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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

Evaluation of Platelet Parameters in Children

Ralf Knoefler, MD, Stefanie Hackel, Julia Staechele, MD, Judith Lohse, MD, Ursula Range, Meinolf Suttorp, PhD MD, Oliver Tiebel, MD

Blood (2017) 130 (Supplement 1): 4842.

https://doi.org/10.1182/blood.V130.Suppl_1.4842.4842

Published: 2017

Journal Articles

Inherited Giant Platelet Disorder, Kashmiri Thrombocytopenia, a Common Syndrome Found in Srinagar, India

Felipe R Lorenzo, PhD, Tsewang Tashi, MD, Parvaiz Koul, MD, Nicola J Camp, PhD, Perumal Thiagarajan, MD, Josef T. Prchal, MD

Blood (2014) 124 (21): 4211.

https://doi.org/10.1182/blood.V124.21.4211.4211

Published: 2014

Journal Articles

Platelet-Like-Particles Sheared From Myosin-II-Inhibited Megakaryocytes Highlights The Elevated Thrombocrit Of May-Hegglin Anomaly

Kyle R Spinler, B.S., Jae-Won Shin, Ph.D., Dennis E Discher, Ph.D.

Blood (2013) 122 (21): 2426.

https://doi.org/10.1182/blood.V122.21.2426.2426

Published: 2013

Journal Articles

Hemorrhagic Complications With Adenotonsillectomy In Children and Young Adults With Bleeding Disorders

Deepti M. Warad, M.B.B.S., Fareeda TN. Hussain, MD, Shelagh A. Cofer, MD, Vilmarie Rodriguez, MD

Blood (2013) 122 (21): 3611.

https://doi.org/10.1182/blood.V122.21.3611.3611

Published: 2013

Journal Articles

May-Hegglin anomaly

Cyrus C. Hsia, Anargyros Xenocostas

Blood (2012) 119 (2): 328.

https://doi.org/10.1182/blood-2010-12-325431

Published: 2012

Journal Articles

Myh9 Q1443L Is a Novel Mouse Model of MYH9-Related Disorders

Blood (2010) 116 (21): 2527.

https://doi.org/10.1182/blood.V116.21.2527.2527

Published: 2010

Journal Articles

Differential expression of wild-type and mutant NMMHC-IIA polypeptides in blood cells suggests cell-specific regulation mechanisms in MYH9 disorders

Shinji Kunishima, Motohiro Hamaguchi, Hidehiko Saito

Blood (2008) 111 (6): 3015–3023.

https://doi.org/10.1182/blood-2007-10-116194

Published: 2008

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

Loss of Non-Muscle Myosin Heavy Chain IIA Function Does Not Restrict Megakaryocyte Maturation or Spontaneous Platelet Release and Likely Affects Non-Cell-Autonomous Aspects of Thrombopoiesis.

Zhao Chen, PhD, Alessandra Balduini, MD, Mary Anne Conti, PH.D, Robert S. Adelstein, PH.D, Ramesh A. Shivdasani, MD PH. D

Blood (2006) 108 (11): 701.

https://doi.org/10.1182/blood.V108.11.701.701

Published: 2006

Journal Articles

Initial Laboratory Findings Useful for Predicting the Diagnosis of Chronic ITP: Results of a Multicenter Prospective Study.

Masataka Kuwana, MD, Yoshiyuki Kurata, MD, Kingo Fujimura, MD, Koji Fujisawa, MD, Hideo Wada, MD, Toshiro Nagasawa, MD, Shosaku Nomura, MD, Tetsuhito Kojima, MD, Hideo Yagi, MD, Yasuo Ikeda, MD

Blood (2004) 104 (11): 2061.

https://doi.org/10.1182/blood.V104.11.2061.2061

Published: 2004

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

The E1841K Mutation in MYH-9 of a Patient with May-Hegglin Anomaly Inhibits the Disassembly of Non-Muscle Myosin IIA (MYH-9) Responsible for the Phenotype of the Disease.

Koji Miyazaki, MD, PhD, Satoshi Komatsu, PhD, Mariko Watanabe, Naoya Nakadate, MD, PhD, Mitsuo Ikebe, PhD, Masaaki Higashihara, MD, PhD

Blood (2004) 104 (11): 736.

https://doi.org/10.1182/blood.V104.11.736.736

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

Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome)

Shinji Kunishima, Tetsuhito Kojima, Tadashi Matsushita, Toshihiro Tanaka, Masahito Tsurusawa, Yoshio Furukawa, Yukitsugu Nakamura, Takashi Okamura, Norihiko Amemiya, Takayuki Nakayama, Tadashi Kamiya, Hidehiko Saito

Blood (2001) 97 (4): 1147–1149.

https://doi.org/10.1182/blood.V97.4.1147

Published: 2001

NARROW

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

Evaluation of Platelet Parameters in Children

Inherited Giant Platelet Disorder, Kashmiri Thrombocytopenia, a Common Syndrome Found in Srinagar, India

Platelet-Like-Particles Sheared From Myosin-II-Inhibited Megakaryocytes Highlights The Elevated Thrombocrit Of May-Hegglin Anomaly

Hemorrhagic Complications With Adenotonsillectomy In Children and Young Adults With Bleeding Disorders

May-Hegglin anomaly

Myh9 Q1443L Is a Novel Mouse Model of MYH9-Related Disorders

Differential expression of wild-type and mutant NMMHC-IIA polypeptides in blood cells suggests cell-specific regulation mechanisms in MYH9 disorders

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

Loss of Non-Muscle Myosin Heavy Chain IIA Function Does Not Restrict Megakaryocyte Maturation or Spontaneous Platelet Release and Likely Affects Non-Cell-Autonomous Aspects of Thrombopoiesis.

Initial Laboratory Findings Useful for Predicting the Diagnosis of Chronic ITP: Results of a Multicenter Prospective Study.

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.

The E1841K Mutation in MYH-9 of a Patient with May-Hegglin Anomaly Inhibits the Disassembly of Non-Muscle Myosin IIA (MYH-9) Responsible for the Phenotype of the Disease.

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

Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome)

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American Society of Hematology

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ASH Publications

American Society of Hematology

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