Clinical aspects and genetic analysis of Taiwanese patients with the phenotype of hyper-immunoglobulin E recurrent infection syndromes (HIES).
Lee, Wen-I; Huang, Jing-Long; Lin, Shy-Jae; Yeh, Kuo-Wei; Chen, Li-Chen; Hsieh, Meng-Ying; Huang, Yhu-Chering; Kuo, Ho-Chang; Yang, Kunder D; Yu, Hong-Ren; Jaing, Tang-Her; Yang, Chih-Hsun.
J Clin Immunol
; 31(2): 272-80, 2011 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-21120687
[THE DISEASE OF JOB].
Hyper IgE syndromes: clinical and molecular characteristics.
Autosomal recessive hyper-IgE syndrome successfully treated with hematopoietic stem cell transplantation.
Hyper-IgE syndromes: recent advances in pathogenesis, diagnostics and clinical care.
Hyper-IgE Syndrome in an Infant.
DOCK8 mutation diagnosed using whole-exome sequencing of the dried blood spot-derived DNA: a case report of an Iraqi girl diagnosed in Japan.
Squamous Cell Carcinoma With Hyper-IgE Syndrome: A Case Report.
Clinical Manifestation of Hyper IgE Syndrome Including Otitis Media.
Clinical Manifestations and Genetic Analysis of 17 Patients with Autosomal Dominant Hyper-IgE Syndrome in Mainland China: New Reports and a Literature Review.
A deep intronic splice mutation of <i>STAT3</i> underlies hyper IgE syndrome by negative dominance.