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Abnormal hemoglobin anti-Lepore Hong Kong compound with β0-thalassemia ameliorate thalassemia severity when co-inherited with α-thalassemia

Scientific reports, 2024-03, Vol.14 (1), p.6682-6682, Article 6682

2024

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Comparison of cord blood hematological parameters among normal, α-thalassemia, and β-thalassemia fetuses between 17 and 38 weeks of gestation

Scientific reports, 2021-02, Vol.11 (1), p.3844-3844, Article 3844

2021

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Magnetic resonance imaging-guided disc–condyle relationship adjustment via articulation: a technical note and case series

Journal of international medical research, 2020-08, Vol.48 (8), p.300060520951052-300060520951052

2020

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Hb Q-Thailand heterozygosity unlinked with the (-α4.2/) α+-thalassemia deletion allele identified by long-read SMRT sequencing: hematological and molecular analyses

Hematology (Luxembourg), 2023-12, Vol.28 (1), p.2184118-2184118

2023

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Compound heterozygosity for hemoglobin variant Hb-Broomhill and the Southeast Asian α-thalassemia deletion does not worsen outcome: a case report of two unrelated patients

Journal of international medical research, 2020-11, Vol.48 (11), p.300060520967825-300060520967825

2020

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The prevalence and molecular spectrum of α- and β-globin gene mutations in 14,332 families of Guangdong Province, China

PloS one, 2014-02, Vol.9 (2), p.e89855-e89855

2014

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Severe fetal anemia and hydrops fetalis associated with compound heterozygosity for Hb Zurich-Albisrieden (HBA2:c.178G>C) and Hb Quong Sze (HBA2:c.377T>C)

Journal of international medical research, 2021-07, Vol.49 (7), p.30006052110314-3000605211031429

2021

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First study to describe a novel HbA2: c.400A > C mutation and Hb Dongguan heterozygote in two unrelated Chinese families

Hematology (Luxembourg), 2022-12, Vol.27 (1), p.867-873

2022

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Accurate detection of α-globin gene copy number variants with two reactions using droplet digital PCR

Hematology (Luxembourg), 2022-12, Vol.27 (1), p.198-203

2022

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Identification of four novel large deletions and complex variants in the α-globin locus in Chinese population

Human genomics, 2023-04, Vol.17 (1), p.38-38, Article 38

2023

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The first Chinese case of unstable Hemoglobin Santa Ana detected by capillary electrophoresis: a case report and literature review

Hematology (Luxembourg), 2022-12, Vol.27 (1), p.258-262

2022

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Two novel deletion mutations in β-globin gene cause β-thalassemia trait in two Chinese families

Human genomics, 2023-12, Vol.17 (1), p.111-111, Article 111

2023

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Characterisation of two unusual cases of haemoglobin Bart’s hydrops foetalis caused by –SEA and large novel α-globin gene cluster deletions

Journal of international medical research, 2021-02, Vol.49 (2), p.300060521993642-300060521993642

2021

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Characterisation of two unusual cases of haemoglobin Bart’s hydrops foetalis caused by – and large novel α-globin gene cluster deletions

Journal of international medical research, 2021-02, Vol.49

2021

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The -α3.7III subtype of α+-thalassemia was identified in China

Hematology (Luxembourg), 2022-12, Vol.27 (1), p.826-830

2022

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Compounded with hemoglobin Port Phillip and ‐α4.2 or ‐‐SEA deletions were identified in Chinese population

Molecular genetics & genomic medicine, 2021-09, Vol.9 (9), p.e1699-n/a

2021

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Ferroptosis and central nervous system demyelinating diseases

Journal of neurochemistry, 2023-06, Vol.165 (6), p.759-771

2023

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Exosomal miR-23a-3p derived from human umbilical cord mesenchymal stem cells promotes remyelination in central nervous system demyelinating diseases by targeting Tbr1/Wnt pathway

The Journal of biological chemistry, 2024-01, Vol.300 (1), p.105487-105487, Article 105487

2024

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Molecular and prenatal diagnosis of a rare mutation IVS1-116（A→G）of α2-globin gene

Zhōnghuá xuèyèxué zázhì, 2015-09, Vol.36 (9), p.791-792

2015

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Diagnosis and prenatal diagnosis to a family of hemoglobin variant with α-thalassemia

Zhonghua yi xue yi chuan xue za zhi, 2015-04, Vol.32 (2), p.226

2015

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Soft tissue chondrosarcoma occurred in the left parotid region: a case report

Hua xi kou qiang yi xue za zhi, 2015-02, Vol.33 (1), p.104-106

2015

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Ossifying fibromyxoid tumor in the mandible: a case report

Hua xi kou qiang yi xue za zhi, 2014-04, Vol.32 (2), p.200-202

2014

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Both of adenolymphoma and pleomorphic adenoma occurred in unilateral parotid gland: a case report

Hua xi kou qiang yi xue za zhi, 2012-08, Vol.30 (4), p.444-445

2012

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Tongue osteocartilaginous choristoma: a case report

Hua xi kou qiang yi xue za zhi, 2014-02, Vol.32 (1), p.96-98

2014

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High serum creatinine is associated with reduction of psychiatric symptoms in female patients with anti-NMDAR encephalitis

Neuroscience letters, 2021-02, Vol.746, p.135650-135650, Article 135650

2021

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Abnormal hemoglobin anti-Lepore Hong Kong compound with β0-thalassemia ameliorate thalassemia severity when co-inherited with α-thalassemia

Comparison of cord blood hematological parameters among normal, α-thalassemia, and β-thalassemia fetuses between 17 and 38 weeks of gestation

Magnetic resonance imaging-guided disc–condyle relationship adjustment via articulation: a technical note and case series

Hb Q-Thailand heterozygosity unlinked with the (-α4.2/) α+-thalassemia deletion allele identified by long-read SMRT sequencing: hematological and molecular analyses

Compound heterozygosity for hemoglobin variant Hb-Broomhill and the Southeast Asian α-thalassemia deletion does not worsen outcome: a case report of two unrelated patients

The prevalence and molecular spectrum of α- and β-globin gene mutations in 14,332 families of Guangdong Province, China

Severe fetal anemia and hydrops fetalis associated with compound heterozygosity for Hb Zurich-Albisrieden (HBA2:c.178G>C) and Hb Quong Sze (HBA2:c.377T>C)

First study to describe a novel HbA2: c.400A > C mutation and Hb Dongguan heterozygote in two unrelated Chinese families

Accurate detection of α-globin gene copy number variants with two reactions using droplet digital PCR

Identification of four novel large deletions and complex variants in the α-globin locus in Chinese population

The first Chinese case of unstable Hemoglobin Santa Ana detected by capillary electrophoresis: a case report and literature review

Two novel deletion mutations in β-globin gene cause β-thalassemia trait in two Chinese families

Characterisation of two unusual cases of haemoglobin Bart’s hydrops foetalis caused by –SEA and large novel α-globin gene cluster deletions

Characterisation of two unusual cases of haemoglobin Bart’s hydrops foetalis caused by – and large novel α-globin gene cluster deletions

The -α3.7III subtype of α+-thalassemia was identified in China

Compounded with hemoglobin Port Phillip and ‐α4.2 or ‐‐SEA deletions were identified in Chinese population

Ferroptosis and central nervous system demyelinating diseases

Exosomal miR-23a-3p derived from human umbilical cord mesenchymal stem cells promotes remyelination in central nervous system demyelinating diseases by targeting Tbr1/Wnt pathway

Molecular and prenatal diagnosis of a rare mutation IVS1-116（A→G）of α2-globin gene

Diagnosis and prenatal diagnosis to a family of hemoglobin variant with α-thalassemia

Soft tissue chondrosarcoma occurred in the left parotid region: a case report

Ossifying fibromyxoid tumor in the mandible: a case report

Both of adenolymphoma and pleomorphic adenoma occurred in unilateral parotid gland: a case report

Tongue osteocartilaginous choristoma: a case report

High serum creatinine is associated with reduction of psychiatric symptoms in female patients with anti-NMDAR encephalitis

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