Francesca Aiello (F Aiello)

Publication Activity (10 Years)

Years Active: 2022-2023
Publications (10 Years): 5

Top Topics

Pulmonary Embolism

End Stage Renal Disease

Ejection Fraction

Top Venues

Journal of endocrinological investigation

Journal of pediatric endocrinology & metabolism : JPEM

This page only lists publications with an associated author ORCID identifier.

Publications

Francesca Aiello, Stefania Palumbo, Grazia Cirillo, Gianluca Tornese, Daniela Fava, Malgorzata Gabriela Wasniewska, Maria Felicia Faienza, Mauro Bozzola, C Luongo, Adalgisa Festa, Emanuele Miraglia Del Giudice, Anna Grandone
MKRN3 circulating levels in girls with central precocious puberty caused by MKRN3 gene mutations. Journal of endocrinological investigation 47 (6) (2023)
Francesca Aiello, Stefania Palumbo, Grazia Cirillo, Gianluca Tornese, Daniela Fava, Malgorzata Gabriela Wasniewska, Maria Felicia Faienza, Mauro Bozzola, C Luongo, Adalgisa Festa, Emanuele Miraglia Del Giudice, Anna Grandone
MKRN3 circulating levels in girls with central precocious puberty caused by MKRN3 gene mutations. Journal of endocrinological investigation 47 (6) (2023)
Francesca Aiello, Stefania Palumbo, Grazia Cirillo, Gianluca Tornese, Daniela Fava, Malgorzata Gabriela Wasniewska, Maria Felicia Faienza, Mauro Bozzola, C Luongo, Adalgisa Festa, Emanuele Miraglia Del Giudice, Anna Grandone
MKRN3 circulating levels in girls with central precocious puberty caused by MKRN3 gene mutations. Journal of endocrinological investigation 47 (6) (2023)
Francesca Aiello, Stefania Palumbo, Grazia Cirillo, Gianluca Tornese, Daniela Fava, Malgorzata Gabriela Wasniewska, Maria Felicia Faienza, Mauro Bozzola, C Luongo, Adalgisa Festa, Emanuele Miraglia Del Giudice, Anna Grandone
MKRN3 circulating levels in girls with central precocious puberty caused by MKRN3 gene mutations. Journal of endocrinological investigation (2023)
Francesca Aiello, Daniela Pasquali, Federico Baronio, Alessandra Cassio, Cesare Rossi, Rosa Di Fraia, Raffaela Carotenuto, Lucia Digitale, Adalgisa Festa, Caterina Luongo, Giulio Maltoni, Roberta Schiano di Cola, Emanuele Miraglia Del Giudice, Anna Grandone
Rare PHEX intron variant causes complete and severe phenotype in a family with hypophosphatemic rickets: a case report. Journal of pediatric endocrinology & metabolism : JPEM (2022)