Table of Contents, Volume Six, 1970 [PDF]
, 1970 Table of contents for MCV/Q, Medical College of Virginia Quarterly, 1970, Volume ...
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Hematological and biochemical parameters in hereditary spherocytosis under oxidative stress [PDF]
, 1999 Barbot, José +7 more
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Pattern of Splenectomy Indications in Kashan Shahid-Beheshti Hospital : A 5-Year Study [PDF]
, 2013 Background: The spleen is amongst the most vulnerable organs which are easily injured in abdominal trauma. Nowadays, blunt trauma is the most prevalent indication of splenectomy.
Alizargar, J. +2 more
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New Thoughts on Hereditary Spherocytosis [PDF]
, 1970 In addition to its accentuated pattern of rigidity at decreasing ATP/Ca ratios, the hereditary spherocyte poses a special challenge within the splenic pulp because of its shape.
Weed, Robert I.
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Análise do polimorfismo TA6/TA7 na região promotora do gene UGT1A1, em pacientes com anemia e traço falciforme de dois hospitais da cidade de Porto Alegre – RS [PDF]
, 2011 A doença de células falciformes é uma anemia hemolítica crônica de caráter autossômico recessivo, causada por uma mutação pontual no cromossomo 11. Esta mutação provoca a substituição de um ácido glutâmico por uma valina na posição seis da cadeia da ...
Antunes, Liana
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Acute childhood ischemic stroke: a pakistani tertiary care hospital experience [PDF]
, 2016 Stroke in pediatric population is increasingly recognized and has diverse clinical presentation and risk factor profile. Majority of patients survive acute stroke but remain disabled.
Arain, Fazal +4 more
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Mean corpuscular volume of control red blood cells determines the interpretation of eosin-5′-maleimide (EMA) test result in infants aged less than 6 months [PDF]
, 2015 core +1 more source
Kathmandu University medical journal (KUMJ), 2005 Hereditary spherocytosis is a congenital haemolytic anaemia due to defect in spectrin-a RBC membrane protein and is transmitted as autosomal dominant. Due to this defect there is presence of characteristic spherical cell in peripheral blood smear and osmotic fragility is increased.
B L, Bajracharya, A, Giri, M R, Baral
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Correction: Identification of a novel <i>ANK1</i> gene variant c.1504-9G>A and its mechanism of intron retention in hereditary spherocytosis. [PDF]
Front GenetXiong T +6 more
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Hereditary Spherocytosis: Linking Ion Transport Defects to Osmotic Gradient Ektacytometry Profiles-A Review. [PDF]
Int J Mol SciVives-Corrons JL, Krishnevskaya E.
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