Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Razq Hakem"'
Autor:
Coline H M van Moorsel, Ana Montes-Worboys, Razq Hakem, E. Ellen Billett, Carmen Herranz, Eline Blommaert, Oscar Yanes, Antonio Roman, Julio Ancochea, Álvaro Casanova, Raúl Rigo-Bonnin, Harilaos Filippakis, Berta Saez, August Vidal, Alexandra Baiges, Antoni Xaubet, Suzanne Miller, Antonio Gomez, Roderic Espín, Joanne J van der Vis, José A Rodríguez-Portal, Chiara Gorrini, Jaume Bordas, Marian J R Quanjel, Aleix Noguera-Castells, Luis Palomero, Eva Revilla-López, Josep M. Cruzado, Xiaohu Zhang, Enrique Lastra, Nadia García, Elżbieta Radzikowska, Marc Ferrer, Simon R. Johnson, Christophe Bontoux, Maria Molina-Molina, Alexandra Junza, Javier A. Menendez, Ana I. Extremera, Piedad Ussetti, Rosalía Laporta, Álvaro Lahiguera, Miquel Angel Pujana, Susana Gómez-Ollés, Daniel Cuadras, Mario Mancino, Claudia Valenzuela, Tamara Alonso, Jose C. Perales, Francesca Mateo, Francesc Viñals, Aslihan Ugun-Klusek, Gorka Ruiz de Garibay, Roser Guiteras, Jordi Capellades, Concettina La Motta, Carlos Machahua
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
EMBO Molecular Medicine
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Scientia
DDFV. Repositorio Institucional de la Universidad Francisco de Vitoria
Dipòsit Digital de la UB
Universidad de Barcelona
EMBO Molecular Medicine, Vol 13, Iss 9, Pp n/a-n/a (2021)
instname
EMBO Molecular Medicine
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Scientia
DDFV. Repositorio Institucional de la Universidad Francisco de Vitoria
Dipòsit Digital de la UB
Universidad de Barcelona
EMBO Molecular Medicine, Vol 13, Iss 9, Pp n/a-n/a (2021)
Inhibition of mTOR is the standard of care for lymphangioleiomyomatosis (LAM). However, this therapy has variable tolerability and some patients show progressive decline of lung function despite treatment. LAM diagnosis and monitoring can also be cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3528695e98889a787bd38a10b1b3e32
http://hdl.handle.net/10261/265901
http://hdl.handle.net/10261/265901
Autor:
Matthew D. Liptak, David H. McMillan, Sarah Abdalla, James D. Nolin, Jose L. Gomez, Morgan E. Cousins, Markus Bachschmid, Charles G. Irvin, Vikas Anathy, Yvonne M. W. Janssen-Heininger, David J. Seward, Jos van der Velden, Reem Aboushousha, Razq Hakem, Sidra M. Hoffman, Naftali Kaminski, Shi B. Chia, David G. Chapman, Ye-Shih Ho, Albert van der Vliet, Karolyn G. Lahue, Evan Elko, Robert W. Schneider, Kevin K. Brown, Jane T. Jones, Dylan T. Casey, Douglas J. Taatjes, Ralph C. Budd, Elle C. Roberson, Kelly J. Butnor, Reiko Matsui
© 2018, The Author(s). Idiopathic pulmonary fibrosis is characterized by excessive deposition of collagen in the lung, leading to chronically impaired gas exchange and death 1–3 . Oxidative stress is believed to be critical in this disease pathoge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd38dbe553d5b60503766effcf205466
https://hdl.handle.net/10453/130981
https://hdl.handle.net/10453/130981
Autor:
Stéphane Carpentier, Shaalee Dworski, Thierry Levade, James C.M. Wang, Virginie Garcia, Jeffrey A. Medin, Razq Hakem, Abdu Alayoubi, Bryan Au, Samah El-Ghmrsni
Publikováno v:
Molecular Genetics and Metabolism. 105:S16
these two groups, those with HCT did better than ERT. Conclusion: With the exception of slight increased risk for hydrocephalus/shunt in the attenuated group, similar patterns of disease were found. Adaptive functions were better in the HCT group. Ea