Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Luisa Nanni"'
Autor:
Federica Sentinelli, Ilenia Minicocci, Anna Montali, Luisa Nanni, Stefano Romeo, Michela Incani, M. Gisella Cavallo, Andrea Lenzi, Marcello Arca, Marco G. Baroni
Publikováno v:
Journal of Lipids, Vol 2013 (2013)
Background. Familial combined hyperlipidemia (FCHL), the most common genetic form of hyperlipdemia, is characterized by a strong familial clustering and by premature coronary heart disease. The FCHL locus has been mapped to human chromosome 1q21-q23.
Externí odkaz:
https://doaj.org/article/2554692d7cf84ffa89061d9f661b2768
Autor:
Sentinelli, Federica, Minicocci, Ilenia, Montali, Anna, Nanni, Luigia, Luisa, Nanni, Stefano, Romeo, Michela, Incani, Cavallo, Maria Gisella, Maria Gisella Cavallo, Lenzi, Andrea, Arca, Marcello, Baroni, Marco Giorgio
Publikováno v:
Journal of Lipids
Journal of Lipids, Vol 2013 (2013)
Journal of Lipids, Vol 2013 (2013)
Background. Familial combined hyperlipidemia (FCHL), the most common genetic form of hyperlipdemia, is characterized by a strong familial clustering and by premature coronary heart disease. The FCHL locus has been mapped to human chromosome 1q21-q23.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5376ffe9357f2da8225b3c82ab11aab2
https://doi.org/10.1155/2013/517943
https://doi.org/10.1155/2013/517943
Publikováno v:
Journal of Molecular and Cellular Cardiology. 41:934-948
Gene expression profiling by microarray technologies has been successfully applied to study the transcriptional changes that occur in tissues such as heart, vessels and blood cells in different cardiovascular disorders. Such studies have been perform
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa134c571a3012740c1fa1db12359444
https://doi.org/10.1016/j.yjmcc.2006.08.009
https://doi.org/10.1016/j.yjmcc.2006.08.009
Autor:
Luisa Nanni, Michael J. Aldred, Y. Du, Roger K. Hall, Jeffrey E. Ming, Maximilian Muenke, Agnes Bankier
Publikováno v:
American Journal of Medical Genetics. 102:1-10
Solitary median maxillary central incisor (SMMCI) or single central incisor is a rare dental anomaly. It has been reported in holoprosencephaly (HPE) cases with severe facial anomalies or as a microform in autosomal dominant HPE (ADHPE). In our revie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::debc2bce737969acf1d430ed40701eba
https://doi.org/10.1002/1096-8628(20010722)102:1<1::aid-ajmg1336>3.0.co
https://doi.org/10.1002/1096-8628(20010722)102:1<1::aid-ajmg1336>3.0.co
Publikováno v:
American Journal of Medical Genetics. 90:315-319
Holoprosencephaly (HPE) is a common developmental anomaly of the forebrain and midface in which the cerebral hemispheres fail to separate into distinct left and right halves. HPE is extremely heterogeneous. In addition to teratogenic agents, several
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26d4e9aaa9deb27378100734d4aaacb9
https://doi.org/10.1002/(sici)1096-8628(20000214)90:4<315::aid-ajmg10>3.0.co
https://doi.org/10.1002/(sici)1096-8628(20000214)90:4<315::aid-ajmg10>3.0.co
Publikováno v:
Pediatric Pathology & Molecular Medicine. 19:1-19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5998604546299befb68ae464dcf14453
https://doi.org/10.1080/15227950050033747
https://doi.org/10.1080/15227950050033747
Autor:
Italo, Porto, Antonio Maria, Leone, Luisa, Nanni, Alessandro, Sciahbasi, Maria, De Vita, Gaetano Antonio, Lanza, Felicita, Andreotti
Publikováno v:
Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis. 16(2)
Platelets play a pivotal role in thrombus formation in patients with coronary artery disease (CAD), since the high shear generated in the presence of severe coronary stenoses can increase platelet reactivity (PR) and trigger thrombogenesis. Several r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5310b230361d5c989262a97d08a760d0
https://pubmed.ncbi.nlm.nih.gov/15741796
https://pubmed.ncbi.nlm.nih.gov/15741796
Autor:
Alessandro Sciahbasi, Italo Porto, Antonio Maria Leone, Luisa Nanni, Gaetano Antonio Lanza, Felicita Andreotti, Maria De Vita
Publikováno v:
Scopus-Elsevier
Platelets play a pivotal role in thrombus formation in patients with coronary artery disease (CAD), since the high shear generated in the presence of severe coronary stenoses can increase platelet reactivity (PR) and trigger thrombogenesis. Several r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2715ded59ded8c1576ce391b921468ac
https://hdl.handle.net/11567/936696
https://hdl.handle.net/11567/936696
Autor:
Luisa Nanni, Rosanna Zimbello, Andrea Frustaci, Gerolamo Lanfranchi, Maurizio Pieroni, Barbara Simionati, Cristina Chimenti, Attilio Maseri
About 10% of cases of hypertrophic cardiomyopathy (HCM) evolve into dilated cardiomyopathy (DCM) with unknown causes. We studied 11 unrelated patients (pts) with HCM who progressed to DCM (group A) and 11 who showed "typical" HCM (group B). Mutationa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97bdb7c148517e2cec43823e946c70f4
http://hdl.handle.net/11573/133596
http://hdl.handle.net/11573/133596
Autor:
Luisa Nanni, Erich Roessler, Diana W. Bianchi, Christine E. M. de Die-Smulders, Mary Ella M Pierpont, Kathryn A. Steinhaus, Nathaniel H. Robin, Rick A. Martin, Miguel Del Campo, Ian D. Young, Kenneth L. Jones, Maximilian Muenke, Aldo Giannotti, Peter Meinecke, Jeffrey E. Ming, Maureen Bocian, Kiyoshi Imaizumi
Publikováno v:
Human molecular genetics. 8(13)
Holoprosencephaly (HPE) is a common developmental anomaly of the human forebrain and midface where the cerebral hemispheres fail to separate into distinct left and right halves. We have previously reported haploinsufficiency for Sonic Hedgehog ( SHH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b3bff939ab61236af4b4d9403e8a318
https://pubmed.ncbi.nlm.nih.gov/10556296
https://pubmed.ncbi.nlm.nih.gov/10556296