Results 151 to 160 of about 5,131 (194)
Some of the next articles are maybe not open access.
A Splenunculus in Hereditary Spherocytosis
British Journal of Haematology, 1968Studies on a patient with hereditary spherocytosis and a functioning splenunculus are reported. An inverse relationship between splenic size and red cell survival was observed. Evidence was obtained which further verified that red cell survival in hereditary spherocytosis is not related to the shape or to the osmotic sensitivity of the cell and that ...
M P, Westerman, J L, Jenkins, K M, Bron
openaire +2 more sources
Hereditary spherocytosis and hemochromatosis
Annals of Hematology, 2002A 37-year-old male, splenectomized at the age of 1 year, was admitted to the ward with severe chest pain and signs of cardiogenic shock. Clinical investigations revealed the presence of both hemochromatosis and hereditary spherocytosis (HS). HLA typing showed A3,B7 and A24,B57 haplotypes and genetic analysis revealed homozygosity for the C282Y mutation.
Brandenberg JB +3 more
openaire +3 more sources
Hereditary Spherocytosis And Polycythemia
Archives of Internal Medicine, 1965POLYCYTHEMIA that was clinically indistinguishable from polycythemia vera was observed in a patient who had splenectomy to palliate the anemia and hemolysis of hereditary spherocytosis. Polycythemia occurred 14 years after splenectomy, and the rubrocytes retained the spherocytic shape.
T W, CLARK, R W, EWER
openaire +2 more sources
Hereditary spherocytosis in the elderly
The American Journal of Medicine, 1988Five patients with hereditary spherocytosis diagnosed in their seventh to ninth decades of life are presented. These patients are remarkable for absent or mild clinical manifestations of disease. Splenectomy is the recommended treatment for hereditary spherocytosis to avoid the complications of aplastic or hemolytic crisis.
E W, Friedman +2 more
openaire +2 more sources
HLA and Hereditary Spherocytosis
Vox Sanguinis, 1977Abstract. The HLA types of two families with hereditary spherocytosis (HS) suggest that the HS gene(s) may be linked with the HLA locus. If substantiated by further family studies, this linkage would place HS on chromosome 6.; Accepted: February 14 ...
D P, Sengar +3 more
openaire +2 more sources
NeoReviews, 2016
Neonatal jaundice is commonly encountered in the neonatal period. Although it is mostly asymptomatic, severe cases may present as encephalopathy or kernicterus. Hereditary spherocytosis (HS) is the most common cause of nonimmune hemolytic anemia and the third most common cause of kernicterus after glucose-6-phosphate-dehydrogenase deficiency and ABO ...
Vasudha Mahajan, Sunil K. Jain
openaire +1 more source
Neonatal jaundice is commonly encountered in the neonatal period. Although it is mostly asymptomatic, severe cases may present as encephalopathy or kernicterus. Hereditary spherocytosis (HS) is the most common cause of nonimmune hemolytic anemia and the third most common cause of kernicterus after glucose-6-phosphate-dehydrogenase deficiency and ABO ...
Vasudha Mahajan, Sunil K. Jain
openaire +1 more source
Combination of hereditary elliptocytosis and hereditary spherocytosis
Clinical Genetics, 1974A girl with the combination of hereditary spherocytosis and hereditary elliptocytosis is presented. She had a moderately severe haemolytic anaemia. This was the result either of a summation of the clinical effects of the involved genes or of the mutual enhancement of any of genes involved in the two conditions.
M, Aksoy +5 more
openaire +2 more sources
2006
Abstract A 25-year-old Japanese man was admitted to the hospital because of fever, sore throat, and general malaise. He had been febrile for several days and had noticed that the color of his urine was unusually dark. On admission, his temperature was 37.8°C.
openaire +2 more sources
Abstract A 25-year-old Japanese man was admitted to the hospital because of fever, sore throat, and general malaise. He had been febrile for several days and had noticed that the color of his urine was unusually dark. On admission, his temperature was 37.8°C.
openaire +2 more sources
Archives of Internal Medicine, 1965
A LARGE family study of hereditary spherocytosis (HS) has not been reported since Race's classic work in 1942. 1 Since then new hematologic methods, including Coombs' test, the radioactive chromium ( 51 Cr) erythrocyte survival test, the mechanical fragility test, and autohemolysis have become widely used.
openaire +3 more sources
A LARGE family study of hereditary spherocytosis (HS) has not been reported since Race's classic work in 1942. 1 Since then new hematologic methods, including Coombs' test, the radioactive chromium ( 51 Cr) erythrocyte survival test, the mechanical fragility test, and autohemolysis have become widely used.
openaire +3 more sources