Disease: Bone Marrow failure syndromes
- A CRISPR base editing approach for the functional assessment of telomere biology disorder-related genes in human health and aging
- A minimal Fanconi Anemia complex in early diverging fungi
- A murine model to evaluate immunotherapy effectiveness for human Fanconi anemia-mutated acute myeloid leukemia
- A naturally occurring canine model of syndromic congenital microphthalmia
- A Rare Inherited Bone Marrow Failure Syndrome Disclosed by Reanalysis of the Exome Data of a Patient Evaluated for Cytopenia and Dysmorphic Features
- A Review of the Repair of DNA Double Strand Breaks in the Development of Oral Cancer
- A way to "mimic" the pathophysiology of acquired SAA
- Activity and safety of eltrombopag in combination with cyclosporin A as first‑line treatment of adults with severe aplastic anaemia (SOAR): a phase 2, single-arm study
- Adenocarcinoma with Aplastic Anemia as an Immune-related Adverse Event Caused by Pembrolizumab: Report of a Case
- Advances in nutritional support for children undergoing hematopoietic stem cell transplantation
- Alloengraftment without significant toxicity or GVHD in CD45 antibody-drug conjugate conditioned Fanconi anemia mice
- Aplastic anaemia following antibiotic use for urinary tract infection
- Aplastic Anaemia in Pregnancy: A Case-Based Comprehensive Review of the Literature
- Aplastic anemia: history and recent developments in diagnosis and treatment
- Cardiovascular Management of Patients Undergoing Hematopoietic Stem Cell Transplantation: From Pretransplantation to Survivorship: A Scientific Statement From the American Heart Association
- Case Report: Profound newborn leukopenia related to a novel RAC2 variant
- Caspase 8 deletion causes infection/inflammation-induced bone marrow failure and MDS-like disease in mice
- Characteristic phenotypes of ADH5/ALDH2 deficiency during childhood
- Clinical and genetic characteristics of Chinese patients with Shwachman Diamond syndrome: a literature review of Chinese publication
- Clinical impact and characteristics of erythroid dysplasia in adult aplastic anaemia: Results from a multicentre registry
- Clinical mutations in the TERT and TERC genes coding for telomerase components induced oxidative stress, DNA damage at telomeres and cell apoptosis besides decreased telomerase activity
- Clonal hematopoiesis in children with predisposing conditions
- Combating bone marrow failure with polymer materials
- Consideration of ATG-free therapy with eltrombopag and cyclosporine for severe aplastic anaemia
- Demographic and disease-related factors impact bone turnover and vitamin D in children with hemato-oncological diseases
- Deregulated protein homeostasis constrains fetal hematopoietic stem cell pool expansion in Fanconi anemia
- Diagnosis, treatment, and surveillance of Diamond-Blackfan anaemia syndrome: international consensus statement
- Diagnostic guidance for hereditary neutropenia in children: Narrative literature review
- Diamond-Blackfan anemia, the archetype of ribosomopathy: How distinct is it from the other constitutional ribosomopathies?
- Dioscin alleviates aplastic anemia through regulatory T cells promotion
- Discerning clinicopathological features of congenital neutropenia syndromes: an approach to diagnostically challenging differential diagnoses
- Donor-type bone marrow aplasia following hematopoietic stem cell transplantation in a child with a novel SAMD9L variant
- Ectopic expression of the transcription factor ONECUT3 drives a complex karyotype in myelodysplastic syndromes
- Ectopic expression of transcription factor ONECUT3 drives complex karyotype in Myelodysplastic Syndromes
- Efficacy and safety of immunosuppressive therapy combined with eltrombopag for severe aplastic anemia: a systematic review and meta-analysis
- Erratum to: Utility of clinical comprehensive genomic characterization for diagnostic categorization in patients presenting with hypocellular bone marrow failure syndromes
- Et barn med langvarig anemi
- Exploring strategies to optimise outcomes in hepatitis-associated aplastic anaemia patients following haematopoietic stem cell transplantation
- Fertility Potential and Gonadal Function in Survivors of Reduced Intensity HCT
- Fertility Potential and Gonadal Function in Survivors of Reduced-Intensity Hematopoietic Stem Cell Transplantation
- Fosl2 Deficiency Predisposes Mice to Osteopetrosis, Leading to Bone Marrow Failure
- Genetic and clinical analysis of a child with Shwachman-Diamond syndrome due to compound heterozygous variants of SBDS gene
- Germline biallelic BRCA2 pathogenic variants and medulloblastoma: an international cohort study
- Germline predisposition to myeloid neoplasms: Characteristics and management of high versus variable penetrance disorders
- Growth Charts for Shwachman-Diamond Syndrome at Ages 0 to 18 Years
- Haploidentical Hematopoietic Stem Cell Transplantation for Patients with Severe Aplastic Anemia-Single-Centre Experience
- Harmonizing definitions for hematopoietic recovery, graft rejection, graft failure, poor graft function, and donor chimerism in allogeneic hematopoietic cell transplantation: a report on behalf of the EBMT, ASTCT, CIBMTR, and APBMT
- Hematopoietic stem cell transplantation in two sisters with bone marrow failure associated with POLE gene variants
- HERVs may perform as the initial trigger for acquired aplastic anemia
- High-Specific-Activity 131I-MIBG for the Treatment of Advanced Pheochromocytoma and Paraganglioma
- HLA-haploidentical stem cell transplantation in children with inherited bone marrow failure syndromes: A retrospective analysis on behalf of EBMT severe aplastic Anemia and pediatric diseases working parties
- How to think about the clinical classifications of acquired aplastic anemia
- Immune-driven clonal cell selection at the intersection among cancer, infections, autoimmunity and senescence
- Impact of newborn screening for fatty acid oxidation disorders on neurological outcome: A Belgian retrospective and multicentric study
- Impaired Mitochondrial Function and Marrow Failure in Patients Carrying a Variant of the SRSF4 Gene
- Inherited bone marrow failure syndromes: phenotype as a tool for early diagnostic suspicion at a major reference center in Mexico
- Interleukin-6 and interleukin-8 levels in children with aplastic anemia and its correlation with disease severity and response to immunosuppressive therapy
- Langerhans cell histiocytosis: NACHO update on progress, chaos, and opportunity on the path to rational cures
- Linking Gene Fusions to Bone Marrow Failure and Malignant Transformation in Dyskeratosis Congenita
- Loeys-Dietz syndrome with concomitant aplastic anemia
- Low-dose non-steroidal anti-inflammatory drugs: a promising approach for the treatment of symptomatic bone marrow failure in Ghosal hematodiaphyseal dysplasia
- Macrocytic anemias
- Malignant progression of pre-leukemic disorders
- Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesis
- Metagenomic Next-Generation Sequencing (mNGS) of cerebrospinal fluid for diagnosis of human herpesvirus 6B encephalitis following transplantation for severe aplastic anemia
- Modified Delphi Panel Consensus Recommendations for Management of Severe Aplastic Anemia
- Moyamoya Disease in a Child With Fanconi Anemia: An Anomaly or a Complication
- Myelodysplastic neoplasms evolving from inherited bone marrow failure syndromes / germline predisposition syndromes: Back under the microscope
- Nomogram establishment for short-term survival prediction in ICU patients with aplastic anemia based on the MIMIC-IV database
- Novel compound heterozygous variants in FANCI cause premature ovarian insufficiency
- Novel Presentation of Major Histocompatibility Complex Class II Deficiency with Hemophagocytic Lymphohistiocytosis
- Of gains and losses: SAMD9/SAMD9L and monosomy 7 in myelodysplastic syndrome
- Oh rats! Intracellular rod-like inclusions in an adolescent with Shwachman-Diamond syndrome
- Oral cancer and oral potentially malignant disorders in patients with Fanconi anemia - A systematic review
- Osteopetrosis and related osteoclast disorders in adults: A review and knowledge gapsOn behalf of the European calcified tissue society and ERN BOND
- Pancancer analysis of the prognostic and immunological role of FANCD2: a potential target for carcinogenesis and survival
- Pancytopenia with aplastic anemia in systemic lupus erythematosus: case series and literature review
- Pathogenesis of myelodysplastic syndromes by excessive mitochondrial fragmentation
- Pediatric acute promyelocytic leukemia and Fanconi anemia: Case report and literature review
- Pre-existing Immunocompromising Conditions and Outcomes of Acute COVID-19 Patients Admitted for Pediatric Intensive Care
- Progress in medical therapy in aplastic anemia: why it took so long?
- Recombinant Human Thrombopoietin Promotes Platelet Engraftment in Severe Aplastic Anemia Patients Following Treatment With Haploid Hematopoietic Stem Cell Transplantation using Modified Post-Transplantation Cyclophosphamide
- Reduced toxicity matched sibling bone marrow transplant results in excellent outcomes for severe congenital neutropenia
- Revisiting the most often used item in the haematological tool box-The extent of haemodilution in bone marrow aspirates
- Role of miRNAs in T-cell activation and Th17/Treg-cell imbalance in acquired aplastic anemia
- Safety and efficacy of eltrombopag in patients with aplastic anemia: a systematic review and meta-analysis of randomized controlled trials
- Screening and Identification of lncRNA Related to Adipocity of Bone Marrow Microenvironment in Aplastic Anemia
- Single non-blood-related umbilical cord blood transplantation using a reduced-intensity conditioning regimen for the treatment of severe aplastic anemia
- Spurious High Platelet Count without PLT Flag(S) in a Patient with Severe Aplastic Anaemia
- Strategic infection prevention after genetically modified hematopoietic stem cell therapies: recommendations from the International Society for Cell & Gene Therapy Stem Cell Engineering Committee
- Telomere Biology Disorder: A Focus on Gastrointestinal and Hepatic Manifestations
- The state of the art in the treatment of severe aplastic anemia: immunotherapy and hematopoietic cell transplantation in children and adults
- To determine the frequency of aldehyde dehydrogenase type 2 (aldh2) deficiency in aplastic anaemia: A single center experience from pakistan
- Tracer-based lipidomics enables the discovery of disease-specific candidate biomarkers in mitochondrial beta-oxidation disorders
- Tracer-based lipidomics enables the discovery of disease-specific candidate biomarkers in mitochondrial β-oxidation disorders
- Transformation of Severe Aplastic Anemia into Donor Cell Leukemia after Allogeneic Hematopoietic Stem Cell Transplantation: A Rare Case Report
- Umbilical Cord Blood Transplantation for Fanconi Anemia With a Special Focus on Late Complications: a Study on Behalf of Eurocord and SAAWP-EBMT
- Unrelated donor hematopoietic stem cell transplantation compared to immunosuppressive therapy plus eltrombopag as first-line treatment for adults with severe aplastic anemia
- Variability in evaluation and follow-up of newborns with CRMS/CFSPID in New York State
- When inflammatory stressors dramatically change, disease phenotypes may transform between autoimmune hematopoietic failure and myeloid neoplasms