• 36th International Symposium on Intensive Care and Emergency Medicine : Brussels, Belgium. 15-18 March 2016
• A case of adult-onset Still's disease accompanied by pseudo-gray platelet syndrome
• A Case of Chronic Thrombocytopenia in a 17-Year-Old Female
• A case of EDTA-related in vitro platelet degranulation
• A case report of pseudo grey platelet syndrome with citrate-induced pseudothrombocytopenia: those artifacts may interfere in the platelet numeration and lead to critical misdiagnosis
• A Comprehensive Review of Congenital Platelet Disorders, Thrombocytopenias and Thrombocytopathies
• A Deep Dive into the Pathology of Gray Platelet Syndrome: New Insights on Immune Dysregulation
• A Dominant-Negative GFI1B Mutation in the Gray Platelet Syndrome
• A novel nonsense NBEAL2 gene mutation causing severe bleeding in a patient with gray platelet syndrome
• Abnormal proplatelet formation and emperipolesis in cultured human megakaryocytes from gray platelet syndrome patients
• Acquired Gray Platelet Syndrome Associated with Primary Myelofibrosis
• Advances in Clinical Cardiology 2016: A Summary of the Key Clinical Trials
• Aetiology and outcomes of secondary myelofibrosis occurring in the context of inherited platelet disorders: A single institutional study of four patients
• An oligogenic case of severe neonatal thrombocytopenia and a purportedly benign variant in <em>GFI1B</em> requiring reinterpretation
• Annual Incidence of Confirmed Stent Thrombosis and Clinical Predictors in Patients With ACS Treated With Ticagrelor or Prasugrel
• Association between the severity of liver fibrosis and cardiovascular outcomes in patients with type 2 diabetes
• BEACHcombing for α-granules
• Cell Surface Platelet Tissue Factor Expression: Regulation by P2Y(12) and Link to Residual Platelet Reactivity
• Cell Surface Platelet Tissue Factor Expression: Regulation by P2Y₁₂ and Link to Residual Platelet Reactivity
• Clinical Diagnosis and Magnetic Resonance Imaging in Patients With Transient and Minor Neurological Symptoms: A Prospective Cohort Study
• Comparison of assays measuring extracellular vesicle tissue factor in plasma samples: communication from the ISTH SSC Subcommittee on Vascular Biology
• Comparison of effectiveness and safety between ticagrelor and clopidogrel in patients with acute coronary syndrome and on dialysis in Taiwan
• Complex head and neck microsurgery/neurosurgery in Gray platelet syndrome
• Correction of Severe Myelofibrosis, Impaired Platelet Functions and Abnormalities in a Patient with Gray Platelet Syndrome Successfully Treated by Stem Cell Transplantation
• Corrigendum: Abnormal proplatelet formation and emperipolesis in cultured human megakaryocytes from gray platelet syndrome patients
• Defective Zn²⁺ homeostasis in mouse and human platelets with α- and δ-storage pool diseases
• Determinants of ST-segment elevation myocardial infarction as clinical presentation of acute coronary syndrome
• Diagnosis of inherited platelet disorders on a blood smear: a tool to facilitate worldwide diagnosis of platelet disorders
• Diagnostic workup of inherited platelet disorders
• Early delivery or expectant management for late preterm preeclampsia: A meta-analysis of randomized controlled trials
• EDTA-related degranulation mimicking Storage Pool Disease
• Generation and characterization of a human iPSC line SANi006-A from a Gray Platelet Syndrome patient
• Genetic classification and confirmation of inherited platelet disorders: current status in Korea
• Gray platelet syndrome can mimic autoimmune lymphoproliferative syndrome
• Gray Platelet Syndrome in a Neonate With VACTERL Association: A Novel Homozygous Pathogenic Variant c.5257C&gt;T in the NBEAL2 Gene
• Gray Platelet Syndrome in a Neonate With VACTERL Association: A Novel Homozygous Pathogenic Variant c.5257C>T in the NBEAL2 Gene
• Gray platelet syndrome mimicking atypical autoimmune lymphoproliferative syndrome: the key is in the blood smear
• Gray Platelet Syndrome Presenting With Pancytopenia, Splenomegaly, and Bone Marrow Fibrosis
• Gray Platelet Syndrome with Severe Thrombocytopenia: A Novel <em>NBEAL2</em> Gene Variant from India
• Gray Platelet Syndrome with Severe Thrombocytopenia: A Novel NBEAL2 Gene Variant from India
• Gray Platelet Syndrome-Unusual Presentation with Spontaneous Splenic Rupture: A Case Report and Literature Review
• Gray platelet syndrome, more than just a bleeding disorder
• Gray platelet syndrome: immunity goes awry
• Gray platelet syndrome: Management of perioperative bleeding in redo cardiac surgery
• Gray platelet syndrome: NBEAL2 mutations are associated with pathology beyond megakaryocyte and platelet function defects
• Gray platelet syndrome: Novel mutations of the NBEAL2 gene
• Gray platelets - artifact or real?
• Grey platelet syndrome misdiagnosed as ITP
• Grey zones on dual antiplatelet therapy. Expert opinion
• Hermansky-Pudlak syndrome: Report of two patients with updated genetic classification and management recommendations
• Human platelets contain a pool of free zinc in dense granules
• Hysteresis-like binding of coagulation factors X/Xa to procoagulant activated platelets and phospholipids results from multistep association and membrane-dependent multimerization
• Identifying Patients With Kawasaki Disease Safe for Early Discharge: Development of a Risk Prediction Model at a US Children's Hospital
• Idiopathic Purpura With Gray Platelets: an Acquired Form of Gray Platelet Syndrome
• Immune dysregulation, autoimmunity, and granule defects in gray platelet syndrome
• Infantile-onset inflammatory bowel disease in a patient with Hermansky-Pudlak syndrome: a case report
• Liver stiffness and fibrosis-4 alone better predict liver events compared with aspartate aminotransferase to platelet ratio index in a cohort of human immunodeficiency virus and hepatitis C virus co-infected patients from ANRS CO13 HEPAVIH cohort
• Mitral annuloplasty detachment secondary to unnoticed unruptured left sinus Valsalva aneurysm
• Mutations in Neurobeachin-like 2 do not impact Weibel-Palade body biogenesis and von Willebrand factor secretion in gray platelet syndrome Endothelial Colony Forming Cells
• NBEAL2 deficiency in humans leads to low CTLA-4 expression in activated conventional T cells
• Nbeal2 Deficiency Increases Organ Damage but Does Not Affect Host Defense During Gram-Negative Pneumonia-Derived Sepsis
• Nbeal2 interacts with Dock7, Sec16a, and Vac14
• NBEAL2 is required for neutrophil and NK cell function and pathogen defense
• NBEAL2 mutations and bleeding in patients with gray platelet syndrome
• Neutrophil specific granule and NETosis defects in gray platelet syndrome
• Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome
• Onyx embolization of an intraosseous pseudoaneurysm of the middle meningeal artery in a patient with meningiomatosis, McCune-Albright syndrome, and gray platelet syndrome
• Platelet alpha-granules modulate the inflammatory response under systemic lipopolysaccharide injection in mice
• Platelet granules - secretory and secretive
• Platelet proteome and function in X-linked thrombocytopenia with thalassemia and <em>in silico</em> comparisons with gray platelet syndrome
• Platelet proteome and function in X-linked thrombocytopenia with thalassemia and in silico comparisons with gray platelet syndrome
• Platelet Releasate Proteome Profiling Reveals a Core Set of Proteins with Low Variance between Healthy Adults
• Platelet secretion paves the way
• Platelet α-granules modulate the inflammatory response under systemic lipopolysaccharide injection in mice
• Platelet-Derived Growth Factor Predicts Vulnerable Plaque in Patients with Non-ST Elevation Acute Coronary Syndrome
• Polycystic Ovarian Syndrome Physiologic Pathways Implicated Through Clustering of Genetic Loci
• Polycystic Ovary Syndrome Physiologic Pathways Implicated Through Clustering of Genetic Loci
• Prediction of Post-Discharge Bleeding in Elderly Patients with Acute Coronary Syndromes: Insights from the BleeMACS Registry
• Pseudo gray platelet syndrome: the first case report in Korea
• Pseudo-grey platelet syndrome in a pregnant patient
• Repercussion of Megakaryocyte-Specific Gata1 Loss on Megakaryopoiesis and the Hematopoietic Precursor Compartment
• Rerouting DOT1L inhibitors in leukemia
• Should any genetic defect affecting alpha-granules in platelets be classified as gray platelet syndrome?
• Single-cell multi-omics analysis of the immune response in COVID-19
• Sorting machineries: how platelet-dense granules differ from alpha-granules
• Sorting machineries: how platelet-dense granules differ from α-granules
• Spontaneous 8bp Deletion in Nbeal2 Recapitulates the Gray Platelet Syndrome in Mice
• Striking emperipolesis in megakaryocytes of gray platelet syndrome
• Super-resolution microscopy in the diagnosis of platelet granule disorders
• Syntaxin 12 and COMMD3 are new factors that function with VPS33B in the biogenesis of platelet alpha-granules
• Syntaxin 12 and COMMD3 are new factors that function with VPS33B in the biogenesis of platelet α-granules
• The cisd gene family regulates physiological germline apoptosis through ced-13 and the canonical cell death pathway in Caenorhabditis elegans
• The endoplasmic reticulum protein SEC22B interacts with NBEAL2 and is required for megakaryocyte α-granule biogenesis
• The Neurobeachin-like 2 Protein Regulates Mast Cell Homeostasis
• The Role of Platelets and epsilon-Aminocaproic Acid in Arthrogryposis, Renal Dysfunction, and Cholestasis (ARC) Syndrome Associated Hemorrhage
• The transcription factor GATA1 regulates NBEAL2 expression through a long-distance enhancer
• Thrombocytopenia in a child with polyarthritis: A pointer to gray platelet syndrome
• Ticagrelor Versus Clopidogrel in Older Patients with NSTE-ACS Using Oral Anticoagulation: A Sub-Analysis of the POPular Age Trial
• Zebrafish for thrombocytopoiesis- and hemostasis-related researches and disorders
• α-granule biogenesis: from disease to discovery