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Hemoglobin C Disease
Known as:
Hemoglobin-C Disease
, Hemoglobin C Diseases
, Hemoglobin C Disease [Disease/Finding]
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A disease characterized by compensated hemolysis with a normal hemoglobin level or a mild to moderate anemia. There may be intermittent abdominal…
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National Institutes of Health
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Related topics
Related topics
16 relations
Conditions tested for in this newborn screening study:ID:Pt:Bld.dot:Nom
HBB gene
HBB wt Allele
Hematopoietic and Lymphoid Cell
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
1991
1991
Effect of transport time and FiO2 on SpO2 during transport from the OR to the PACU.
C. Hoffman
,
D. Nakamoto
,
R. Okal
,
J. Clochesy
Nurse anesthesia
1991
Corpus ID: 40183139
Early postoperative hypoxemia may be due to a reduced functional residual capacity, hypoventilation, and ventilation-perfusion…
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1979
1979
Hemoglobin Cowtown (beta 146 HC3 His-Leu): a mutant with high oxygen affinity and erythrocytosis.
R. Schneider
,
J. Bremner
,
B. Brimhall
,
R. Jones
,
T. Shih
American Journal of Clinical Pathology
1979
Corpus ID: 44292951
A new mutant, hemoglobin Cowtown, has been found in a white man and his father, both of whom have erythrocytosis. The father had…
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1975
1975
Heats of carbon monoxide binding by hemoglobin M Iwate.
H. Gaud
,
S. Gill
,
B. Barisas
,
K. Gersonde
Biochemistry
1975
Corpus ID: 41063949
The heat of reaction of CO gas with the alpha2Mmetbeta2 and alpha2Mbeta2 species of the alpha-chain mutant hemoglobin M Iwate has…
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1973
1973
The interaction of hemoglobin E with beta thalassemia: a study of hemoglobin synthesis in a family of mixed Burmese and Iranian origin.
R. Feldman
,
R. F. Rieder
Blood
1973
Corpus ID: 30617143
A 5-yr-old girl with hemoglobin E-β thalassemia was discovered in a family of mixed origin. The father is Iranian (β-thalassemia…
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1967
1967
Hemoglobin M's of the Japanese.
S. Shibata
,
T. Miyaji
,
I. Iuchi
,
Y. Ohba
,
Kiyomi Yamamoto
1967
Corpus ID: 68744252
Highly Cited
1966
Highly Cited
1966
Studies on relationships between structure and function of hemoglobin M-Iwate.
N. Hayashi
,
Y. Motokawa
,
G. Kikuchi
Journal of Biological Chemistry
1966
Corpus ID: 11764224
Abstract Functional properties of hemoglobin Miwate (α287 tyrβ2a) were studied with particular reference to their relations with…
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Highly Cited
1963
Highly Cited
1963
Roentgenologic demonstration of renal papillary necrosis in sickle-cell trait.
B. Harrow
,
J. A. Sloane
,
N. Liebman
New England Journal of Medicine
1963
Corpus ID: 26268609
THE presence of S-type hemoglobin in the red blood cell has, in recent years, been demonstrated as the etiologic factor in…
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1956
1956
Thalassemia-hemoglobin C disease in white siblings.
M. Erlandson
,
C. Smith
,
I. Schulman
Pediatrics
1956
Corpus ID: 895323
Two white sisters of Italian parentage in whom thalassemia-hemoglobin C disease was found, have been presented. This is the third…
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1955
1955
SICKLE CELL-HEMOGLOBIN C DISEASE
E. F. Hays
,
R. Engle
1955
Corpus ID: 71049860
Excerpt Recent studies have shown that sickle hemoglobin can be differentiated electrophoretically from normal adult hemoglobin,1…
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1955
1955
Hemoglobin C disease: report of four cases.
W. Hartz
,
S. Schwartz
Blood
1955
Corpus ID: 46683327
1. The cases of four Negro patients with splenomegaly and targeting of the red cells are reported. 2. Electrophoretic analysis…
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