Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Anna Filomena Guglielmi"'
Autor:
Giovanna Forte, Filomena Cariola, Antonia Lucia Buonadonna, Anna Filomena Guglielmi, Andrea Manghisi, Katia De Marco, Valentina Grossi, Candida Fasano, Martina Lepore Signorile, Paola Sanese, Rosanna Bagnulo, Nicoletta Resta, Vittoria Disciglio, Cristiano Simone
Publikováno v:
Genes and Diseases, Vol 11, Iss 2, Pp 1084- (2024)
Externí odkaz:
https://doaj.org/article/85689712f5434c3caf431daeca8fc522
Autor:
Giovanna Forte, Antonia Lucia Buonadonna, Candida Fasano, Paola Sanese, Filomena Cariola, Andrea Manghisi, Anna Filomena Guglielmi, Martina Lepore Signorile, Katia De Marco, Valentina Grossi, Vittoria Disciglio, Cristiano Simone
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 14, p 7939 (2024)
Juvenile polyposis syndrome (JPS) is an inherited autosomal dominant condition that predisposes to the development of juvenile polyps throughout the gastrointestinal (GI) tract, and it poses an increased risk of GI malignancy. Germline causative vari
Externí odkaz:
https://doaj.org/article/997e30fbf6b448178cbf5ce9f1180fff
Autor:
Giovanna Forte, Filomena Cariola, Antonia Lucia Buonadonna, Anna Filomena Guglielmi, Andrea Manghisi, Katia De Marco, Valentina Grossi, Candida Fasano, Martina Lepore Signorile, Paola Sanese, Rosanna Bagnulo, Nicoletta Resta, Vittoria Disciglio, Cristiano Simone
Publikováno v:
Genes and Diseases, Vol 10, Iss 4, Pp 1187-1189 (2023)
Externí odkaz:
https://doaj.org/article/98534bd75c294ac18e9690010718e4ac
Autor:
Giovanna Forte, Antonia Lucia Buonadonna, Antonino Pantaleo, Candida Fasano, Donatella Capodiferro, Valentina Grossi, Paola Sanese, Filomena Cariola, Katia De Marco, Martina Lepore Signorile, Andrea Manghisi, Anna Filomena Guglielmi, Simonetta Simonetti, Nicola Laforgia, Vittoria Disciglio, Cristiano Simone
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 24, p 17388 (2023)
Classic galactosemia is an autosomal recessive inherited liver disorder of carbohydrate metabolism caused by deficient activity of galactose-1-phosphate uridylyltransferase (GALT). While a galactose-restricted diet is lifesaving, most patients still
Externí odkaz:
https://doaj.org/article/3fd2a20a98514403a8a3907c11b120ef
Autor:
Giovanna Forte, Filomena Cariola, Antonia Lucia Buonadonna, Anna Filomena Guglielmi, Andrea Manghisi, Katia De Marco, Valentina Grossi, Candida Fasano, Martina Lepore Signorile, Paola Sanese, Rosanna Bagnulo, Nicoletta Resta, Vittoria Disciglio, Cristiano Simone
Publikováno v:
Genes & Diseases.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96342a1972069b6c16e55e0a65d0fb22
https://doi.org/10.1016/j.gendis.2022.11.017
https://doi.org/10.1016/j.gendis.2022.11.017