Immunofluorescence Analysis of Neutrophil Nonmuscle Myosin Heavy Chain-A in MYH9 Disorders: Association of Subcellular Localization with MYH9 Mutations-Reference-Cited by-同舟云学术

Immunofluorescence Analysis of Neutrophil Nonmuscle Myosin Heavy Chain-A in MYH9 Disorders: Association of Subcellular Localization with MYH9 Mutations

Published:2003-01 Issue:1 Volume:83 Page:115-122
ISSN:0023-6837
Container-title:Laboratory Investigation
language:
Short-container-title:Lab Invest

Author:

Kunishima Shinji,Matsushita Tadashi,Kojima Tetsuhito,Sako Masahiro,Kimura Fumihiro,Jo Eun-Kyeong,Inoue Chikako,Kamiya Tadashi,Saito Hidehiko

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Molecular Biology,Pathology and Forensic Medicine

Reference24 articles.

1. Hereditary Thrombocytopenia, Deafness, and Renal Disease

2. Hereditary macrothrombocytopathia, nephritis and deafness

3. Sebastian platelet syndrome: A new variant of hereditary macrothrombocytopenia with leukocyte inclusions

4. Nonmuscle Myosin Heavy Chain IIA Mutations Define a Spectrum of Autosomal Dominant Macrothrombocytopenias: May-Hegglin Anomaly and Fechtner, Sebastian, Epstein, and Alport-Like Syndromes

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3. Case Report: MYH9-related disease caused by Ala44Pro mutation in a child with a previous diagnosis of chronic immune thrombocytopenia;Frontiers in Pediatrics;2024-05-17

4. Diagnostic delay of MYH9‐related disorder in Japan;British Journal of Haematology;2024-04-22

5. A single-center experience of using immunofluorescence staining of blood smears for the diagnosis of hereditary thrombocytopathies;Pediatric Hematology/Oncology and Immunopathology;2023-10-01