Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Patrizia Matarazzo"'
Autor:
Luisa De Sanctis, Patrizia Matarazzo, Daniele Tessaris, Massimiliano Bergallo, Ilaria Galliano, Paola Montanari
Publikováno v:
Hormone Research in Paediatrics. 87:342-349
Background/Aim: The McCune-Albright syndrome (MAS) is a potentially severe disorder hallmarked by fibrous bone dysplasia, café-au-lait skin spots, and endocrine hyperfunction. It is caused by postzygotic activating mutations at the R201 codon of the
McCune-Albright syndrome (MAS) is characterized by the triad of polyostotic bone fibrous dysplasia (PFD), endocrine disorders, and café-au-lait skin pigmentation. Ninety percent of MAS patients have fibrous dysplasia (FD) craniofacial lesions. Osteo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9465729ada82c97e244819440187310f
http://hdl.handle.net/2318/1556588
http://hdl.handle.net/2318/1556588
Autor:
Daniele Tessaris, Patrizia Matarazzo, L. de Sanctis, Malgorzata Wasniewska, Andrea Corrias, Roberto Lala, M. F. Messina, Maria Cristina Vigone
Publikováno v:
Hormone Research in Paediatrics. 78:151-157
Background: To date, there is no agreement about the frequency or the features of thyroid abnormalities in McCune-Albright syndrome (MAS). The aim of our study was to detect thyroid abnormalities in a cohort of MAS children and adolescents and to giv
Autor:
Roberto Lala, Luisa De Sanctis, Riccardo Guanà, Laura Valfrè, Patrizia Matarazzo, Roberto Gesmundo, Daniela Marzari
Publikováno v:
Scopus-Elsevier
Ovarian cysts are common in peripheral precocious puberty in McCune-Albright syndrome (MAS). The clinical course of these cysts is unpredictable due to episodes of hyperestrogenism typical of MAS ovarian hyperfunction. In persistent and recurrent lar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::966820022402f58b7d06abb4f8116799
http://hdl.handle.net/2318/110533
http://hdl.handle.net/2318/110533