Results 91 to 100 of about 6,512 (195)

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HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Extramedullary paraspinal hematopoiesis in hereditary spherocytosis

Annals of Thoracic Medicine, 2008
Hereditary spherocytosis (HS) is a common inherited hemolytic anemia due to red cell membrane defects. Extramedullary hematopoiesis is a compensatory response to insufficient bone marrow blood cell production.
Gogia P, Goel R, Nayar S
doaj  

Partial deficiency of erythrocyte spectrin in hereditary spherocytosis.

, 1985
Hereditary spherocytosis (HS) is a common, clinically heterogeneous haemolytic anaemia in which the primary erythrocyte defect is believed to be some abnormality in the spectrin-actin membrane skeleton, leading to loss of surface membrane.
William H. Zinkham, Peter Agre, James F. Casella, Casella, James F., McMillan, Campbell, Vann Bennett, Bennett, Vann, Zinkham, William H., Agre, Peter, Campbell McMillan   +9 more
core   +1 more source

Hereditary Spherocytosis: Recent Experience and Current Concepts of Pathophysiology

, 1986
Hereditary spherocytosis is a clinically heterogeneous, genetically determined red blood cell membrane disorder resulting in hemolytic anemia. A deficiency of spectrin, the largest and most abundant structural protein of the erythrocyte membrane skeleton,
CROOM, ROBERT, SHELDON, GEORGE, ORRINGER, EUGENE, MCMILLAN, CAMPBELL   +3 more
core   +1 more source

SCREENING TESTS FOR SPHEROCYTOSIS [PDF]

British Journal of Haematology, 1981
A, Zanella, G, Sirchia
openaire   +2 more sources

The sphericity of erythrocytes and its communication with biochemical, hemostasis and rheological by properties of blood at the patients with coronary disease and arterial hypertension

Acta Biomedica Scientifica, 2013
The aim of the work was to study the peculiarities of the influence of bloodfactors on the development of spherocytosis in patients with coronary disease and arterial hypertension.
Y. I. Pivovarov, T. Y. Kurilskaya, A. S. Sergeyeva, L. B. Koryakina   +3 more
doaj  

Spherocytosis [PDF]

, 2020
openaire   +1 more source

Open heart surgery in presence of hereditary spherocytosis

, 1995
A patient with ostium secundum atrial septal defect was operated upon despite having hereditary spherocytosis, without any hemolytic effects of cardiopulmonary bypass.

core  

Marked reduction of spectrinin hereditary spherocytosis in the common house mouse.

, 1978
In contrast to the disease in humans, hereditary spherocytosis in the common house mouse produces an extreme spherocytosis. The cells show a broad distribution in size ranging from microcytic to macrocytic.
Shohet, S B, Bernstein, S E, Greenquist, A C   +2 more
core  

A novel <i>ANK1</i> gene mutation associated with hereditary spherocytosis: a case report. [PDF]

Front Pediatr
Lai M, Luo Z, Yang Z, Pan R, Huang W, Zhang W, Ma G, Chen R.   +7 more
europepmc   +1 more source