Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Acidified glycerol lysis test"'
Publikováno v:
Translational Medicine. 6:51-59
Hereditary spherocytosis (HS) is the most common cause of hemolytic anemia of varying severity can lead to complications such as cholelithiasis, sepsis, etc. Difficulties in diagnosis are asymptomatic and atypical cases HS. It is important to search
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d9048d78809cb0a6acbeedaff3eb687
https://doi.org/10.18705/2311-4495-2019-6-6-51-59
https://doi.org/10.18705/2311-4495-2019-6-6-51-59
Autor:
Elisa Fermo, Agostino Cortelezzi, Paola Bianchi, Cristina Vercellati, Anna Paola Marcello, Wilma Barcellini, Laura Porretti, Alberto Zanella
Publikováno v:
Haematologica. 97:516-523
Background The laboratory diagnosis of hereditary spherocytosis commonly relies on NaCl-based or glycerol-based red cell osmotic fragility tests; more recently, an assay directly targeting the hereditary spherocytosis molecular defect (eosin-5′-mal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f020010025e1beca673cc5d89ef2709
https://doi.org/10.3324/haematol.2011.052845
https://doi.org/10.3324/haematol.2011.052845
Publikováno v:
European Journal of Haematology. 40:227-231
In this study we compared the results of the acidified glycerol lysis test, the Pink test and the osmotic fragility test in 38 patients with hereditary spherocytosis and in healthy controls. The sensitivity of the acidified glycerol lysis test was 81
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::366668aea1ac37864228665d7f7946a1
https://doi.org/10.1111/j.1600-0609.1988.tb00828.x
https://doi.org/10.1111/j.1600-0609.1988.tb00828.x
Autor:
Corinne Guitton, Véronique Picard, Caroline Mayeur-Rousse, Mélanie Gentil, Madeleine Fénéant Thibaut, Jérémie Botton
The laboratory diagnosis of hereditary spherocytosis commonly relies on NaCl-based or glycerol-based red cell osmotic fragility tests; more recently, an assay directly targeting the hereditary spherocytosis molecular defect (eosin-5'-maleimide-bindin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db4b50a99dce8d9e8c050738d7ea46b6
https://europepmc.org/articles/PMC3590076/
https://europepmc.org/articles/PMC3590076/
Autor:
SR Mehdi
Publikováno v:
Laboratory Procedures in Haematology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e99ec9c7d7d371dedf7776a96b07e17
https://doi.org/10.5005/jp/books/10437_7
https://doi.org/10.5005/jp/books/10437_7
Publikováno v:
European journal of haematology. 47(5)
The usefulness of the pre-incubated acidified glycerol lysis test (AGLT), a laboratory test for spherocytosis, has been investigated in a selected hospital population of 348 patients with haemolytic and non-haemolytic anaemia. The AGLT was positive i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::117d8c7d4775d2c48b319bd5928a59db
https://pubmed.ncbi.nlm.nih.gov/1761123
https://pubmed.ncbi.nlm.nih.gov/1761123
Publikováno v:
British Journal of Haematology. 65:252-252
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60dc6bc41e890d47c9c60517885225f1
https://doi.org/10.1111/j.1365-2141.1987.00248.x-i1
https://doi.org/10.1111/j.1365-2141.1987.00248.x-i1
Publikováno v:
Clinical & Laboratory Haematology. 8:261-264
In hereditary spherocytosis (HS) there is an abnormality in the erythrocyte membrane resulting in an abnormal erythrocyte form and increased haemolysis. Spectrin deficiency and spectrin abnormalities are described as the principal underlying cause of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1182ff4e337b289c483007841de3e39
https://doi.org/10.1111/j.1365-2257.1986.tb00103.x
https://doi.org/10.1111/j.1365-2257.1986.tb00103.x
Akademický článek
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Publikováno v:
British Journal of Haematology. 63:119-121
Summary The acidified glycerol lysis test (AGLT), as a screening procedure for spherocytosis, has been assessed for sensitivity and specificity. AGLT identified 24 of 26 subjects with hereditary spherocytosis and produced 19 abnormal AGLTs out of a t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3398fef377b6e687d184ef0ac430acab
https://doi.org/10.1111/j.1365-2141.1986.tb07501.x
https://doi.org/10.1111/j.1365-2141.1986.tb07501.x