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Hereditary elliptocytosis in a child with an autosomal recessive <i>SPTA1</i> mutation: a case report from Saudi Arabia. [PDF]
J Med LifeAlamr F.
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The Lancet, 2008
Hereditary spherocytosis is a common inherited disorder that is characterised by anaemia, jaundice, and splenomegaly. It is reported worldwide and is the most common inherited anaemia in individuals of northern European ancestry. Clinical severity is variable with most patients having a well-compensated haemolytic anaemia.
PERROTTA, Silverio +2 more
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Hereditary spherocytosis is a common inherited disorder that is characterised by anaemia, jaundice, and splenomegaly. It is reported worldwide and is the most common inherited anaemia in individuals of northern European ancestry. Clinical severity is variable with most patients having a well-compensated haemolytic anaemia.
PERROTTA, Silverio +2 more
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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
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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
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JAMA: The Journal of the American Medical Association, 1989
Hereditary spherocytosis is the most common inherited anemia in persons of northern European descent. In 75 percent of cases, the condition is inherited in an autosomal dominant fashion. Patients usually present with splenomegaly, jaundice and anemia.
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Hereditary spherocytosis is the most common inherited anemia in persons of northern European descent. In 75 percent of cases, the condition is inherited in an autosomal dominant fashion. Patients usually present with splenomegaly, jaundice and anemia.
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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.
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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
Annals of African Medicine, 2009
Hereditary spherocytosis (HS) is a familial hemolytic disorder with marked heterogeneity of clinical features, ranging from an asymptomatic condition to a fulminant hemolytic anemia. Although a positive family history of spherocytosis increases the risk for this disorder, it may be sporadic in some cases. In severe cases the disorder may be detected in
Dieter Metze +199 more
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Hereditary spherocytosis (HS) is a familial hemolytic disorder with marked heterogeneity of clinical features, ranging from an asymptomatic condition to a fulminant hemolytic anemia. Although a positive family history of spherocytosis increases the risk for this disorder, it may be sporadic in some cases. In severe cases the disorder may be detected in
Dieter Metze +199 more
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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.
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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