162 related articles for article (PubMed ID: 31338855)
21. Cutaneous manifestations of DOCK8 deficiency syndrome.
Chu EY; Freeman AF; Jing H; Cowen EW; Davis J; Su HC; Holland SM; Turner ML
Arch Dermatol; 2012 Jan; 148(1):79-84. PubMed ID: 21931011
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. The Potential and Limits of Hematopoietic Stem Cell Transplantation for the Treatment of Autosomal Dominant Hyper-IgE Syndrome.
Yanagimachi M; Ohya T; Yokosuka T; Kajiwara R; Tanaka F; Goto H; Takashima T; Morio T; Yokota S
J Clin Immunol; 2016 Jul; 36(5):511-6. PubMed ID: 27091139
[TBL] [Abstract][Full Text] [Related]
24. [Hyper IgE syndrome: atopic dermatitis as first manifestation. Case report].
Carrera Dangond MM; Schellnast Faure A; Fernanda Vargas M; Regairaz L; Cabanillas D
Arch Argent Pediatr; 2021 Aug; 119(4):e370-e374. PubMed ID: 34309321
[TBL] [Abstract][Full Text] [Related]
25. Hematopoietic stem cell transplant effectively rescues lymphocyte differentiation and function in DOCK8-deficient patients.
Pillay BA; Avery DT; Smart JM; Cole T; Choo S; Chan D; Gray PE; Frith K; Mitchell R; Phan TG; Wong M; Campbell DE; Hsu P; Ziegler JB; Peake J; Alvaro F; Picard C; Bustamante J; Neven B; Cant AJ; Uzel G; Arkwright PD; Casanova JL; Su HC; Freeman AF; Shah N; Hickstein DD; Tangye SG; Ma CS
JCI Insight; 2019 Apr; 5(11):. PubMed ID: 31021819
[TBL] [Abstract][Full Text] [Related]
26. Treatment options for DOCK8 deficiency-related severe dermatitis.
Ollech A; Mashiah J; Lev A; Simon AJ; Somech R; Adam E; Barzilai A; Hagin D; Greenberger S
J Dermatol; 2021 Sep; 48(9):1386-1393. PubMed ID: 34043252
[TBL] [Abstract][Full Text] [Related]
27. Successful engraftment of donor marrow after allogeneic hematopoietic cell transplantation in autosomal-recessive hyper-IgE syndrome caused by dedicator of cytokinesis 8 deficiency.
McDonald DR; Massaad MJ; Johnston A; Keles S; Chatila T; Geha RS; Pai SY
J Allergy Clin Immunol; 2010 Dec; 126(6):1304-5.e3. PubMed ID: 20810158
[TBL] [Abstract][Full Text] [Related]
28. Autosomal recessive hyper-IgE syndrome in two brothers of a Chinese family with a novel mutation in DOCK8 gene.
Wang S; Mou W; Xu Z; Gui J; Ma L
J Eur Acad Dermatol Venereol; 2018 Aug; 32(8):e302-e304. PubMed ID: 29419892
[No Abstract] [Full Text] [Related]
29. Hyper-IgE Syndromes and the Lung.
Freeman AF; Olivier KN
Clin Chest Med; 2016 Sep; 37(3):557-67. PubMed ID: 27514600
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. [Hyper IgE syndrome. Opportune diagnosis and management].
Orozco CV; Velásquez LH; Méndez NH; Augusto B; Salazar T
Rev Alerg Mex; 2008; 55(1):38-45. PubMed ID: 18697452
[TBL] [Abstract][Full Text] [Related]
32. [Hyper-IgE syndrome with mutation in STAT3 gene - case report and literature review].
Heropolitańska-Pliszka E; Pietrucha B; Mikołuć B; Bernatowska E
Med Wieku Rozwoj; 2009; 13(1):19-25. PubMed ID: 19648655
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. [Combined immunodeficiency due to DOCK8 deficiency. State of the art].
Liquidano-Pérez E; Maza-Ramos G; Yamazaki-Nakashimada MA; Barragán-Arévalo T; Lugo-Reyes SO; Scheffler-Mendoza S; Espinosa-Padilla SE; González-Serrano ME
Rev Alerg Mex; 2022 Jul; 69(1):31-47. PubMed ID: 36927749
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. The hyperimmunoglobulin E syndrome--clinical manifestation diversity in primary immune deficiency.
Szczawinska-Poplonyk A; Kycler Z; Pietrucha B; Heropolitanska-Pliszka E; Breborowicz A; Gerreth K
Orphanet J Rare Dis; 2011 Nov; 6():76. PubMed ID: 22085750
[TBL] [Abstract][Full Text] [Related]
37. [Hyper-IgE syndrome. Lessons from function and defects of STAT-3 or DOCK-8].
Alcántara-Montiel JC; Vega-Torres BI
Rev Alerg Mex; 2016; 63(4):385-396. PubMed ID: 27795219
[TBL] [Abstract][Full Text] [Related]
38. Clinical Manifestations and Genetic Analysis of 17 Patients with Autosomal Dominant Hyper-IgE Syndrome in Mainland China: New Reports and a Literature Review.
Wu J; Chen J; Tian ZQ; Zhang H; Gong RL; Chen TX; Hong L
J Clin Immunol; 2017 Feb; 37(2):166-179. PubMed ID: 28197791
[TBL] [Abstract][Full Text] [Related]
39. Squamous Cell Carcinoma With Hyper-IgE Syndrome: A Case Report.
Sasihuseyinoglu AS; Yilmaz M; Altintaş DU; Dogruel D; Serbes M; Uğuz AH; Kiroğlu M
J Pediatr Hematol Oncol; 2018 Aug; 40(6):e380-e382. PubMed ID: 28902078
[TBL] [Abstract][Full Text] [Related]
40. A novel large deletion of the DOCK8 gene in a Chinese family with autosomal-recessive hyper-IgE syndrome.
Xue L; Yang Y; Wang S
J Eur Acad Dermatol Venereol; 2015 Mar; 29(3):599-601. PubMed ID: 24673638
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
