1. A disorder of surfactant metabolism without identified genetic mutations. Issue 1 (December 2015) Authors: Montella, Silvia; Vece, Timothy; Langston, Claire; Carrera, Paola; Nogee, Lawrence; Hamvas, Aaron; Manna, Angelo; Cervasio, Mara; Santamaria, Francesca Journal: Italian journal of pediatrics Issue: Volume 41:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A disorder of surfactant metabolism without identified genetic mutations. Issue 1 (December 2015) Authors: Montella, Silvia; Vece, Timothy; Langston, Claire; Carrera, Paola; Nogee, Lawrence; Hamvas, Aaron; Manna, Angelo; Cervasio, Mariarosaria; Santamaria, Francesca Journal: Italian journal of pediatrics Issue: Volume 41:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A disorder of surfactant metabolism without identified genetic mutations. Issue 1 (December 2015) Authors: Montella, Silvia; Vece, Timothy; Langston, Claire; Carrera, Paola; Nogee, Lawrence; Hamvas, Aaron; Manna, Angelo; Cervasio, Mariarosaria; Santamaria, Francesca Journal: Italian journal of pediatrics Issue: Volume 41:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Biallelic variants of ATP13A3 cause dose-dependent childhood-onset pulmonary arterial hypertension characterised by extreme morbidity and mortality. Issue 9 (7th September 2021) Authors: Machado, Rajiv D; Welch, Carrie L; Haimel, Matthias; Bleda, Marta; Colglazier, Elizabeth; Coulson, John D; Debeljak, Marusa; Ekstein, Josef; Fineman, Jeffrey R; Golden, William Christopher; Griffin, Emily L; Hadinnapola, Charaka; Harris, Michael A; Hirsch, Yoel; Hoover-Fong, Julie Elizabeth; Noge... Journal: Journal of medical genetics Issue: Volume 59:Issue 9(2022) Page Start: 906 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Biallelic variants of ATP13A3 cause dose-dependent childhood-onset pulmonary arterial hypertension characterised by extreme morbidity and mortality. Issue 9 (7th September 2021) Authors: Machado, Rajiv D; Welch, Carrie L; Haimel, Matthias; Bleda, Marta; Colglazier, Elizabeth; Coulson, John D; Debeljak, Marusa; Ekstein, Josef; Fineman, Jeffrey R; Golden, William Christopher; Griffin, Emily L; Hadinnapola, Charaka; Harris, Michael A; Hirsch, Yoel; Hoover-Fong, Julie Elizabeth; Noge... Journal: Journal of medical genetics Issue: Volume 59:Issue 9(2022) Page Start: 906 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Erratum to: A disorder of surfactant metabolism without identified genetic mutations. Issue 1 (December 2015) Authors: Montella, Silvia; Vece, Timothy; Langston, Claire; Carrera, Paola; Nogee, Lawrence; Hamvas, Aaron; Manna, Angelo; Cervasio, Mariarosaria; Santamaria, Francesca Journal: Italian journal of pediatrics Issue: Volume 41:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Premature Identical Twin Neonates With Sleep Apnea. (October 2017) Authors: Ramesh, Anirudh; Diaz, Johanna; Nogee, Lawrence; Duis, Jessica; Jang, Dae Song; Lawson, Cathleen; Maegawa, Gustavo Journal: Clinical pediatrics Issue: Volume 56:Number 11(2017) Page Start: 1075 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗