(Q44625632)

English

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

scientific article published on 12 September 2012

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

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author name string

Zobaida Alsum

1

1 reference

Europe PubMed Central

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4 December 2017

Abbas Hawwari

2

1 reference

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4 December 2017

Osama Alsmadi

3

1 reference

Europe PubMed Central

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4 December 2017

Safa Al-Hissi

4

1 reference

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4 December 2017

Esteban Borrero

5

1 reference

Europe PubMed Central

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4 December 2017

Asma' Abu-Staiteh

6

1 reference

Europe PubMed Central

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4 December 2017

Hanif G Khalak

7

1 reference

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4 December 2017

Salma Wakil

8

1 reference

Europe PubMed Central

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4 December 2017

Abdelmoneim M Eldali

9

1 reference

Europe PubMed Central

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4 December 2017

Rand Arnaout

10

1 reference

Europe PubMed Central

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4 December 2017

Abdulaziz Al-Ghonaium

11

1 reference

Europe PubMed Central

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4 December 2017

Saleh Al-Muhsen

12

1 reference

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4 December 2017

Hasan Al-Dhekri

13

1 reference

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4 December 2017

Bandar Al-Saud

14

1 reference

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4 December 2017

Hamoud Al-Mousa

15

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4 December 2017

publication date

12 September 2012

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4 December 2017

Journal of Clinical Immunology

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4 December 2017

33

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4 December 2017

1

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4 December 2017

55-67

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4 December 2017

https://scigraph.springernature.com/pub.10.1007/s10875-012-9769-x

0 references

The hyper-IgE syndromes

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9769-X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9769-X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9769-X

21 January 2018

Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9769-X

21 January 2018

Human tyrosine kinase 2 deficiency reveals its requisite roles in multiple cytokine signals involved in innate and acquired immunity

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9769-X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9769-X

21 January 2018

Dedicator of cytokinesis 8 (DOCK8) deficiency

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9769-X

21 January 2018

Dock8 mutations cripple B cell immunological synapses, germinal centers and long-lived antibody production.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9769-X

21 January 2018

Interplay of polarity proteins and GTPases in T-lymphocyte function.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9769-X

21 January 2018

DOCK8 is essential for T-cell survival and the maintenance of CD8+ T-cell memory

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9769-X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9769-X

21 January 2018

Genetic linkage of hyper-IgE syndrome to chromosome 4.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9769-X

21 January 2018

Additional diverse findings expand the clinical presentation of DOCK8 deficiency

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9769-X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9769-X

21 January 2018

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.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9769-X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10875-012-9769-X

21 January 2018

Genetic, clinical, and laboratory markers for DOCK8 immunodeficiency syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22968740

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Successful bone marrow transplantation for DOCK8 deficient hyper IgE syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22968740

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical aspects and genetic analysis of Taiwanese patients with the phenotype of hyper-immunoglobulin E recurrent infection syndromes (HIES).

1 reference

https://pubmed.ncbi.nlm.nih.gov/22968740

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defects along the T(H)17 differentiation pathway underlie genetically distinct forms of the hyper IgE syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22968740

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22968740

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22968740

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Consanguinity and major genetic disorders in Saudi children: a community-based cross-sectional study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22968740

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Combined immunodeficiency associated with DOCK8 mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/22968740

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Successful allogeneic hematopoietic stem cell transplantation for DOCK8 deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/22968740

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10875-012-9769-X

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

ResearchGate publication ID

0 references

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