Pages that link to "Q52573741"
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The following pages link to Successful bone marrow transplantation for IPEX syndrome after reduced-intensity conditioning. (Q52573741):
Displaying 50 items.
- IPEX as a result of mutations in FOXP3 (Q21342967) (← links)
- FOXP3: genetic and epigenetic implications for autoimmunity (Q27003398) (← links)
- Use of sirolimus in IPEX and IPEX-like children (Q28280196) (← links)
- Genetic control of the inflammatory T-cell response in regulatory T-cell deficient scurfy mice (Q30431210) (← links)
- Type 1 diabetes and autoimmune polyendocrine syndromes (Q33379406) (← links)
- IPEX syndrome and human Treg cells (Q33391755) (← links)
- Improving cellular therapy for primary immune deficiency diseases: recognition, diagnosis, and management (Q33700953) (← links)
- Banting Lecture 2009: An unfinished journey: molecular pathogenesis to prevention of type 1A diabetes (Q33750667) (← links)
- Autoimmune polyendocrine syndromes: clues to type 1 diabetes pathogenesis (Q33811669) (← links)
- Stable hematopoietic cell engraftment after low-intensity nonmyeloablative conditioning in patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (Q34233378) (← links)
- Hematopoietic cell transplantation for treatment of primary immune deficiencies (Q34383907) (← links)
- Clues to immune tolerance: the monogenic autoimmune syndromes (Q34440616) (← links)
- From IPEX syndrome to FOXP3 mutation: a lesson on immune dysregulation (Q34515848) (← links)
- IPEX, FOXP3 and regulatory T-cells: a model for autoimmunity. (Q34583514) (← links)
- Hematopoietic stem cell transplantation for primary immunodeficiencies (Q34630754) (← links)
- Exome sequencing identifies a novel FOXP3 mutation in a 2-generation family with inflammatory bowel disease (Q34778685) (← links)
- Therapeutic in vivo selection of thymic-derived natural T regulatory cells following non-myeloablative hematopoietic stem cell transplant for IPEX (Q35435153) (← links)
- Fatal autoimmunity in mice reconstituted with human hematopoietic stem cells encoding defective FOXP3 (Q35757391) (← links)
- Etiopathogenesis of insulin autoimmunity (Q35910119) (← links)
- Regulatory T cells in asthma (Q36064548) (← links)
- Immune dysregulation, polyendocrinopathy, enteropathy, x-linked syndrome: a paradigm of immunodeficiency with autoimmunity (Q36282394) (← links)
- Unrelated donor cord blood transplantation for children with severe sickle cell disease: results of one cohort from the phase II study from the Blood and Marrow Transplant Clinical Trials Network (BMT CTN) (Q36745209) (← links)
- Clinical heterogeneity in patients with FOXP3 mutations presenting with permanent neonatal diabetes (Q37022929) (← links)
- Primary immune deficiency disorders presenting as autoimmune diseases: IPEX and APECED. (Q37081019) (← links)
- Diagnosis and treatment of gastrointestinal disorders in patients with primary immunodeficiency (Q37238684) (← links)
- Hematopoietic cell transplantation for correction of primary immunodeficiencies (Q37251051) (← links)
- Impairing oral tolerance promotes allergy and anaphylaxis: a new murine food allergy model (Q37453377) (← links)
- Resetting microbiota by Lactobacillus reuteri inhibits T reg deficiency-induced autoimmunity via adenosine A2A receptors. (Q37549749) (← links)
- Hematopoietic stem cell transplantation for pediatric autoimmune disease: where we stand and where we need to go. (Q37549888) (← links)
- Gastrointestinal manifestations in primary immune disorders (Q37564321) (← links)
- Regulatory T cells as therapeutic targets in rheumatoid arthritis (Q37607071) (← links)
- Pathogenic mechanisms of allergic inflammation: atopic asthma as a paradigm (Q37748077) (← links)
- The relationship of x-linked primary immune deficiencies and autoimmunity (Q37767175) (← links)
- Monogenic Autoimmunity (Q37973770) (← links)
- Recent advances in transplantation for primary immune deficiency diseases: a comprehensive review (Q38119863) (← links)
- ICON: the early diagnosis of congenital immunodeficiencies (Q38195246) (← links)
- Hematopoietic stem cell transplantation in patients with gain-of-function signal transducer and activator of transcription 1 mutations (Q38732260) (← links)
- Rare phenotypes in the understanding of autoimmunity (Q38937349) (← links)
- Successful Hematopoietic Stem Cell Transplantation in a Patient with LPS-Responsive Beige-Like Anchor (LRBA) Gene Mutation. (Q39793998) (← links)
- Gut immune reconstitution in immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome after hematopoietic stem cell transplantation. (Q43089114) (← links)
- Single centre experience of haematopoietic SCT for patients with immunodysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (Q43971473) (← links)
- Long-term follow up of IPEX syndrome patients after different therapeutic strategies: an international multicenter retrospective study. (Q45875838) (← links)
- FOXP3 expression following bone marrow transplantation for IPEX syndrome after reduced-intensity conditioning. (Q45995235) (← links)
- Type 1 diabetes as an autoimmune disease: the evidence (Q50474708) (← links)
- A novel mutation and unusual clinical features in a patient with immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome (Q50525033) (← links)
- Alternative Splicing of FOXP3-Virtue and Vice. (Q55495606) (← links)
- Identification of FOXP3-negative regulatory T-like (CD4 CD25 CD127low) cells in patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (Q56963542) (← links)
- Digestive histopathological presentation of IPEX syndrome (Q57078467) (← links)
- The diagnosis and management of monogenic diabetes in children and adolescents (Q57303417) (← links)
- Autoimmune Enteropathy: An Updated Review with Special Focus on Stem Cell Transplant Therapy (Q58555924) (← links)