings in the case are presented.
E C, BURKE, A H, BAGGENSTOSS, C A, OWEN, M H, POWER, O W, LOHR   +4 more
openaire   +2 more sources