DOCK8 deficiency: clinical and immunological phenotype and treatment options-a review of 136 patients

SE Aydin, SS Kilic, C Aytekin, A Kumar… - Journal of clinical …, 2015 - Springer
Mutations in DOCK8 result in autosomal recessive Hyper-IgE syndrome with combined
immunodeficiency (CID). However, the natural course of disease, long-term prognosis, and …
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DOCK8 deficiency: clinical and immunological phenotype and treatment options: a review of 136 patients

SE Aydin, SS Kilic, C Aytekin, A Kumar, O Porras… - 2015 - opus.bibliothek.uni-augsburg.de
OPUS 4 | DOCK8 deficiency: clinical and immunological phenotype and treatment options: a
review of 136 patients Deutsch Login Open Access Home Search Browse Publish/report a …

DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options-a Review of 136 Patients

SE Aydin, SS Kilic, C Aytekin, A Kumar… - Journal of Clinical …, 2015 - search.proquest.com
Mutations in DOCK8 result in autosomal recessive Hyper-IgE syndrome with combined
immunodeficiency (CID). However, the natural course of disease, long-term prognosis, and …

[引用][C] DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options-a Review of 136 Patients

SE Aydin, SS Kilic, C Aytekin, A Kumar… - Journal of Clinical …, 2015 - cir.nii.ac.jp
DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review
of 136 Patients | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ …

DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options-a Review of 136 Patients

SE Aydin, SS Kilic, C Aytekin, A Kumar… - Journal of Clinical …, 2015 - eprints.ncl.ac.uk
Abstract© 2015, Springer Science+ Business Media New York. Mutations in DOCK8 result in
autosomal recessive Hyper-IgE syndrome with combined immunodeficiency (CID) …

DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options-a Review of 136 Patients

SE Aydin, SS Kilic, C Aytekin… - Journal of …, 2015 - researchinformation.amsterdamumc …
Mutations in DOCK8 result in autosomal recessive Hyper-IgE syndrome with combined
immunodeficiency (CID). However, the natural course of disease, long-term prognosis, and …

DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options-a Review of 136 Patients

SE Aydin, SS Kilic, C Aytekin, A Kumar… - Journal of Clinical …, 2015 - infona.pl
Mutations in DOCK8 result in autosomal recessive Hyper-IgE syndrome with combined
immunodeficiency (CID). However, the natural course of disease, long-term prognosis, and …

DOCK8 deficiency: clinical and immunological phenotype and treatment options-a review of 136 patients

SE Aydin, SS Kilic, C Aytekin… - Journal of clinical …, 2015 - pubmed.ncbi.nlm.nih.gov
Mutations in DOCK8 result in autosomal recessive Hyper-IgE syndrome with combined
immunodeficiency (CID). However, the natural course of disease, long-term prognosis, and …

DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options-a Review of 136 Patients

S Aydin, S Kilic, C Aytekin, A Kumar… - JOURNAL OF …, 2015 - avesis.uludag.edu.tr
Mutations in DOCK8 result in autosomal recessive Hyper-IgE syndrome with combined
immunodeficiency (CID). However, the natural course of disease, long-term prognosis, and …

DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options-a Review of 136 Patients

SE Aydin, J Sawalle-Belohradsky, G Notheis… - Journal of Clinical …, 2015 - elibrary.ru
Mutations in DOCK8 result in autosomal recessive Hyper-IgE syndrome with combined
immunodeficiency (CID). However, the natural course of disease, long-term prognosis, and …