Manifestaciones cutáneas en lactante con síndrome de hiper-IgE
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Published in | Anales de pediatría (Barcelona, Spain : 2003) Vol. 90; no. 5; pp. 319 - 320 |
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Main Authors | , , , |
Format | Journal Article |
Language | Spanish |
Published |
Elsevier España, S.L.U
01.05.2019
Elsevier |
Subjects | |
Online Access | Get full text |
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Author | García-Fernández, Manuel Emilio Peña-López, Sandra Monteagudo, Benigno Fernández-Jorge, Beatriz |
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Author_xml | – sequence: 1 fullname: Peña-López, Sandra – sequence: 2 fullname: Monteagudo, Benigno – sequence: 3 fullname: Fernández-Jorge, Beatriz – sequence: 4 fullname: García-Fernández, Manuel Emilio |
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Cites_doi | 10.1016/j.jaad.2010.09.714 10.1001/archderm.140.9.1119 10.1097/MD.0b013e31825f95b9 |
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DocumentTitleAlternate | Cutaneous manifestations in an infant with hyper-IgE syndrome |
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References | Chandesris, Melki, Natividad, Puel, Fieschi, Yun (bib0020) 2012; 91 Eberting, Davis, Puck, Holland, Turner (bib0025) 2004; 140 Olaiwan, Chandesris, Fraitag, Lortholary, Hermine, Fisher (bib0030) 2011; 65 Eberting (10.1016/j.anpedi.2018.03.015_bib0025) 2004; 140 Olaiwan (10.1016/j.anpedi.2018.03.015_bib0030) 2011; 65 Chandesris (10.1016/j.anpedi.2018.03.015_bib0020) 2012; 91 |
References_xml | – volume: 140 start-page: 1119 year: 2004 end-page: 1125 ident: bib0025 article-title: Dermatitis and the newborn rash of hyper-IgE syndrome publication-title: Arch Dermatol contributor: fullname: Turner – volume: 91 start-page: 1 year: 2012 end-page: 19 ident: bib0020 article-title: Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: Molecular, cellular, and clinical features from a French national survey publication-title: Medicine (Baltimore) contributor: fullname: Yun – volume: 65 start-page: 1167 year: 2011 end-page: 1172 ident: bib0030 article-title: Cutaneous findings in sporadic and familial autosomal dominant hyper-IgE syndrome: A retrospective, single-center study of 21 patients diagnosed using molecular analysis publication-title: J Am Acad Dermatol contributor: fullname: Fisher – volume: 65 start-page: 1167 year: 2011 ident: 10.1016/j.anpedi.2018.03.015_bib0030 article-title: Cutaneous findings in sporadic and familial autosomal dominant hyper-IgE syndrome: A retrospective, single-center study of 21 patients diagnosed using molecular analysis publication-title: J Am Acad Dermatol doi: 10.1016/j.jaad.2010.09.714 contributor: fullname: Olaiwan – volume: 140 start-page: 1119 year: 2004 ident: 10.1016/j.anpedi.2018.03.015_bib0025 article-title: Dermatitis and the newborn rash of hyper-IgE syndrome publication-title: Arch Dermatol doi: 10.1001/archderm.140.9.1119 contributor: fullname: Eberting – volume: 91 start-page: 1 year: 2012 ident: 10.1016/j.anpedi.2018.03.015_bib0020 article-title: Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: Molecular, cellular, and clinical features from a French national survey publication-title: Medicine (Baltimore) doi: 10.1097/MD.0b013e31825f95b9 contributor: fullname: Chandesris |
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Title | Manifestaciones cutáneas en lactante con síndrome de hiper-IgE |
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