MYH9-related disorder, a probable May–Hegglin anomaly case series: A tertiary care experience-Reference-Cited by-同舟云学术

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MYH9-related disorder, a probable May–Hegglin anomaly case series: A tertiary care experience

Published:2016-12 Issue:4 Volume:9 Page:137-140
ISSN:1658-3876
Container-title:Hematology/Oncology and Stem Cell Therapy
language:en
Short-container-title:Hematology/Oncology and Stem Cell Therapy

Author:

Kamath Vandana,Gnanasekaran Kiruthiga Kala,Mammen Joy

Publisher

Elsevier BV

Subject

Oncology,Hematology,General Medicine

Reference19 articles.

1. Perioperative management of a patient with May–Hegglin anomaly requiring craniotomy;Sehbai;Am J Hematol,2005

2. A Chinese adolescent girl with Fechtner-like syndrome;Leung;Acta Paediatr,1998

3. Historical hematology: May–Hegglin anomaly;Saito;Am J Hematol,2008

4. May-Hegglin anomaly: a rare cause of thrombocytopenia;Greinacher;Eur J Pediatr,1992

5. Autosomal dominant macrothrombocytopenia with leukocyte inclusions (May–Hegglin anomaly) is linked to chromosome 22q12–13;Kelley;Hum Genet,2000

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1. Disorders of white blood cells and platelets;Atlas of Hematopathology with 100 Case Studies;2024

2. Granulocytic Disorders;Atlas of Hematopathology;2018

3. Challenges on the diagnostic approach of inherited platelet function disorders: Is a paradigm change necessary?;Platelets;2017-11-01

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