164 related articles for article (PubMed ID: 22926906)
1. [The incidence of alpha-1-antitrypsin (A1AT) deficiency alleles in population of Central Poland--preliminary results from newborn screening].
Chorostowska-Wynimko J; Struniawski R; Popławska B; Borszewska-Kornacka M
Pneumonol Alergol Pol; 2012; 80(5):450-3. PubMed ID: 22926906
[TBL] [Abstract][Full Text] [Related]
2. Pulmonary langerhans cell histiocytosis - insight into the incidence of alfa-1-antitrypsin (A1ATD) deficiency alleles.
Radzikowska E; Struniawski R; Chorostowska-Wynimko J; Wiatr E; Roszkowski-Śliż K
Adv Respir Med; 2017; 85(6):297-300. PubMed ID: 29288477
[TBL] [Abstract][Full Text] [Related]
3. Frequency of Rare Alpha-1 Antitrypsin Variants in Polish Patients with Chronic Respiratory Disorders.
Duk K; Zdral A; Szumna B; Roży A; Chorostowska-Wynimko J
Adv Exp Med Biol; 2016; 910():47-53. PubMed ID: 26987331
[TBL] [Abstract][Full Text] [Related]
4. Incidence of alpha-1 antitrypsin Z and S alleles in patients with granulomatosis with polyangiitis--pilot study.
Chorostowska-Wynimko J; Gawryluk D; Struniawski R; Popławska B; Fijołek J
Pneumonol Alergol Pol; 2013; 81(4):319-22. PubMed ID: 23744167
[TBL] [Abstract][Full Text] [Related]
5. [Genetic variants of alpha-1 antitrypsin: classification and clinical implications].
Popławska B; Janciauskiene S; Chorostowska-Wynimko J
Pneumonol Alergol Pol; 2013; 81(1):45-54. PubMed ID: 23258471
[TBL] [Abstract][Full Text] [Related]
6. α-1 Antitrypsin Genotype-Phenotype Discrepancy in a 42-Year-Old Man Who Carries the Null-Allele.
Pavičić T; Ćelap I; Njegovan M; Tešija Kuna A; Štefanović M
Lab Med; 2020 May; 51(3):301-305. PubMed ID: 31583408
[TBL] [Abstract][Full Text] [Related]
7. The prevalence of alpha(1)-antitrypsin deficiency in a representative population sample from Poland.
Kaczor MP; Sanak M; Libura-Twardowska M; Szczeklik A
Respir Med; 2007 Dec; 101(12):2520-5. PubMed ID: 17693072
[TBL] [Abstract][Full Text] [Related]
8. Frequency of alleles and genotypes associated with alpha-1 antitrypsin deficiency in clinical and general populations: Revelations about underdiagnosis.
Hernández-Pérez JM; Ramos-Díaz R; Vaquerizo-Pollino C; Pérez JA
Pulmonology; 2023; 29(3):214-220. PubMed ID: 35346640
[TBL] [Abstract][Full Text] [Related]
9. Rapid DNA extraction protocol for detection of alpha-1 antitrypsin deficiency from dried blood spots by real-time PCR.
Struniawski R; Szpechcinski A; Poplawska B; Skronski M; Chorostowska-Wynimko J
Adv Exp Med Biol; 2013; 756():29-37. PubMed ID: 22836616
[TBL] [Abstract][Full Text] [Related]
10. Alpha-1-antitrypsin deficiency in Serbian adults with lung diseases.
Topic A; Stankovic M; Divac-Rankov A; Petrovic-Stanojevic N; Mitic-Milikic M; Nagorni-Obradovic L; Radojkovic D
Genet Test Mol Biomarkers; 2012 Nov; 16(11):1282-6. PubMed ID: 22971141
[TBL] [Abstract][Full Text] [Related]
11. The prevalence of PI*S and PI*Z SERPINA1 alleles in healthy individuals and COPD patients in Saudi Arabia: A case-control study.
Al-Jameil N; Hassan AA; Hassanato R; Isac SR; Otaiby MA; Al-Shareef F; Al-Maarik B; Ajeyan IA; Al-Bahloul K; Ghani S; Al-Torbak D
Medicine (Baltimore); 2017 Oct; 96(42):e8320. PubMed ID: 29049242
[TBL] [Abstract][Full Text] [Related]
12. Alpha-1 antitrypsin deficiency: From the lung to the heart?
Curjuric I; Imboden M; Bettschart R; Caviezel S; Dratva J; Pons M; Rothe T; Schmidt-Trucksäss A; Stolz D; Thun GA; von Eckardstein A; Kronenberg F; Ferrarotti I; Probst-Hensch NM
Atherosclerosis; 2018 Mar; 270():166-172. PubMed ID: 29432934
[TBL] [Abstract][Full Text] [Related]
13. Sensitivity of alpha-1 antitrypsin level for inherited deficiency detection in COPD patients.
Serapinas D; Sakalauskas R
Pneumologia; 2012; 61(1):34-6. PubMed ID: 22545487
[TBL] [Abstract][Full Text] [Related]
14. Linkage analysis of alpha 1-antitrypsin deficiency: lessons for complex diseases.
Silverman EK; Mosley JD; Rao DC; Palmer LJ; Province MA; Elston RC; Weiss ST; Campbell EJ
Hum Hered; 2001; 52(4):223-32. PubMed ID: 11713419
[TBL] [Abstract][Full Text] [Related]
15. Rapid screening for alpha1-antitrypsin deficiency in patients with chronic obstructive pulmonary disease using dried blood specimens.
Rodriguez F; Jardí R; Costa X; Cotrina M; Galimany R; Vidal R; Miravitlles M
Am J Respir Crit Care Med; 2002 Sep; 166(6):814-7. PubMed ID: 12231490
[TBL] [Abstract][Full Text] [Related]
16. Is an integrative laboratory algorithm more effective in detecting alpha-1-antitrypsin deficiency in patients with premature chronic obstructive pulmonary disease than AAT concentration based screening approach?
Beletic A; Dudvarski-Ilic A; Milenkovic B; Nagorni-Obradovic L; Ljujic M; Djordjevic V; Mirkovic D; Radojkovic D; Majkic-Singh N
Biochem Med (Zagreb); 2014; 24(2):293-8. PubMed ID: 24969923
[TBL] [Abstract][Full Text] [Related]
17. Prevalence of alpha-1 antitrypsin deficiency and allele frequency in patients with COPD in Brazil.
Russo R; Zillmer LR; Nascimento OA; Manzano B; Ivanaga IT; Fritscher L; Lundgren F; Miravitlles M; Gondim HD; Santos G; Alves MA; Oliveira MV; Souza AA; Sales MP; Jardim JR
J Bras Pneumol; 2016; 42(5):311-316. PubMed ID: 27812629
[TBL] [Abstract][Full Text] [Related]
18. Null
Chen S; DeMarco ML; Estey MP; Kyle B; Parker ML; Agbor TA; Kawada P; Speevak M; Nelson TN; Mattman A
Clin Biochem; 2020 May; 79():23-27. PubMed ID: 32087139
[TBL] [Abstract][Full Text] [Related]
19. How Can We Improve the Detection of Alpha1-Antitrypsin Deficiency?
Ferrarotti I; Poplawska-Wisniewska B; Trevisan MT; Koepke J; Dresel M; Koczulla R; Ottaviani S; Baldo R; Gorrini M; Sala G; Cavallon L; Welte T; Chorostowska-Wynimko J; Luisetti M; Janciauskiene S
PLoS One; 2015; 10(8):e0135316. PubMed ID: 26270547
[TBL] [Abstract][Full Text] [Related]
20. [Place of genotyping in addition to the phenotype and the assay of serum α-1 antitrypsin].
Joly P; Francina A; Lacan P; Heraut J; Chapuis-Cellier C
Ann Biol Clin (Paris); 2011; 69(5):571-6. PubMed ID: 22008137
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
