Results 141 to 150 of about 5,131 (199)

Splenic Artery Embolization as a Primary Treatment for Hereditary Spherocytosis: A Case Report. [PDF]

Cureus
Mahamat HA, Alamin SM, Alrawi A, Al Mohammad OA, Alsaadi A, Balila S.   +5 more
europepmc   +1 more source

Biliary obstruction in pediatric hereditary spherocytosis: a clinical review of 16 cases. [PDF]

BMC Pediatr
Huang X, Peng C, Chen Y, Wu D, Chen W, Wang Z, Wang K.   +6 more
europepmc   +1 more source

Transcatheter edge-to-edge repair for post-surgical recurrent mitral regurgitation in hereditary spherocytosis: a case report. [PDF]

Eur Heart J Case Rep
Yagasaki H, Umeda Y, Suzuki T, Watanabe R, Noda T.   +4 more
europepmc   +1 more source

Low Hemoglobin A1c (HbA1c) Revealing Hemolytic Anemia in a Growth Hormone-Treated Child: A Case Report. [PDF]

Cureus
Ito T, Oda Y, Kato S, Shindo T, Namai Y.
europepmc   +1 more source

Effect of case-based learning biochemistry among first-year medical students. [PDF]

Bioinformation
Singh M, Singh G.
europepmc   +1 more source

Hereditary spherocytosis.

Indian pediatrics, 1985
C S, Kamala, A, Hussain, C S, Ravinarayan, S, Umadevi   +3 more
openaire   +1 more source

Hereditary spherocytosis

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, GALLAGHER P. G., MOHANDAS N.   +2 more
core   +6 more sources

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Hereditary Spherocytosis

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.
openaire   +4 more sources

Hereditary spherocytosis in infancy

The Journal of Pediatrics, 1957
Summary A case of hereditary spherocytosis posed a difficult diagnostic problem during the first months of life. Spherocytosis was not observed during the neonatal period. The classification of the hemolytic anemia was partially obscured by the presence of a large proportion of donor blood.
Geoffrey C. Robinson, J.M. McKenty
openaire   +2 more sources