Found: 63
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Reduced-intensity conditioning in unrelated donor cord blood transplantation for familial hemophagocytic lymphohistiocytosis.
- Published in:
- American Journal of Hematology, 2012, v. 87, n. 6, p. 637, doi. 10.1002/ajh.23190
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- Publication type:
- Article
Case Report: A Pediatric Case of Familial Mediterranean Fever Concurrent With Autoimmune Hepatitis.
- Published in:
- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.917398
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- Publication type:
- Article
Induced Pluripotent Stem Cell-Derived Monocytes/Macrophages in Autoinflammatory Diseases.
- Published in:
- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.870535
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- Publication type:
- Article
Case Report: A Case of Epstein-Barr Virus-Associated Acute Liver Failure Requiring Hematopoietic Cell Transplantation After Emergent Liver Transplantation.
- Published in:
- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.825806
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- Publication type:
- Article
A nationwide survey of Aicardi–Goutières syndrome patients identifies a strong association between dominant TREX1 mutations and chilblain lesions: Japanese cohort study.
- Published in:
- Rheumatology, 2014, v. 53, n. 3, p. 448, doi. 10.1093/rheumatology/ket372
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- Publication type:
- Article
Heterozygous TREX1 p.Asp18Asn mutation can cause variable neurological symptoms in a family with Aicardi–Goutières syndrome/familial chilblain lupus.
- Published in:
- 2013
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- Publication type:
- Journal Article
Heterozygous TREX1 p.Asp18Asn mutation can cause variable neurological symptoms in a family with Aicardi–Goutières syndrome/familial chilblain lupus.
- Published in:
- Rheumatology, 2013, v. 52, n. 2, p. 406, doi. 10.1093/rheumatology/kes181
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- Publication type:
- Article
Gastric ulcer and gastroenteritis caused by Epstein–Barr virus during immunosuppressive therapy for a child with systemic juvenile idiopathic arthritis.
- Published in:
- 2012
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- Publication type:
- Journal Article
Gastric ulcer and gastroenteritis caused by Epstein–Barr virus during immunosuppressive therapy for a child with systemic juvenile idiopathic arthritis.
- Published in:
- 2012
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- Publication type:
- Case Study
A case of early-onset sarcoidosis with a six-base deletion in the NOD2 gene.
- Published in:
- 2010
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- Publication type:
- Letter
Transitioning from paediatric to adult rheumatological healthcare: English summary of the Japanese Transition Support Guide.
- Published in:
- Modern Rheumatology, 2022, v. 32, n. 2, p. 248, doi. 10.1093/mr/roab071
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- Publication type:
- Article
National survey of Japanese patients with mevalonate kinase deficiency reveals distinctive genetic and clinical characteristics.
- Published in:
- Modern Rheumatology, 2019, v. 29, n. 1, p. 181, doi. 10.1080/14397595.2018.1442639
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- Publication type:
- Article
Patient with neonatal-onset chronic hepatitis presenting with mevalonate kinase deficiency with a novel MVK gene mutation.
- Published in:
- Modern Rheumatology, 2011, v. 21, n. 6, p. 641, doi. 10.3109/s10165-011-0442-7
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- Publication type:
- Article
FR901228 induces tumor regression associated with induction of Fas ligand and activation of Fas signaling in human osteosarcoma cells.
- Published in:
- Oncogene, 2003, v. 22, n. 58, p. 9231, doi. 10.1038/sj.onc.1207184
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- Publication type:
- Article
Augmentation of Stimulator of Interferon Genes–Induced Type I Interferon Production in COPA Syndrome.
- Published in:
- Arthritis & Rheumatology, 2021, v. 73, n. 11, p. 2105, doi. 10.1002/art.41790
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- Publication type:
- Article
Enhanced Chondrogenesis of Induced Pluripotent Stem Cells From Patients With Neonatal-Onset Multisystem Inflammatory Disease Occurs via the Caspase 1-Independent cAMP/Protein Kinase A/CREB Pathway.
- Published in:
- Arthritis & Rheumatology, 2015, v. 67, n. 1, p. 302, doi. 10.1002/art.38912
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- Publication type:
- Article
Regulation of trunk neural crest delamination by δ EF1 and Sip1 in the chicken embryo.
- Published in:
- Development, Growth & Differentiation, 2016, v. 58, n. 2, p. 205, doi. 10.1111/dgd.12256
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- Publication type:
- Article
Tocilizumab modifies clinical and laboratory features of macrophage activation syndrome complicating systemic juvenile idiopathic arthritis.
- Published in:
- Pediatric Rheumatology, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s12969-020-0399-1
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- Publication type:
- Article
Clinical features and characteristics of uveitis associated with juvenile idiopathic arthritis in Japan: first report of the pediatric rheumatology association of Japan (PRAJ).
- Published in:
- Pediatric Rheumatology, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s12969-019-0318-5
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- Publication type:
- Article
Detection of Base Substitution-Type Somatic Mosaicism of the NLRP3 Gene with >99.9% Statistical Confidence by Massively Parallel Sequencing.
- Published in:
- DNA Research, 2012, v. 19, n. 2, p. 143, doi. 10.1093/dnares/dsr047
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- Publication type:
- Article
Partial Trisomy 9p with Clinical Symptoms Resembling Interferonopathies.
- Published in:
- 2022
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- Publication type:
- Letter
Rapid Flow Cytometry-Based Assay for the Functional Classification of MEFV Variants.
- Published in:
- Journal of Clinical Immunology, 2021, v. 41, n. 6, p. 1187, doi. 10.1007/s10875-021-01021-7
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- Publication type:
- Article
Correction to: Helicobacter cinaedi-Associated Refractory Cellulitis in Patients with X-Linked Agammaglobulinemia.
- Published in:
- 2021
- By:
- Publication type:
- Correction Notice
Helicobacter cinaedi-Associated Refractory Cellulitis in Patients with X-Linked Agammaglobulinemia.
- Published in:
- Journal of Clinical Immunology, 2020, v. 40, n. 8, p. 1132, doi. 10.1007/s10875-020-00830-6
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- Publication type:
- Article
A CD57 CTL Degranulation Assay Effectively Identifies Familial Hemophagocytic Lymphohistiocytosis Type 3 Patients.
- Published in:
- Journal of Clinical Immunology, 2017, v. 37, n. 1, p. 92, doi. 10.1007/s10875-016-0357-3
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- Publication type:
- Article
A Female Patient with Incomplete Hemophagocytic Lymphohistiocytosis Caused by a Heterozygous XIAP Mutation Associated with Non-Random X-Chromosome Inactivation Skewed Towards the Wild-Type XIAP Allele.
- Published in:
- Journal of Clinical Immunology, 2015, v. 35, n. 3, p. 244, doi. 10.1007/s10875-015-0144-6
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- Publication type:
- Article
Autosomal Dominant Anhidrotic Ectodermal Dysplasia with Immunodeficiency Caused by a Novel NFKBIA Mutation, p.Ser36Tyr, Presents with Mild Ectodermal Dysplasia and Non-Infectious Systemic Inflammation.
- Published in:
- Journal of Clinical Immunology, 2013, v. 33, n. 7, p. 1165, doi. 10.1007/s10875-013-9924-z
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- Publication type:
- Article
Multiple Reversions of an IL2RG Mutation Restore T cell Function in an X-linked Severe Combined Immunodeficiency Patient.
- Published in:
- Journal of Clinical Immunology, 2012, v. 32, n. 4, p. 690, doi. 10.1007/s10875-012-9684-1
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- Publication type:
- Article
RUNX inhibitor suppresses graft‐versus‐host disease through targeting RUNX‐NFATC2 axis.
- Published in:
- EJHaem, 2021, v. 2, n. 3, p. 449, doi. 10.1002/jha2.230
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- Publication type:
- Article
EBV‐associated lymphoproliferative disorder in a patient with X‐linked severe combined immunodeficiency with multiple reversions of an IL2RG mutation in T cells.
- Published in:
- EJHaem, 2020, v. 1, n. 2, p. 581, doi. 10.1002/jha2.119
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- Publication type:
- Article
Robust and Highly-Efficient Differentiation of Functional Monocytic Cells from Human Pluripotent Stem Cells under Serum- and Feeder Cell-Free Conditions.
- Published in:
- PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0059243
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- Publication type:
- Article
Subtypes of Familial Hemophagocytic Lymphohistiocytosis in Japan Based on Genetic and Functional Analyses of Cytotoxic T Lymphocytes.
- Published in:
- PLoS ONE, 2010, v. 5, n. 11, p. 1, doi. 10.1371/journal.pone.0014173
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- Publication type:
- Article
Laboratory parameters identify familial haemophagocytic lymphohistiocytosis from other forms of paediatric haemophagocytosis.
- Published in:
- British Journal of Haematology, 2015, v. 170, n. 4, p. 532, doi. 10.1111/bjh.13461
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- Publication type:
- Article
Successful cord blood transplantation using reduced intensity conditioning in a 5‐month‐old patient with IL‐10RA deficiency.
- Published in:
- Pediatric Blood & Cancer, 2024, v. 71, n. 8, p. 1, doi. 10.1002/pbc.31056
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- Publication type:
- Article
An efficient diagnosis: A patient with X‐linked inhibitor of apoptosis protein (XIAP) deficiency in the setting of infantile hemophagocytic lymphohistiocytosis was diagnosed using high serum interleukin‐18 combined with common laboratory parameters
- Published in:
- Pediatric Blood & Cancer, 2022, v. 69, n. 8, p. 1, doi. 10.1002/pbc.29606
- By:
- Publication type:
- Article
A case of fetal-onset type 3 familial hemophagocytic lymphohistiocytosis surviving without severe complications after early diagnosis and treatment.
- Published in:
- 2021
- By:
- Publication type:
- case study
Lipid A Analogue, ONO-4007, Inhibits IgE Response and Antigen-Induced Eosinophilic Recruitment into Airways in BALB/c Mice.
- Published in:
- International Archives of Allergy & Immunology, 2002, v. 127, n. 3, p. 217, doi. 10.1159/000053866
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- Publication type:
- Article
Rare diseases presenting with hemophagocytic lymphohistiocytosis.
- Published in:
- Pediatrics International, 2023, v. 65, n. 1, p. 1, doi. 10.1111/ped.15516
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- Publication type:
- Article
Low-frequency mosaicism in cryopyrin-associated periodic fever syndrome: mosaicism in systemic autoinflammatory diseases.
- Published in:
- International Immunology, 2019, v. 31, n. 10, p. 649, doi. 10.1093/intimm/dxz047
- By:
- Publication type:
- Article
The CD40–CD40L axis and IFN-γ play critical roles in Langhans giant cell formation.
- Published in:
- International Immunology, 2012, v. 24, n. 1, p. 5, doi. 10.1093/intimm/dxr088
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- Publication type:
- Article
Hereditary angioedema with a novel mutation, c.1481G>C, in the SERPING1 gene.
- Published in:
- 2021
- By:
- Publication type:
- Case Study
Successful reduced-intensity stem cell transplantation for GATA2 deficiency before progression of advanced MDS.
- Published in:
- Pediatric Transplantation, 2016, v. 20, n. 2, p. 333, doi. 10.1111/petr.12667
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- Publication type:
- Article
Diagnostic accuracy of endoscopic features of pediatric acute gastrointestinal graft-versus-host disease.
- Published in:
- Digestive Endoscopy, 2016, v. 28, n. 5, p. 548, doi. 10.1111/den.12604
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- Publication type:
- Article
Early hematopoietic cell transplantation for familial hemophagocytic lymphohistiocytosis in a regional treatment network in Japan.
- Published in:
- International Journal of Hematology, 2024, v. 119, n. 5, p. 592, doi. 10.1007/s12185-024-03721-3
- By:
- Publication type:
- Article
Outcomes in children with hemophagocytic lymphohistiocytosis treated using HLH-2004 protocol in Japan.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Comprehensive molecular diagnosis of Epstein-Barr virus-associated lymphoproliferative diseases using next-generation sequencing.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Influence of post-transplant mucosal-associated invariant T cell recovery on the development of acute graft-versus-host disease in allogeneic bone marrow transplantation.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Hematopoietic stem cell transplantation with reduced intensity conditioning from a family haploidentical donor in an infant with familial hemophagocytic lymphohistocytosis.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Second transplantation from HLA 2-loci-mismatched mother for graft failure due to hemophagocytic syndrome after cord blood transplantation.
- Published in:
- 2004
- By:
- Publication type:
- journal article
A sporadic case of CTLA4 haploinsufficiency manifesting as Epstein-Barr virus-positive diffuse large B-cell lymphoma.
- Published in:
- Journal of Clinical & Experimental Hematopathology, 2022, v. 62, n. 1, p. 52, doi. 10.3960/jslrt.21026
- By:
- Publication type:
- Article