Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Rosaria Teresa, Basile"'
Autor:
Maurizio Clementi, Elena Di Gianantonio, Romano Tenconi, Isabella Mammi, Rosaria Teresa Basile, Elisabetta Pelo
Publikováno v:
American Journal of Medical Genetics. 83:43-46
We report on a further case of congenital anomalies in a child exposed to methimazole during the first trimester of pregnancy (from first to seventh gestational week), and define a specific malformation pattern related to prenatal methimazole exposur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::094ea097ba3085e5328e57f6668bb31b
https://doi.org/10.1002/(sici)1096-8628(19990305)83:1<43::aid-ajmg8>3.0.co
https://doi.org/10.1002/(sici)1096-8628(19990305)83:1<43::aid-ajmg8>3.0.co
Autor:
Ernestina Saulle, Rosaria Teresa Basile, Romano Tenconi, Piero A. Battaglia, Concezio Di Rocco, F. Velardi, Marco Tartaglia, Veronica Bordoni
Publikováno v:
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. 15(8)
A number of craniosynostotic disorders have recently been ascribed to mutations in genes coding for the fibroblast growth factor receptors(FGFRs). The common feature of these FGFR-associated conditions is the unilateral or bilateral premature ossific
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::497d17246895531cd7953b82049a0ce9
https://pubmed.ncbi.nlm.nih.gov/10447608
https://pubmed.ncbi.nlm.nih.gov/10447608
Autor:
Isabella, Mammi, Mammi, Isabella, Rosaria Teresa, Basile, Basile Rosaria, Teresa, Silvano, Bellato, Bellato, Silvano, Serena, Belli, Belli, Serena, Francesco, Benedicenti, Benedicenti, Francesco, Stefania, Boni, Boni, Stefania, Claudio, Castellan, Castellan, Claudio, Maurizio, Clementi, Clementi, Maurizio, Elena, Di Gianantonio, Di Gianantonio, Elena, Marilena, Petrella, Petrella, Marilena, Licia, Turolla, Turolla, Licia, Romano, Tenconi, Tenconi, Romano
Publikováno v:
Scopus-Elsevier
Congenital malformations (CM) affect 2-3% of all births, the cause of which, when known, is genetic in 80-90% of cases. A genetic consultation (GC) is indicated for the parents of a child affected by a CM. This study analyzes the parental utilization
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0e6912d7469712aea2f67f85678cd79
http://www.scopus.com/inward/record.url?eid=2-s2.0-0041694105&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0041694105&partnerID=MN8TOARS
