Zobrazeno 1 - 10
of 9 749
pro vyhledávání: '"Immune thrombocytopenia"'
Autor:
Maaz Khan Afghan, Areeb Lutfi, Fatima Qadri, Sahrish Khan, Sana Javaid, Brian Michael Currie, Juan Pablo Rocca, Benjamin Samstein, Erika Hissong, Pashtoon Murtaza Kasi
Publikováno v:
Case Reports in Oncology, Vol 17, Iss 1, Pp 1183-1193 (2024)
Introduction: Immune thrombocytopenia (ITP) secondary to durvalumab, a programmed cell death ligand 1 inhibitor, is a rare but clinically significant immune-related adverse event. Herein, we present 2 patients with cholangiocarcinoma who developed IT
Externí odkaz:
https://doaj.org/article/bcc347cfacc545d0bcda994c01558e05
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-8 (2024)
Abstract Immune checkpoint inhibitors (ICIs) have become an important treatment modality for various malignancies. Due to excessive inflammatory and immune responses, immune-related adverse events (irAEs), such as rash, pruritis, pneumonitis, hepatit
Externí odkaz:
https://doaj.org/article/e7732f0860fa4210a5885d0bb91aa11e
Publikováno v:
National Board of Examinations Journal of Medical Sciences, Vol Volume 2, Iss Issue 10, Pp 1032-1037 (2024)
Introduction: In neonatal intensive care units, neonatal thrombocytopenia is one of the common hematological abnormality seen. Neonatal autoimmune thrombocytopenia should be considered in any neonate who is born to a known case of immune thrombocytop
Externí odkaz:
https://doaj.org/article/590f32355e5b4bb5b49fe86f6b229fab
Autor:
S. G. Zakharov
Publikováno v:
Онкогематология, Vol 19, Iss 3, Pp 34-44 (2024)
Immune thrombocytopenia (ITP) is an autoimmune disease characterized by a decrease in platelet count, which often leads to bleeding. Evidence suggests that low platelet counts in ITP are the result of multiple factors, including impaired thrombocytop
Externí odkaz:
https://doaj.org/article/bfc3a5276b034fba847d3ad99247c4fc
Autor:
Seham Mohamed Ragab, Wafaa Moustafa Abo ElFotoh, Mahmoud Ahmed El-Hawy, Eman Abdelfatah Badr, Saara Khairat Ali Mostafa, Mai El-Sayad Abd El-Hamid
Publikováno v:
Clinical and Experimental Pediatrics, Vol 67, Iss 9, Pp 465-473 (2024)
Background The pathophysiology and susceptibility of children to primary immune thrombocytopenia (ITP) are linked to polymorphisms of the interleukin (IL)-1B and IL-1 receptor (IL-1R) antagonist genes. Purpose To investigate the association between t
Externí odkaz:
https://doaj.org/article/e921a9ac3d62407ea5d81e2f6b622413
Publikováno v:
Neurological Research and Practice, Vol 6, Iss 1, Pp 1-4 (2024)
Abstract Guillain-Barré syndrome is the most common acute inflammatory demyelinating peripheral nerve condition. Occasionally, other autoimmune conditions can mimic Guillain-Barré syndrome but may require different diagnostic workup and treatment.
Externí odkaz:
https://doaj.org/article/521532a00170449e9096356ac1129f48
Autor:
Elif Gülsüm Ümit, Ahmet Muzaffer Demir, Muhlis Cem Ar, Mesut Ayer, Meltem Aylı, Volkan Karakuş, Emin Kaya, Fahir Özkalemkaş, Nilgün Sayınalp, Mehmet Sönmez, Fahri Şahin, Selami Koçak Toprak, Tayfur Toptaş, İrfan Yavaşoğlu, Ümran Çalış
Publikováno v:
Turkish Journal of Hematology, Vol 41, Iss 3, Pp 141-145 (2024)
Objective: Primary immune thrombocytopenia (ITP) is an acquired disorder of platelets with a complex and unclear mechanism of increased immune destruction or impaired production of platelets. While the management of ITP is evolving, there is still a
Externí odkaz:
https://doaj.org/article/054d63ab37a14969ae51686eef5b3e9e
Publikováno v:
İstanbul Medical Journal, Vol 25, Iss 3, Pp 241-244 (2024)
Introduction: This study aimed to evaluate the results obtained with the preference of eltrombopag according to the line of treatment in patients diagnosed with ITP. Methods: This retrospective study included 51 patients who were treated with eltrom
Externí odkaz:
https://doaj.org/article/4c38683d785f449b83616bb0b28335d8
Autor:
Ibrahim Hawwari, Lukas Rossnagel, Nathalia Rosero, Salie Maasewerd, Matilde B Vasconcelos, Marius Jentzsch, Agnieszka Demczuk, Lino L Teichmann, Lisa Meffert, Damien Bertheloot, Lucas S Ribeiro, Sebastian Kallabis, Felix Meissner, Moshe Arditi, Asli E Atici, Magali Noval Rivas, Bernardo S Franklin
Publikováno v:
EMBO Molecular Medicine, Vol 16, Iss 8, Pp 1901-1929 (2024)
Abstract In humans, blood Classical CD14+ monocytes contribute to host defense by secreting large amounts of pro-inflammatory cytokines. Their aberrant activity causes hyper-inflammation and life-threatening cytokine storms, while dysfunctional monoc
Externí odkaz:
https://doaj.org/article/3f0b496722be4a4a8de3b39c4dca46e8
Autor:
N. V. Davydova, N. V. Zinovieva, S. B. Zimin, O. V. Shvez, E. V. Galeeva, Yu. E. Konoplyannikova, O. V. Molochnikova, Yu. V. Petrova, G. N. Gildeeva, I. G. Kozlov
Publikováno v:
Медицинская иммунология, Vol 26, Iss 4, Pp 777-786 (2024)
Patients with 22q11.2 deletion syndrome (DiGeorge syndrome) are characterized by a combination of a wide range of pediatric problems with an immunodeficiency. Defects are characterized by T cell lymphopenia, changes in the functions and subpopulation
Externí odkaz:
https://doaj.org/article/731131c1a2c447c68987f8fb68c7ac5d