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Journal Articles

Providing Primary Care to Children Diagnosed with Myosin Heavy Chain 9-Related Platelet Disorder: A Case Report and Review of Literature

Ka Li, Rafat Ahmed, MBBS

Blood (2018) 132 (Supplement 1): 5828.

https://doi.org/10.1182/blood-2018-99-113967

Published: 2018

Journal Articles

Gene Heterogenicity Diagnosis on Children with Complicated Immunological and Hematological Abnormalities

Chunfu Li, MD, Haixia Guo, MD PhD

Blood (2017) 130 (Supplement 1): 4946.

https://doi.org/10.1182/blood.V130.Suppl_1.4946.4946

Published: 2017

Journal Articles

Assessment of MYH9- Related Syndromes among a Series of Patients with Constitutional Macrothrombocytopenia (MT).

Nicole Schlegel, Beatrice Saposnik, Sylvie Binard, Sandrine Elbaz, Odile Fenneteau, Valerie Bardet, Benedicte Gerard, Paquita Nurden, French Ref Center for Inherited Plat Disorders

Blood (2006) 108 (11): 700.

https://doi.org/10.1182/blood.V108.11.700.700

Published: 2006

Journal Articles

Congenital Macrothrombocytopenia and Defective Localization of the Nonmuscle Myosin Heavy Chain IIA in Leukocytes and Megakaryocytes with a Normal MYH9 Gene.

Walter H. Kahr, MD, PhD, FRCPC, Ling Li, MD, MSc, Chanchai Traivaree, MD, Hilary Christensen, BA, MLTU, Tara Paton, PhD, Sheila E. Butchard, RN, Julie Curtin, MBBS, PhD, Victor S. Blanchette, FRCP

Blood (2004) 104 (11): 3032.

https://doi.org/10.1182/blood.V104.11.3032.3032

Published: 2004

Journal Articles

A Novel Frameshift Mutation in a Case of Familial May-Hegglin Anomaly.

Jacky A. Cutler, Mike J. Mitchell, Geoffrey F. Savidge

Blood (2004) 104 (11): 3033.

https://doi.org/10.1182/blood.V104.11.3033.3033

Published: 2004

Journal Articles

Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome

Samuel Deutsch, Alexandra Rideau, Marie-Luce Bochaton-Piallat, Giuseppe Merla, Antoine Geinoz, Giulio Gabbiani, Torsten Schwede, Thomas Matthes, Stylianos E. Antonarakis, Photis Beris

Blood (2003) 102 (2): 529–534.

https://doi.org/10.1182/blood-2002-09-2783

Published: 2003

Journal Articles

Autosomal-dominant giant platelet syndromes: a hint of the same genetic defect as in Fechtner syndrome owing to a similar genetic linkage to chromosome 22q11-13

Amos Toren, Galit Rozenfeld-Granot, Bianca Rocca, Charles J. Epstein, Ninette Amariglio, Ferdinando Laghi, Raffaele Landolfi, Frida Brok-Simoni, Lena E. Carlsson, Gideon Rechavi, Andreas Greinacher

Blood (2000) 96 (10): 3447–3451.

https://doi.org/10.1182/blood.V96.10.3447

Published: 2000

NARROW

Providing Primary Care to Children Diagnosed with Myosin Heavy Chain 9-Related Platelet Disorder: A Case Report and Review of Literature

Gene Heterogenicity Diagnosis on Children with Complicated Immunological and Hematological Abnormalities

Assessment of MYH9- Related Syndromes among a Series of Patients with Constitutional Macrothrombocytopenia (MT).

Congenital Macrothrombocytopenia and Defective Localization of the Nonmuscle Myosin Heavy Chain IIA in Leukocytes and Megakaryocytes with a Normal MYH9 Gene.

A Novel Frameshift Mutation in a Case of Familial May-Hegglin Anomaly.

Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome

Autosomal-dominant giant platelet syndromes: a hint of the same genetic defect as in Fechtner syndrome owing to a similar genetic linkage to chromosome 22q11-13

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ASH Publications

American Society of Hematology

Providing Primary Care to Children Diagnosed with Myosin Heavy Chain 9-Related Platelet Disorder: A Case Report and Review of Literature

Gene Heterogenicity Diagnosis on Children with Complicated Immunological and Hematological Abnormalities

Assessment of MYH9- Related Syndromes among a Series of Patients with Constitutional Macrothrombocytopenia (MT).

Congenital Macrothrombocytopenia and Defective Localization of the Nonmuscle Myosin Heavy Chain IIA in Leukocytes and Megakaryocytes with a Normal MYH9 Gene.

A Novel Frameshift Mutation in a Case of Familial May-Hegglin Anomaly.

Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome

Autosomal-dominant giant platelet syndromes: a hint of the same genetic defect as in Fechtner syndrome owing to a similar genetic linkage to chromosome 22q11-13

Email alerts

ASH Publications

American Society of Hematology

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