Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Gary R. Albert"'
Autor:
John E. Moran, Gary R. Albert, Lyne Gagnon, Nasreen Khalil, Martin Kolb, Frank Cesari, Joseph M. Parker, Christopher J. Ryerson, Renata Sawtell, Paul Hernandez, Aline Hagerimana, Pierre Laurin, Eric Turcotte, Shane Shapera, Hélène Manganas, André M. Cantin
Publikováno v:
The European Respiratory Journal
PBI-4050 is a novel orally active small-molecule compound with demonstrated anti-fibrotic activity in several models of fibrosis, including lung fibrosis. We present results from our first clinical study of PBI-4050 in patients with idiopathic pulmon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::410340e43330324b8fe13d84beff9849
http://europepmc.org/articles/PMC6422836
http://europepmc.org/articles/PMC6422836
Autor:
Gary R. Albert, Joseph M. Parker, John E. Moran, Brandon M. Hardesty, Pierre Laurin, Neelam Thukral, Per Morten Sandset, Charles Nakar, Karen Thibaudeau, Amy D. Shapiro
Publikováno v:
Blood. 131(12)
Congenital plasminogen deficiency is caused by mutations in PLG, the gene coding for production of the zymogen plasminogen, and is an ultrarare disorder associated with abnormal accumulation or growth of fibrin-rich pseudomembranous lesions on mucous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cec892cf0c83322b7d97ac76a9d032d
https://pubmed.ncbi.nlm.nih.gov/29567753
https://pubmed.ncbi.nlm.nih.gov/29567753
Autor:
Joseph M. Parker, Amy D. Shapiro, Per Morten Sandset, Pierre Laurin, Brandon M. Hardesty, Gary R. Albert, Charles Nakar, Neelam Thakral, John Moran
Publikováno v:
Blood. 130:84-84
Background: Congenital plasminogen deficiency (PLGD) caused by mutations in the PLG gene is a rare genetic disorder that leads to clinical manifestations due to extravascular fibrinous deposits on mucous membranes with disruption of tissue or organ f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b03baffa21338fa9ddfee69624fc2e53
https://doi.org/10.1182/blood.v130.suppl_1.84.84
https://doi.org/10.1182/blood.v130.suppl_1.84.84
Publikováno v:
Monatsschrift Kinderheilkunde; Sep2019 Supplement 4, Vol. 167, p197-278, 82p