| P50 | author | Pauline Iorio | Q89629632 |
| P2093 | author name string | Nathalie Boddaert | |
| | Rémi Salomon | |
| | Laurence Heidet | |
| | Vincent Morinière | |
| | Marie-Pierre Audrézet | |
| | Nicolas Garcelon | |
| | Laureline Berteloot | |
| | Caroline Rutten | |
| P2860 | cites work | Liver and kidney disease in ciliopathies | Q24633724 |
| | ARPKD and early manifestations of ADPKD: the original polycystic kidney disease and phenocopies | Q26824716 |
| | Diagnosis and screening of autosomal dominant polycystic kidney disease | Q33736708 |
| | Cystic kidney disease: a primer | Q34481318 |
| | Autosomal dominant polycystic kidney disease: the changing face of clinical management | Q34481426 |
| | Rationale, design and objectives of ARegPKD, a European ARPKD registry study | Q35176977 |
| | Cystic and inherited kidney diseases | Q35600180 |
| | Improving a full-text search engine: the importance of negation detection and family history context to identify cases in a biomedical data warehouse | Q36322199 |
| | Role of primary cilia in the pathogenesis of polycystic kidney disease | Q36788907 |
| | Color comet-tail artifact: clinical applications | Q37355422 |
| | Cystic diseases of the kidney: molecular biology and genetics | Q37724268 |
| | Imaging and classification of congenital cystic renal diseases | Q38005065 |
| | Ciliopathies - from rare inherited cystic kidney diseases to basic cellular function | Q38626551 |
| | Inherited renal cystic diseases | Q38831807 |
| | Ciliopathies | Q38994215 |
| | Motile and non-motile cilia in human pathology: from function to phenotypes | Q39012190 |
| | Genetic spectrum of Saudi Arabian patients with antenatal cystic kidney disease and ciliopathy phenotypes using a targeted renal gene panel | Q40890886 |
| | Gene mutation analysis in Iranian children with nephronophthisis: a two-center study | Q43406365 |
| | Sonography of infantile polycystic kidney disease | Q44356454 |
| | Clinical Significance of US Artifacts. | Q51831399 |
| | Sonographic assessment of renal length in normal children. | Q52432462 |
| | Anomalies of the TCF2 Gene Are the Main Cause of Fetal Bilateral Hyperechogenic Kidneys | Q57718701 |
| | Imaging of Kidney Cysts and Cystic Kidney Diseases in Children: An International Working Group Consensus Statement | Q64026793 |
| | Renal involvement in children with HNF1β mutation: early sonographic appearances and long-term follow-up | Q86632434 |
| | New Insights into Cystic Kidney Diseases | Q88591276 |
| | International consensus statement on the diagnosis and management of autosomal dominant polycystic kidney disease in children and young people | Q92227120 |
| P577 | publication date | 2020-02-10 | |
| P1433 | published in | Pediatric Nephrology | Q15749796 |
| P1476 | title | The "salt and pepper" pattern on renal ultrasound in a group of children with molecular-proven diagnosis of ciliopathy-related renal diseases | |