Zobrazeno 1 - 10
of 155
pro vyhledávání: '"idiopathic CD4+lymphocytopenia"'
Autor:
Amar Kumar Mishra, Sanjay Kumar, Niraja Agasti, Gautam Guha, Saikat Ghosh, Bijendra Mohanty, Pideno S Ngullie, Joydeep Mukherjee
Publikováno v:
Asian Journal of Medical Sciences, Vol 13, Iss 10, Pp 288-292 (2022)
Progressive multifocal leukoencephalopathy (PML) is a rare subacute-onset fatal demyelinating disease of the central nervous system caused by the John Cunningham (JC) virus. It usually occurs in impaired cell-mediated immunity settings such as lympho
Externí odkaz:
https://doaj.org/article/3b8f75cedb244b4f93ebac67b1fef6e3
Autor:
Koji Maruyama, Daisuke Chujo, Koji Watanabe, Akitsu Kawabe, Takehiro Sugiyama, Mitsuru Ohsugi, Akiyo Tanabe, Kohjiro Ueki, Hiroshi Kajio
Publikováno v:
Journal of Diabetes Investigation, Vol 10, Iss 4, Pp 1108-1111 (2019)
Abstract A 64‐year‐old woman developed type 1 diabetes 23 years after the diagnosis of idiopathic CD4 lymphocytopenia. To investigate the etiological interaction between idiopathic CD4 lymphocytopenia and type 1 diabetes, we carried out a longitu
Externí odkaz:
https://doaj.org/article/d9a5b07dd1ea4d64889d3f539ea23588
Publikováno v:
Journal of Indian Academy of Oral Medicine and Radiology, Vol 30, Iss 4, Pp 412-416 (2018)
Idiopathic CD4+ T-cell lymphocytopenia (ICL) is a rare disorder of immune system with heterogeneous clinical manifestations and immunologic profile. This is a rare condition, which was first defined in 1992 by the Centers for Disease Control and Prev
Externí odkaz:
https://doaj.org/article/9ad3eb734ebb4cc6a1872f0261f78dcd
Akademický článek
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Autor:
Rosa Anita Fernandes, Martin Perez-Andres, Elena Blanco, Maria Jara-Acevedo, Ignacio Criado, Julia Almeida, Vitor Botafogo, Ines Coutinho, Artur Paiva, Jacques J. M. van Dongen, Alberto Orfao, Emilia Faria
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Idiopathic T-CD4 lymphocytopenia (ICL) is a rare and heterogeneous syndrome characterized by opportunistic infections due to reduced CD4 T-lymphocytes (
Externí odkaz:
https://doaj.org/article/3c26d0b96d3e436c8bb5c832e3ad336a
Publikováno v:
Annals of Indian Academy of Neurology, Vol 19, Iss 3, Pp 381-384 (2016)
A, 21-years-old, male, presented with acute onset, gradually progressive, predominantly distal, symmetrical weakness of both upper and lower limbs with arreflexia. He had impaired sensations in glove and stocking distribution with distal gradient. He
Externí odkaz:
https://doaj.org/article/74c7c21be1b146599543379976e4b758
Publikováno v:
Avicenna Journal of Medicine, Vol 03, Iss 02, Pp 37-47 (2013)
Idiopathic CD4 lymphocytopenia (ICL) was first defined in 1992 by the US Centers for Disease Control and Prevention (CDC) as the repeated presence of a CD4+ T lymphocyte count of fewer than 300 cells per cubic millimeter or of less than 20% of total
Externí odkaz:
https://doaj.org/article/358b6a4db52243f3a5fac7f14441550e
Publikováno v:
Medical Mycology Case Reports, Vol 6, Iss C, Pp 73-75 (2014)
Idiopathic CD4 lymphocytopenia (ICL) is characterized by a low CD4+ lymphocyte count in the absence of HIV or other underlying etiologies. We report a case of a 57-year old man with ICL and giant cell arteritis (GCA) who developed pulmonary mucormyco
Externí odkaz:
https://doaj.org/article/59c9fe61f9aa433d884860e5b3bdf3f1
Autor:
Alessandro Montanelli, Viviana Giustini, Matteo Filippini, Luisa Imberti, Stefano Belleri, Alessandra Sottini, Marco Maria Fontanella, Diego Bertoli, Aldo M. Roccaro
Publikováno v:
Journal of Neurosurgical Sciences. 65
Cryptococcal meningoencephalitis is the most common infective complication observed in patients with CD4 lymphocytopenia, including sarcoidosis. T-cell immunity is well characterized in HIV-related infections and data regarding immunity in cryptococc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f1a934c799cd8d44d588799247882e9
https://doi.org/10.23736/s0390-5616.18.04375-8
https://doi.org/10.23736/s0390-5616.18.04375-8
Publikováno v:
Cureus
Idiopathic CD4 T-lymphocytopenia (ICL) is a rare entity that is associated with decreased immunity which predisposes affected individuals to opportunistic infections and malignancies. Autoimmune conditions are common in patients with ICL and they are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85beb6ad55edbf905ff77694e7737237
https://doi.org/10.7759/cureus.19748
https://doi.org/10.7759/cureus.19748