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DC Field | Value | Language |
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dc.contributor | Sistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP | |
dc.contributor.author | SOARES, Diogo C. | |
dc.contributor.author | DANTAS, Anelisa G. | |
dc.contributor.author | MATTA, Marina C. | |
dc.contributor.author | PASTORINO, Antonio C. | |
dc.contributor.author | MELARAGNO, Maria Isabel | |
dc.contributor.author | KULIKOWSKI, Leslie | |
dc.contributor.author | MONTENEGRO, Marilia | |
dc.contributor.author | KIM, Chong A. | |
dc.contributor.author | CARNEIRO-SAMPAIO, Magda | |
dc.contributor.author | TORRES, Leuridan C. | |
dc.date.accessioned | 2020-12-16T14:56:47Z | - |
dc.date.available | 2020-12-16T14:56:47Z | - |
dc.date.issued | 2020 | |
dc.identifier.citation | CLINICAL IMMUNOLOGY, v.220, article ID 108590, 3p, 2020 | |
dc.identifier.issn | 1521-6616 | |
dc.identifier.uri | https://observatorio.fm.usp.br/handle/OPI/38505 | - |
dc.description.abstract | 22q11.2 deletion syndrome (22q11.2DS) has a heterogeneous presentation that includes multiple congenital anomalies and immunodeficiency, one of the most striking features. Usually, it is characterized by T cell lymphopenia, B cell dysfunction and autoimmunity. Here, we describe an unusual case of 22q11.2DS in a patient with lymphoproliferative disorder, polyautoimmunity and hypogammaglobulinemia. | eng |
dc.description.sponsorship | FAPESPFundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [2014/11572-8, 2014/50489-9] | |
dc.description.sponsorship | CAPESCAPES [001] | |
dc.language.iso | eng | |
dc.publisher | ACADEMIC PRESS INC ELSEVIER SCIENCE | eng |
dc.relation.ispartof | Clinical Immunology | |
dc.rights | restrictedAccess | eng |
dc.subject | DiGeorge syndrome | eng |
dc.subject | 22q11.2 deletion syndrome | eng |
dc.subject | Immunodeficiency | eng |
dc.subject | Autoimmunity | eng |
dc.subject | Hypogammaglobulinemia | eng |
dc.subject.other | responses | eng |
dc.title | Lymphoproliferative disorder with polyautoimmunity and hypogammaglobulinemia: An unusual presentation of 22q11.2 deletion syndrome | eng |
dc.type | article | eng |
dc.rights.holder | Copyright ACADEMIC PRESS INC ELSEVIER SCIENCE | eng |
dc.identifier.doi | 10.1016/j.clim.2020.108590 | |
dc.identifier.pmid | 32920211 | |
dc.subject.wos | Immunology | eng |
dc.type.category | letter | eng |
dc.type.version | publishedVersion | eng |
hcfmusp.author.external | DANTAS, Anelisa G.:Univ Fed Sao Paulo UNIFESP, Div Genet, Dept Morphol & Genet, Sao Paulo, SP, Brazil | |
hcfmusp.author.external | MATTA, Marina C.:Inst Med Integral Prof Fernando Figueira IMIP, Translat Res Lab, Recife, PE, Brazil | |
hcfmusp.author.external | MELARAGNO, Maria Isabel:Univ Fed Sao Paulo UNIFESP, Div Genet, Dept Morphol & Genet, Sao Paulo, SP, Brazil | |
hcfmusp.author.external | TORRES, Leuridan C.:Inst Med Integral Prof Fernando Figueira IMIP, Translat Res Lab, Recife, PE, Brazil | |
hcfmusp.description.articlenumber | 108590 | |
hcfmusp.description.volume | 220 | |
hcfmusp.origem | WOS | |
hcfmusp.origem.id | WOS:000582396200009 | |
hcfmusp.origem.id | 2-s2.0-85091232100 | |
hcfmusp.publisher.city | SAN DIEGO | eng |
hcfmusp.publisher.country | USA | eng |
hcfmusp.relation.reference | De Dios Jose Angelo A, 2012, Conn Med, V76, P15 | eng |
hcfmusp.relation.reference | Finocchi A, 2006, PEDIATR ALLERGY IMMU, V17, P382, DOI 10.1111/j.1399-3038.2006.00409.x | eng |
hcfmusp.relation.reference | Gennery AR, 2012, CELL MOL LIFE SCI, V69, P17, DOI 10.1007/s00018-011-0842-z | eng |
hcfmusp.relation.reference | Mather MW, 2015, J ALLERGY CLIN IMMUN, V135, P559, DOI 10.1016/j.jaci.2014.07.025 | eng |
hcfmusp.relation.reference | McDonald-McGinn DM, 2015, NAT REV DIS PRIMERS, V1, DOI 10.1038/nrdp.2015.71 | eng |
hcfmusp.relation.reference | Nain E, 2019, SCAND J IMMUNOL, V90, DOI 10.1111/sji.12809 | eng |
hcfmusp.relation.reference | Sood AK, 2018, CURR ALLERGY ASTHM R, V18, DOI 10.1007/s11882-018-0769-7 | eng |
hcfmusp.relation.reference | Sullivan KE, 2019, IMMUNOL REV, V287, P186, DOI 10.1111/imr.12701 | eng |
hcfmusp.relation.reference | Tam PYI, 2015, CLIN PEDIATR, V54, P1290, DOI 10.1177/0009922814565885 | eng |
dc.description.index | MEDLINE | eng |
dc.identifier.eissn | 1521-7035 | |
hcfmusp.citation.scopus | 1 | - |
hcfmusp.scopus.lastupdate | 2024-03-29 | - |
Appears in Collections: | Artigos e Materiais de Revistas Científicas - FM/MPE Artigos e Materiais de Revistas Científicas - HC/ICr Artigos e Materiais de Revistas Científicas - LIM/03 Artigos e Materiais de Revistas Científicas - LIM/36 Artigos e Materiais de Revistas Científicas - ODS/03 |
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art_SOARES_Lymphoproliferative_disorder_with_polyautoimmunity_and_hypogammaglobulinemia_An_unusual_2020.PDF.pdf Restricted Access | publishedVersion (English) | 1 MB | Adobe PDF | View/Open Request a copy |
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