Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1969 1
1970 3
1971 2
1972 1
1973 3
1974 4
1975 14
1976 14
1977 6
1978 10
1979 2
1980 12
1981 9
1982 6
1983 10
1984 17
1985 9
1986 13
1987 18
1988 8
1989 19
1990 14
1991 22
1992 16
1993 14
1994 17
1995 14
1996 20
1997 13
1998 15
1999 18
2000 31
2001 28
2002 18
2003 26
2004 25
2005 29
2006 28
2007 34
2008 41
2009 29
2010 31
2011 28
2012 33
2013 42
2014 46
2015 55
2016 48
2017 62
2018 50
2019 44
2020 52
2021 53
2022 44
2023 45
2024 19

Text availability

Article attribute

Article type

Publication date

Search Results

1,207 results

Results by year

Filters applied: . Clear all
Page 1
Alpha(1)-Antitrypsin Deficiency.
Strnad P, McElvaney NG, Lomas DA. Strnad P, et al. N Engl J Med. 2020 Apr 9;382(15):1443-1455. doi: 10.1056/NEJMra1910234. N Engl J Med. 2020. PMID: 32268028 Review. No abstract available.
Alpha-1 antitrypsin deficiency.
Dasí F. Dasí F. Med Clin (Barc). 2024 Apr 12;162(7):336-342. doi: 10.1016/j.medcli.2023.10.014. Epub 2023 Nov 22. Med Clin (Barc). 2024. PMID: 37993348 Free article. Review. English, Spanish.
Alpha-1 antitrypsin deficiency (AATD) is a rare hereditary condition caused by decreased plasma and tissue levels of alpha-1 antitrypsin (AAT) that can lead to serious lung and liver disease in children and adults. ...
Alpha-1 antitrypsin deficiency (AATD) is a rare hereditary condition caused by decreased plasma and tissue level
Alpha-1 antitrypsin deficiency.
Dasí F. Dasí F. Med Clin (Barc). 2023 Mar 10;160(5):203-205. doi: 10.1016/j.medcli.2022.09.001. Epub 2022 Oct 14. Med Clin (Barc). 2023. PMID: 36253208 English, Spanish. No abstract available.
Alpha-1-antitrypsin deficiency.
Bals R. Bals R. Best Pract Res Clin Gastroenterol. 2010 Oct;24(5):629-33. doi: 10.1016/j.bpg.2010.08.006. Best Pract Res Clin Gastroenterol. 2010. PMID: 20955965 Free article. Review.
Alpha-1-antitrypsin deficiency (AATD) is a rare genetic disorder associated with the development of liver and lung disease. ...
Alpha-1-antitrypsin deficiency (AATD) is a rare genetic disorder associated with the development of liver and lu
Alpha-1 antitrypsin deficiency-associated panniculitis.
Franciosi AN, Ralph J, O'Farrell NJ, Buckley C, Gulmann C, O'Kane M, Carroll TP, McElvaney NG. Franciosi AN, et al. J Am Acad Dermatol. 2022 Oct;87(4):825-832. doi: 10.1016/j.jaad.2021.01.074. Epub 2021 Jan 29. J Am Acad Dermatol. 2022. PMID: 33516773 Free article. Review.
BACKGROUND: Panniculitis represents a rare and potentially lethal manifestation of alpha-1 antitrypsin deficiency (AATD). Evidence regarding management is limited to case reports and small case series. ...SEARCH METHODOLOGY: Articles and abstracts publ …
BACKGROUND: Panniculitis represents a rare and potentially lethal manifestation of alpha-1 antitrypsin deficiency
Alpha-1-Antitrypsin Deficiency Liver Disease.
Patel D, Teckman JH. Patel D, et al. Clin Liver Dis. 2018 Nov;22(4):643-655. doi: 10.1016/j.cld.2018.06.010. Epub 2018 Aug 22. Clin Liver Dis. 2018. PMID: 30266154 Review.
α1-Antitrypsin Deficiency.
Hatipoğlu U, Stoller JK. Hatipoğlu U, et al. Clin Chest Med. 2016 Sep;37(3):487-504. doi: 10.1016/j.ccm.2016.04.011. Epub 2016 Jun 25. Clin Chest Med. 2016. PMID: 27514595 Review.
Alpha1-antitrypsin deficiency and asthma.
Pini L, Paoletti G, Heffler E, Tantucci C, Puggioni F; Asthma and Alpha1-Antitrypsin Research Group. Pini L, et al. Curr Opin Allergy Clin Immunol. 2021 Feb 1;21(1):46-51. doi: 10.1097/ACI.0000000000000711. Curr Opin Allergy Clin Immunol. 2021. PMID: 33284159 Review.
Alpha-1-antitrypsin deficiency.
Perlmutter DH. Perlmutter DH. Semin Liver Dis. 1998;18(3):217-25. doi: 10.1055/s-2007-1007158. Semin Liver Dis. 1998. PMID: 9773422 Review.
Homozygous PIZZ alpha 1-antitrypsin deficiency, which has an incident of 1 in 1600 to 1 in 2000 live births, is the most common genetic cause of liver disease in children. ...
Homozygous PIZZ alpha 1-antitrypsin deficiency, which has an incident of 1 in 1600 to 1 in 2000 live births, is …
1,207 results