282 related articles for article (PubMed ID: 31242861)
21. Atopic dermatitis, STAT3- and DOCK8-hyper-IgE syndromes differ in IgE-based sensitization pattern.
Boos AC; Hagl B; Schlesinger A; Halm BE; Ballenberger N; Pinarci M; Heinz V; Kreilinger D; Spielberger BD; Schimke-Marques LF; Sawalle-Belohradsky J; Belohradsky BH; Przybilla B; Schaub B; Wollenberg A; Renner ED
Allergy; 2014 Jul; 69(7):943-53. PubMed ID: 24898675
[TBL] [Abstract][Full Text] [Related]
22. Confirmation of Hyperimmunoglobulin E Syndrome in Two Patients with an Ocular Problem: Detection of Two New DOCK8 Mutations.
Saghafi S; Zandieh F; Fazlollahi MR; Glocker C; Frede N; Buchta M; Yang L; Mahmoudi AH; Houshmand M; Pourpak Z; Grimbacher B; Moin M
Iran J Allergy Asthma Immunol; 2022 Jun; 21(3):355-363. PubMed ID: 35822685
[TBL] [Abstract][Full Text] [Related]
23. Diagnostic challenge in a series of eleven patients with hyper IgE syndromes.
Yaakoubi R; Mekki N; Ben-Mustapha I; Ben-Khemis L; Bouaziz A; Ben Fraj I; Ammar J; Hamzaoui A; Turki H; Boussofara L; Denguezli M; Haddad S; Ouederni M; Bejaoui M; Chan KW; Lau YL; Mellouli F; Barbouche MR; Ben-Ali M
Front Immunol; 2022; 13():1057679. PubMed ID: 36703986
[TBL] [Abstract][Full Text] [Related]
24. Successful long-term correction of autosomal recessive hyper-IgE syndrome due to DOCK8 deficiency by hematopoietic stem cell transplantation.
Bittner TC; Pannicke U; Renner ED; Notheis G; Hoffmann F; Belohradsky BH; Wintergerst U; Hauser M; Klein B; Schwarz K; Schmid I; Albert MH
Klin Padiatr; 2010 Nov; 222(6):351-5. PubMed ID: 21058221
[TBL] [Abstract][Full Text] [Related]
25. The first cohort of Iranian patients with hyper immunoglobulin E syndrome: A long-term follow-up and genetic analysis.
Tavassoli M; Abolhassani H; Yazdani R; Ghadami M; Azizi G; Abdolrahim Poor Heravi S; Moeini Shad T; Kokabee M; Movahedi M; Abdshahzadeh H; Gharagozlou M; Rezaei N; Esmaeilzadeh H; Aleyasin S; Aghamohammadi A
Pediatr Allergy Immunol; 2019 Jun; 30(4):469-478. PubMed ID: 30801830
[TBL] [Abstract][Full Text] [Related]
26. Clinical, immunological, and genetic description of a Mexican cohort of patients with DOCK8 deficiency.
Liquidano-Perez E; Maza-Ramos G; Perez Arias BA; Lugo Reyes SO; Barragan Arevalo T; Solorzano-Morales SA; Venegas Montoya E; Staines-Boone AT; Guzmán Cotaya R; Okada S; Picard C; Patin E; Ramirez-Uribe N; Bustamante-Ogando JC; Scheffler-Mendoza SC; Yamazaki-Nakashimada MA; Saez-de-Ocariz M; Espinosa Padilla SE; Gonzalez-Serrano ME
Pediatr Allergy Immunol; 2024 Feb; 35(2):e14073. PubMed ID: 38351896
[TBL] [Abstract][Full Text] [Related]
27. Genetic, clinical, and laboratory markers for DOCK8 immunodeficiency syndrome.
Zhang Q; Davis JC; Dove CG; Su HC
Dis Markers; 2010; 29(3-4):131-9. PubMed ID: 21178272
[TBL] [Abstract][Full Text] [Related]
28. Successful interferon-alpha 2b therapy for unremitting warts in a patient with DOCK8 deficiency.
Al-Zahrani D; Raddadi A; Massaad M; Keles S; Jabara HH; Chatila TA; Geha R
Clin Immunol; 2014 Jul; 153(1):104-108. PubMed ID: 24743019
[TBL] [Abstract][Full Text] [Related]
29. Novel DOCK8 gene mutations lead to absence of protein expression in patients with hyper-IgE syndrome.
Qin T; An Y; Liu C; Wu J; Dai R; Liu D; Li X; Jiang L; Wu D; Tang X; Song W; Wang T; Zhao X
Immunol Res; 2016 Feb; 64(1):260-71. PubMed ID: 26659092
[TBL] [Abstract][Full Text] [Related]
30. Phenotyping and long-term follow up of patients with hyper IgE syndrome.
Alyasin S; Esmaeilzadeh H; Ebrahimi N; Nabavizadeh SH; Kashef S; Esmaeilzadeh E; Babaei M; Amin R
Allergol Immunopathol (Madr); 2019; 47(2):152-158. PubMed ID: 30279075
[TBL] [Abstract][Full Text] [Related]
31. Hyper IgE Syndrome Associated With Warts: A First Case of Dedicator of Cytokinesis 8 Deficiency in the Philippines.
Villanueva JCMM; Chan KW; Ong RC; Andaya AG; Lau YL; van Zelm MC; Kanegane H
Front Pediatr; 2020; 8():604725. PubMed ID: 33251169
[TBL] [Abstract][Full Text] [Related]
32. Key findings to expedite the diagnosis of hyper-IgE syndromes in infants and young children.
Hagl B; Heinz V; Schlesinger A; Spielberger BD; Sawalle-Belohradsky J; Senn-Rauh M; Magg T; Boos AC; Hönig M; Schwarz K; Dückers G; von Bernuth H; Pache C; Karitnig-Weiss C; Belohradsky BH; Frank J; Niehues T; Wahn V; Albert MH; Wollenberg A; Jansson AF; Renner ED
Pediatr Allergy Immunol; 2016 Mar; 27(2):177-84. PubMed ID: 26592211
[TBL] [Abstract][Full Text] [Related]
33. [Hyper-IgE syndromes].
He YY; Liu B; Xiao XP
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2017 Jun; 31(11):892-896. PubMed ID: 29775011
[TBL] [Abstract][Full Text] [Related]
34. Clinical, immunological and molecular characterization of DOCK8 and DOCK8-like deficient patients: single center experience of twenty-five patients.
Alsum Z; Hawwari A; Alsmadi O; Al-Hissi S; Borrero E; Abu-Staiteh A; Khalak HG; Wakil S; Eldali AM; Arnaout R; Al-Ghonaium A; Al-Muhsen S; Al-Dhekri H; Al-Saud B; Al-Mousa H
J Clin Immunol; 2013 Jan; 33(1):55-67. PubMed ID: 22968740
[TBL] [Abstract][Full Text] [Related]
35. DOCK8 deficiency in a boy who presented with a giant aortic aneurysm between aortic root and iliac bifurcation.
Patıroğlu T; Akar HH; Doğan MS; Üzüm K
Turk Kardiyol Dern Ars; 2016 Jun; 44(4):342-5. PubMed ID: 27372622
[TBL] [Abstract][Full Text] [Related]
36. Case Report: DOCK8 Deficiency Without Hyper-IgE in a Child With a Large Deletion.
Venegas-Montoya E; Staines-Boone AT; Sánchez-Sánchez LM; García-Campos JA; Córdova-Gurrola RA; Salazar-Galvez Y; Múzquiz-Zermeño D; González-Serrano ME; Lugo Reyes SO
Front Pediatr; 2021; 9():635322. PubMed ID: 34195158
[TBL] [Abstract][Full Text] [Related]
37. Acute eosinophilic pneumonia occurring in a dedicator of cytokinesis 8 (DOCK8) deficient patient.
Tsuge I; Ito K; Ohye T; Kando N; Kondo Y; Nakajima Y; Inuo C; Kurahashi H; Urisu A
Pediatr Pulmonol; 2014 Mar; 49(3):E52-5. PubMed ID: 24106060
[TBL] [Abstract][Full Text] [Related]
38. Flow cytometry diagnosis of dedicator of cytokinesis 8 (DOCK8) deficiency.
Pai SY; de Boer H; Massaad MJ; Chatila TA; Keles S; Jabara HH; Janssen E; Lehmann LE; Hanna-Wakim R; Dbaibo G; McDonald DR; Al-Herz W; Geha RS
J Allergy Clin Immunol; 2014 Jul; 134(1):221-3. PubMed ID: 24698323
[No Abstract] [Full Text] [Related]
39. EBV Negative Lymphoma and Autoimmune Lymphoproliferative Syndrome Like Phenotype Extend the Clinical Spectrum of Primary Immunodeficiency Caused by STK4 Deficiency.
Schipp C; Schlütermann D; Hönscheid A; Nabhani S; Höll J; Oommen PT; Ginzel S; Fleckenstein B; Stork B; Borkhardt A; Stepensky P; Fischer U
Front Immunol; 2018; 9():2400. PubMed ID: 30386345
[TBL] [Abstract][Full Text] [Related]
40. DOCK8 deficiency: clinical and immunological phenotype and treatment options - a review of 136 patients.
Aydin SE; Kilic SS; Aytekin C; Kumar A; Porras O; Kainulainen L; Kostyuchenko L; Genel F; Kütükcüler N; Karaca N; Gonzalez-Granado L; Abbott J; Al-Zahrani D; Rezaei N; Baz Z; Thiel J; Ehl S; Marodi L; Orange JS; Sawalle-Belohradsky J; Keles S; Holland SM; Sanal Ö; Ayvaz DC; Tezcan I; Al-Mousa H; Alsum Z; Hawwari A; Metin A; Matthes-Martin S; Hönig M; Schulz A; Picard C; Barlogis V; Gennery A; Ifversen M; van Montfrans J; Kuijpers T; Bredius R; Dückers G; Al-Herz W; Pai SY; Geha R; Notheis G; Schwarze CP; Tavil B; Azik F; Bienemann K; Grimbacher B; Heinz V; Gaspar HB; Aydin R; Hagl B; Gathmann B; Belohradsky BH; Ochs HD; Chatila T; Renner ED; Su H; Freeman AF; Engelhardt K; Albert MH;
J Clin Immunol; 2015 Feb; 35(2):189-98. PubMed ID: 25627830
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]