Zobrazeno 1 - 10
of 27
pro vyhledávání: '"STK4 deficiency"'
Autor:
Assiya El Kettani, Hind Ouair, Farida Marnissi, Jalila El Bakkouri, Rémi Chevalier, Lazaro Lorenzo, Halima Kholaiq, Vivien Béziat, Emmanuelle Jouanguy, Jean-Laurent Casanova, Ahmed Aziz Bousfiha
Publikováno v:
Viruses, Vol 16, Iss 9, p 1415 (2024)
Epidermodysplasia verruciformis (EV) is a rare genodermatosis caused by β-human papillomaviruses (HPV) in immunodeficient patients. EV is characterized by flat warts and pityriasis-like lesions and might be isolated or syndromic, associated with som
Externí odkaz:
https://doaj.org/article/78144104671a4232ad911ced41934618
Akademický článek
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Autor:
Cyrill Schipp, David Schlütermann, Andrea Hönscheid, Schafiq Nabhani, Jessica Höll, Prasad T. Oommen, Sebastian Ginzel, Bernhard Fleckenstein, Björn Stork, Arndt Borkhardt, Polina Stepensky, Ute Fischer
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
Serine/threonine kinase 4 (STK4) deficiency is an autosomal recessive genetic condition that leads to primary immunodeficiency (PID) typically characterized by lymphopenia, recurrent infections and Epstein Barr Virus (EBV) induced lymphoproliferation
Externí odkaz:
https://doaj.org/article/70159e89017049b38b7be46a22af2a70
Autor:
Vedat Uygun, Sevgi Keleş, Hayriye Daloğlu, Seda Öztürkmen, Koray Yalçın, Gülsün Karasu, Akif Yeşilipek
Publikováno v:
Pediatric Transplantation. 27
Background Serine/threonine kinase 4 (STK4) deficiency is a combined immunodeficiency (CID) characterized by early onset recurrent bacterial, viral, and fungal infections. Allogeneic hematopoietic stem cell transplantation (HSCT) is a curative therap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::580db6123f0587e15db07f6d54570525
https://doi.org/10.1111/petr.14439
https://doi.org/10.1111/petr.14439
Akademický článek
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Autor:
Guennoun, Andrea, Bougarn, Salim, Khan, Taushif, Mackeh, Rafah, Rahman, Mahbuba, Al-Ali, Fatima, Ata, Manar, Aamer, Waleed, Prosser, Debra, Habib, Tanwir, Chin-Smith, Evonne, Al-Darwish, Khawla, Zhang, Qian, Al-Shakaki, Alya, Robay, Amal, Crystal, Ronald G., Fakhro, Khalid, Al-Naimi, Amal, Al Maslamani, Eman, Tuffaha, Amjad, Janahi, Ibrahim, Janahi, Mohammad, Love, Donald R., Karim, Mohammed Yousuf, Lo, Bernice, Hassan, Amel, Adeli, Mehdi, Marr, Nico
Publikováno v:
Journal of Clinical Immunology
Purpose Human serine/threonine kinase 4 (STK4) deficiency is a rare, autosomal recessive genetic disorder leading to combined immunodeficiency; however, the extent to which immune signaling and host defense are impaired is unclear. We assessed the fu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c47c08ce0af77243cffe4ab87a96a51
https://pubmed.ncbi.nlm.nih.gov/34427831
https://pubmed.ncbi.nlm.nih.gov/34427831
Autor:
Bernhard Fleckenstein, Sebastian Ginzel, David Schlütermann, Schafiq Nabhani, Andrea Hönscheid, Polina Stepensky, Prasad T. Oommen, Cyrill Schipp, Arndt Borkhardt, Björn Stork, Ute Fischer, Jessica I. Höll
Publikováno v:
Frontiers in Immunology
Front. Immunol. 9:2400
Frontiers in Immunology, Vol 9 (2018)
Front. Immunol. 9:2400
Frontiers in Immunology, Vol 9 (2018)
Serine/threonine kinase 4 (STK4) deficiency is an autosomal recessive genetic condition that leads to primary immunodeficiency (PID) typically characterized by lymphopenia, recurrent infections and Epstein Barr Virus (EBV) induced lymphoproliferation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdb05e0dd3d93323c046dc053521dfe4
https://doi.org/10.3389/fimmu.2018.02400
https://doi.org/10.3389/fimmu.2018.02400
Autor:
Cagman Sun-Tan, Baran Erman, Köksal R. Özgül, Sevil Oskay Halacli, Ilhan Tezcan, Elif Uz, Ozden Sanal, Deniz Cagdas Ayvaz, Didem Yücel Yılmaz
Publikováno v:
Clinical Immunology. 161:316-323
Combined immunodeficiencies (CIDs) are heterogeneous group of disorders characterized by abrogated/impaired T cell development and/or functions that resulted from diverse genetic defects. In addition to the susceptibility to infections with various m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee94198c32ae9f98a8655b1c8364421a
https://doi.org/10.1016/j.clim.2015.06.010
https://doi.org/10.1016/j.clim.2015.06.010
Autor:
Sherkat, Roya, Sabri, Mohammad Reza, Dehghan, Bahar, Bigdelian, Hamid, Reisi, Nahid, Afsharmoghadam, Nooshin, Rahimi, Hamid, Rahmanian, Narges, Klein, Cristoph
Publikováno v:
Medicine
Rationale: Primary cardiac lymphoma (PLC) is an extremely uncommon malignancy. PCL is more common in secondary immunodeficient patients. In this report, we describe a unique case of PLC who had been diagnosed as a STK4 deficient patient. This case is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a4ad5e5c2ca229f05a47c6007431e844
http://europepmc.org/articles/PMC5728766
http://europepmc.org/articles/PMC5728766
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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