Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Margherita, Vinciguerra"'
Autor:
A.G. Antonino Giambona, F.L. Filippo Leto, F.C. Filippo Cassara, V.T. Viviana Tartaglia, V.C. Valentina Cigna, G.C. Gaspare Cucinella, E.O. Emanuela Orlandi, F.P. Francesco Picciotto, M.V. Margherita Vinciguerra, A.M. Aurelio Maggio
Publikováno v:
HemaSphere, Vol 7, Iss S1, Pp 22-23 (2023)
Externí odkaz:
https://doaj.org/article/9cd8e50f282b476aab5375fa45207950
Autor:
Margherita Vinciguerra, Filippo Leto, Filippo Cassarà, Viviana Tartaglia, Michela Malacarne, Domenico Coviello, Valentina Cigna, Emanuela Orlandi, Francesco Picciotto, Gaspare Cucinella, Emanuela Salzano, Maria Piccione, Aurelio Maggio, Antonino Giambona
Publikováno v:
Life, Vol 13, Iss 1, p 20 (2022)
Background: Turner syndrome is a rare genetic condition in which a female is partly or completely missing an X chromosome. Signs and symptoms vary among those affected. In fetuses that survive at birth and without congenital malformations, the progno
Externí odkaz:
https://doaj.org/article/21ef2c14625d4b9c833b954c392163ac
Autor:
Antonino Giambona, Filippo Leto, Filippo Cassarà, Viviana Tartaglia, Rosario Campisi, Corrado Campisi, Valentina Cigna, Elena Mugavero, Gaspare Cucinella, Emanuela Orlandi, Francesco Picciotto, Aurelio Maggio, Margherita Vinciguerra
Publikováno v:
Hemoglobin. 46:297-302
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21158a91afec2fad1e3e51c24892c947
https://doi.org/10.1080/03630269.2023.2167659
https://doi.org/10.1080/03630269.2023.2167659
Autor:
Antonino Giambona, Filippo Leto, Filippo Cassarà, Viviana Tartaglia, Giuseppe Marchese, Emanuela Orlandi, Valentina Cigna, Francesco Picciotto, Aurelio Maggio, Margherita Vinciguerra
Publikováno v:
International Journal of Laboratory Hematology. 44:796-802
Analysis of fetal DNA in at risk couples for thalassemia is performed from fetal trophoblast or amniotic fluid cells. Although these procedures are in common use, the main limitation is essentially due to the late gestation week in which diagnosis is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6a3bf1f7d316df5efdd2be2afd5fbe0
https://doi.org/10.1111/ijlh.13837
https://doi.org/10.1111/ijlh.13837
Autor:
Antonino Giambona, Margherita Vinciguerra, Filippo Leto, Filippo Cassarà, Viviana Tartaglia, Valentina Cigna, Emanuela Orlandi, Francesco Picciotto, Nourah H. Al Qahtani, Eman S. Alsulmi, Noor B. Almandil, Sayed AbdulAzeez, J. Francis Borgio, Aurelio Maggio
Publikováno v:
Molecular Diagnosis & Therapy. 26:239-252
Celomic fluid can be considered as an ultra-filtrate of maternal serum, containing a high protein concentration, urea, and many other molecules. It is an important transfer interface and a reservoir of nutrients for the embryo. Celomic fluid contains
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16b8c2a88f9295b1b3134ffdc04d5488
https://doi.org/10.1007/s40291-022-00577-3
https://doi.org/10.1007/s40291-022-00577-3
Autor:
Margherita Vinciguerra, Filippo Leto, Filippo Cassarà, Viviana Tartaglia, Michela Malacarne, Domenico Coviello, Valentina Cigna, Emanuela Orlandi, Francesco Picciotto, Gaspare Cucinella, Emanuela Salzano, Maria Piccione, Aurelio Maggio, Antonino Giambona
Publikováno v:
Life; Volume 13; Issue 1; Pages: 20
Background: Turner syndrome is a rare genetic condition in which a female is partly or completely missing an X chromosome. Signs and symptoms vary among those affected. In fetuses that survive at birth and without congenital malformations, the progno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b2dd98503fdb30921e201fb7097a5ad
https://hdl.handle.net/10447/582570
https://hdl.handle.net/10447/582570
Autor:
Antonino Giambona, Filippo Leto, Filippo Cassarà, Viviana Tartaglia, Giuseppe Marchese, Emanuela Orlandi, Valentina Cigna, Francesco Picciotto, Aurelio Maggio, Margherita Vinciguerra
Publikováno v:
International Journal of Laboratory Hematology. 45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d8ee6691cc0881b680cc47c5a72d1f2
https://doi.org/10.1111/ijlh.13961
https://doi.org/10.1111/ijlh.13961
Autor:
Valentina Cigna, Aurelio Maggio, Filippo Cassarà, Gianfranca Damiani, Filippo Leto, Kypros H. Nicolaides, Antonino Giambona, C Jakil, Francesco Picciotto, George Makrydimas, Giovanna Schillaci, Margherita Vinciguerra, Manuela Orlandi
Publikováno v:
Ultrasound in Obstetrics & Gynecology. 56:672-677
OBJECTIVE Celocentesis is an invasive technique that can provide prenatal diagnosis of single-gene disorders, from as early as 7 weeks' gestation. The objective of this study was to examine the safety of celocentesis. METHODS In this prospective stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::530ab87b648f31649937def50d5af0b0
https://doi.org/10.1002/uog.22059
https://doi.org/10.1002/uog.22059
Autor:
Antonino Giambona, Margherita Vinciguerra, Filippo Leto, Filippo Cassarà, Gaspare Cucinella, Valentina Cigna, Emanuela Orlandi, Maria Piccione, Francesco Picciotto, Aurelio Maggio
Cockayne’s syndrome (CS) is a rare autosomal recessive multisystem disease characterised by early severe progression of symptoms. This study reports the feasibility of earlier prenatal diagnosis of CS by coelocentesis at 8 weeks of gestation respec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68bc46052201507e8e8c39b20a58b0c3
http://hdl.handle.net/10447/547097
http://hdl.handle.net/10447/547097
Autor:
Carmen Lo Pinto, Filippo Leto, Riccardo Ganci, Filippo Cassarà, Cristina Passarello, Aurelio Maggio, Lorella Pitrolo, Antonino Giambona, Margherita Vinciguerra, Paola Licari, Monica Cannata
Publikováno v:
Hemoglobin. 43:210-213
The evaluation of a 10-month-old girl of Sicilian origin with a clinical phenotype of severe thalassemia led to the identification of two β-globin gene defects, a β-thalassemia (β-thal), mutation a...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac5f80dfd011684882a4be60ba2db263
https://doi.org/10.1080/03630269.2019.1655030
https://doi.org/10.1080/03630269.2019.1655030