Results 11 to 20 of about 89,859 (293)

Clinical observation of Сhronic granulomatous disease in a 6-year-old child

Детские инфекции (Москва), 2020
Chronic granulomatous disease (CGD) is a hereditary disease caused by a genetic defect of violations of oxygen — dependent mechanisms of phagocytosis.
G. A. Kharchenko, O. G. Kimirilova
doaj   +1 more source

Immunopathogenesis of canine chronic ulcerative stomatitis. [PDF]

, 2020
Canine Chronic Ulcerative Stomatitis is a spontaneously occurring inflammatory disease of the oral mucosa. An immune-mediated pathogenesis is suspected though not yet proven.
Anderson, JG, Bizikova, P, Ford, K, Jimenez, RJ, Kol, A, Murphy, BG, Stapelton, BP, Vasilatis, D, Villarreal, A   +8 more
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Clinic manifestations in granulomatosis with polyangiitis [PDF]

, 2016
Granulomatosis with polyangiitis (GPA), formerly Wegener's granulomatosis (WG), is an uncommon immunologically mediated systemic small-vessel vasculitis that is pathologically characterised by an inflammatory reaction pattern (necrosis, granulomatous ...
De Vincentiis, Marco, De Virgilio, Armando, Fusconi, Massimo, Gallo, Andrea, Greco, Antonio, Macri, Gian Franco, Marinelli, Caterina, Zambetti, Giampietro   +7 more
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Case report: HLA-haploidentical HSCT rescued with donor lymphocytes infusions in a patient with X-linked chronic granulomatous disease

Frontiers in Immunology, 2023
Chronic granulomatous disease is an inborn error of immunity due to disrupted function of the nicotinamide adenine dinucleotide phosphate (NADPH) oxidase complex.
Julia Scheiermann, Julia Scheiermann, Annette Künkele, Annette Künkele, Annette Künkele, Annette Künkele, Arend von Stackelberg, Angelika Eggert, Angelika Eggert, Angelika Eggert, Angelika Eggert, Peter Lang, Peter Lang, Felix Zirngibl, Luise Martin, Johannes Hubertus Schulte, Johannes Hubertus Schulte, Johannes Hubertus Schulte, Johannes Hubertus Schulte, Horst von Bernuth, Horst von Bernuth, Horst von Bernuth, Horst von Bernuth   +22 more
doaj   +1 more source

Chronic Granulomatous Disease: the Experience of Diagnosis and Treatment in Children

Zdorovʹe Rebenka, 2013
Chronic granulomatous disease — primary immunodeficiency with X-linked and autosomal recessive inheritance, characterized by impaired bactericidal function of phagocytic immune system.
L.I. Chernyshova, A.P. Volokha, A.V. Bondarenko, A.M. Gilfanova, V.P. Chernyshov   +4 more
doaj   +1 more source

Lacrimal gland tumors in Turkey: types, frequency, and outcomes. [PDF]

, 2018
AIM: To evaluate the clinical, radiological, and treatment features of lacrimal gland tumors. METHODS: Retrospective review of 99 eyes of 92 patients with lacrimal gland tumors diagnosed and managed in a single institution between January 1999 and March ...
Erden, Esra, Gündüz, Ahmet Kaan, Shields, Carol L., Yeşiltaş, Yağmur Seda   +3 more
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Topical tacrolimus 0.1% ointment for treatment of cutaneous Crohn's Disease [PDF]

, 2013
Peer reviewedPublisher ...
El-Omar, Emad, Keenan, Ronald A, Ormerod, Anthony D, Rice, Shantini A, Woo, Pick N   +4 more
core   +2 more sources

Sarcoidosis Presenting as Acute Respiratory Distress Syndrome. [PDF]

, 2018
Sarcoidosis is a multisystem granulomatous disease of unknown origin. It typically involves the lungs and mediastinal lymph nodes in a chronic fashion. However, acute syndrome has been reported possibly in response to systemic release of proinflammatory ...
Chan, Vincent, Lashari, Bilal, Raza, Ahmad, Ward, William   +3 more
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Chronic Granulomatous Disease

Hematology/Oncology Clinics of North America, 2009
Chronic granulomatous disease (CGD) was first described in the 1950s and has become a paradigm for genetic neutrophil diseases. It is characterized by recurrent infections with a narrow spectrum of bacteria and fungi as well as a common set of inflammatory complications most notably including inflammatory bowel disease. Over the last half century major
B H, Segal, L, Romani, P, Puccetti
  +8 more sources

Differential Kinetics of Aspergillus nidulans and Aspergillus fumigatus Phagocytosis [PDF]

, 2017
Acknowledgements: The authors would like to acknowledge Fraser P. Coxon and Ian Ganley for providing LC3-GFP-mCherry BMDMs. M.S.G. was supported by an FEMS research grant and F.L.v.d.V.
Alonso, M Fernanda, Bain, Judith M, Becker, Katharina L, Erwig, Lars P, Gresnigt, Mark S, Leenders, Floris, Meis, Jacques F, van de Veerdonk, Frank L, Wang, Xiaowen   +8 more
core   +2 more sources