Literature DB >> 22981789

Challenges of genetic counseling in patients with autosomal dominant diseases, such as the hyper-IgE syndrome (STAT3-HIES).

Benedikt D Spielberger, Cristina Woellner, Gregor Dueckers, Julie Sawalle-Belohradsky, Beate Hagl, Katja Anslinger, Birgit Bayer, Kathrin Siepermann, Tim Niehues, Bodo Grimbacher, Bernd H Belohradsky, Ellen D Renner.   

Abstract

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Year:  2012        PMID： 22981789     DOI： 10.1016/j.jaci.2012.07.030

Source DB:  PubMed          Journal:  J Allergy Clin Immunol        ISSN： 0091-6749            Impact factor:   10.793


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  3 in total

Review 1.  Human hyper-IgE syndrome: singular or plural?

Authors:  Qian Zhang; Bertrand Boisson; Vivien Béziat; Anne Puel; Jean-Laurent Casanova
Journal:  Mamm Genome       Date:  2018-08-09       Impact factor: 2.957

2.  Intermediate phenotypes in patients with autosomal dominant hyper-IgE syndrome caused by somatic mosaicism.

Authors:  Amy P Hsu; Kathryn J Sowerwine; Monica G Lawrence; Joie Davis; Carolyn J Henderson; Kol A Zarember; Mary Garofalo; John I Gallin; Douglas B Kuhns; Theo Heller; Joshua D Milner; Jennifer M Puck; Alexandra F Freeman; Steven M Holland
Journal:  J Allergy Clin Immunol       Date:  2013-04-25       Impact factor: 10.793

3.  Retained primary teeth in STAT3 hyper-IgE syndrome: early intervention in childhood is essential.

Authors:  Iris Meixner; Beate Hagl; Carolin I Kröner; Benedikt D Spielberger; Ekaterini Paschos; Gregor Dückers; Tim Niehues; Ronny Hesse; Ellen D Renner
Journal:  Orphanet J Rare Dis       Date:  2020-09-10       Impact factor: 4.123
  3 in total

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