(Q38334918)

2 September 2017

title

DOCK8 deficiency: clinical and immunological phenotype and treatment options - a review of 136 patients (English)

1 reference

2 September 2017

1 reference

1 reference

14

1 reference

2 September 2017

33

1 reference

2 September 2017

Roland Aydin

52

0 references

Beate Hagl

Beate Hagl

53

0 references

Jordan Abbott

Jordan Abbott

12

0 references

Leena Kainulainen

Leena Kainulainen

6

0 references

Stephan Ehl

Stephan Ehl

17

0 references

Abbas Hawwari

Abbas Hawwari

Luis Ignacio Gonzalez-Granado

28

0 references

Luis Gonzalez-Granado

11

0 references

Fatih Azik

Fatih Azik

47

0 references

Jordan S. Orange

Jordan S Orange

19

0 references

Talal A Chatila

Talal Chatila

57

0 references

Caner Aytekin

3

Caner Aytekin

1 reference

2 September 2017

38

Taco Kuijpers

1 reference

2 September 2017

56

Hans D Ochs

1 reference

2 September 2017

Deniz C Ayvaz

24

0 references

Andrew R Gennery

35

Andrew Gennery

1 reference

2 September 2017

49

Bodo Grimbacher

1 reference

2 September 2017

Neslihan Edeer Karaca

10

Neslihan Karaca

1 reference

2 September 2017

8

Ferah Genel

1 reference

2 September 2017

21

Sevgi Keles

1 reference

2 September 2017

34

Vincent Barlogis

1 reference

2 September 2017

46

Betül Tavil

1 reference

2 September 2017

43

Raif Geha

1 reference

2 September 2017

Susanne E Aydin

1

1 reference

2 September 2017

Sara Sebnem Kilic

2

1 reference

2 September 2017

Ashish Kumar

4

1 reference

2 September 2017

Oscar Porras

5

1 reference

2 September 2017

Larysa Kostyuchenko

7

1 reference

2 September 2017

Necil Kütükcüler

9

1 reference

2 September 2017

Daifulah Al-Zahrani

13

1 reference

2 September 2017

Zeina Baz

15

1 reference

2 September 2017

Jens Thiel

16

1 reference

2 September 2017

László Marodi

18

1 reference

2 September 2017

Julie Sawalle-Belohradsky

20

1 reference

2 September 2017

Steven M Holland

22

1 reference

2 September 2017

Özden Sanal

23

1 reference

2 September 2017

Ilhan Tezcan

25

1 reference

2 September 2017

Hamoud Al-Mousa

26

1 reference

2 September 2017

Zobaida Alsum

27

1 reference

2 September 2017

Ayse Metin

29

1 reference

2 September 2017

Susanne Matthes-Martin

30

1 reference

2 September 2017

Manfred Hönig

31

1 reference

2 September 2017

Ansgar Schulz

32

1 reference

2 September 2017

Marianne Ifversen

36

1 reference

2 September 2017

Joris van Montfrans

37

1 reference

2 September 2017

Robbert Bredius

39

1 reference

2 September 2017

Gregor Dückers

40

1 reference

2 September 2017

Waleed Al-Herz

41

1 reference

2 September 2017

Sung-Yun Pai

42

1 reference

2 September 2017

Gundula Notheis

44

1 reference

2 September 2017

Carl-Philipp Schwarze

45

1 reference

2 September 2017

Kirsten Bienemann

48

1 reference

2 September 2017

Valerie Heinz

50

1 reference

2 September 2017

H Bobby Gaspar

51

1 reference

2 September 2017

Benjamin Gathmann

54

1 reference

2 September 2017

Bernd H Belohradsky

55

1 reference

2 September 2017

Ellen D Renner

58

1 reference

2 September 2017

Helen Su

59

1 reference

2 September 2017

Alexandra F Freeman

60

1 reference

2 September 2017

Karin Engelhardt

61

1 reference

2 September 2017

Michael H Albert

62

1 reference

2 September 2017

inborn errors working party of EBMT

63

1 reference

2 September 2017

publication date

28 January 2015

1 reference

Journal of Clinical Immunology

2 September 2017

published in

1 reference

2 September 2017

volume

35

1 reference

2 September 2017

issue

2

1 reference

2 September 2017

page(s)

189-198

1 reference

https://scigraph.springernature.com/pub.10.1007/s10875-014-0126-0

2 September 2017

exact match

0 references

cites work

Hyper-IgE syndrome with recurrent infections--an autosomal dominant multisystem disorder

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

STAT3 mutations in the hyper-IgE syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

STAT3Mutation in the Original Patient with Job's Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

Combined immunodeficiency associated with DOCK8 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

Successful interferon-alpha 2b therapy for unremitting warts in a patient with DOCK8 deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

Plasmacytoid dendritic cell depletion in DOCK8 deficiency: rescue of severe herpetic infections with IFN-α 2b therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

Beneficial IFN-α treatment of tumorous herpes simplex blepharoconjunctivitis in dedicator of cytokinesis 8 deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

Successful long-term correction of autosomal recessive hyper-IgE syndrome due to DOCK8 deficiency by hematopoietic stem cell transplantation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

Clinical and immunological correction of DOCK8 deficiency by allogeneic hematopoietic stem cell transplantation following a reduced toxicity conditioning regimen.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

Successful allogeneic hematopoietic stem cell transplantation for DOCK8 deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

Haploidentical stem cell transplantation in DOCK8 deficiency - Successful control of pre-existing severe viremia with a TCRaß/CD19-depleted graft and antiviral treatment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

Hypomorphic homozygous mutations in phosphoglucomutase 3 (PGM3) impair immunity and increase serum IgE levels

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

DOCK8 is critical for the survival and function of NKT cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

Dedicator of cytokinesis 8 interacts with talin and Wiskott-Aldrich syndrome protein to regulate NK cell cytotoxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

Defective actin accumulation impairs human natural killer cell function in patients with dedicator of cytokinesis 8 deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

Cutaneous manifestations of DOCK8 deficiency syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

Deficient T Cell Receptor Excision Circles (TRECs) in autosomal recessive hyper IgE syndrome caused by DOCK8 mutation: implications for pathogenesis and potential detection by newborn screening.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

Successful engraftment of donor marrow after allogeneic hematopoietic cell transplantation in autosomal-recessive hyper-IgE syndrome caused by dedicator of cytokinesis 8 deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

DOCK8 deficiency impairs CD8 T cell survival and function in humans and mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

Additional diverse findings expand the clinical presentation of DOCK8 deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

Clinical, immunological and molecular characterization of DOCK8 and DOCK8-like deficient patients: single center experience of twenty-five patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

Clinical, immunologic and genetic profiles of DOCK8-deficient patients in Kuwait

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

MST1 mutations in autosomal recessive primary immunodeficiency characterized by defective naive T-cell survival

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

Somatic reversion in dedicator of cytokinesis 8 immunodeficiency modulates disease phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

Targeted next-generation sequencing: a novel diagnostic tool for primary immunodeficiencies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

STAT3 is a central regulator of lymphocyte differentiation and function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

Clinical spectrum, pathophysiology and treatment of the Wiskott-Aldrich syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

Aberrant humoral immune reactivity in DOCK8 deficiency with follicular hyperplasia and nodal plasmacytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

DOCK8 is a Cdc42 activator critical for interstitial dendritic cell migration during immune responses

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0126-0

Successful bone marrow transplantation for DOCK8 deficient hyper IgE syndrome

21 January 2018

1 reference

12 December 2020

Job's Syndrome. Recurrent, "cold", staphylococcal abscesses

1 reference

12 December 2020

Curative treatment of autosomal-recessive hyper-IgE syndrome by hematopoietic cell transplantation

1 reference

12 December 2020

Flow cytometry diagnosis of dedicator of cytokinesis 8 (DOCK8) deficiency.

1 reference

12 December 2020

Extreme hyperimmunoglobulinemia E and undue susceptibility to infection

1 reference

12 December 2020

10.1007/S10875-014-0126-0

Identifiers

DOI

1 reference

Dimensions Publication ID

2 September 2017

1046798042

0 references

1 reference