These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

294 related articles for article (PubMed ID: 28070732)

  • 1. The clinical and laboratory spectrum of dedicator of cytokinesis 8 immunodeficiency syndrome in patients with a unique mutation.
    Broides A; Mandola AB; Levy J; Yerushalmi B; Pinsk V; Eldan M; Shubinsky G; Hadad N; Levy R; Nahum A; Ben-Harosh M; Lev A; Simon A; Somech R
    Immunol Res; 2017 Jun; 65(3):651-657. PubMed ID: 28070732
    [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. 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]  

  • 4. Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome.
    Engelhardt KR; McGhee S; Winkler S; Sassi A; Woellner C; Lopez-Herrera G; Chen A; Kim HS; Lloret MG; Schulze I; Ehl S; Thiel J; Pfeifer D; Veelken H; Niehues T; Siepermann K; Weinspach S; Reisli I; Keles S; Genel F; Kutukculer N; Camcioğlu Y; Somer A; Karakoc-Aydiner E; Barlan I; Gennery A; Metin A; Degerliyurt A; Pietrogrande MC; Yeganeh M; Baz Z; Al-Tamemi S; Klein C; Puck JM; Holland SM; McCabe ER; Grimbacher B; Chatila TA
    J Allergy Clin Immunol; 2009 Dec; 124(6):1289-302.e4. PubMed ID: 20004785
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. [Severe atopy and allergy--rare hyper-IgE syndrome caused by the DOCK8 mutation as underlying condition].
    Koskenvuo M; Kainulainen L; Vanto T; Lukkarinen H; Lähteenmäki P; Ruuskanen O
    Duodecim; 2015; 131(6):541-4. PubMed ID: 26237897
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. DOCK8 Deficiency Presenting as an IPEX-Like Disorder.
    Alroqi FJ; Charbonnier LM; Keles S; Ghandour F; Mouawad P; Sabouneh R; Mohammed R; Almutairi A; Chou J; Massaad MJ; Geha RS; Baz Z; Chatila TA
    J Clin Immunol; 2017 Nov; 37(8):811-819. PubMed ID: 29058101
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Dedicator of cytokinesis 8 (DOCK8) deficiency.
    Su HC
    Curr Opin Allergy Clin Immunol; 2010 Dec; 10(6):515-20. PubMed ID: 20864884
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 15.