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Literature DB >> 9133954

Systemic lupus erythematosus complicating hyper IgE syndrome.

J North, S Kotecha, P Houtman, K Whaley.

Abstract

Entities: Disease

Mesh：

Substances：
Immunoglobulin E

Year: 1997 PMID： 9133954 DOI： 10.1093/rheumatology/36.2.297

Source DB: PubMed Journal: Br J Rheumatol ISSN： 0263-7103

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Cited

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7 in total

Review 1. Autoimmunity in Primary Immunodeficiencies (PID).

Authors: Grace T Padron; Vivian P Hernandez-Trujillo
Journal: Clin Rev Allergy Immunol Date: 2022-06-01 Impact factor: 8.667

Review 2. A review on the vascular features of the hyperimmunoglobulin E syndrome.

Authors: H Yavuz; R Chee
Journal: Clin Exp Immunol Date: 2009-11-12 Impact factor: 4.330

Review 3. The hyperimmunoglobulin E syndrome--clinical manifestation diversity in primary immune deficiency.

Authors: Aleksandra Szczawinska-Poplonyk; Zdzislawa Kycler; Barbara Pietrucha; Edyta Heropolitanska-Pliszka; Anna Breborowicz; Karolina Gerreth
Journal: Orphanet J Rare Dis Date: 2011-11-15 Impact factor: 4.123

Review 4. Hyper-IgE syndrome and autoimmunity in Mexican children.

Authors: Marco Yamazaki-Nakashimada; Samuel Zaltzman-Girshevich; Silvestre Garcia de la Puente; Beatriz De Leon-Bojorge; Sara Espinosa-Padilla; Marimar Saez-de-Ocariz; Daniel Carrasco-Daza; Victor Hernandez-Bautista; Lorenzo Pérez-Fernandez; Francisco Espinosa-Rosales
Journal: Pediatr Nephrol Date: 2006-06-22 Impact factor: 3.651

Systemic lupus erythematosus complicating hyper IgE syndrome.

Review 1. Autoimmunity in Primary Immunodeficiencies (PID).

Review 2. A review on the vascular features of the hyperimmunoglobulin E syndrome.

Review 3. The hyperimmunoglobulin E syndrome--clinical manifestation diversity in primary immune deficiency.

Review 4. Hyper-IgE syndrome and autoimmunity in Mexican children.

5. Hyperimmunoglobulin E-recurrent infection syndrome in a patient with juvenile dermatomyositis.

Review 6. Hyperimmunoglobulin E syndrome: Genetics, immunopathogenesis, clinical findings, and treatment modalities.

Review 7. An update on the hyper-IgE syndromes.