Literature DB >> 15491395

Refractory autoimmune hemolytic anemia in a patient with chromosome 22q11.2 deletion syndrome.

Osamu Sakamoto1, Masue Imaizumi, Ari Suzuki, Atsushi Sato, Takashi Tanaka, Eishin Ogawa, Satoru Kumaki, Kazuie Iinuma.   

Abstract

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Year:  2004        PMID： 15491395     DOI： 10.1111/j.1442-200x.2004.01940.x

Source DB:  PubMed          Journal:  Pediatr Int        ISSN： 1328-8067            Impact factor:   1.524


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  4 in total

1.  Evans syndrome and antibody deficiency: an atypical presentation of chromosome 22q11.2 deletion syndrome.

Authors:  Gloria Colarusso; Eleonora Gambineri; Elisabetta Lapi; Tommaso Casini; Fabio Tucci; Francesca Lippi; Chiara Azzari
Journal:  Pediatr Rep       Date:  2010-09-06

Review 2.  From murine to human nude/SCID: the thymus, T-cell development and the missing link.

Authors:  Rosa Romano; Loredana Palamaro; Anna Fusco; Leucio Iannace; Stefano Maio; Ilaria Vigliano; Giuliana Giardino; Claudio Pignata
Journal:  Clin Dev Immunol       Date:  2012-03-05

3.  Recurrent Evans Syndrome in a Patient With 22q11.2 Deletion Syndrome: An Uncommon Hematological Presentation.

Authors:  Hector A Oliveras-Cordero; Enid Rivera-Jiménez
Journal:  Cureus       Date:  2020-11-16

Review 4.  Immunodeficiency in DiGeorge Syndrome and Options for Treating Cases with Complete Athymia.

Authors:  E Graham Davies
Journal:  Front Immunol       Date:  2013-10-31       Impact factor: 7.561
  4 in total

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