187 related articles for article (PubMed ID: 34893131)
61. Hydrops Fetalis Associated with Compound Heterozygosity for Hb Zurich-Albisrieden (HBA2: C.178G > C) and the Southeast Asian (- -
Yang X; Yan JM; Li J; Xie XM; Zhou JY; Li Y; Li DZ
Hemoglobin; 2016 Sep; 40(5):353-355. PubMed ID: 27686733
[TBL] [Abstract][Full Text] [Related]
62. Second trimester maternal serum markers and a predictive model for predicting fetal hemoglobin Bart's disease.
Tongprasert F; Srisupundit K; Luewan S; Tongsong T
J Matern Fetal Neonatal Med; 2013 Jan; 26(2):146-9. PubMed ID: 22989193
[TBL] [Abstract][Full Text] [Related]
63. Application of an expanded multiplex genotyping assay for the simultaneous detection of Hemoglobin Constant Spring and common deletional alpha-thalassemia mutations.
Kidd JL; Azimi M; Lubin B; Vichinsky E; Hoppe C
Int J Lab Hematol; 2010 Aug; 32(4):373-80. PubMed ID: 19919622
[TBL] [Abstract][Full Text] [Related]
64. Clinical and molecular genetic features of Hb H and AE Bart's diseases in central Thai children.
Traivaree C; Boonyawat B; Monsereenusorn C; Rujkijyanont P; Photia A
Appl Clin Genet; 2018; 11():23-30. PubMed ID: 29662324
[TBL] [Abstract][Full Text] [Related]
65. Hemoglobin Q-Thailand related disorders: origin, molecular, hematological and diagnostic aspects.
Singsanan S; Karnpean R; Fucharoen G; Sanchaisuriya K; Sae-Ung N; Fucharoen S
Blood Cells Mol Dis; 2010 Oct; 45(3):210-4. PubMed ID: 20615730
[TBL] [Abstract][Full Text] [Related]
66. Hb Bart's level in cord blood and deletions of alpha-globin genes.
Lie-Injo LE; Solai A; Herrera AR; Nicolaisen L; Kan YW; Wan WP; Hasan K
Blood; 1982 Feb; 59(2):370-6. PubMed ID: 6895707
[TBL] [Abstract][Full Text] [Related]
67. Detection of alpha(0)-thalassemia South-East Asian-type deletion by droplet digital PCR.
Pornprasert S; Prasing W
Eur J Haematol; 2014 Mar; 92(3):244-8. PubMed ID: 24330258
[TBL] [Abstract][Full Text] [Related]
68. Detection of alpha-thalassemia in beta-thalassemia carriers and prevention of Hb Bart's hydrops fetalis through prenatal screening.
Li D; Liao C; Li J; Xie X; Huang Y; Zhong H
Haematologica; 2006 May; 91(5):649-51. PubMed ID: 16627247
[TBL] [Abstract][Full Text] [Related]
69. Second trimester maternal serum inhibin-A in fetal anemia secondary to hemoglobin Bart's disease.
Tongprasert F; Srisupundit K; Luewan S; Tongsong T
J Matern Fetal Neonatal Med; 2014 Jul; 27(10):1005-9. PubMed ID: 24107149
[TBL] [Abstract][Full Text] [Related]
70. Prenatal diagnosis of hemoglobin Bart's hydrops fetalis by HPLC analysis of hemoglobin in fetal blood samples.
Sanguansermsri T; Thanaratanakorn P; Steger HF; Tongsong T; Sirivatanapa P; Wanapirak C; Sirichotiyakul S; Chanprapas P; Flatz G
Southeast Asian J Trop Med Public Health; 2001 Mar; 32(1):180-5. PubMed ID: 11485083
[TBL] [Abstract][Full Text] [Related]
71. Ten years' experience in prenatal diagnosis of α-thalassemia in a municipal hospital and retrospective analysis of ultrasonic abnormalities.
Li H; Wang J; Wang D; Gan Y; Xiong Y
Int J Hematol; 2023 Sep; 118(3):355-363. PubMed ID: 37477864
[TBL] [Abstract][Full Text] [Related]
72. Comparison of maternal serum PlGF and sFlt-1 between pregnancies with and without fetal hemoglobin Bart's disease.
Tongprasert F; Srisupundit K; Luewan S; Tongsong T
Prenat Diagn; 2013 Dec; 33(13):1272-5. PubMed ID: 24122800
[TBL] [Abstract][Full Text] [Related]
73. Prenatal and postnatal diagnoses of thalassemias and hemoglobinopathies by HPLC.
Fucharoen S; Winichagoon P; Wisedpanichkij R; Sae-Ngow B; Sriphanich R; Oncoung W; Muangsapaya W; Chowthaworn J; Kanokpongsakdi S; Bunyaratvej A; Piankijagum A; Dewaele C
Clin Chem; 1998 Apr; 44(4):740-8. PubMed ID: 9554484
[TBL] [Abstract][Full Text] [Related]
74. Thalassemia intermedia associated with the Hb Constant Spring EE Bart's disease in pregnancy: a molecular and hematological analysis.
Fucharoen S; Fucharoen G; Sae-ung N; Sanchaisuriya K
Blood Cells Mol Dis; 2007; 39(2):195-8. PubMed ID: 17587614
[TBL] [Abstract][Full Text] [Related]
75. [Multiplex PCR for detecting genotypes of deletional alpha-thalassemia].
Wu JY; Liao C; Li J; Huang YN
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2004 Aug; 12(4):472-4. PubMed ID: 15363134
[TBL] [Abstract][Full Text] [Related]
76. Molecular characterization of a novel 83.9-kb deletion of the α-globin upstream regulatory elements by long-read sequencing.
Feng J; Mao A; Lu Y; Shi H; Meng W; Liang C
Blood Cells Mol Dis; 2023 Nov; 103():102764. PubMed ID: 37336681
[TBL] [Abstract][Full Text] [Related]
77. Hematological characterization of compound heterozygous hemoglobin Hope/E patients with and without alpha-thalassemia-1 SEA type deletion.
Pornprasert S
Clin Lab; 2013; 59(9-10):1183-5. PubMed ID: 24273946
[TBL] [Abstract][Full Text] [Related]
78. Chicken Egg Yolk Antibodies Specific for the γ Chain of Human Hemoglobin for Diagnosis of Thalassemia.
Jintaridth P; Srisomsap C; Vichittumaros K; Kalpravidh RW; Winichagoon P; Fucharoen S; Svasti MRJ; Kasinrerk W
Int J Hematol; 2006 Jun; 83(5):408-414. PubMed ID: 29349701
[TBL] [Abstract][Full Text] [Related]
79. Potential new approaches to the management of the Hb Bart's hydrops fetalis syndrome: the most severe form of α-thalassemia.
King AJ; Higgs DR
Hematology Am Soc Hematol Educ Program; 2018 Nov; 2018(1):353-360. PubMed ID: 30504332
[TBL] [Abstract][Full Text] [Related]
80. [Gene Mutation Types of Thalassemia in Chongzuo Childbearing-age Population of Guangxi Zhuang Autonomous Region of China].
Li DM; Huang XN; Zhao H; Chen X; Yang WW; Peng ZR; Liang LF; Chen BY; He S
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2023 Dec; 31(6):1804-1810. PubMed ID: 38071064
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
