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Ilaria Ferrarotti

Showing results (1-10 of 87) with videos related to

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The Lancet. Respiratory Medicine|March 14, 2014
COPD: no gene left unturnedIlaria Ferrarotti, Maurizio Luisetti
The European Respiratory Journal|January 2, 2016
Efficacy of augmentation therapy for emphysema associated with α1-antitrypsin deficiency: enough is enoughBruno Balbi, Ilaria Ferrarotti, Marc Miravitlles
Methods in Molecular Biology (Clifton, N.J.)|December 18, 2023
Sanger and Next-Generation Sequencing of AATValentina Barzon, Ilaria Ferrarotti, Stefania Ottaviani
Orphanet Journal of Rare Diseases|February 22, 2024
Rare variants in alpha 1 antitrypsin deficiency: a systematic literature reviewIlaria Ferrarotti, Marion Wencker, Joanna Chorostowska-Wynimko
Respiratory Medicine|August 30, 2005
CR1 gene polymorphism in FinlandMichele Zorzetto, Ilaria Ferrarotti, Ilaria Campo, et al.
The European Respiratory Journal|September 5, 2014
Rare α₁-antitrypsin genotype in a grass seed workerTine H Malling, Line Sloth Carlsen, Ilaria Ferrarotti, et al.
European Journal of Human Genetics : EJHG|January 21, 2011
Clinical utility gene card for: α-1-antitrypsin deficiencySabina Janciauskiene, Ilaria Ferrarotti, Florian Laenger, et al.
Breathe (Sheffield, England)|August 23, 2018
Update on α<sub>1</sub>-antitrypsin deficiencyIlaria Ferrarotti, Stefania Ottaviani, Annalisa De Silvestri, et al.
Chest|November 6, 2013
α₁-Antitrypsin level and pheno/genotypesIlaria Ferrarotti, Gian Andri Thun, Nicole M Probst-Hensch, et al.
Respirology Case Reports|February 21, 2020
Clinical manifestations in patients with PI*MM<sub>Malton</sub> genotypes. A matter still unsolved in alpha-1 antitrypsin deficiencyMarina Aiello, Alberto Fantin, Chiara Longo, et al.
Pageof 9

Showing results (1-10 of 87) with videos related to

Sort By:
Pageof 9
The Lancet. Respiratory Medicine|March 14, 2014
COPD: no gene left unturnedIlaria Ferrarotti, Maurizio Luisetti
The European Respiratory Journal|January 2, 2016
Efficacy of augmentation therapy for emphysema associated with α1-antitrypsin deficiency: enough is enoughBruno Balbi, Ilaria Ferrarotti, Marc Miravitlles
Methods in Molecular Biology (Clifton, N.J.)|December 18, 2023
Sanger and Next-Generation Sequencing of AATValentina Barzon, Ilaria Ferrarotti, Stefania Ottaviani
Orphanet Journal of Rare Diseases|February 22, 2024
Rare variants in alpha 1 antitrypsin deficiency: a systematic literature reviewIlaria Ferrarotti, Marion Wencker, Joanna Chorostowska-Wynimko
Respiratory Medicine|August 30, 2005
CR1 gene polymorphism in FinlandMichele Zorzetto, Ilaria Ferrarotti, Ilaria Campo, et al.
The European Respiratory Journal|September 5, 2014
Rare α₁-antitrypsin genotype in a grass seed workerTine H Malling, Line Sloth Carlsen, Ilaria Ferrarotti, et al.
European Journal of Human Genetics : EJHG|January 21, 2011
Clinical utility gene card for: α-1-antitrypsin deficiencySabina Janciauskiene, Ilaria Ferrarotti, Florian Laenger, et al.
Breathe (Sheffield, England)|August 23, 2018
Update on α<sub>1</sub>-antitrypsin deficiencyIlaria Ferrarotti, Stefania Ottaviani, Annalisa De Silvestri, et al.
Chest|November 6, 2013
α₁-Antitrypsin level and pheno/genotypesIlaria Ferrarotti, Gian Andri Thun, Nicole M Probst-Hensch, et al.
Respirology Case Reports|February 21, 2020
Clinical manifestations in patients with PI*MM<sub>Malton</sub> genotypes. A matter still unsolved in alpha-1 antitrypsin deficiencyMarina Aiello, Alberto Fantin, Chiara Longo, et al.
Pageof 9