MYH9 Related Thrombocytopenia Latest Advances

The application of thrombopoietin receptor agonists in the treatment of non-muscle myosin heavy chain 9-related disease

Journal: Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi

Published: April 16, 2026

A Case Report of Thrombocytopenia Caused by a May-Hegglin Anomaly in a Young Saudi Female.

Journal: Journal of investigative medicine high impact case reports

Published: February 21, 2026

Inherited Platelet Disorders During Pregnancy and Delivery: Overview of Management Strategies and Emerging Therapeutic Considerations.

Journal: Hematology reports

Published: December 22, 2025

Corrigendum to "Natural history of the severe subtype of MYH9-related disease (Epstein syndrome)" [European Journal of Internal Medicine 138 (2025) 6354].

Journal: European journal of internal medicine

Published: December 11, 2025

A novel variant of MYH9 mutation associated macro-thrombocytopenia: A case series.

Journal: Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis

Published: August 26, 2025

Re-evaluating the MYH9 p.I1816V variant in a patient with atypical clinical presentation.

Journal: Pediatric nephrology (Berlin, Germany)

Published: August 13, 2025

Analysis of Platelet Membrane Glycoproteins and The Specific Antibodies in MYH9-Related Diseases.

Journal: International journal of general medicine

Published: August 01, 2025

Identification of a de novo MYH9 mutation in a Chinese family with MYH9-related disease.

Journal: Hematology (Amsterdam, Netherlands)

Published: July 21, 2025

Thrombocytopenia, renal failure and hearing loss in a young patient: MYH9-related disorder.

Journal: BMJ case reports

Published: June 24, 2025

First Report of MYH9 E1841K Variant in an Indian Family: A Case of Familial Macrothrombocytopenia and Review of Literature.

Journal: Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion

Published: June 19, 2025

Successful kidney transplantation using eltrombopag in a patient with MYH9-related disease.

Journal: CEN case reports

Published: June 05, 2025

Pulled-in-two syndrome in a young woman with restrictive strabismus and rare genetic mutation.

Journal: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus

Published: March 23, 2025

MYH9 Related Thrombocytopenia Latest Advances

Find the Latest Research About MYH9 Related Thrombocytopenia

The application of thrombopoietin receptor agonists in the treatment of non-muscle myosin heavy chain 9-related disease

The application of thrombopoietin receptor agonists in the treatment of non-muscle myosin heavy chain 9-related disease

A Case Report of Thrombocytopenia Caused by a May-Hegglin Anomaly in a Young Saudi Female.

A Case Report of Thrombocytopenia Caused by a May-Hegglin Anomaly in a Young Saudi Female.

Inherited Platelet Disorders During Pregnancy and Delivery: Overview of Management Strategies and Emerging Therapeutic Considerations.

Inherited Platelet Disorders During Pregnancy and Delivery: Overview of Management Strategies and Emerging Therapeutic Considerations.

Corrigendum to "Natural history of the severe subtype of MYH9-related disease (Epstein syndrome)" [European Journal of Internal Medicine 138 (2025) 6354].

Corrigendum to "Natural history of the severe subtype of MYH9-related disease (Epstein syndrome)" [European Journal of Internal Medicine 138 (2025) 6354].

A novel variant of MYH9 mutation associated macro-thrombocytopenia: A case series.

A novel variant of MYH9 mutation associated macro-thrombocytopenia: A case series.

Re-evaluating the MYH9 p.I1816V variant in a patient with atypical clinical presentation.

Re-evaluating the MYH9 p.I1816V variant in a patient with atypical clinical presentation.

Analysis of Platelet Membrane Glycoproteins and The Specific Antibodies in MYH9-Related Diseases.

Analysis of Platelet Membrane Glycoproteins and The Specific Antibodies in MYH9-Related Diseases.

Identification of a de novo MYH9 mutation in a Chinese family with MYH9-related disease.

Identification of a de novo MYH9 mutation in a Chinese family with MYH9-related disease.

Thrombocytopenia, renal failure and hearing loss in a young patient: MYH9-related disorder.

Thrombocytopenia, renal failure and hearing loss in a young patient: MYH9-related disorder.

First Report of MYH9 E1841K Variant in an Indian Family: A Case of Familial Macrothrombocytopenia and Review of Literature.

First Report of MYH9 E1841K Variant in an Indian Family: A Case of Familial Macrothrombocytopenia and Review of Literature.

Successful kidney transplantation using eltrombopag in a patient with MYH9-related disease.

Successful kidney transplantation using eltrombopag in a patient with MYH9-related disease.

Pulled-in-two syndrome in a young woman with restrictive strabismus and rare genetic mutation.

Pulled-in-two syndrome in a young woman with restrictive strabismus and rare genetic mutation.