Results 171 to 180 of about 54,540 (236)
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[Congenital hemolytic anemias].

Acta medica Austriaca, 1981
During the last years our knowledge of the structural composition of erythrocyte membranes has markedly increased. It is the aim of this review to discuss hereditary changes of the erythrocyte membrane of pathophysiological significance on the basis of these recent biochemical findings.
J D, Schwarzmeier, K, Moser, A, Pohl
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Congenital Nonspherocytic Hemolytic Anemias

Postgraduate Medicine, 1967
A specific diagnosis must be established in congenital nonspherocytic hemolytic anemia, for guidance in therapy and family counseling. Diagnostic methods have recently progressed rapidly and include determination of deficiencies in the activity of certain enzymes. Further definitions of enzymatic deficiencies are anticipated.
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Transfusion Therapy in Congenital Hemolytic Anemias

Hematology/Oncology Clinics of North America, 1994
Transfusion with red blood cells is a mainstay in the prevention or treatment of complications associated with the more serious congenital hemolytic anemias. These disorders include hemoglobinopathies, red cell enzyme deficiency disorders, and abnormalities of the red cell membrane.
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[Diagnosis of congenital hemolytic anemia by comprehensive gene analysis: significance and limitations].

[Rinsho ketsueki] The Japanese journal of clinical hematology, 2021
H. Kanno, H. Ogura
semanticscholar   +1 more source

CRYPTOCOCCUS MENINGITIS IN A CASE OF CONGENITAL HEMOLYTIC ANEMIA

Annals of Internal Medicine, 1956
Excerpt The following case of cryptococcus meningitis is reported because of three interesting facets: its occurrence in a patient with congenital hemolytic anemia, an associated leukemoid reaction...
J B, ATKINSON, W E, DELANEY, F R, MILLER
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Congenital Hemolytic Anemia Due to Hexokinase Deficiency

Archives of Pediatrics & Adolescent Medicine, 1978
In 1965, Lohr et al 1 described three male subjects belonging to two families in whom erythrocytes, leukocytes, and platelets possessed diminished hexokinase (HK) activity accompanied by abnormal enzyme kinetics. Each had multiple congenital anomalies, panmyelopathy, and chromosomal aberrations characteristic of classic Fanconi's syndrome.
F, Gilsanz   +3 more
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Hemochromatosis and Congenital Nonspherocytic Hemolytic Anemia in Siblings

JAMA: The Journal of the American Medical Association, 1963
The unusual occurrence of both congenital nonspherocytic hemolytic anemia and hemochromatosis in a brother and sister is reported. The strikingly similar clinicopathologic abnormalities, including extraordinarily severe cardiac lesions in these relatively young siblings, is discussed.
G, REEVES   +4 more
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Transplantation studies in mice with congenital hemolytic anemia

Clinical Immunology and Immunopathology, 1990
Sphha/sphha anemic mice have an abnormality in the erythroid membrane protein, alpha spectrin, and exhibit multiple related clinical abnormalities, including spherocytosis, shortened red cell survival, chronic hemolysis, hemosiderosis, and extramedullary hematopoiesis.
L, Maggio-Price   +5 more
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Coombs positive hemolytic anemia in congenital rubella

The Journal of Pediatrics, 1979
tered antibiotics. '~ Ampicillin, which attains a relatively high intraventricular concentration during acute meningitis, may penetrate poorly when inflammation is not so extensive. ' Lumbar intrathecal treatment does not enhance resolution of ventriculitis or produce increased intraventricular concentrations of antibiotics.
S, Miyazaki   +4 more
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Congenital Nonspherocytic Hemolytic Anemia

American Journal of Diseases of Children, 1961
It has been well demonstrated in man and in other species that the fundamental expression of a hereditary chemical disorder may be the deletion of a single metabolic or enzymic step. The extent to which such loss in enzymic activity is due to dimimished amounts or to a qualitative inefficiency of the enzyme has been a matter of considable interest. The
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