Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Maura Mingoia"'
Autor:
Valeria Orrù, Valentina Serra, Michele Marongiu, Sandra Lai, Valeria Lodde, Magdalena Zoledziewska, Maristella Steri, Annalisa Loizedda, Monia Lobina, Maria Grazia Piras, Francesca Virdis, Giuseppe Delogu, Maria Giuseppina Marini, Maura Mingoia, Matteo Floris, Marco Masala, M. Paola Castelli, Rafaela Mostallino, Jessica Frau, Lorena Lorefice, Gabriele Farina, Marzia Fronza, Daniele Carmagnini, Elisa Carta, Silvy Pilotto, Paola Chessa, Marcella Devoto, Paolo Castiglia, Paolo Solla, Roberto Ignazio Zarbo, Maria Laura Idda, Maristella Pitzalis, Eleonora Cocco, Edoardo Fiorillo, Francesco Cucca
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
IntroductionDisease-modifying therapies (DMTs) have been shown to improve disease outcomes in multiple sclerosis (MS) patients. They may also impair the immune response to vaccines, including the SARS-CoV-2 vaccine. However, available data on both th
Externí odkaz:
https://doaj.org/article/f41a064daa884909ab3e4b4c89e00533
Autor:
Michela Simbula, Maria Francesca Manchinu, Maura Mingoia, Mauro Pala, Isadora Asunis, Cristian Antonio Caria, Lucia Perseu, Manan Shah, Merlin Crossley, Paolo Moi, Maria Serafina Ristaldi
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 34, Iss , Pp 102025- (2023)
Hemoglobin switching is a complex biological process not yet fully elucidated. The mechanism regulating the suppression of fetal hemoglobin (HbF) expression is of particular interest because of the positive impact of HbF on the course of diseases suc
Externí odkaz:
https://doaj.org/article/51a79e8cc1744969890ec07116199680
Autor:
Maria Laura Idda, Maristella Pitzalis, Valeria Lodde, Annalisa Loizedda, Jessica Frau, Monia Lobina, Magdalena Zoledziewska, Francesca Virdis, Giuseppe Delogu, Maria Giuseppina Marini, Maura Mingoia, Marco Masala, Lorena Lorefice, Marzia Fronza, Daniele Carmagnini, Elisa Carta, Silvy Pilotto, Paolo Castiglia, Paola Chessa, Sergio Uzzau, Gabriele Farina, Paolo Solla, Maristella Steri, Marcella Devoto, Edoardo Fiorillo, Matteo Floris, Roberto Ignazio Zarbo, Eleonora Cocco, Francesco Cucca
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Monitoring immune responses to SARS-CoV-2 vaccination and its clinical efficacy over time in Multiple Sclerosis (MS) patients treated with disease-modifying therapies (DMTs) help to establish the optimal strategies to ensure adequate COVID-19 protect
Externí odkaz:
https://doaj.org/article/428af1285e0f426b860885e0acd1d04d
Autor:
Maristella Pitzalis, Maria Laura Idda, Valeria Lodde, Annalisa Loizedda, Monia Lobina, Magdalena Zoledziewska, Francesca Virdis, Giuseppe Delogu, Federica Pirinu, Maria Giuseppina Marini, Maura Mingoia, Jessica Frau, Lorena Lorefice, Marzia Fronza, Daniele Carmagnini, Elisa Carta, Valeria Orrù, Sergio Uzzau, Paolo Solla, Federica Loi, Marcella Devoto, Maristella Steri, Edoardo Fiorillo, Matteo Floris, Ignazio Roberto Zarbo, Eleonora Cocco, Francesco Cucca
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
ObjectivesVaccination against COVID-19 is highly recommended to patients affected by multiple sclerosis (MS); however, the impact of MS disease-modifying therapies (DMTs) on the immune response following vaccination has been only partially investigat
Externí odkaz:
https://doaj.org/article/976ec4d72e4d4da4a9dfc6d093da9193
Publikováno v:
Journal of Pediatric and Neonatal Individualized Medicine, Vol 10, Iss 1, Pp e100113-e100113 (2020)
We report the case of a pregnant woman who underwent prenatal diagnosis by chorionic villi sampling for increased risk of trisomy 21 due to advanced age and abnormal results of the first trimester combined screening test. Karyotype analysis of the ch
Externí odkaz:
https://doaj.org/article/db186c6df655467e88c755bad9e7ab14
Autor:
Viola Alesi, Francesca Sessini, Silvia Genovese, Giusy Calvieri, Ester Sallicandro, Laura Ciocca, Maura Mingoia, Antonio Novelli, Paolo Moi
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 4, p 2106 (2021)
Distal Arthrogryposis type 5D (DA5D) is characterized by congenital contractures involving the distal joints, short stature, scoliosis, ptosis, astigmatism, and dysmorphic features. It is inherited in an autosomal recessive manner, and it is a result
Externí odkaz:
https://doaj.org/article/101af6808e8a44b5b84e28de109ef196
Autor:
Farid Boulad, Aurelio Maggio, Xiuyan Wang, Paolo Moi, Santina Acuto, Friederike Kogel, Chayamon Takpradit, Susan Prockop, Jorge Mansilla-Soto, Annalisa Cabriolu, Ashlesha Odak, Jinrong Qu, Keyur Thummar, Fang Du, Lingbo Shen, Simona Raso, Rita Barone, Rosario Di Maggio, Lorella Pitrolo, Antonino Giambona, Maura Mingoia, John K. Everett, Pascha Hokama, Aoife M. Roche, Vito Adrian Cantu, Hriju Adhikari, Shantan Reddy, Eric Bouhassira, Narla Mohandas, Frederic D. Bushman, Isabelle Rivière, Michel Sadelain
Publikováno v:
Nature Medicine. 28:63-70
Autor:
Jiaming Wang, M Franca Marongiu, Maura Mingoia, Laura Manunza, Isadora Asunis, M. Giuseppina Marini, Yuet Wai Kan, Yukio Nakamura, Annalisa Cabriolu, Paolo Moi, Cristian Antonio Caria, Francesco Cucca, Lin Ye, Ryo Kurita, M Carla Sollaino
Publikováno v:
British Journal of Haematology. 192:395-404
Hereditary persistence of fetal haemoglobin (HPFH) is the major modifier of the clinical severity of β-thalassaemia. The homozygous mutation c.-196 C>T in the Aγ-globin (HBG1) promoter, which causes Sardinian δβ0 -thalassaemia, is able to complet
Autor:
Francesca Sessini, Maura Mingoia, Paolo Moi, Ester Sallicandro, Viola Alesi, Laura Ciocca, Silvia Genovese, Antonio Novelli, Giusy Calvieri
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 2106, p 2106 (2021)
International Journal of Molecular Sciences
International Journal of Molecular Sciences
Distal Arthrogryposis type 5D (DA5D) is characterized by congenital contractures involving the distal joints, short stature, scoliosis, ptosis, astigmatism, and dysmorphic features. It is inherited in an autosomal recessive manner, and it is a result
Autor:
Maura, Mingoia, Cristian A, Caria, Lin, Ye, Isadora, Asunis, M Franca, Marongiu, Laura, Manunza, M Carla, Sollaino, Jiaming, Wang, Annalisa, Cabriolu, Ryo, Kurita, Yukio, Nakamura, Francesco, Cucca, Yuet W, Kan, M Giuseppina, Marini, Paolo, Moi
Publikováno v:
British journal of haematologyReferences. 192(2)
Hereditary persistence of fetal haemoglobin (HPFH) is the major modifier of the clinical severity of β-thalassaemia. The homozygous mutation c.-196 CT in the Aγ-globin (HBG1) promoter, which causes Sardinian δβ