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Plenary Paper

Diagnosis and treatment of MYH9-RD in an Australasian cohort with thrombocytopenia

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Pages 793-800 | Received 03 Jun 2017, Accepted 06 Jul 2017, Published online: 01 Nov 2017

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Wenchao Zhang, Xiaoqiang Lian, Yifeng Sun & Jihong Hao. (2020) A sporadic MYH9-related disease in a Chinese boy with p.A95T mutation. Hematology 25:1, pages 34-36.
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Articles from other publishers (8)

Jian Li, Liucheng Rong, Jun Wang & Yongjun Fang. (2022) Umbilical cord blood transplantation for MYH9‐related disorders. Pediatric Blood & Cancer 69:11.
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Carlo L. Balduini. (2022) Treatment of inherited thrombocytopenias. Haematologica 107:6, pages 1278-1292.
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Limy Wong, Louis L. Huang, Marija Nedeljkovic, Ashley Irish & Lawrence P. McMahon. (2021) Nephritis and Hearing Loss—Not All Roads Lead to Alport Syndrome. Kidney International Reports 6:11, pages 2922-2925.
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Xiaoqiang Lian, Yuxin Wang, Jie Gao, Heqiong Liu, Jihong Hao & Shinji Kunishima. (2021) Novel variant of MYH9 associated with mild evaluation of MYH9 related disorder in a Chinese family . Clinical Chemistry and Laboratory Medicine (CCLM) 59:10, pages e398-e400.
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Rungrote Natesirinilkul, Darintr Sosothikul, Patcharee Komwilaisak, Bunchoo Pongtanakul, Nattee Narkbunnum, Najwa Yudhasompop, Pimsiri Mekjarusgool, Pimjai Niparuck, Kochawan Boonyawat, Shinji Kunishima & Nongnuch Sirachainan. (2021) MYH9 disorder : Identification and a novel mutation in patients with macrothrombocytopenia . Pediatric Blood & Cancer 68:7.
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José María Bastida, José Ramón Gonzalez-Porras, José Rivera & María Luisa Lozano. (2021) Role of Thrombopoietin Receptor Agonists in Inherited Thrombocytopenia. International Journal of Molecular Sciences 22:9, pages 4330.
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Brett J. Wakefield, Rachel Diehl, Anne T. Neff, Suzanne Bakdash, Gosta B. Pettersson & Anand R. Mehta. (2021) Perioperative Management of a Patient With Profound Thrombocytopenia Secondary to MYH9-RD Presenting for Thoracic Aortic Aneurysm Repair and Aortic Valve Replacement. Journal of Cardiothoracic and Vascular Anesthesia 35:4, pages 1154-1160.
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Kun Li, Runming Jin, Wenfu Xu, Yaqing Shen, Ke Lu & Xiaoyan Wu. (2021) A De Novo Mutation in MYH9 in a Child With Severe and Prolonged Macrothrombocytopenia. Journal of Pediatric Hematology/Oncology 43:1, pages e7-e10.
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