Related references
Note: Only part of the references are listed.Primary immune deficiency disorders presenting as autoimmune diseases: IPEX and APECED
D. Moraes-Vasconcelos et al.
JOURNAL OF CLINICAL IMMUNOLOGY (2008)
Insulin mutation screening in 1,044 patients with diabetes:: Mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood
Emma L. Edghill et al.
DIABETES (2008)
Developmental changes of FOXP3-expressing CD4+CD25+ regulatory T cells and their impairment in patients with FOXP3 gene mutations
Tatsuya Fuchizawa et al.
CLINICAL IMMUNOLOGY (2007)
CD4+ CD25+ FoxP3+ regulatory T cells in autoimmune diseases
Xavier Valencia et al.
NATURE CLINICAL PRACTICE RHEUMATOLOGY (2007)
Immunodysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome: an unusual cause of proteinuria in infancy
Asha Moudgil et al.
PEDIATRIC NEPHROLOGY (2007)
Permanent neonatal diabetes caused by dominant, recessive, or compound heterozygous SUR1 mutations with opposite functional effects
Sian Ellard et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Mutations in ATP-sensitive K+ channel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthood
Sarah E. Flanagan et al.
DIABETES (2007)
CD25 deficiency causes an immune dysregulation, polyendocrinopathy, enteropathy, X-linked-like syndrome, and defective IL-10 expression from CD4 lymphocytes
Amy A. Caudy et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY (2007)
Circulating antibodies to nephrin in patients with type 1 diabetes
Petri Aaltonen et al.
NEPHROLOGY DIALYSIS TRANSPLANTATION (2007)
Successful bone marrow transplantation for IPEX syndrome after reduced-intensity conditioning
Aarati Rao et al.
BLOOD (2007)
Analysis of FOXP3 reveals multiple domains required for its function as a transcriptional repressor
Jared E. Lopes et al.
JOURNAL OF IMMUNOLOGY (2006)
Defective regulatory and effector T cell functions in patients with FOXP3 mutations
Rosa Bacchetta et al.
JOURNAL OF CLINICAL INVESTIGATION (2006)
HLA genotyping supports a nonautoimmune etiology in patients diagnosed with diabetes under the age of 6 months
Emma L. Edghill et al.
DIABETES (2006)
Mechanistic associations of a mild phenotype of immunodysregulation, polyendocrinopathy, enteropathy, X-linked syndrome
Fabrizio De Benedetti et al.
CLINICAL GASTROENTEROLOGY AND HEPATOLOGY (2006)
The SWISS-MODEL workspace: a web-based environment for protein structure homology modelling
K Arnold et al.
BIOINFORMATICS (2006)
Permanent diabetes mellitus in the first year of life
D Iafusco et al.
DIABETOLOGIA (2002)
Novel mutations of FOXP3 in two Japanese patients with immune dysregulation, polyendocrinopathy, enteropathy, X linked syndrome (IPEX)
I Kobayashi et al.
JOURNAL OF MEDICAL GENETICS (2001)
X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy
RS Wildin et al.
NATURE GENETICS (2001)
The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3
CL Bennett et al.
NATURE GENETICS (2001)
JM2, encoding a fork head-related protein, is mutated in X-linked autoimmunity-allergic disregulation syndrome
TA Chatila et al.
JOURNAL OF CLINICAL INVESTIGATION (2000)
Neonatal Type I diabetes associated with maternal echovirus 6 infection:: a case report
T Otonkoski et al.
DIABETOLOGIA (2000)
Share Paper
