Výsledky vyhledávání - "membranopathy"

Akademický článek

Mechanisms of oxidative stress in the pathogenesis of chronic bacterial prostatitis (literature review)

Autor: O. I. Bratchikov, P. A. Dubonos, I. A. Tyuzikov, E. A. Schumakova

Publikováno v: Андрология и генитальная хирургия, Vol 23, Iss 3, Pp 19-28 (2022)

The review article, based on the results of modern clinical and experimental studies, discusses general issues of the pathophysiology of oxidative stress as a universal pathogenetic factor of human diseases and particular pathophysiological aspects o

Externí odkaz: https://doaj.org/article/df7c674e7d3b41daa14bc1ec5856c947

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Akademický článek

Improving the EMA Binding Test by Using Commercially Available Fluorescent Beads

Autor: Andreas Glenthøj, Alaa Sharfo, Christian Brieghel, Amina Nardo-Marino, Henrik Birgens, Jesper Brix Petersen

Publikováno v: Frontiers in Physiology, Vol 11 (2020)

Hereditary spherocytosis (HS) is a common anemia caused by germline mutations in red blood cell cytoskeleton proteins. The flow cytometry-based eosin-5′-maleimide (EMA) binding test is most frequently employed for reliable diagnostics. To perform t

Externí odkaz: https://doaj.org/article/3357ba8f78404d60b93a2a6f9faa397c

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Akademický článek

IDENTIFICATION AND VERIFICATION OF HEREDITARY SPHEROCYTOSIS BY MEANS OF LABORATORY DIAGNOSIS

Autor: Yu. A. Prokhorova, E. E. Zueva, N. E. Sokolova, G. N. Salogub, V. I. Golubeva

Publikováno v: Педиатрическая фармакология, Vol 11, Iss 4, Pp 67-74 (2014)

Aim. Hereditary spherocytosis (HS) is the most commonly encountered erythrocyte membranopathy. Frequency of occurrence of the disease makes one case per 2000−5000 newborns. Hereditary spherocytosis often causes a complex of clinical signs, includin

Externí odkaz: https://doaj.org/article/8bf3f6b21a944d37afb8ac59741ddc0c

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Akademický článek

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Clinical and laboratory profile of hereditary spherocytosis

Autor: Larisa Gaikovaya, Marina N. Zenina, Nataliya Yu. Chernysh, Tatevik T. Asatryan

Publikováno v: Vestnik severo-zapadnogo gosudarstvennogo medicinskogo universiteta im. I.I. Mečnikova, Vol 11, Iss 1, Pp 65-72 (2019)

Diagnostics of hereditary spherocytosis is usually based on clinical picture, family history and laboratory tests. The list of laboratory tests includes osmotic fragility test, a glycerol lysis test, an eosin-5-maleimide binding test and others. None

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9169f59e6eae63e8ea1d56ae4a1bff3a
https://journals.eco-vector.com/vszgmu/article/viewFile/10724/9258

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Improving the EMA Binding Test by Using Commercially Available Fluorescent Beads

Autor: Henrik Birgens, Christian Brieghel, Amina Nardo-Marino, Jesper Brix Petersen, Andreas Glenthøj, Alaa Sharfo

Publikováno v: Frontiers in Physiology
Frontiers in Physiology, Vol 11 (2020)
Glenthøj, A, Sharfo, A, Brieghel, C, Nardo-Marino, A, Birgens, H & Petersen, J B 2020, ' Improving the EMA Binding Test by Using Commercially Available Fluorescent Beads ', Frontiers in Physiology, vol. 11, 569289 . https://doi.org/10.3389/fphys.2020.569289

Hereditary spherocytosis (HS) is a common anemia caused by germline mutations in red blood cell cytoskeleton proteins. The flow cytometry-based eosin-5'-maleimide (EMA) binding test is most frequently employed for reliable diagnostics. To perform thi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52913b7b33a5095cec520d95cab8e786
http://europepmc.org/articles/PMC7522531

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