Zobrazeno 1 - 10
of 11
pro vyhledávání: '"hereditary spherocytosi"'
Publikováno v:
British Journal of Haematology. 187:13-24
Hereditary erythrocyte membrane disorders are caused by mutations in genes encoding various transmembrane or cytoskeletal proteins of red blood cells. The main consequences of these genetic alterations are decreased cell deformability and shortened e
Autor:
S.-H. Lee, James D. Hoyer, Paola Bianchi, Véronique Picard, L. Garçon, M.-J. King, Achille Iolascon, G. Stewart, Alberto Zanella
SummaryIntroduction Hereditary spherocytosis (HS), hereditary elliptocytosis (HE), and hereditary stomatocytosis (HSt) are inherited red cell disorders caused by defects in various membrane proteins. The heterogeneous clinical presentation, biochemic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5930ac59cbca9c5dbee4b82b6d708963
http://hdl.handle.net/11588/661104
http://hdl.handle.net/11588/661104
Autor:
Maddalena Casale, Silverio Perrotta
Publikováno v:
Expert review of hematology. 4(6)
Hereditary spherocytosis (HS) is an hematologic disorder, common in the Northern European population, which is characterized by hemolytic anemia and splenomegaly. The pathophysiological bedrock of HS consists of the retention and damage of abnormal r
Autor:
Silverio Perrotta, Alessandra F. Perna, Patrizia Galletti, Giovanna D’Urzo, E. Miraglia del Giudice, Vincenzo Zappia, Achille Iolascon, Stefania D'Angelo, Diego Ingrosso
Publikováno v:
British journal of haematology. 93(1)
Based on quantitative analysis of red cell membrane proteins, hereditary spherocytosis (HS) can be divided into two main groups including isolated or ankyrin combined spectrin deficiency and band 3 reduction. Protein methyl esterification catalysed b
Autor:
Francesco Salvatore, Stefania Orrù, Gordon W. Stewart, Achille Iolascon, Luigi Del Vecchio, Silverio Perrotta, Marianna Caterino, Margherita Ruoppolo, Marcella Savoia
Publikováno v:
FEBS Letters. (28-29):6527-6532
Fresh human blood samples were collected from healthy controls and splenectomized and unsplenectomized patients with hereditary spherocytosis due to band 3 or ankyrin and spectrin deficiency. The erythrocytes were separated into age-related fractions
Autor:
Kaloterakis, A., Filiotou, A., Konstantopoulos, K., Rombos, Y., Bossinakou, I., Hadziyannis, S.
Publikováno v:
Haematologia; 2001, Vol. 31 Issue 2, p153-159, 7p
Autor:
Mansouri, Ali, Perry, Carol A.
Publikováno v:
Hemoglobin; 1987, Vol. 11 Issue 4, p353-371, 19p
Publikováno v:
Hemoglobin; 1980, Vol. 4 Issue 5/6, p717-734, 18p
Autor:
Beutler, E.
Publikováno v:
Hemoglobin; 1980, Vol. 4 Issue 5/6, p805-819, 15p