BPG is committed to discovery and dissemination of knowledge
Cited by in CrossRef
For: Rametta R, Nebbia G, Dongiovanni P, Farallo M, Fargion S, Valenti L. A novel alpha1-antitrypsin null variant (PiQ0Milano). World J Hepatol 2013; 5(8): 458-461 [PMID: 24023986 DOI: 10.4254/wjh.v5.i8.458]
URL: https://www.wjgnet.com/1948-5182/full/v5/i8/458.htm
Number Citing Articles
1
Marian Hill, Noor Kalsheker. Alpha-1-antitrypsin Deficiency2017; : 37 doi: 10.1016/B978-0-12-803942-7.00004-0
2
Arif Bashir, Naveed Nazir Shah, Younis Mohammad Hazari, Mudasir Habib, Samirul Bashir, Nazia Hilal, Mariam Banday, Syed Asrafuzzaman, Khalid Majid Fazili. Novel variants of SERPIN1A gene: Interplay between alpha1-antitrypsin deficiency and chronic obstructive pulmonary diseaseRespiratory Medicine 2016; 117: 139 doi: 10.1016/j.rmed.2016.06.005
3
Ignacio Blanco. Blanco's Overview of Alpha-1 Antitrypsin Deficiency2017; : 67 doi: 10.1016/B978-0-12-809530-0.00006-4
4
Beatriz Lara, Maria Teresa Martínez, Ignacio Blanco, Cristina Hernández-Moro, Eladio A Velasco, Ilaria Ferrarotti, Francisco Rodriguez-Frias, Laura Perez, Irene Vazquez, Javier Alonso, Manuel Posada, Beatriz Martínez-Delgado. Severe alpha-1 antitrypsin deficiency in composite heterozygotes inheriting a new splicing mutation QOMadridRespiratory Research 2014; 15(1) doi: 10.1186/s12931-014-0125-y
5
Ilaria Ferrarotti, Tomás P Carroll, Stefania Ottaviani, Anna M Fra, Geraldine O’Brien, Kevin Molloy, Luciano Corda, Daniela Medicina, David R Curran, Noel G McElvaney, Maurizio Luisetti. Identification and characterisation of eight novel SERPINA1 Null mutationsOrphanet Journal of Rare Diseases 2014; 9(1) doi: 10.1186/s13023-014-0172-y
6
Marc Miravitlles, Mike Herepath, Asim Priyendu, Sheetal Sharma, Tatiana Vilchez, Oliver Vit, Michaela Haensel, Virginie Lepage, Helena Gens, Timm Greulich. Disease burden associated with alpha-1 antitrypsin deficiency: systematic and structured literature reviewsEuropean Respiratory Review 2022; 31(163): 210262 doi: 10.1183/16000617.0262-2021