Clinical and molecular genetic features of Hb H and AE Bart's diseases in central Thai children.

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Efficacy of Oral Acetaminophen and Intravenous Chlorpheniramine Maleate versus Placebo to Prevent Red Cell Transfusion Reactions in Children and Adolescent with Thalassemia: A Prospective, Randomized, Double-Blind Controlled Trial

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Clinical and molecular genetic features of Hb H and AE Bart's diseases in central Thai children.

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http://www.wikidata.org/entity/Q54943903

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

@wuu

2018年学术文章

@zh-cn

2018年学术文章

@zh-hans

2018年学术文章

@zh-my

2018年学术文章

@zh-sg

2018年學術文章

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2018年學術文章

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2018年學術文章

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name

Clinical and molecular genetic ...... ases in central Thai children.

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Clinical and molecular genetic ...... ases in central Thai children.

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type

Item

label

Clinical and molecular genetic ...... ases in central Thai children.

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Clinical and molecular genetic ...... ases in central Thai children.

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Clinical and molecular genetic ...... ases in central Thai children.

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Clinical and molecular genetic ...... ases in central Thai children.

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Clinical and molecular genetic ...... ases in central Thai children.

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Apichat Photia

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Boonchai Boonyawat

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Chalinee Monsereenusorn

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Piya Rujkijyanont

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P2860

Identification and key management of non-transfusion-dependent thalassaemia patients: not a rare but potentially under-recognised condition

Hemoglobin H disease: not necessarily a benign disorder.

Hb H disease: clinical course and disease modifiers.

Single-tube multiplex-PCR screen for common deletional determinants of alpha-thalassemia.

Clinical presentation and molecular identification of four uncommon alpha globin variants in Thailand. Initiation codon mutation of α2-globin Gene (HBA2:c.1delA), donor splice site mutation of α1-globin gene (IVSI-1, HBA1:c.95 + 1G>A), hemoglobin Qu

Different hematologic phenotypes are associated with the leftward (-alpha 4.2) and rightward (-alpha 3.7) alpha+-thalassemia deletions.

Hemoglobin E levels in double heterozygotes of hemoglobin E and SEA-type alpha-thalassemia.

Hemoglobin Constant Spring is markedly high in women of an ethnic minority group in Vietnam: a community-based survey and hematologic features.

Heterogeneity of hemoglobin H disease in childhood.

Clinical features and molecular analysis in Thai patients with HbH disease.

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23-30

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scholarly article

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10.2147/TACG.S161152

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P478

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Chanchai Traivaree

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2018-04-03T00:00:00Z

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29662324

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P921

An Téalainn

P932

5892615

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Clinical and molecular genetic features of Hb H and AE Bart's diseases in central Thai children.

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P2860

P2860

Clinical and molecular genetic features of Hb H and AE Bart's diseases in central Thai children.

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P1433

P1476

P2093

P2860

P304

P31

P356

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P50

P577

P698

P921

P932