Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Kaveh Samii"'
Autor:
Maria Mavromati, Verdiana Caironi, Essia Saiji, Maria-Isabel Vargas, Shahan Momjian, Stephanie Andrade-Lopes, Capucine Gubert, Marco Stefano Demarchi, Ismini Mainta, François R Jornayvaz, Kaveh Samii, Grégoire Stalder, Sophie Leboulleux
Publikováno v:
European Thyroid Journal, Vol 13, Iss 3, Pp 1-6 (2024)
Langerhans cell histiocytosis (LCH) may present as unifocal disease of the suprasellar region, with symptoms and signs of hypopituitarism, arginine vasopressin deficiency (AVP-D), and weight gain. Transcranial biopsy is necessary to define diagnosis
Externí odkaz:
https://doaj.org/article/8a9f8f7fbea84dfbad174aac584778ab
Publikováno v:
healthbook TIMES. Oncology Hematology, Vol 20, Iss 2 (2024)
Multiple myeloma (MM) is an incurable hematological malignancy of the plasma cells. Most patients with MM are older than 65 years. Therefore, it is highly important to perform a frailty assessment to identify which patients are especially vulnerable
Externí odkaz:
https://doaj.org/article/3a8a58b8607f4d99be043350b6352eba
Publikováno v:
Thrombosis Journal, Vol 20, Iss 1, Pp 1-4 (2022)
Abstract Background Some conventional vaccines have been recognized as a cause of secondary immune thrombocytopenia (ITP). According to recent publications, mRNA vaccines are probably associated with an increased risk of ITP. Case presentation Our pa
Externí odkaz:
https://doaj.org/article/06d80d70b10240c8a50d0596d3fc14ee
Autor:
Kaveh Samii
Publikováno v:
healthbook TIMES. Oncology Hematology (2022)
Externí odkaz:
https://doaj.org/article/ddc921577f9c4ed1a3a9df6f1a7f19e4
Autor:
Axel Rüfer, Hubert Angermann, Rudolf Benz, Nicolas Bonadies, Antonello Calderoni, Nathan Cantoni, Anna Efthymiou, Robert Escher, Geneviève Favre, Dorothea Friess, Andreas Gschwend, Andreas Himmelmann, Andreas Holbro, Peter Keller, Eirini Kouroupi, Thomas Lehmann, Nikolaus Pedarnig, Véronique Rigamonti, Kaveh Samii, Adrian Schmidt, Hans-Peter Schäfer, Roland Sperb, Georg Stüssi, Annette Winkler, Reinhard Zenhäusern, Jeroen S. Goede, on behalf of the SLIM-Registry Investigators
Publikováno v:
HemaSphere, Vol 6, Iss 7, p e741 (2022)
Externí odkaz:
https://doaj.org/article/96e57933677a4445bcd61d39ea571d5b
Autor:
Kaveh Samii
Publikováno v:
healthbook TIMES. Oncology Hematology (2022)
Externí odkaz:
https://doaj.org/article/783c929b892b4c2f80638b4d49351d9d
Autor:
Alicia Rovó, Nathan Cantoni, Kaveh Samii, Axel Rüfer, Giedre Koenen, Sandra Ivic, Davide Cavanna, Rudolf Benz
Publikováno v:
PLoS ONE, Vol 17, Iss 4, p e0267342 (2022)
Aims of the studyThrombopoietin receptor agonists (TPO-RAs) are approved for immune thrombocytopenia (ITP), but their impact on health-related quality of life (HRQoL) remains poorly investigated in clinical practice. This observational study aimed to
Externí odkaz:
https://doaj.org/article/f412851071b14047afa86e101bf9f96f
Autor:
André Truffert, Ruxandra Iancu Ferfoglia, Johannes Alexander Lobrinus, Kaveh Samii, André Kohler
Publikováno v:
European Journal of Translational Myology (2020)
Monoclonal gammopathy of undetermined significance (MGUS) associated to sporadic late onset nemaline myopathy (SLONM) is a rare and severely disabling condition of quickly progressive limb girdle acquired myopathy. It is believed by some authors to b
Externí odkaz:
https://doaj.org/article/68779f81851747d48b67d3b4d3b92a7a
Autor:
Axel Rüfer, Christine Bapst, Rudolf Benz, Jens Bremerich, Nathan Cantoni, Laura Infanti, Kaveh Samii, Mathias Schmid, Jean-Paul Vallée
Publikováno v:
Swiss Medical Weekly, Vol 147, Iss 4546 (2017)
Hyperferritinaemia is a frequent clinical problem. Elevated serum ferritin levels can be detected in different genetic and acquired diseases and can occur with or without anaemia. It is therefore important to determine whether hyperferritinaemia is d
Externí odkaz:
https://doaj.org/article/c4d3afd29f3d4618b108c59f4a995f49
Autor:
Céline Louis, Sandrine Vijgen, Kaveh Samii, Yves Chalandon, Louis Terriou, David Launay, David C. Fajgenbaum, Jörg D. Seebach, Yannick D. Muller
Publikováno v:
Frontiers in Medicine, Vol 4 (2017)
BackgroundTAFRO syndrome has been reported in Japan among human herpesvirus 8 (HHV-8)-negative/idiopathic multicentric Castleman’s disease (iMCD) patients. To date, the majority of iMCD patients with TAFRO syndrome originate from Japan.Case present
Externí odkaz:
https://doaj.org/article/799ec65fc9744d1ab6f79528b2c69b5b