Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Daniela Sansone"'
Autor:
Elena Botta, Tiziana Nardo, Anja Raams, Judith Offman, Daniela Sansone, Wim J. Kleijer, Alain Sarasin, Nicolaas G. J. Jaspers, Giovanna Zambruno, Alan R. Lehmann, Paolo Balestri, Miria Stefanini, Roberta Ricotti
Publikováno v:
Human Mutation, 28(1), 92-96. Wiley-Liss Inc.
Trichothiodystrophy (TTD) is a rare autosomal recessive disorder whose defining feature is brittle hair. Associated clinical symptoms include physical and mental retardation of different severity, ichthyosis, premature aging, and, in half of the pati
Autor:
Antonio Bizzarro, Annamaria De Bellis, Mariangela Guaglione, Silvia Perrino, Antonio Bellastella, Concetta Coronella, Stefano Solimeno, Jack R. Wall, Daniela Sansone, Marisa Conte
Publikováno v:
Clinical Endocrinology. 59:388-395
Summary objective To investigate whether variations over time of TSH-receptor antibodies (TRAb) and antibodies against G2s (G2sAb) and extraocular muscles (EMAb) can predict worsening of ophthalmopathy in Graves’ patients treated with intravenous g
Autor:
Massimo Tonacchera, Daniela Sansone, Paolo Vitti, Aldo Pinchera, E. Ferrarini, Alessandra Capodanno, Antonio Dimida, Paola Collecchi, Giuseppina De Marco, Patrizia Agretti
Loss-of-function mutations of the thyrotropin receptor (TSHr) may be responsible for congenital hypothyroidism or isolated hyperthyreotropinemia. To study cell surface expression of inactivating TSHr mutations detected in patients with isolated hyper
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5434a9b142df8a0a9bc68f059be8d00
http://hdl.handle.net/11568/194774
http://hdl.handle.net/11568/194774
Autor:
Patrizia Agretti, Giuseppina De Marco, Alessandra Capodanno, Eleonora Ferrarini, Antonio Dimida, Daniela Sansone, Paola Collecchi, Aldo Pinchera, Paolo Vitti, Massimo Tonacchera
Publikováno v:
Thyroid; Sep2007, Vol. 17 Issue 9, p861-868, 8p