Chronic Graft Versus Host Disease
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Last Posted: Jun 14, 2024
- MICB Genetic Variants and Its Protein Soluble Level Are Associated with the Risk of Chronic GvHD and CMV Infection after Allogeneic HSCT.
Jagoda Siemaszko, et al. Archivum immunologiae et therapiae experimentalis 2024 0 (1) - Effect of IL-2 polymorphism rs2069762 on single-unit cord blood transplant outcomes.
Takaaki Konuma, et al. Cytokine 2024 0 156636 - Prognostic impact of HLA supertype mismatch in single-unit cord blood transplantation.
Takeshi Sugio, et al. Bone marrow transplantation 2024 0 - Clonal hematopoiesis of a novel dic(18;20) clone following allogeneic hematopoietic stem cell transplantation.
Makoto Ito, et al. International journal of hematology 2023 0 - Identification of single nucleotide polymorphisms (SNPs) associated with chronic graft-versus-host disease in patients undergoing allogeneic hematopoietic cell transplantation.
Jean-Luc C Mougeot, et al. Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer 2023 0 (10) 587 - The impact of NKG2A and NKG2D receptors and HLA-E and MICA ligands polymorphisms on post-transplant complications after paediatric allogeneic HSCT: a single-centre experience.
Jagoda Siemaszko, et al. Frontiers in genetics 2023 0 1186123 - Circulating cell-free mitochondrial DNA as a diagnostic and prognostic biomarker in chronic and late acute graft-versus-host disease in children.
Azadpour Shima, et al. Experimental hematology 2023 0 - Characteristics and risk of chronic graft-versus-host disease of liver in allogeneic hematopoietic stem cell transplant recipients.
Chen Chien-Ting, et al. PloS one 2017 0 (9) e0185210 - Donor characteristics and hematopoietic stem cell transplantation outcome: experience of a single center in Southern Brazil.
Paz Alessandra, et al. Hematology, transfusion and cell therapy 2018 0 (2) 136-142 - Kinetics and Risk Factors of Relapse after Allogeneic Stem Cell Transplantation in Children with Leukemia: A Long-Term Follow-Up Single-Center Study.
Molina Blanca, et al. Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation 2018 0 (1) 100-106
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Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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