Zobrazeno 1 - 6
of 6
pro vyhledávání: '"MESH: Bronchopulmonary Dysplasia"'
Autor:
Alison, Marianne, Tilea, Bogdana, Toumazi, Artemis, Biran, Valérie, Mohamed, Damir, Alberti, Corinne, Bourmaud, Aurélie, Baud, Olivier, PREMILOC Trial group
Publikováno v:
Archives of Disease in Childhood Fetal and Neonatal Edition (2020)
Archives of disease in childhood. Fetal and neonatal edition
Archives of disease in childhood. Fetal and neonatal edition, BMJ Publishing Group, 2020, 105 (5), pp.520-525. ⟨10.1136/archdischild-2019-317720⟩
Archives of disease in childhood.Fetal and neonatal edition
Archives of disease in childhood.Fetal and neonatal edition, BMJ Publishing Group, 2020, 105 (5), pp.520-525. ⟨10.1136/archdischild-2019-317720⟩
Archives of disease in childhood. Fetal and neonatal edition
Archives of disease in childhood. Fetal and neonatal edition, BMJ Publishing Group, 2020, 105 (5), pp.520-525. ⟨10.1136/archdischild-2019-317720⟩
Archives of disease in childhood.Fetal and neonatal edition
Archives of disease in childhood.Fetal and neonatal edition, BMJ Publishing Group, 2020, 105 (5), pp.520-525. ⟨10.1136/archdischild-2019-317720⟩
ObjectiveTo determine whether early low-dose hydrocortisone treatment in extremely preterm infants is associated with brain damage assessed by MRI at term equivalent of age (TEA).Patients and outcomesThis is a predefined secondary analysis of brain a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5eb6be7a7c2f966726d0e3372a5ab47
https://archive-ouverte.unige.ch/unige:137352
https://archive-ouverte.unige.ch/unige:137352
Autor:
François Goffinet, Monique Kaminski, Jennifer Zeitlin, Anne Ego, Cécile Lebeaux, Pierre-Yves Ancel, Pierre-Henri Jarreau, Isabelle Monier
Publikováno v:
American Journal of Obstetrics and Gynecology
American Journal of Obstetrics and Gynecology, Elsevier, 2017, 216 (5), pp.516.e1-516.e10. ⟨10.1016/j.ajog.2017.02.001⟩
American Journal of Obstetrics and Gynecology, Elsevier, 2017, 216 (5), pp.516.e1-516.e10. ⟨10.1016/j.ajog.2017.02.001⟩
Fetal growth restriction is defined using ultrasound parameters during pregnancy or as a low birthweight for gestational age after birth, but these definitions are not always concordant.The purpose of this study was to investigate fetal and neonatal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5df8649656db4f8804c0c1d3fefed7f
http://hal.univ-grenoble-alpes.fr/hal-02007822
http://hal.univ-grenoble-alpes.fr/hal-02007822
Autor:
Pierre-Henri Jarreau, Emmanuelle Bouzigon, Johanna M. Huusko, Roberto Incitti, Ines Layouni, Jacques R. Bourbon, Richard Lenclen, Claude Danan, Florence Demenais, Mikko Hallman, Alice Hadchouel, Juliana Patkai, Christophe Delacourt, Xavier Durrmeyer, Marie-Laure Franco-Montoya
Publikováno v:
American Journal of Respiratory and Critical Care Medicine
American Journal of Respiratory and Critical Care Medicine, American Thoracic Society, 2011, 184 (10), pp.1164-70. ⟨10.1164/rccm.201103-0548OC⟩
American Journal of Respiratory and Critical Care Medicine, 2011, 184 (10), pp.1164-70. ⟨10.1164/rccm.201103-0548OC⟩
American Journal of Respiratory and Critical Care Medicine, American Thoracic Society, 2011, 184 (10), pp.1164-70. 〈10.1164/rccm.201103-0548OC〉
American Journal of Respiratory and Critical Care Medicine, American Thoracic Society, 2011, 184 (10), pp.1164-70. ⟨10.1164/rccm.201103-0548OC⟩
American Journal of Respiratory and Critical Care Medicine, 2011, 184 (10), pp.1164-70. ⟨10.1164/rccm.201103-0548OC⟩
American Journal of Respiratory and Critical Care Medicine, American Thoracic Society, 2011, 184 (10), pp.1164-70. 〈10.1164/rccm.201103-0548OC〉
International audience; RATIONALE: Bronchopulmonary dysplasia is the most common chronic respiratory disease in premature infants. Genetic factors might contribute to bronchopulmonary dysplasia susceptibility. OBJECTIVES: To identify genetic variants
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a85f2b310a0163bd5d2b5d8dbdb8e0d0
https://www.hal.inserm.fr/inserm-00617002/document
https://www.hal.inserm.fr/inserm-00617002/document
Autor:
Isabelle Halphen, Marie-Laure Franco-Montoya, Pierre-Henri Jarreau, Claude Danan, Fabrice Decobert, Jacques R. Bourbon, Emmanuel Martin, Alice Hadchouel, Olivier Boucherat, Serge Amselem, Alexandra Benachi, Christophe Delacourt
Publikováno v:
PLoS ONE
PLoS ONE, Public Library of Science, 2008, 3 (9), pp.e3188. 〈10.1371/journal.pone.0003188〉
PLoS ONE, Public Library of Science, 2008, 3 (9), pp.e3188. ⟨10.1371/journal.pone.0003188⟩
PLoS ONE, Vol 3, Iss 9, p e3188 (2008)
PLoS ONE, 2008, 3 (9), pp.e3188. ⟨10.1371/journal.pone.0003188⟩
PLoS ONE, Public Library of Science, 2008, 3 (9), pp.e3188. 〈10.1371/journal.pone.0003188〉
PLoS ONE, Public Library of Science, 2008, 3 (9), pp.e3188. ⟨10.1371/journal.pone.0003188⟩
PLoS ONE, Vol 3, Iss 9, p e3188 (2008)
PLoS ONE, 2008, 3 (9), pp.e3188. ⟨10.1371/journal.pone.0003188⟩
International audience; BACKGOUND: Alveolarization requires coordinated extracellular matrix remodeling, a process in which matrix metalloproteinases (MMPs) play an important role. We postulated that polymorphisms in MMP genes might affect MMP functi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::566615578b49b7af41337c527c8e1a3c
http://www.hal.inserm.fr/inserm-00447737
http://www.hal.inserm.fr/inserm-00447737
Autor:
Hadchouel, Alice, Durrmeyer, Xavier, Bouzigon, Emmanuelle, Incitti, Roberto, Huusko, Johanna, Jarreau, Pierre-Henri, Lenclen, Richard, Demenais, Florence, Franco-Montoya, Marie-Laure, Layouni, Ines, Patkai, Juliana, Bourbon, Jacques, Hallman, Mikko, Danan, Claude, Delacourt, Christophe
Publikováno v:
American Journal of Respiratory and Critical Care Medicine
American Journal of Respiratory and Critical Care Medicine, American Thoracic Society, 2011, 184 (10), pp.1164-70. ⟨10.1164/rccm.201103-0548OC⟩
American Journal of Respiratory and Critical Care Medicine, American Thoracic Society, 2011, 184 (10), pp.1164-70. ⟨10.1164/rccm.201103-0548OC⟩
International audience; RATIONALE: Bronchopulmonary dysplasia is the most common chronic respiratory disease in premature infants. Genetic factors might contribute to bronchopulmonary dysplasia susceptibility. OBJECTIVES: To identify genetic variants
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1398::b811c8fda91211adf37b0dac80ec4292
https://www.hal.inserm.fr/inserm-00617002/document
https://www.hal.inserm.fr/inserm-00617002/document
Autor:
Jacques R. Bourbon, Bruno Crestani, Jorge Boczkowski, Christophe Delacourt, Olivier Boucherat
Publikováno v:
Trends in Molecular Medicine
Trends in Molecular Medicine, Elsevier, 2009, 15 (4), pp.169-79. ⟨10.1016/j.molmed.2009.02.003⟩
Trends in Molecular Medicine, 2009, 15 (4), pp.169-79. ⟨10.1016/j.molmed.2009.02.003⟩
Trends in Molecular Medicine, Elsevier, 2009, 15 (4), pp.169-79. ⟨10.1016/j.molmed.2009.02.003⟩
Trends in Molecular Medicine, 2009, 15 (4), pp.169-79. ⟨10.1016/j.molmed.2009.02.003⟩
International audience; Bronchopulmonary dysplasia of the premature neonate and emphysema of the adult lung are common diseases that are characterized by increased airspace size and respiratory insufficiency and that presently lack efficient treatmen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c9e1fe24c04976490c03ecc91ecc7cf
https://www.hal.inserm.fr/inserm-00371860
https://www.hal.inserm.fr/inserm-00371860