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Dordoni, Chiara
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1

Clinical Significance of the Cystic Phenotype in Alport Syn..:

Zeni, Letizia ; Mescia, Federica ; Toso, Diego...
American Journal of Kidney Diseases.  , 2024
Link: https://doi.org/10.1053/..
 
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2

Monoallelic pathogenic IFT140 variants are a common cause o..:

Dordoni, Chiara ; Zeni, Letizia ; Toso, Diego...
Clinical Kidney Journal.  17 (2024)  2 - p. , 2024
Link: https://doi.org/10.1093/..
 
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3

Identification of bi‐allelic LFNG variants in three patient..:

Lecca, Mauro ; Bedeschi, Maria Francesca ; Izzi, Claudia...
Clinical Genetics.  104 (2023)  2 - p. 230-237 , 2023
Link: https://doi.org/10.1111/..
 
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4

#4215 MONOALLELIC IFT140-RELATED POLYCYSTIC KIDNEY DISEASE ..:

Dordoni, Chiara ; Zeni, Letizia ; Mazza, Cinzia...
Nephrology Dialysis Transplantation.  38 (2023)  Supplement_1 - p. , 2023
Link: https://doi.org/10.1093/..
 
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5

#5542 THE ITALIAN REGISTRY OF POLYCYSTIC KIDNEY DISEASE (RI..:

Cortinovis, Roberta ; Dordoni, Chiara ; Mescia, Federica...
Nephrology Dialysis Transplantation.  38 (2023)  Supplement_1 - p. , 2023
Link: https://doi.org/10.1093/..
 
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6

#6036 CYSTIC KIDNEY PHENOTYPE IS A FREQUENT, AGE- AND EGFR-..:

Zeni, Letizia ; Mescia, Federica ; Toso, Diego...
Nephrology Dialysis Transplantation.  38 (2023)  Supplement_1 - p. , 2023
Link: https://doi.org/10.1093/..
 
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7

Lessons From the Clinic: ADPKD Genetic Test Unraveling Seve..:

Izzi, Claudia ; Dordoni, Chiara ; Delbarba, Elisa...
Kidney International Reports.  7 (2022)  4 - p. 895-898 , 2022
Link: https://doi.org/10.1016/..
 
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8

Expanding the variability of the ADPKD-GANAB clinical pheno..:

Delbarba, Elisa ; Econimo, Laura ; Dordoni, Chiara...
Journal of Nephrology.  35 (2021)  2 - p. 645-652 , 2021
Link: https://doi.org/10.1007/..
 
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9

P0074EXPANDING THE VARIABILITY OF THE ADPKD-GANAB CLINICAL ..:

Izzi, Claudia ; Scolari, Francesco ; Dallera, Nadia...
Nephrology Dialysis Transplantation.  35 (2020)  Supplement_3 - p. , 2020
Link: https://doi.org/10.1093/..
 
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10

Variable Expressivity of HNF1B Nephropathy, From Renal Cyst..:

Izzi, Claudia ; Dordoni, Chiara ; Econimo, Laura...
Kidney International Reports.  5 (2020)  12 - p. 2341-2350 , 2020
Link: https://doi.org/10.1016/..
 
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11

P0057ADPKD: COMPLEX GENOTYPES MAY EXPLAIN SEVERE PHENOTYPE ..:

Scolari, Francesco ; Dallera, Nadia ; Mazza, Cinzia...
Nephrology Dialysis Transplantation.  35 (2020)  Supplement_3 - p. , 2020
Link: https://doi.org/10.1093/..
 
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12

Prenatal findings in oral‐facial‐digital syndrome type VI: ..:

Dordoni, Chiara ; Prefumo, Federico ; Iascone, Maria...
Prenatal Diagnosis.  39 (2019)  8 - p. 652-655 , 2019
Link: https://doi.org/10.1002/..
 
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13

A classical Ehlers-Danlos syndrome family with incomplete p..:

Colombi, Marina ; Dordoni, Chiara ; Cinquina, Valeria..
European Journal of Medical Genetics.  61 (2018)  1 - p. 17-20 , 2018
Link: https://doi.org/10.1016/..
 
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14

Characterization of a Pseudoxanthoma elasticum-like patient..:

Dordoni, Chiara ; Gatti, Marta ; Venturini, Marina...
Journal of Dermatological Science.  89 (2018)  2 - p. 201-204 , 2018
Link: https://doi.org/10.1016/..
 
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15

A novel MAP3K7 splice mutation causes cardiospondylocarpofa..:

Morlino, Silvia ; Castori, Marco ; Dordoni, Chiara...
European Journal of Human Genetics.  26 (2018)  4 - p. 582-586 , 2018
Link: https://doi.org/10.1038/..
 
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