Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Carlota, Rovira Zurriaga"'
Autor:
Montserrat Izquierdo Renau, Elsa García González, Isabel Iglesias Platas, Alba Vergès Castells, Victoria Aldecoa-Bilbao, Carlota Rovira Zurriaga
Publikováno v:
The Journal of Maternal-Fetal & Neonatal Medicine. 34:1780-1785
Postnatal growth restriction remains one of the most common problems of very preterm infants (VPI). Chorioamnionitis is a frequent cause of prematurity. Both have been related to worse postnatal outcomes.To evaluate the influence of histological chor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::674e483d25e355d281b21c5471a39155
https://doi.org/10.1080/14767058.2019.1648423
https://doi.org/10.1080/14767058.2019.1648423
Autor:
Gudrun E. Moore, Miho Ishida, Miguel Alsina Casanova, Julio Moreno Hernando, Franck Court, Ana Monteagudo-Sánchez, Luciana Rodiguez Guerineau, Elisenda Moliner Calderon, David Monk, Carlota Rovira Zurriaga, M. Castañón, Loreto Martorell, Isabel Gazquez Serrano
Publikováno v:
Human Mutation. 38:615-620
Alveolar capillary dysplasia with misalignment of pulmonary veins (ACDMPV) is a rare cause of pulmonary hypertension in newborns. Maternally inherited point mutations in Forkhead Box F1 gene (FOXF1), deletions of the gene, or its long-range enhancers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::292d054b18e4d55c1970645b03b46342
https://doi.org/10.1002/humu.23213
https://doi.org/10.1002/humu.23213
Publikováno v:
Gynecology and Obstetrics Research - Open Journal. 3:26-31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1864f594519e95feaf360cb8f1ec7a05
https://doi.org/10.17140/goroj-3-133
https://doi.org/10.17140/goroj-3-133
Autor:
Diego Gutiérrez de la Iglesia, Antonia González Enseñat, Laura M. Pérez López, Loreto Martorell Sampol, Marisa Cabrera González, Carlota Rovira Zurriaga
Publikováno v:
HAND. 8:473-478
Digitocutaneous dysplasia, also termed osseous terminal dysplasia with pigmentary defects, is a recently described pathology. In 1974, Bloem et al. [5] discussed the association between digital fibromas and pigmentary lesions. In 1998, Horii et al. [
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f1a1f19649c16bce42cebf025457d23
https://doi.org/10.1007/s11552-013-9515-8
https://doi.org/10.1007/s11552-013-9515-8
Autor:
Miguel, Alsina Casanova, Ana, Monteagudo-Sánchez, Luciana, Rodiguez Guerineau, Franck, Court, Isabel, Gazquez Serrano, Loreto, Martorell, Carlota, Rovira Zurriaga, Gudrun E, Moore, Miho, Ishida, Montserrat, Castañon, Elisenda, Moliner Calderon, David, Monk, Julio, Moreno Hernando
Publikováno v:
Human mutation. 38(6)
Alveolar capillary dysplasia with misalignment of pulmonary veins (ACDMPV) is a rare cause of pulmonary hypertension in newborns. Maternally inherited point mutations in Forkhead Box F1 gene (FOXF1), deletions of the gene, or its long-range enhancers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8a73fd270ab6dd9fb4515c52c9d84bd2
https://pubmed.ncbi.nlm.nih.gov/28256047
https://pubmed.ncbi.nlm.nih.gov/28256047