142 related articles for article (PubMed ID: 24517560)
1. Grave aortic aneurysmal dilatation in DOCK8 deficiency.
Al Mutairi M; Al-Mousa H; AlSaud B; Hawwari A; AlJoufan M; AlWesaibi A; AlHalees Z; Al-Mayouf SM
Mod Rheumatol; 2014 Jul; 24(4):690-3. PubMed ID: 24517560
[TBL] [Abstract][Full Text] [Related]
2. The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency.
Engelhardt KR; Gertz ME; Keles S; Schäffer AA; Sigmund EC; Glocker C; Saghafi S; Pourpak Z; Ceja R; Sassi A; Graham LE; Massaad MJ; Mellouli F; Ben-Mustapha I; Khemiri M; Kilic SS; Etzioni A; Freeman AF; Thiel J; Schulze I; Al-Herz W; Metin A; Sanal Ö; Tezcan I; Yeganeh M; Niehues T; Dueckers G; Weinspach S; Patiroglu T; Unal E; Dasouki M; Yilmaz M; Genel F; Aytekin C; Kutukculer N; Somer A; Kilic M; Reisli I; Camcioglu Y; Gennery AR; Cant AJ; Jones A; Gaspar BH; Arkwright PD; Pietrogrande MC; Baz Z; Al-Tamemi S; Lougaris V; Lefranc G; Megarbane A; Boutros J; Galal N; Bejaoui M; Barbouche MR; Geha RS; Chatila TA; Grimbacher B
J Allergy Clin Immunol; 2015 Aug; 136(2):402-12. PubMed ID: 25724123
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Ten-year follow-up of a DOCK8-deficient child with features of systemic lupus erythematosus.
Jouhadi Z; Khadir K; Ailal F; Bouayad K; Nadifi S; Engelhardt KR; Grimbacher B
Pediatrics; 2014 Nov; 134(5):e1458-63. PubMed ID: 25332498
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. CNS vasculitis and stroke as a complication of DOCK8 deficiency: a case report.
AlKhater SA
BMC Neurol; 2016 Apr; 16():54. PubMed ID: 27113444
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. DOCK8 deficiency with hypereosinophilia and the syndrome of inappropriate antidiuretic hormone secretion during herpes infection.
Yeşil AM; Kayaoğlu B; Gül E; Gönç N; Özön A; Tezcan İ; Gürsel M; Çağdaş D
Turk J Pediatr; 2023; 65(3):536-541. PubMed ID: 37395973
[TBL] [Abstract][Full Text] [Related]
9. Novel mutation in DOCK8-HIES with severe phenotype and successful transplantation.
Al Shekaili L; Sheikh F; Al Gazlan S; Al Dhekri H; Al Mousa H; Al Ghonaium A; Al Saud B; Al Mohsen S; Rehan Khaliq AM; Al Sumayli S; Al Zahrani M; Dababo A; AlKawi A; Hawwari A; Arnaout R
Clin Immunol; 2017 May; 178():39-44. PubMed ID: 27890707
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Dedicator of cytokinesis 8 regulates signal transducer and activator of transcription 3 activation and promotes T
Keles S; Charbonnier LM; Kabaleeswaran V; Reisli I; Genel F; Gulez N; Al-Herz W; Ramesh N; Perez-Atayde A; Karaca NE; Kutukculer N; Wu H; Geha RS; Chatila TA
J Allergy Clin Immunol; 2016 Nov; 138(5):1384-1394.e2. PubMed ID: 27350570
[TBL] [Abstract][Full Text] [Related]
12. The Surgical Repair of a Hyperimmunoglobulin E Syndrome Associated Ascending Aortic Aneurysm.
Battaloglu B; Colak C; Disli OM; Akca B; Erdil N; Karakurt C
Ann Thorac Surg; 2017 Jan; 103(1):e65-e67. PubMed ID: 28007278
[TBL] [Abstract][Full Text] [Related]
13. Critical aneurysmal dilatation of the thoracic aorta in young adolescents with variant hyperimmunoglobulin E syndrome.
van der meer JW; Weemaes CM; van Krieken JH; Blomjous CE; van Die CE; Netea MG; Bredie SJ
J Intern Med; 2006 Jun; 259(6):615-8. PubMed ID: 16704563
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. 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]
17. Autosomal recessive hyper-IgE syndrome caused by DOCK8 gene mutation with new clinical features: a case report.
Yang J; Liu Y
BMC Neurol; 2021 Jul; 21(1):288. PubMed ID: 34301197
[TBL] [Abstract][Full Text] [Related]
18. Successful hematopoietic stem cell transplantation after myeloablative conditioning in three patients with dedicator of cytokinesis 8 deficiency (DOCK8) related Hyper IgE syndrome.
Kuşkonmaz B; Ayvaz D; Tezcan İ; Yüce A; Sanal Ö; Çetinkaya DU
Bone Marrow Transplant; 2018 Mar; 53(3):339-343. PubMed ID: 29269803
[No Abstract] [Full Text] [Related]
19. 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]
20. Novel Variants of DOCK8 Deficiency in a Case Series of Iranian Patients.
Momtazmanesh S; Rayzan E; Zoghi S; Shahkarami S; Molatefi R; Mohammadzadeh I; Ghaffari J; Mahmoudi H; Dmytrus J; Segarra-Roca A; Somekh I; Witzel M; Hauck F; Boztug K; Klein C; Rezaei N
Endocr Metab Immune Disord Drug Targets; 2022; 22(1):159-168. PubMed ID: 33634762
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
