Successful treatment with infliximab for inflammatory colitis in a patient with X-linked anhidrotic ectodermal dysplasia with immunodeficiency. (Q51851019)

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scientific article published on 13 October 2011

Language	Label	Description	Also known as
English	Successful treatment with infliximab for inflammatory colitis in a patient with X-linked anhidrotic ectodermal dysplasia with immunodeficiency.	scientific article published on 13 October 2011

Statements

scholarly article

1 reference

Europe PubMed Central

14 April 2018

http://europepmc.org/abstract/MED/21993693

Successful treatment with infliximab for inflammatory colitis in a patient with X-linked anhidrotic ectodermal dysplasia with immunodeficiency. (English)

1 reference

Europe PubMed Central

14 April 2018

http://europepmc.org/abstract/MED/21993693

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based on heuristic

inferred from title

Anhidrotic ectodermal dysplasia

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author name string

Tomoyuki Mizukami

1

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Europe PubMed Central

14 April 2018

http://europepmc.org/abstract/MED/21993693

Megumi Obara

2

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Europe PubMed Central

14 April 2018

http://europepmc.org/abstract/MED/21993693

Ryuta Nishikomori

3

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Europe PubMed Central

14 April 2018

http://europepmc.org/abstract/MED/21993693

Tomoki Kawai

4

1 reference

Europe PubMed Central

14 April 2018

http://europepmc.org/abstract/MED/21993693

Yoshihiro Tahara

5

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Europe PubMed Central

14 April 2018

http://europepmc.org/abstract/MED/21993693

Naoki Sameshima

6

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Europe PubMed Central

14 April 2018

http://europepmc.org/abstract/MED/21993693

Kousuke Marutsuka

7

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Europe PubMed Central

14 April 2018

http://europepmc.org/abstract/MED/21993693

Hiroshi Nakase

8

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Europe PubMed Central

14 April 2018

http://europepmc.org/abstract/MED/21993693

Nobuhiro Kimura

9

1 reference

Europe PubMed Central

14 April 2018

http://europepmc.org/abstract/MED/21993693

Toshio Heike

10

1 reference

Europe PubMed Central

14 April 2018

http://europepmc.org/abstract/MED/21993693

Hiroyuki Nunoi

11

1 reference

Europe PubMed Central

14 April 2018

http://europepmc.org/abstract/MED/21993693

publication date

13 October 2011

1 reference

Europe PubMed Central

14 April 2018

http://europepmc.org/abstract/MED/21993693

Journal of Clinical Immunology

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Europe PubMed Central

14 April 2018

http://europepmc.org/abstract/MED/21993693

32

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http://europepmc.org/abstract/MED/21993693

1

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http://europepmc.org/abstract/MED/21993693

39-49

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Europe PubMed Central

14 April 2018

http://europepmc.org/abstract/MED/21993693

https://scigraph.springernature.com/pub.10.1007/s10875-011-9600-0

0 references

A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO)

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9600-0

21 January 2018

X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9600-0

21 January 2018

Specific missense mutations in NEMO result in hyper-IgM syndrome with hypohydrotic ectodermal dysplasia

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9600-0

21 January 2018

Deficient natural killer cell cytotoxicity in patients with IKK-gamma/NEMO mutations

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9600-0

21 January 2018

The presentation and natural history of immunodeficiency caused by nuclear factor kappaB essential modulator mutation

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9600-0

21 January 2018

Allogeneic transplantation successfully corrects immune defects, but not susceptibility to colitis, in a patient with nuclear factor-kappaB essential modulator deficiency

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9600-0

21 January 2018

X-linked ectodermal dysplasia with immunodeficiency caused by NEMO mutation: early recognition and diagnosis

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9600-0

21 January 2018

Challenges in the use of allogeneic hematopoietic SCT for ectodermal dysplasia with immune deficiency.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9600-0

21 January 2018

Allogeneic hematopoietic stem cell transplantation for X-linked ectodermal dysplasia and immunodeficiency: case report and review of outcomes.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9600-0

21 January 2018

Persistent systemic inflammation and atypical enterocolitis in patients with NEMO syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9600-0

21 January 2018

Hypomorphic nuclear factor-kappaB essential modulator mutation database and reconstitution system identifies phenotypic and immunologic diversity

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9600-0

21 January 2018

NEMO mutation as a cause of familial occurrence of Behçet's disease in female patients.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9600-0

21 January 2018

Inflammatory bowel disease in CGD reproduces the clinicopathological features of Crohn's disease

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9600-0

21 January 2018

Sequences and repertoire of the human T cell receptor alpha and beta chain variable region genes in thymocytes

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9600-0

21 January 2018

Spontaneous in vivo reversion of an inherited mutation in the Wiskott-Aldrich syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9600-0

21 January 2018

X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 production

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9600-0

21 January 2018

Skin lesion development in a mouse model of incontinentia pigmenti is triggered by NEMO deficiency in epidermal keratinocytes and requires TNF signaling.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9600-0

21 January 2018

Infliximab but not etanercept induces apoptosis in lamina propria T-lymphocytes from patients with Crohn's disease

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9600-0

21 January 2018

Complications of tumor necrosis factor-α blockade in chronic granulomatous disease-related colitis

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9600-0

21 January 2018

Hepatosplenic T cell lymphoma associated with infliximab use in young patients treated for inflammatory bowel disease

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9600-0

21 January 2018

Hepatosplenic T cell lymphoma associated with infliximab use in young patients treated for inflammatory bowel disease: update.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9600-0

21 January 2018

Epithelial NEMO links innate immunity to chronic intestinal inflammation

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9600-0

21 January 2018

Clonal expansion of alphabeta-T lymphocytes with inverted Jbeta1 bias in familial hemophagocytic lymphohistiocytosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/21993693

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Anti-tumour necrosis factor-alpha therapy for severe enteropathy in patients with common variable immunodeficiency (CVID)

1 reference

https://pubmed.ncbi.nlm.nih.gov/21993693

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Atypical X-Linked Severe Combined Immunodeficiency Due to Possible Spontaneous Reversion of the Genetic Defect in T Cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/21993693

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Correction of immunodeficiency associated with NEMO mutation by umbilical cord blood transplantation using a reduced-intensity conditioning regimen

1 reference

https://pubmed.ncbi.nlm.nih.gov/21993693

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked ectodermal dysplasia and immunodeficiency caused by reversion mosaicism of NEMO reveals a critical role for NEMO in human T-cell development and/or survival

1 reference

https://pubmed.ncbi.nlm.nih.gov/21993693

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oligoclonal expansion of T lymphocytes with multiple second-site mutations leads to Omenn syndrome in a patient with RAG1-deficient severe combined immunodeficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/21993693

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spontaneous in vivo reversion to normal of an inherited mutation in a patient with adenosine deaminase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/21993693

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intracellular cytokine patterns of peripheral blood T cells as a useful indicator of activeness of Crohn's disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21993693

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Crohn's disease in common variable immunodeficiency: treatment with antitumor necrosis factor alpha

1 reference

https://pubmed.ncbi.nlm.nih.gov/21993693

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of T lymphocytes with a second-site mutation in skin lesions of atypical X-linked severe combined immunodeficiency mimicking Omenn syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21993693

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tumor necrosis factor alpha blockers and malignancy in children: forty-eight cases reported to the Food and Drug Administration

1 reference

https://pubmed.ncbi.nlm.nih.gov/21993693

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10875-011-9600-0

1 reference

Europe PubMed Central

14 April 2018

http://europepmc.org/abstract/MED/21993693

1 reference

Europe PubMed Central

14 April 2018

http://europepmc.org/abstract/MED/21993693

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