179 related articles for article (PubMed ID: 21636698)
1. Simultaneous phenotyping and quantification of α-1-antitrypsin by liquid chromatography-tandem mass spectrometry.
Chen Y; Snyder MR; Zhu Y; Tostrud LJ; Benson LM; Katzmann JA; Bergen HR
Clin Chem; 2011 Aug; 57(8):1161-8. PubMed ID: 21636698
[TBL] [Abstract][Full Text] [Related]
2. Diagnosis of alpha-1-antitrypsin deficiency: An algorithm of quantification, genotyping, and phenotyping.
Snyder MR; Katzmann JA; Butz ML; Wiley C; Yang P; Dawson DB; Halling KC; Highsmith WE; Thibodeau SN
Clin Chem; 2006 Dec; 52(12):2236-42. PubMed ID: 17053153
[TBL] [Abstract][Full Text] [Related]
3. Quantitation of circulating wild-type alpha-1-antitrypsin in heterozygous carriers of the S and Z deficiency alleles.
Donato LJ; Karras RM; Katzmann JA; Murray DL; Snyder MR
Respir Res; 2015 Aug; 16(1):96. PubMed ID: 26243289
[TBL] [Abstract][Full Text] [Related]
4. Alpha-1-Antitrypsin (A1AT) Proteotyping by LC-MS/MS.
Kemp J; Ladwig PM; Snyder MR
Methods Mol Biol; 2024; 2750():95-106. PubMed ID: 38108970
[TBL] [Abstract][Full Text] [Related]
5. 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]
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. [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]
8. [Development of a laboratory test on dried blood spots for facilitating early diagnosis of alpha-1-antitrypsin deficiency].
Balduyck M; Chapuis Cellier C; Roche D; Odou MF; Joly P; Madelain V; Vergne A; Nouadje G; Lafitte JJ; Porchet N; Beaune P; Zerimech F
Ann Biol Clin (Paris); 2014; 72(6):689-704. PubMed ID: 25486665
[TBL] [Abstract][Full Text] [Related]
9. Reference and interpretive ranges for α(1)-antitrypsin quantitation by phenotype in adult and pediatric populations.
Donato LJ; Jenkins SM; Smith C; Katzmann JA; Snyder MR
Am J Clin Pathol; 2012 Sep; 138(3):398-405. PubMed ID: 22912357
[TBL] [Abstract][Full Text] [Related]
10. Liquid Chromatography-Tandem Mass Spectrometry-Based α1-Antitrypsin (AAT) Testing.
Murray JD; Willrich MA; Krowka MJ; Bobr A; Murray DL; Halling KC; Graham RP; Snyder MR
Am J Clin Pathol; 2021 Mar; 155(4):547-552. PubMed ID: 33083828
[TBL] [Abstract][Full Text] [Related]
11. Quantitative Analysis of α-1-Antitrypsin Glycosylation Isoforms in HCC Patients Using LC-HCD-PRM-MS.
Yin H; Zhu J; Wang M; Yao ZP; Lubman DM
Anal Chem; 2020 Jun; 92(12):8201-8208. PubMed ID: 32426967
[TBL] [Abstract][Full Text] [Related]
12. Alpha-1-antitrypsin molecular testing in Canada: A seven year, multi-centre comparison.
Mattman A; Gilfix BM; Chen SX; DeMarco ML; Kyle BD; Parker ML; Agbor TA; Jung B; Selvarajah S; Barakauskas VE; Vaags AK; Estey MP; Nelson TN; Speevak MD
Clin Biochem; 2020 Jul; 81():27-33. PubMed ID: 32387440
[TBL] [Abstract][Full Text] [Related]
13. A step toward simplicity for a complex analyte.
Bystrom CE
Clin Chem; 2011 Aug; 57(8):1091-2. PubMed ID: 21666071
[No Abstract] [Full Text] [Related]
14. A rare variant of α 1 antitrypsin mutations detected in Vietnamese children with liver disease.
Hoàng TH; Phạm TN; Nguyễn GK; Lê QH
Ann Clin Biochem; 2013 Jul; 50(Pt 4):339-44. PubMed ID: 23766346
[TBL] [Abstract][Full Text] [Related]
15. Isoelectric focusing phenotyping and denaturing gradient gel electrophoresis genotyping: a comparison of two methods in detection of alpha-1-antitrypsin variants.
Ljujic M; Topic A; Divac A; Nikolic A; Petrovic-Stanojevic N; Surlan M; Mitic-Milikic M; Radojkovic D
Transl Res; 2008 May; 151(5):255-9. PubMed ID: 18433707
[TBL] [Abstract][Full Text] [Related]
16. Polymerase chain reaction-mediated site-directed mutagenesis detection of Z and S alpha-1-antitrypsin alleles in family members.
Hammerberg G; Keren DF
J Clin Lab Anal; 1996; 10(6):384-8. PubMed ID: 8951606
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Clinical heterogeneity and potential high pathogenicity of the Mmalton Alpha 1 antitrypsin allele at the homozygous, compound heterozygous and heterozygous states.
Joly P; Guillaud O; Hervieu V; Francina A; Mornex JF; Chapuis-Cellier C
Orphanet J Rare Dis; 2015 Oct; 10():130. PubMed ID: 26446624
[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. Optimizing the screening of alpha-1 antitrypsin deficiency using serum protein electrophoresis.
Wauthier L; Jacques S; Delanghe J; Favresse J
Clin Chem Lab Med; 2023 Feb; 61(3):427-434. PubMed ID: 36420543
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
