Related references
Note: Only part of the references are listed.Tumor Necrosis Factor α Blockers and Malignancy in Children Forty-Eight Cases Reported to the Food and Drug Administration
Peter Diak et al.
ARTHRITIS AND RHEUMATISM (2010)
NEMO mutation as a cause of familial occurrence of Behcet's disease in female patients
H. Takada et al.
CLINICAL GENETICS (2010)
Complications of Tumor Necrosis Factor-α Blockade in Chronic Granulomatous Disease-Related Colitis
Gulbu Uzel et al.
CLINICAL INFECTIOUS DISEASES (2010)
Inflammatory Bowel Disease in CGD Reproduces the Clinicopathological Features of Crohn's Disease
Daniel J. B. Marks et al.
AMERICAN JOURNAL OF GASTROENTEROLOGY (2009)
Challenges in the use of allogeneic hematopoietic SCT for ectodermal dysplasia with immune deficiency
J. D. Fish et al.
BONE MARROW TRANSPLANTATION (2009)
Persistent systemic inflammation and atypical enterocolitis in patients with NEMO syndrome
Laurence E. Cheng et al.
CLINICAL IMMUNOLOGY (2009)
Allogeneic hematopoietic stem cell transplantation for X-linked ectodermal dysplasia and immunodeficiency: case report and review of outcomes
Perdita Permaul et al.
IMMUNOLOGIC RESEARCH (2009)
Hepatosplenic T Cell Lymphoma Associated with Infliximab Use in Young Patients Treated for Inflammatory Bowel Disease: Update
Ann Corken Mackey et al.
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION (2009)
X-linked ectodermal dysplasia with immunodeficiency caused by NEMO mutation - Early recognition and diagnosis
Anthony J. Mancini et al.
ARCHIVES OF DERMATOLOGY (2008)
Detection of T lymphocytes with a second-site mutation in skin lesions of atypical X-linked severe combined immunodeficiency mimicking Omenn syndrome
Taizo Wada et al.
BLOOD (2008)
Allogeneic transplantation successfully corrects immune defects, but not susceptibility to colitis, in a patient with nuclear factor-κB essential modulator deficiency
Sung-Yun Pai et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY (2008)
Hypomorphic nuclear factor-κB essential modulator mutation database and reconstitution system identifies phenotypic and immunologic diversity
Eric P. Hanson et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY (2008)
Anti-tumour necrosis factor-α therapy for severe enteropathy in patients with common variable immunodeficiency (CVID)
I. Chua et al.
CLINICAL AND EXPERIMENTAL IMMUNOLOGY (2007)
Epithelial NEMO links innate immunity to chronic intestinal inflammation
Arianna Nenci et al.
NATURE (2007)
Hepatosplenic T cell lymphoma associated with infliximab use in young patients treated for inflammatory bowel disease
Ann Corken Mackey et al.
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION (2007)
Correction of immunodeficiency associated with NEMO mutation by umbilical cord blood transplantation using a reduced-intensity conditioning regimen
C. Tono et al.
BONE MARROW TRANSPLANTATION (2007)
X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 production
Orchidee Filipe-Santos et al.
JOURNAL OF EXPERIMENTAL MEDICINE (2006)
Skin lesion development in a mouse model of incontinentia pigmenti is triggered by NEMO deficiency in epidermal keratinocytes and requires TNF signaling
A Nenci et al.
HUMAN MOLECULAR GENETICS (2006)
Crohn's disease in common variable immunodeficiency: Treatment with antitumor necrosis factor alpha
Pilar Nos et al.
AMERICAN JOURNAL OF GASTROENTEROLOGY (2006)
Oligoclonal expansion of T lymphocytes with multiple second-site mutations leads to Omenn syndrome in a patient with RAG1-deficient severe combined immunodeficiency
T Wada et al.
BLOOD (2005)
The presentation and natural history of immunodeficiency caused by nuclear factor κB essential modulator mutation
JS Orange et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY (2004)
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
R Nishikomori et al.
BLOOD (2004)
Infliximab but not etanercept induces apoptosis in lamina propria T-lymphocytes from patients with Crohn's disease
JMH Van Den Brande et al.
GASTROENTEROLOGY (2003)
Spontaneous in vivo reversion of an inherited mutation in the Wiskott-Aldrich syndrome
T Ariga et al.
JOURNAL OF IMMUNOLOGY (2001)
Specific missense mutations in NEMO result in hyper-IgM syndrome with hypohydrotic ectodermal dysplasia
A Jain et al.
NATURE IMMUNOLOGY (2001)
X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-κB signaling
R Döffinger et al.
NATURE GENETICS (2001)
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)
J Zonana et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2000)