Disease: May-Hegglin anomaly
- <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
- Gene analysis and clinical features of MYH9-related disease
- Hereditary thrombocytopenia with familial novel mutation in MYH9 gene: A familial case report
- 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
- 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
- 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 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