TY  - GEN
AU  - Soliman,Neveen A
AU  - Nabhan,Marwa M
AU  - Abdelrahman,Safaa M
AU  - Abdelaziz,Hanan
AU  - Helmy,Rasha
AU  - Ghanim,Khaled
AU  - Bazaraa,Hafez M
AU  - Badr,Ahmed M
AU  - Tolba,Omar A
AU  - Kotb,Magd A
AU  - Eweeda,Khaled M
AU  - Fayez,Alaa
TI  - Clinical spectrum of primary hyperoxaluria type 1: Experience of a tertiary center
SN  - 1872-9177
PY  - 2018///0425
KW  - Adult
KW  - Child
KW  - Child, Preschool
KW  - Cohort Studies
KW  - Consanguinity
KW  - Egypt
KW  - Female
KW  - Humans
KW  - Hyperoxaluria, Primary
KW  - diagnosis
KW  - Infant
KW  - Kidney Failure, Chronic
KW  - genetics
KW  - Male
KW  - Mutation
KW  - Nephrocalcinosis
KW  - Nephrolithiasis
KW  - Phenotype
KW  - Pyridoxine
KW  - therapeutic use
KW  - Retrospective Studies
KW  - Risk Factors
KW  - Tertiary Care Centers
KW  - Transaminases
KW  - Treatment Outcome
KW  - Vitamin B Complex
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1016/j.nephro.2016.08.002
ER  -