Results 141 to 150 of about 5,131 (194)

Identification of a novel SPTB gene splicing mutation in hereditary spherocytosis: a case report and diagnostic insights. [PDF]

Front Genet
Li X, Zhang T, Li X, Wang L, Li Q, Liu Q, He C, Zhang L, Liu Y, Tang J.   +9 more
europepmc   +1 more source

Complex heterozygous mutations in hereditary spherocytosis: A case report. [PDF]

World J Clin Cases
He M, Lv YC, Wei YH, Liu LQ, Guo L, Li C.   +5 more
europepmc   +1 more source

An Epidemic of Parvovirus B19-Induced Aplastic Crises in Pediatric Patients with Hereditary Spherocytosis Following the COVID-19 Pandemic: A Single-Center Retrospective Study. [PDF]

Children (Basel)
Giordano P, Palladino V, Lassandro G, Spina S, Del Vecchio GC.   +4 more
europepmc   +1 more source

A Rare Case of Iron Overload in Hereditary Spherocytosis: A Case Report. [PDF]

Cureus
Bui A, Shah AP, Chae MY, Popard P, Telivala B.   +4 more
europepmc   +1 more source

Identification and functional analysis of novel SPTB and ANK1 mutations in hereditary spherocytosis patients. [PDF]

Sci Rep
Panarach C, Netsawang C, Nuchprayoon I, Leecharoenkiat K.   +3 more
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
exaly   +8 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

Hereditary Spherocytosis in the Negro

Archives of Pediatrics & Adolescent Medicine, 1957
Congenital spherocytosis is a disease characterized by a varying degree of anemia, microspherocytes in the peripheral blood smear, splenomegaly, and increased hemolysis in hypotonic saline solutions. Although probably recognized1and treated2in the latter part of the 19th century, it was first accurately described as a clinical entity by Minkowski3in ...
A H, KLINE, G H, HOLMAN
openaire   +2 more sources