• <em>MYH9</em>-Related Disease
• A familial case of MYH9 gene mutation associated with multiple functional and structural platelet abnormalities
• A family with an MYH9-related disorder with different phenotypes masquerading as immune thrombocytopaenia: an underreported disorder in Taiwan
• A gain-of-function variant in the Wiskott-Aldrich syndrome gene is associated with a MYH9-related disease-like syndrome
• A nationwide survey of MYH9-related disease in Japan
• An interesting case of thrombocytopenia in pregnancy
• Analysis of clinical phenotype and gene mutation characteristics of MYH9-related disorder
• Anesthetic considerations for May-Hegglin anomaly
• Avatrombopag improves thrombocytopenia in MYH9-related disorder following eltrombopag treatment failure
• Bernard Soulier syndrome: a rare, frequently misdiagnosed and poorly managed bleeding disorder
• Characterization of Sensorineural Hearing Loss in Patients With MYH9-Related Disease: A Systematic Review
• Clinical and genetic features of seven children with MYH9-related disease
• Defective VWF secretion due to expression of MYH9-RD E1841K mutant in endothelial cells disrupts hemostasis
• Diagnostic delay of MYH9-related disorder in Japan
• Gene analysis and clinical features of MYH9-related disease
• Hereditary thrombocytopenia with familial novel mutation in MYH9 gene: A familial case report
• Identification of a novel MYH9-related disease-associated mutation with multiple faintly staining Döhle-like bodies
• Individualized Bleeding Risk Assessment through Thromboelastography: A Case Report of May-Hegglin Anomaly in Preterm Twin Neonates
• Linking the Landscape of <em>MYH9</em>-Related Diseases to the Molecular Mechanisms that Control Non-Muscle Myosin II-A Function in Cells
• Lower Leg Hyperpigmentation in MYH9-Related Disorder
• Macrothrombocytopenia with leukocyte inclusions in a patient with Wilson disease: a case report and literature review
• Marked Underestimation of Platelet Count and a Characteristic Platelet Histogram as Clues to MYH9-Related Disorders
• May-Hegglin Anomaly
• May-Hegglin Anomaly
• May-Hegglin Anomaly
• MYH9-related disorder with sole presentation of end-stage kidney disease and long-term, recurrence-free living after living donor renal transplantation: a case report
• Post-Kidney Transplant Brief Psychosis in a Patient With MYH9-Related Disease: A Case Report
• Renal Biopsy-induced Hematoma and Infection in a Patient with Asymptomatic May-Hegglin Anomaly
• Renal injury associated with <em>MYH9</em> disorder with 5773delG mutation: A case report
• Spontaneous and recurrent subdural haematoma in a patient with May-Hegglin anomaly
• Successful administration of eltrombopag in preparation for peritoneal dialysis catheter placement in a girl with MYH9-related disease
• Successful Eltrombopag Therapy in a Child with MYH9-Related Inherited Thrombocytopenia
• Successful hematopoietic stem cell transplantation in MYH9-related congenital thrombocytopenia
• Successful living-related kidney transplantation in MYH9-related disorder with macrothrombocytopenia: lessons for the clinical nephrologist
• The curious incident of a cavum velum interpositum cyst in twins of a mother carrying May-Hegglin anomaly: a case report and short literature review
• The May-Hegglin anomaly: a rare cause of a common complaint
• Umbilical cord blood transplantation for MYH9-related disorders
• Unveiling the hidden clues: Dohle body-like inclusions as morphological markers for MYH9-related disorders: A case report