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Identification of a novel WAS mutation and the non-splicing effect of a second-site mutation in a Chinese pedigree with Wiskott-Aldrich syndrome

Orphanet journal of rare diseases, 2022-12, Vol.17 (1), p.447-447, Article 447

2022

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Novel compound heterozygous mutations of the NPC1 gene associated with Niemann-pick disease type C: a case report and review of the literature

BMC infectious diseases, 2024-01, Vol.24 (1), p.145-145, Article 145

2024

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Case Report: Wiskott-Aldrich Syndrome Caused by Extremely Skewed X-Chromosome Inactivation in a Chinese Girl

Frontiers in pediatrics, 2021-07, Vol.9

2021

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Erythrophagocytosis by Neutrophil and Monocyte in Autoimmune Hemolytic Anemia After Infection

Indian journal of hematology & blood transfusion, 2020-04, Vol.36 (2), p.444-445

2020

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Clostridioides difficile infection in infants: a case report and literature review

Gut pathogens, 2023-06, Vol.15 (1), p.31-31, Article 31

2023

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Abnormally Hypersegmented Neutrophilia in Pediatric Acute Myeloid Leukemia Associated With t(2;11)(q31;p15) and NUP98 Rearrangement

Journal of pediatric hematology/oncology, 2021-05, Vol.43 (4), p.156

2021

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Rare inclusion bodies within monocytes at accelerated phase of Chediak-Higashi syndrome

Clinical chemistry and laboratory medicine, 2018-04, Vol.56 (5), p.e105

2018

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Further classification of neutrophil non-muscle myosin heavy chain-IIA localization for efficient genetic diagnosis of MYH9 disorders

Annals of hematology, 2018-04, Vol.97 (4), p.709-711

2018

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The role of Periodic Acid Schiff stain on bone marrow smear to rapid identification of Talaromyces marneffei in a HIV‐positive patient

International journal of laboratory hematology, 2021-06, Vol.43 (3), p.e107-e109

2021

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Aleukemic Variant of Mast Cell Leukemia with del (7)(q31): Rare Case Report of an Elderly Chinese Man

Turkish journal of haematology, 2023-08, Vol.40 (3), p.216-219

2023

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Novel variant of MYH9 associated with mild evaluation of MYH9 related disorder in a Chinese family

Clinical chemistry and laboratory medicine, 2021-09, Vol.59 (10), p.e398

2021

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Aleukemic Variant of Mast Cell Leukemia with del (7)(q31): Rare Case Report of an Elderly Chinese Man

Turkish journal of haematology, 2023-08, Vol.40 (3), p.216-219

2023

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'Rod-Like' Cytoplasmic Crystals of Peripheral Lymphocytes in Chronic Lymphocytic Leukemia

Turkish journal of haematology, 2023-08, Vol.40 (3), p.202-203

2023

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Aleukemic Variant of Mast Cell Leukemia with del (7) (q31): a Rare Case Report in a Chinese Old Male

Turkish journal of haematology, 2023-06

2023

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Erythrophagocytosis of Peripheral Blood Smear in Antiphospholipid Syndrome Associated with B-Cell Lymphoma

Clinical laboratory (Heidelberg), 2021-01, Vol.67 (12)

2021

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Evans syndrome in a female with erythrophagocytosis by monocytes in peripheral blood smear

International journal of laboratory hematology, 2020-08, Vol.42 (4), p.e150-e151

2020

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A D1424N mutation in the MYH9 gene results in macrothrombocytopenia and granulocytic inclusion bodies in a Chinese inherited macrothrombocytopenia pedigree

Clinical chemistry and laboratory medicine, 2018-06, Vol.56 (7), p.e171

2018

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"Rod-like" Cytoplasmic Crystals of Peripheral Lymphocytes in Chronic Lymphocytic Leukemia

Turkish journal of haematology, 2023-08, Vol.40 (3), p.202-203

2023

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A sporadic MYH9-related disease in a Chinese boy with p.A95T mutation

Hematology (Luxembourg), 2020-01, Vol.25 (1), p.34-36

2020

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Role of microRNA-4516 involved autophagy associated with exposure to fine particulate matter

Oncotarget, 2016-07, Vol.7 (29), p.45385-45397

2016

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A large family with MYH9 disorder caused by E1841K mutation suffering from serious kidney and hearing impairment and cataracts

Annals of hematology, 2012-07, Vol.91 (7), p.1147-1148

2012

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Delay Variation Based Endpoint Admission Control in DiffServ

2008 International Conference on Computer Science and Software Engineering, 2008, Vol.5, p.1004-1006

2008

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Synthesis of ditrimethylolpropane tetraacrylate catalyzed with silicotungstic acid supported on activated carbon

He cheng xiang jiao gong ye, 2011-11, Vol.34 (6), p.429-431

2011

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Microalgae as Biofertilizer in Modern Agriculture

Microalgae Biotechnology for Food, Health and High Value Products, p.397-411

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Case Report: Wiskott-Aldrich Syndrome Caused by Extremely Skewed X-Chromosome Inactivation in a Chinese Girl

Frontiers in pediatrics, 2021, Vol.9, p.691524-691524

2021

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Identification of a novel WAS mutation and the non-splicing effect of a second-site mutation in a Chinese pedigree with Wiskott-Aldrich syndrome

Novel compound heterozygous mutations of the NPC1 gene associated with Niemann-pick disease type C: a case report and review of the literature

Case Report: Wiskott-Aldrich Syndrome Caused by Extremely Skewed X-Chromosome Inactivation in a Chinese Girl

Erythrophagocytosis by Neutrophil and Monocyte in Autoimmune Hemolytic Anemia After Infection

Clostridioides difficile infection in infants: a case report and literature review

Abnormally Hypersegmented Neutrophilia in Pediatric Acute Myeloid Leukemia Associated With t(2;11)(q31;p15) and NUP98 Rearrangement

Rare inclusion bodies within monocytes at accelerated phase of Chediak-Higashi syndrome

Further classification of neutrophil non-muscle myosin heavy chain-IIA localization for efficient genetic diagnosis of MYH9 disorders

The role of Periodic Acid Schiff stain on bone marrow smear to rapid identification of Talaromyces marneffei in a HIV‐positive patient

Aleukemic Variant of Mast Cell Leukemia with del (7)(q31): Rare Case Report of an Elderly Chinese Man

Novel variant of MYH9 associated with mild evaluation of MYH9 related disorder in a Chinese family

Aleukemic Variant of Mast Cell Leukemia with del (7)(q31): Rare Case Report of an Elderly Chinese Man

'Rod-Like' Cytoplasmic Crystals of Peripheral Lymphocytes in Chronic Lymphocytic Leukemia

Aleukemic Variant of Mast Cell Leukemia with del (7) (q31): a Rare Case Report in a Chinese Old Male

Erythrophagocytosis of Peripheral Blood Smear in Antiphospholipid Syndrome Associated with B-Cell Lymphoma

Evans syndrome in a female with erythrophagocytosis by monocytes in peripheral blood smear

A D1424N mutation in the MYH9 gene results in macrothrombocytopenia and granulocytic inclusion bodies in a Chinese inherited macrothrombocytopenia pedigree

"Rod-like" Cytoplasmic Crystals of Peripheral Lymphocytes in Chronic Lymphocytic Leukemia

A sporadic MYH9-related disease in a Chinese boy with p.A95T mutation

Role of microRNA-4516 involved autophagy associated with exposure to fine particulate matter

A large family with MYH9 disorder caused by E1841K mutation suffering from serious kidney and hearing impairment and cataracts

Delay Variation Based Endpoint Admission Control in DiffServ

Synthesis of ditrimethylolpropane tetraacrylate catalyzed with silicotungstic acid supported on activated carbon

Microalgae as Biofertilizer in Modern Agriculture

Case Report: Wiskott-Aldrich Syndrome Caused by Extremely Skewed X-Chromosome Inactivation in a Chinese Girl

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