Disseminated BCG infection mimicking metastatic nasopharyngeal carcinoma in an immunodeficient child with a novel hypomorphic NEMO mutation (Q40318502)

19 September 2017

title

Disseminated BCG infection mimicking metastatic nasopharyngeal carcinoma in an immunodeficient child with a novel hypomorphic NEMO mutation (English)

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19 September 2017

9

Hirokazu Kanegane

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19 September 2017

Masaru Imamura

1

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19 September 2017

Tomoki Kawai

2

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19 September 2017

Satoshi Okada

3

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19 September 2017

Kazushi Izawa

4

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19 September 2017

Takayuki Takachi

5

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19 September 2017

Haruko Iwabuchi

6

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19 September 2017

Sakiko Yoshida

7

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19 September 2017

Ryosuke Hosokai

8

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19 September 2017

Tatsuo Yamamoto

10

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19 September 2017

Hajime Umezu

11

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19 September 2017

Ryuta Nishikomori

12

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19 September 2017

Toshio Heike

13

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19 September 2017

Makoto Uchiyama

14

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19 September 2017

Chihaya Imai

15

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19 September 2017

publication date

14 July 2011

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Journal of Clinical Immunology

19 September 2017

published in

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19 September 2017

volume

31

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19 September 2017

issue

5

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19 September 2017

page(s)

802-810

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https://scigraph.springernature.com/pub.10.1007/s10875-011-9568-9

19 September 2017

exact match

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cites work

Multiple pathogenic and benign genomic rearrangements occur at a 35 kb duplication involving the NEMO and LAGE2 genes

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9568-9

Introduction to NF-kappaB: players, pathways, perspectives

21 January 2018

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https://api.crossref.org/works/10.1007%2FS10875-011-9568-9

Nuclear factor kappaB essential modulator-deficient child with immunodeficiency yet without anhidrotic ectodermal dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9568-9

Human nuclear factor kappa B essential modulator mutation can result in immunodeficiency without ectodermal dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9568-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9568-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9568-9

Spectrum of head and neck cancer in children

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9568-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9568-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9568-9

A critical role for I kappaB kinase alpha in the development of human and mouse squamous cell carcinomas

21 January 2018

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https://api.crossref.org/works/10.1007%2FS10875-011-9568-9

Reduction in IkappaB kinase alpha expression promotes the development of skin papillomas and carcinomas

21 January 2018

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https://api.crossref.org/works/10.1007%2FS10875-011-9568-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9568-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9568-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9568-9

NEMO Mutations in 2 Unrelated Boys With Severe Infections and Conical Teeth

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9568-9

Interferon-γ receptor deficiency mimicking Langerhans’ cell histiocytosis

21 January 2018

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https://api.crossref.org/works/10.1007%2FS10875-011-9568-9

Nasopharyngeal tuberculosis

21 January 2018

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12 December 2020

Early and rapid detection of X-linked lymphoproliferative syndrome with SH2D1A mutations by flow cytometry

1 reference

12 December 2020

Pathologic findings for bacille Calmette-Guérin infections in immunocompetent and immunocompromised patients

1 reference

12 December 2020

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

1 reference

12 December 2020

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

12 December 2020

Decreased expression in nuclear factor-κB essential modulator due to a novel splice-site mutation causes X-linked ectodermal dysplasia with immunodeficiency.

1 reference

12 December 2020

Disseminated bacillus Calmette-Guérin infections in patients with primary immunodeficiencies

1 reference

12 December 2020

New mechanism of X-linked anhidrotic ectodermal dysplasia with immunodeficiency: impairment of ubiquitin binding despite normal folding of NEMO protein

1 reference

12 December 2020

10.1007/S10875-011-9568-9

Identifiers

DOI

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Dimensions Publication ID

19 September 2017

1029000233

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