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Bart's Hemoglobinopathy
Known as:
Hemoglobin Bart's Hydrops
, Hemoglobin Barts
A severe and rare form of alpha thalassemia characterized by the absence of alpha globin chains. It results in hydrops fetalis, severe anemia…
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National Institutes of Health
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Related topics
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4 relations
Alpha thalassemia major
Hemoglobin Bart's
Hemoglobin Barts:PrThr:Pt:Bld:Ord:HPLC
Thalassemia
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2010
2010
Homozygosity for the Mediterranean α-thalassemic deletion (hemoglobin Barts hydrops fetalis)
N. Al-Allawi
,
M. Shamdeen
,
N. S. Rasheed
Annals of Saudi Medicine
2010
Corpus ID: 12795172
Hemoglobin Barts hydrops fetalis syndrome is the most severe and generally fatal clinical phenotype of α-thalassemia. We…
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2008
2008
A multicenter trial of the effectiveness of zeta-globin enzyme-linked immunosorbent assay and hemoglobin H inclusion body screening for the detection of alpha0-thalassemia trait.
J. Lafferty
,
D. Barth
,
+4 authors
M. Crowther
American Journal of Clinical Pathology
2008
Corpus ID: 35957971
Routine laboratories use a hemoglobin H (HbH) screen to detect alpha-thalassemia carriers of fatal hemoglobin Bart's hydrops…
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2003
2003
An improved method for detecting red cells with hemoglobin H inclusions that does not require glass capillary tubes.
D. Sabath
,
S. T. Cross
,
L. Mamiya
Clinical and Laboratory Haematology
2003
Corpus ID: 23370758
alpha-Thalassemia trait is the most common inherited abnormality worldwide. Diagnosis of alpha-thalassemia trait can be difficult…
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1998
1998
Synthesized allosteric effectors of the hemoglobin molecule: a possible mechanism for improved erythrocyte oxygen release capability in hemoglobinopathy H disease.
I. Papassotiriou
,
J. Kister
,
+6 authors
C. Poyart
Experimental Hematology
1998
Corpus ID: 12590777
Patients with the nondeletion genotype of hemoglobinopathy H (HbH or beta4) disease have higher proportions of HbH and more…
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1992
1992
[Incidence of malaria and S hemoglobinopathy in the pediatric hospital milieu in Bamako, Mali].
O. Doumbo
,
A. Toure
,
+6 authors
M. Quilici
Medecine tropicale : revue du Corps de sante…
1992
Corpus ID: 30168775
A study on the incidence and gravity of malaria among children suffering of sickle cell anemia was carried out in the pediatric…
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1991
1991
Alpha-thalassemic traits are common in the Taiwanese population: usefulness of a modified hemoglobin H preparation for prevalence studies.
C. K. Lin
,
S. H. Lee
,
C. C. Wang
,
M. Jiang
,
H. Hsu
Journal of Laboratory and Clinical Medicine
1991
Corpus ID: 45508016
The aim of this study was to determine the crude prevalence of alpha-thalassemia traits in Taiwan. A total of 1435 healthy…
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1989
1989
The Antenatal Blood Gas and Acid-Base Status of Normal Fetuses and Hydropic Fetuses With Bart Hemoglobinopathy
F. Hsieh
,
F. Chang
,
T. Ko
,
P. Kuo
,
D. Chang
,
Hsi‐Yao Chen
Obstetrics and Gynecology
1989
Corpus ID: 1903913
Funipuncture offers direct access to the fetal circulation. The blood gas and acid-base status of the fetus can be studied, and…
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Review
1986
Review
1986
Hydrops fetalis secondary to Bart hemoglobinopathy.
R. Nakayama
,
D. Yamada
,
V. Steinmiller
,
E. Hsia
,
R. Hale
Obstetrics and Gynecology
1986
Corpus ID: 41657732
Alpha-thalassemia is the most common cause of hydrops fetalis among Southeast Asians. With the recent influx of Southeast Asian…
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1975
1975
Incidence of hemoglobin Barts in cord blood samples.
S. Vora
,
P. Iyer
,
M. Bhagat
,
J. C. Patel
,
B. Mehta
Indian Journal of Medical Sciences
1975
Corpus ID: 41479017
1973
1973
Alpha thalassemia screening in neonates by mean corpuscular volume and mean corpuscular hemoglobin determination.
A. Schmaier
,
H. Maurer
,
C. Johnston
,
R. Scott
Jornal de Pediatria
1973
Corpus ID: 29797868
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