R. Piumelli

发表

International Child Care Practices Study: infant sleeping environment.

L. Landini, C. Poets, C. Einspieler, 2001, Early human development.

Comparison between pulse oximetry and transthoracic impedance alarm traces during home monitoring

L. Landini, G. Donzelli, N. Nassi, 2007, Archives of Disease in Childhood.

Fog-induced cough with impaired respiratory sensation in congenital central hypoventilation syndrome.

J. Widdicombe, M. Pistolesi, F. Lavorini, 2007, American journal of respiratory and critical care medicine.

Can we still do something-and what? - for a seemingly missing syndrome?: “Yes we can”

Cinzia Arzilli, N. Nassi, C. Ernst, 2019, Italian Journal of Pediatrics.

The multiagency approach to Sudden Unexpected Infant Deaths (SUID): eleven years’ experience in the Tuscany Region

A. Buccoliero, P. Toti, Cinzia Arzilli, 2020, Italian Journal of Pediatrics.

Urinary Biomarkers as a Proxy for Congenital Central Hypoventilation Syndrome Patient Follow-Up

M. Ramazzotti, D. Degl’Innocenti, G. la Marca, 2022, Antioxidants.

Mutational analysis of the RNX gene in congenital central hypoventilation syndrome.

R. Ravazzolo, F. Mosca, L. Gagliardi, 2002, American journal of medical genetics.

Guidelines for diagnosis and management of congenital central hypoventilation syndrome

M. Samuels, A. Pfleger, I. Ceccherini, 2020, Orphanet Journal of Rare Diseases.

A Common 3′UTR Variant of the PHOX2B Gene Is Associated With Infant Life-Threatening and Sudden Death Events in the Italian Population

I. Ceccherini, T. Bachetti, A. Palmieri, 2021, Frontiers in Neurology.

Sleeping problems in mothers and fathers of patients suffering from congenital central hypoventilation syndrome

Gianpaolo Donzelli, Maria Pia Viggiano, Fiorenza Giganti, 2015, Sleep and Breathing.

Apparent Life-Threatening Events (ALTE): Italian guidelines

S. Salvatore, S. De Masi, F. Cardinale, 2017, Italian Journal of Pediatrics.

Telemonitoring for infants at risk of apnoea, bradycardia and hypoxaemia: transmission of data improves the family compliance during home monitoring

G. Donzelli, N. Nassi, G. Liccioli, 2012, Journal of telemedicine and telecare.

Cough in children with congenital central hypoventilation syndrome.

A. Zanasi, F. Lavorini, G. Fontana, 2004, Pulmonary pharmacology & therapeutics.

Head Covering, Sweating, and the Risk of Sudden Infant Death Syndrome

N. Nassi, R. Piumelli, 2008, Pediatrics.

Systemic oxidative stress in congenital central hypoventilation syndrome

M. Ramazzotti, D. Degl’Innocenti, M. Becatti, 2018, European Respiratory Journal.

Guidelines for diagnosis and management of congenital central hypoventilation syndrome

M. Samuels, A. Pfleger, I. Ceccherini, 2020, Orphanet Journal of Rare Diseases.

Generation of two hiPSC lines (UMILi027-A and UMILi028-A) from early and late-onset Congenital Central hypoventilation Syndrome (CCHS) patients carrying a polyalanine expansion mutation in the PHOX2B gene.

S. Corti, R. Guerrini, D. Fornasari, 2022, Stem cell research.