ライフサイエンスコーパス: alpha1-antitrypsin deficiency

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1 dividuals with emphysema secondary to severe alpha1 antitrypsin deficiency.

2 led trial of A1PI treatment in patients with alpha1 antitrypsin deficiency.

3 which underlies misfolding diseases such as alpha1-antitrypsin deficiency.

4 ding Gaucher disease, cystic fibrosis and ZZ alpha1-antitrypsin deficiency.

5 that underlies emphysema in individuals with alpha1-antitrypsin deficiency.

6 stemic inflammatory diseases associated with alpha1-antitrypsin deficiency.

7 apy for treatment of liver diseases, such as alpha1-antitrypsin deficiency.

8 tions in CF, primary ciliary dyskinesia, and alpha1-antitrypsin deficiency.

9 clinically and cost-effective therapies for alpha1-antitrypsin deficiency.

10 re, early-onset COPD probands without severe alpha1-antitrypsin deficiency.

11 a 34-year-old man with cirrhosis related to alpha1-antitrypsin deficiency.

12 ive pulmonary disease (COPD) associated with alpha1-antitrypsin deficiency (AATD).

13 ng, is believed to cause lung destruction in alpha1-antitrypsin deficiency (AATD).

14 Organoids from alpha1-antitrypsin deficiency and Alagille syndrome pati

15 The association between Z alpha1-antitrypsin deficiency and juvenile cirrhosis is

16 studies of gene therapy for cystic fibrosis, alpha1-antitrypsin deficiency and lung cancer.

17 ng of genetic and nongenetic modifiers in ZZ alpha1-antitrypsin deficiency and other disorders of pro

18 the end-stage liver disease associated with alpha1-antitrypsin deficiency and underscore the contrib

19 netic disorders, such as cystic fibrosis and alpha1-antitrypsin deficiency, and for other diseases, i

20 with either alcohol-related liver disease or alpha1-antitrypsin deficiency, and only one of the healt

21 he most frequent mutation that causes severe alpha1-antitrypsin deficiency arises in the SERPINA 1 ge

22 alpha1-Antitrypsin deficiency (ATD) is a common genetic

23 In the classical form of alpha1-antitrypsin deficiency (ATD), aberrant intracellu

24 r injury in patients with the classical form alpha1-antitrypsin deficiency (ATD).

25 Less common causes include hemochromatosis, alpha1-antitrypsin deficiency, autoimmune hepatitis, and

26 Severe alpha1-antitrypsin deficiency caused by the Z variant (G

27 blished pulmonary mechanics in patients with alpha1-antitrypsin deficiency, chronic obstructive pulmo

28 ess of augmentation therapy (Aug) for severe alpha1-antitrypsin deficiency, comparing strategies of:

29 sensitive measure of disease progression in alpha1 antitrypsin deficiency emphysema than spirometry

30 ents with CF, primary ciliary dyskinesia, or alpha1-antitrypsin deficiency exhibited 3-fold higher mu

31 abolic conditions studied in further detail (alpha1-antitrypsin deficiency, familial hypercholesterol

32 netic hemochromatosis, Wilson's disease, and alpha1-antitrypsin deficiency grow significantly.

33 inhibitor (A1PI) augmentation treatment for alpha1 antitrypsin deficiency has not been substantiated

34 mphysema progression in patients with severe alpha1 antitrypsin deficiency in a randomised controlled

35 In alpha1-antitrypsin deficiency, intrahepatocyte accumulat

36 Alpha1-antitrypsin deficiency is a genetic disease that

37 Alpha1-antitrypsin deficiency is a genetic disorder that

38 alpha1-Antitrypsin deficiency is an inherited condition

39 alpha1-Antitrypsin deficiency is one of the most common

40 tients with alcohol-related liver disease or alpha1-antitrypsin-deficiency liver disease, and only on

41 drug-induced acute liver failure (one), and alpha1-antitrypsin deficiency (one).

42 verity and distribution in 119 subjects with alpha1-antitrypsin deficiency (PiZ phenotype) and groupe

43 y centres in 13 countries if they had severe alpha1 antitrypsin deficiency (serum concentration <11 m

44 Severe alpha1-antitrypsin deficiency (typically PiZZ homozygosi

45 The association of alpha1-antitrypsin deficiency with the development of em

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