Clinical, Immunological Features and Follow up of 21 Patients with Dedicator of Cytokinesis 8 (DOCK8) Deficiency

Immunodeficiency

The clinical and immunological features of patients with primary antibody deficiencies

Endocr Metab Immune Disord Drug Targets.

Azizi G, Bagheri Y, Tavakol M, Askarimoghaddam F, Poorrostami K, Rafiemanesh H, Yazdani R, Kiaee F, Habibi S, Abouhamzeh K, Mohammadi H, Qorbani M, Abolhassani H, Aghamohammadi A

doi: 10.2174/

Autoimmune Disease

Clinical and immunological features of antiphospholipid syndrome in the elderly: a retrospective national multicentre study

Rheumatology (Oxford).

Grimaud F, Yelnik C, Pineton de Chambrun M, Amoura Z, Arnaud L, Costedoat Chalumeau N, Hachulla E, Lambert M, Roriz M, Sibilia J, Papo T, Sacre K

doi: 10.1093/rheumatology/key437.

Immunodeficiency

Clinical, Immunological and Genetic findings in Patients with UNC13D Deficiency (FHL3): a Systematic Review

Pediatr Allergy Immunol.

Amirifar P, Ranjouri MR, Abolhassani H, Moeini Shad T, Almasi-Hashiani A, Azizi G, Moamer S, Aghamohammadi A, Yazdani R

doi: 10.1111/pai.13323.

Further Publications Immunology

Clinical, immunological, and genetic features in patients with Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-linked (IPEX) and IPEX-like Syndrome

J Allergy Clin Immunol Pract.

Jamee M, Zaki-Dizaji M, Lo B, Abolhassani H, Aghamahdi F, Mosavian M, Nademi Z, Mohammadi H, Jadidi-Niaragh F, Rojas M, Anaya JM, Azizi G

doi: 10.1016/j.jaip.2020.04.070.

Rheumatoid Arthritis

Does immunological remission, defined as disappearance of autoantibodies, occur with current treatment strategies? A long-term follow-up study in rheumatoid arthritis patients who achieved sustained DMARD-free status

Ann Rheum Dis.

Boeters DM, Burgers LE, Toes RE, van der Helm-van Mil A

doi: 10.1136/annrheumdis-2018-214868.

Immunodeficiency

Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2

Front Immunol.

Klemann C, Camacho-Ordonez N, Yang L, Eskandarian Z, Rojas-Restrepo JL, Frede N, Bulashevska A, Heeg M, Al-Ddafari MS, Premm J, Seidl M, Ammann S, Sherkat R, Radhakrishnan N, Warnatz K, Unger S, Kobbe R, Hüfner A, Leahy TR, Ip W, Burns SO, Fliegauf M, Grimbacher B

doi: 10.3389/fimmu.2019.00297.

Immunodeficiency

Immunological and Clinical Phenotyping in Primary Antibody Deficiencies: a Growing Disease Spectrum

J Clin Immunol.

Shin JJ, Liauw D, Siddiqui S, Lee J, Chung EJ, Steele R, Hsu FI, Price C, Kang I

doi: 10.1007/s10875-020-00773-y.

Immunodeficiency

Modulation of the Interleukin-21 Pathway with Interleukin-4 Distinguishes Common Variable Immunodeficiency Patients with More Non-infectious Clinical Complications

J Clin Immunol.

Desjardins M, Béland M, Dembele M, Lejtenyi D, Drolet JP, Lemire M, Tsoukas C, Ben-Shoshan M, Noya FJD, Alizadehfar R, McCusker CT, Mazer BD

doi: 10.1007/s10875-017-0452-0.

Psoriasis

Association of IL36RN mutation with clinical features, therapeutic response to acitretin, and frequency of recurrence in patients with generalized pustular psoriasis

Eur J Dermatol.

Zhu T, Jin H, Shu D, Li F, Wu C

doi: 10.1684/ejd.2018.3245.

Related content

The clinical and immunological features of patients with primary antibody deficiencies

Clinical and immunological features of antiphospholipid syndrome in the elderly: a retrospective national multicentre study

Clinical, Immunological and Genetic findings in Patients with UNC13D Deficiency (FHL3): a Systematic Review

Clinical, immunological, and genetic features in patients with Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-linked (IPEX) and IPEX-like Syndrome

Does immunological remission, defined as disappearance of autoantibodies, occur with current treatment strategies? A long-term follow-up study in rheumatoid arthritis patients who achieved sustained DMARD-free status

Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2

Immunological and Clinical Phenotyping in Primary Antibody Deficiencies: a Growing Disease Spectrum

Modulation of the Interleukin-21 Pathway with Interleukin-4 Distinguishes Common Variable Immunodeficiency Patients with More Non-infectious Clinical Complications

Association of IL36RN mutation with clinical features, therapeutic response to acitretin, and frequency of recurrence in patients with generalized pustular psoriasis