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10. 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]
11. Current Status of Dedicator of Cytokinesis-Associated Immunodeficiency: DOCK8 and DOCK2. Dimitrova D; Freeman AF Dermatol Clin; 2017 Jan; 35(1):11-19. PubMed ID: 27890234 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. Clinical and immunological correction of DOCK8 deficiency by allogeneic hematopoietic stem cell transplantation following a reduced toxicity conditioning regimen. Boztug H; Karitnig-Weiß C; Ausserer B; Renner ED; Albert MH; Sawalle-Belohradsky J; Belohradsky BH; Mann G; Horcher E; Rümmele-Waibel A; Geyeregger R; Lakatos K; Peters C; Lawitschka A; Matthes-Martin S Pediatr Hematol Oncol; 2012 Oct; 29(7):585-94. PubMed ID: 22897717 [TBL] [Abstract][Full Text] [Related]
14. Hypomorphic function and somatic reversion of DOCK8 cause combined immunodeficiency without hyper-IgE. Kienzler AK; van Schouwenburg PA; Taylor J; Marwah I; Sharma RU; Noakes C; Thomson K; Sadler R; Segal S; Ferry B; Taylor JC; Blair E; Chapel H; Patel SY Clin Immunol; 2016 Feb; 163():17-21. PubMed ID: 26680607 [TBL] [Abstract][Full Text] [Related]
15. Early Diagnosis in Dedicator of Cytokinesis 8 (DOCK8) Deficiency. Chang DR; Toh J; de Vos G; Gavrilova T J Pediatr; 2016 Dec; 179():33-35. PubMed ID: 27671117 [No Abstract] [Full Text] [Related]
16. Somatic reversion in dedicator of cytokinesis 8 immunodeficiency modulates disease phenotype. Jing H; Zhang Q; Zhang Y; Hill BJ; Dove CG; Gelfand EW; Atkinson TP; Uzel G; Matthews HF; Mustillo PJ; Lewis DB; Kavadas FD; Hanson IC; Kumar AR; Geha RS; Douek DC; Holland SM; Freeman AF; Su HC J Allergy Clin Immunol; 2014 Jun; 133(6):1667-75. PubMed ID: 24797421 [TBL] [Abstract][Full Text] [Related]
17. DOCK8 mutation diagnosed using whole-exome sequencing of the dried blood spot-derived DNA: a case report of an Iraqi girl diagnosed in Japan. Al-Kzayer LFY; Al-Aradi HMH; Shigemura T; Sano K; Tanaka M; Hamada M; Ali KH; Aldaghir OM; Nakazawa Y; Okuno Y BMC Med Genet; 2019 Jun; 20(1):114. PubMed ID: 31242861 [TBL] [Abstract][Full Text] [Related]
18. DOCK8 deficiency. Su HC; Jing H; Zhang Q Ann N Y Acad Sci; 2011 Dec; 1246():26-33. PubMed ID: 22236427 [TBL] [Abstract][Full Text] [Related]
19. Clinical, immunological and molecular profiles of DOCK8 deficiency in six patients from a tertiary care centre in North India. Kumar Jindal A; Sil A; Aggarwal R; Tyagi R; Mondal S; Singh A; Barman P; Chawla S; Loganathan SK; Gupta K; Vinay K; Mahajan R; Saikia B; Kaur G; Sharma R; Saka R; Bhatia A; Sankhyan N; Pandiarajan V; Pilania R; Dhaliwal M; Sharma S; Vyas S; Suri D; Rawat A; Singh S Clin Exp Dermatol; 2024 Feb; 49(3):226-234. PubMed ID: 37815217 [TBL] [Abstract][Full Text] [Related]
20. Exome-first Approach Identified Novel Homozygous Dedicator of Cytokinesis 8 (DOCK8) Mutations in Three Unrelated Iranian Pedigrees Suspected with Hyper-IgE Syndrome. Aghebati-Maleki A; Shahani T; Momen T; Alyasin S; Changi-Ashtiani M; Biglari A; Shahrooei M; Javanian AS; Amini S; Bossuyt X; Rokni-Zadeh H Iran J Allergy Asthma Immunol; 2020 Apr; 19(2):193-199. PubMed ID: 32372632 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]