Literature DB >> 29182883

Clinical Experience with SERPINA1 DNA Sequencing to Detect Alpha-1 Antitrypsin Deficiency.

François Maltais1, Nathalie Gaudreault1, Christine Racine1, Sébastien Thériault1, Yohan Bossé1.   

Abstract

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Year:  2018        PMID: 29182883     DOI: 10.1513/AnnalsATS.201708-694RL

Source DB:  PubMed          Journal:  Ann Am Thorac Soc        ISSN: 2325-6621


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  5 in total

1.  IntraIndividual Variability in Serum Alpha-1 Antitrypsin Levels.

Authors:  Annie Haillot; Andrée-Anne Pelland; Yohan Bossé; Tomás P Carroll; François Maltais; Ronald J Dandurand
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2.  Fulminant hepatic failure in the setting of progressive ANCA-associated vasculitis associated with a rare alpha-1 antitrypsin phenotype, 'PiEE'.

Authors:  Ronald Reilkoff; Laurel Stephenson
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4.  Thrombotic risk determined by rare and common SERPINA1 variants in a population-based cohort study.

Authors:  Eric Manderstedt; Christer Halldén; Christina Lind-Halldén; Johan Elf; Peter J Svensson; Gunnar Engström; Olle Melander; Aris Baras; Luca A Lotta; Bengt Zöller
Journal:  J Thromb Haemost       Date:  2022-03-19       Impact factor: 16.036

5.  The Clinical Utility of Determining the Allelic Background of Mutations Causing Alpha-1 Antitrypsin Deficiency: The Case with the Null Variant Q0(Mattawa)/Q0(Ourém).

Authors:  Judith Bellemare; Nathalie Gaudreault; Kim Valette; Irene Belmonte; Alexa Nuñez; Marc Miravitlles; François Maltais; Yohan Bossé
Journal:  Chronic Obstr Pulm Dis       Date:  2021-01
  5 in total

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