Results 31 to 40 of about 9,034 (208)

Alveolar macrophages develop from fetal monocytes that differentiate into long-lived cells in the first week of life via GM-CSF [PDF]

, 2013
Tissue-resident macrophages can develop from circulating adult monocytes or from primitive yolk sac-derived macrophages. The precise ontogeny of alveolar macrophages (AMFs) is unknown. By performing BrdU labeling and parabiosis experiments in adult mice,
De Kleer, Ismé, De Prijck, Sofie, Deswarte, Kim, Guilliams, Martin, Hammad, Hamida, Henri, Sandrine, Lambrecht, Bart, Malissen, Bernard, Post, Sijranke, Vanhoutte, Leen   +9 more
core   +2 more sources

Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification. [PDF]

, 2020
Since 2013, the International Union of Immunological Societies (IUIS) expert committee (EC) on Inborn Errors of Immunity (IEI) has published an updated phenotypic classification of IEI, which accompanies and complements their genotypic classification ...
Ailal, Fatima, Al-Herz, Waleed, Bousfiha, Aziz, Casanova, Jean-Laurent, Chatila, Talal, Cunningham-Rundles, Charlotte, Etzioni, Amos, Franco, Jose Luis, Holland, Steven M, Jeddane, Leila, Klein, Christoph, Morio, Tomohiro, Ochs, Hans D, Oksenhendler, Eric, Picard, Capucine, Puck, Jennifer, Sullivan, Kathleen E, Tangye, Stuart G, Torgerson, Troy R   +18 more
core  

Proceedings: Regenerative Medicine for Lung Diseases: A CIRM Workshop Report. [PDF]

, 2017
The mission of the California Institute of Regenerative Medicine (CIRM) is to accelerate treatments to patients with unmet medical needs. In September 2016, CIRM sponsored a workshop held at the University of California, Los Angeles, to discuss ...
DeWitt, Natalie D, Gomperts, Brigitte, Kadyk, Lisa C   +2 more
core   +1 more source

Lavagem pulmonar total – A propósito de quatro casos de proteinose alveolar

Revista Portuguesa de Pneumologia, 2009
Resumo: A lavagem pulmonar é uma técnica desenvolvida na década de 60 do século xx com o intuito de remoção física de material proteináceo dos brônquios, em doentes com proteinose alveolar, levando a uma melhoria clínica e funcional. A técnica
M. Aguiar, P. Monteiro, M.M. Marques, S. Feijó, J.M. Rosal, R. Sotto-Mayor, A. Bugalho de Almeida   +6 more
doaj   +1 more source

In Lysinuric Protein Intolerance system y+L activity is defective in monocytes and in GM-CSF-differentiated macrophages [PDF]

, 2010
In the recessive aminoaciduria Lysinuric Protein Intolerance (LPI), mutations of SLC7A7/y+LAT1 impair system y+L transport activity for cationic amino acids.
Amelia Barilli, Bianca Rotoli, Rossana Visigalli, Ovidio Bussolati, Gian C Gazzola, Zamir Kadija, Giuseppe Rodi, Francesca Mariani, Maria Ruzza, Maurizio Luisetti, Valeria Dall'Asta   +10 more
core   +1 more source

Pulmonary Alveolar Proteinosis in an AIDS Patient without Concurrent Pulmonary Infection

Canadian Respiratory Journal, 1995
Patients with acquired immunodeficiency syndrome (AIDS) are potentially at increased risk for developing secondary pulmonary alveolar proteinosis because of underlying immunosuppression and frequent opportunistic lung infections. This condition. however,
Allen T Liu, Lil J Miedzinski, Eric Vallieres, David C Rayner, Dale C Lien   +4 more
doaj   +1 more source

Sirolimus-induced secondary pulmonary alveolar proteinosis

Respiratory Medicine Case Reports, 2022
Pulmonary alveolar proteinosis (PAP) is a rare pulmonary syndrome that is characterized by the accumulation of excess surfactant in the alveolar space, leading to impaired gas exchange. Sirolimus-induced PAP is an extremely rare entity that has only been
Stephanie Wang, MD, Elinor Lee, MD, PhD, Ryan Lau, MD, Tisha Wang, MD   +3 more
doaj   +1 more source

Rituximab therapy in pulmonary alveolar proteinosis improves alveolar macrophage lipid homeostasis [PDF]

, 2012
Rationale Pulmonary Alveolar Proteinosis (PAP) patients exhibit an acquired deficiency of biologically active granulocyte-macrophage colony stimulating factor (GM-CSF) attributable to GM-CSF specific autoantibodies. PAP alveolar macrophages are foamy,
Barna, Barbara P, Huizar, Isham, Karnekar, Reema, Kavuru, Mani S, Malur, Anagha, Marshall, Irene, NC DOCKS at East Carolina University, Thomassen, Mary Jane   +7 more
core   +3 more sources

Simultaneous presentation of two noninflammatory lung diseases in an HIV-infected patient

Annals of Thoracic Medicine, 2017
The simultaneous presentation of two noninflammatory pulmonary diseases, pulmonary alveolar proteinosis and Kaposi's sarcoma (Ks), in an HIV-infected patient, is described.
Rafael Martínez-Girón, Santiago Martínez-Torre   +1 more
doaj   +1 more source

Highlights of the Brazilian Thoracic Association guidelines for interstitial lung diseases [PDF]

, 2012
Interstitial lung diseases (ILDs) are heterogeneous disorders, involving a large number of conditions, the approach to which continues to pose an enormous challenge for pulmonologists.
Aidé, Miguel Abidon, Algranti, Eduardo, Baldi, Bruno Guedes, Bethlem, Eduardo Pamplona, Capitani, Eduardo Mello de, Caramori, Marlova Luzzi, Carvalho, Carlos Roberto Ribeiro, Carvalho, Jozélio Freire de, Coletta, Ester Nei Aparecida Martins, Costa, André Nathan, Ferreira, Rimarcs Gomes, Jezler, Sérgio, Kairalla, Ronaldo Adib, Lima, Mariana Silva, Martinez, José Antônio Baddini, Oliveira, Rudolf Krawczenko Feitoza de, Ota-Arakaki, Jaquelina Sonoe, Pereira, Carlos Alberto de Castro, Pimenta, Suzana Pinheiro, Rocha, Marcelo Jorge Jacó, Rodrigues, Silvia Carla Sousa, Rubin, Adalberto Sperb, Santana, Alfredo Nicodemos da Cruz, Soares, Maria Raquel, Steidle, Leila John Marques   +24 more
core   +3 more sources