Results 151 to 160 of about 7,739 (202)
A 34-year-old man with tea-coloured urine. [PDF]
CMAJBarsanti-Innes B +3 more
europepmc +1 more source
Multigene Panel Testing Reveals Novel Variants in Hereditary Spherocytosis Patients in Türkiye [PDF]
Turk J HaematolDoğru Ö +4 more
europepmc +1 more source
Genetic screening strategy for children with hereditary spherocytosis in Jiangxi Province of China. [PDF]
Front PediatrWu C, Xu Z, Wan Q, Chen F, Ye Y, Wang H.
europepmc +1 more source
Caught by Whole-Exome Sequencing: Hemoglobin Sun Prairie in a Patient With Unexplained Hemolytic Anemia From Nepal. [PDF]
Case Rep HematolUpadhaya P, Shrestha A.
europepmc +1 more source
Shape-Dependent Structural Order of Red Blood Cells. [PDF]
LangmuirPiegols LD +3 more
europepmc +1 more source
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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
exaly +7 more sources
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
exaly +7 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 +2 more sources
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 +2 more sources