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pro vyhledávání: '"Agbariah, Nada"'
Publikováno v:
Case Reports in Hematology. 12/3/2022, Vol. 2022, p1-8. 8p.
Autor:
Buetler, Vanessa Alexandra, Agbariah, Nada, Schild, Deborah Pia, Liechti, Fabian D, Wieland, Anna, Andina, Nicola, Hammann, Felix, Kremer Hovinga, Johanna A
Publikováno v:
Buetler, Vanessa Alexandra; Agbariah, Nada; Schild, Deborah Pia; Liechti, Fabian D; Wieland, Anna; Andina, Nicola; Hammann, Felix; Kremer Hovinga, Johanna A (2022). Immune-Mediated Thrombotic Thrombocytopenic Purpura Following mRNA-Based COVID-19 Vaccine BNT162b2: Case Report and Mini-Review of the Literature. Frontiers in medicine, 9, p. 890661. Frontiers 10.3389/fmed.2022.890661
Introduction An increasing number of case reports have associated vaccinations against coronavirus disease 2019 (COVID-19) with immune-mediated thrombotic thrombocytopenic purpura (iTTP), a very rare but potentially life-threatening thrombotic microa
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https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4463b00c6e7b3ec2b8be1958d1be393a
https://boris.unibe.ch/170493/1/fmed-09-890661.pdf
https://boris.unibe.ch/170493/1/fmed-09-890661.pdf
Akademický článek
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Akademický článek
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Publikováno v:
Agbariah, Nada; Sanz, Javier; Rovó, Alicia (2022). “A Dangerous Black Box:” Idiopathic Hemophagocytic Lymphohistiocytosis in Adult Patients—A Case Report and Review of the Literature. Case reports in hematology, 2022, pp. 1-8. Hindawi 10.1155/2022/5867129
Hemophagocytic lymphohistiocytosis (HLH) is a rare potentially life-threatening condition characterized by aberrant inflammation that can be related to genetic or sporadic forms. In both forms, triggering factors may be involved. Early detection of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbba335aa9910f5bdaf2a30da4a36f36
Autor:
Nada Agbariah, Alicia Rovó
Publikováno v:
Agbariah, Nada; Rovó, Alicia (2022). Breaking stereotypes-Polycythemia secondary to shisha smoking in a middle-age Swiss woman. Acta haematologica, 145(6), pp. 650-654. Karger 10.1159/000526016
The diagnosis of polycythemia, particularly the secondary forms, can be challenging. The distinction between primary and secondary polycythemia is relevant and has management implications. A systematic diagnostic workup algorithm and a good anamnesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3939a094cd65fc6501ad07d4daddb942