Literature DB >> 28414192

Congenital erythroderma should be considered as an urgent warning sign of immunodeficiency: a case of Omenn syndrome.

Edwin Cuperus1, Joris M VAN Montfrans2, Mariëlle E VAN Gijn3, Maarten T Bastiaens4, Mirjam Ma DE Willigen5, Roos J Leguit6, Carla Afm Brijnzeel-Koomen7, Ingrid Mb RusseL8, Suzanne Gma Pasmans9.   

Abstract

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Year:  2017        PMID： 28414192     DOI： 10.1684/ejd.2017.2992

Source DB:  PubMed          Journal:  Eur J Dermatol        ISSN： 1167-1122            Impact factor:   3.328


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  3 in total

1.  A Novel RAG1 Mutation in a Compound Heterozygous Status in a Child With Omenn Syndrome.

Authors:  Juan Shen; Li Jiang; Yifang Gao; Rongqiong Ou; Sifei Yu; Binyan Yang; Changyou Wu; Weiping Tan
Journal:  Front Genet       Date:  2019-10-02       Impact factor: 4.599

Review 2.  Proposal for a 6-step approach for differential diagnosis of neonatal erythroderma.

Authors:  E Cuperus; A Bygum; L Boeckmann; C Bodemer; M C Bolling; M Caproni; A Diociaiuti; S Emmert; J Fischer; A Gostynski; S Guez; M E van Gijn; K Hannulla-Jouppi; C Has; A Hernández-Martín; A E Martinez; J Mazereeuw-Hautier; M Medvecz; I Neri; V Sigurdsson; K Suessmuth; H Traupe; V Oji; S G M A Pasmans
Journal:  J Eur Acad Dermatol Venereol       Date:  2022-03-15       Impact factor: 9.228

3.  Reduced Function and Diversity of T Cell Repertoire and Distinct Clinical Course in Patients With IL7RA Mutation.

Authors:  Atar Lev; Amos J Simon; Ortal Barel; Eran Eyal; Efrat Glick-Saar; Omri Nayshool; Ohad Birk; Tali Stauber; Amit Hochberg; Arnon Broides; Shlomo Almashanu; Ayal Hendel; Yu Nee Lee; Raz Somech
Journal:  Front Immunol       Date:  2019-07-17       Impact factor: 7.561
  3 in total

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