Literature DB >> 25546745

Primary immunodeficiencies screening: neonatal screening for T/B cell disorders - a triplex PCR method for quantitation of TRECs and KRECs in newborns.

L Hammarström1.   

Abstract

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Year:  2014        PMID: 25546745      PMCID: PMC4285474          DOI: 10.1111/cei.12494

Source DB:  PubMed          Journal:  Clin Exp Immunol        ISSN: 0009-9104            Impact factor:   4.330


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  8 in total

1.  Impact of Down syndrome on the performance of neonatal screening assays for severe primary immunodeficiency diseases.

Authors:  Ruud H J Verstegen; Stephan Borte; Levinus A Bok; Paul H Th van Zwieten; Ulrika von Döbeln; Lennart Hammarström; Esther de Vries
Journal:  J Allergy Clin Immunol       Date:  2013-12-09       Impact factor: 10.793

2.  Quantification of κ-deleting recombination excision circles in Guthrie cards for the identification of early B-cell maturation defects.

Authors:  Noriko Nakagawa; Kohsuke Imai; Hirokazu Kanegane; Hiroki Sato; Masafumi Yamada; Kensuke Kondoh; Satoshi Okada; Masao Kobayashi; Kazunaga Agematsu; Hidetoshi Takada; Noriko Mitsuiki; Koichi Oshima; Osamu Ohara; Deepti Suri; Amit Rawat; Surjit Singh; Qiang Pan-Hammarström; Lennart Hammarström; Janine Reichenbach; Reinhard Seger; Tadashi Ariga; Toshiro Hara; Toshio Miyawaki; Shigeaki Nonoyama
Journal:  J Allergy Clin Immunol       Date:  2011-03-11       Impact factor: 10.793

3.  Retrospective analysis of TREC based newborn screening results and clinical phenotypes in infants with the 22q11 deletion syndrome.

Authors:  Jenny Lingman Framme; Stephan Borte; Ulrika von Döbeln; Lennart Hammarström; Sólveig Oskarsdóttir
Journal:  J Clin Immunol       Date:  2014-03-09       Impact factor: 8.317

4.  Development of population-based newborn screening for severe combined immunodeficiency.

Authors:  Kee Chan; Jennifer M Puck
Journal:  J Allergy Clin Immunol       Date:  2005-02       Impact factor: 10.793

5.  Newborn screening for severe T and B cell lymphopenia identifies a fraction of patients with Wiskott-Aldrich syndrome.

Authors:  Stephan Borte; Anders Fasth; Ulrika von Döbeln; Jacek Winiarski; Lennart Hammarström
Journal:  Clin Immunol       Date:  2014-09-15       Impact factor: 3.969

Review 6.  Guidelines for newborn screening of primary immunodeficiency diseases.

Authors:  Stephan Borte; Ulrika von Döbeln; Lennart Hammarström
Journal:  Curr Opin Hematol       Date:  2013-01       Impact factor: 3.284

Review 7.  The case for mandatory newborn screening for severe combined immunodeficiency (SCID).

Authors:  H B Gaspar; L Hammarström; N Mahlaoui; M Borte; S Borte
Journal:  J Clin Immunol       Date:  2014-04-02       Impact factor: 8.317

8.  Neonatal screening for severe primary immunodeficiency diseases using high-throughput triplex real-time PCR.

Authors:  Stephan Borte; Ulrika von Döbeln; Anders Fasth; Ning Wang; Magdalena Janzi; Jacek Winiarski; Ulrich Sack; Qiang Pan-Hammarström; Michael Borte; Lennart Hammarström
Journal:  Blood       Date:  2011-11-30       Impact factor: 22.113

  8 in total
  1 in total

1.  Screening for primary immunodeficiency diseases by next-generation sequencing in early life.

Authors:  Jinqiao Sun; Lin Yang; Yulan Lu; Huijun Wang; Xiaomin Peng; Xinran Dong; Guoqiang Cheng; Yun Cao; Bingbing Wu; Xiaochuan Wang; Wenhao Zhou
Journal:  Clin Transl Immunology       Date:  2020-05-17
  1 in total

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