Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Roser Maria Pons"'
Autor:
Dolores Martínez-Rubio, Isabel Hinarejos, Paula Sancho, Nerea Gorría-Redondo, Raquel Bernadó-Fonz, Cristina Tello, Clara Marco-Marín, Itxaso Martí-Carrera, María Jesús Martínez-González, Ainhoa García-Ribes, Raquel Baviera-Muñoz, Isabel Sastre-Bataller, Irene Martínez-Torres, Anna Duat-Rodríguez, Patrícia Janeiro, Esther Moreno, Leticia Pías-Peleteiro, Mar O’Callaghan Gordo, Ángeles Ruiz-Gómez, Esteban Muñoz, Maria Josep Martí, Ana Sánchez-Monteagudo, Candela Fuster, Amparo Andrés-Bordería, Roser Maria Pons, Silvia Jesús-Maestre, Pablo Mir, Vincenzo Lupo, Belén Pérez-Dueñas, Alejandra Darling, Sergio Aguilera-Albesa, Carmen Espinós
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 19, p 11847 (2022)
Our clinical series comprises 124 patients with movement disorders (MDs) and/or ataxia with cerebellar atrophy (CA), many of them showing signs of neurodegeneration with brain iron accumulation (NBIA). Ten NBIA genes are accepted, although isolated c
Externí odkaz:
https://doaj.org/article/65e1319d27ad461db2e041f1cb14beef
Autor:
George Markousis-Mavrogenis, Michel Noutsias, Angelos G. Rigopoulos, Aikaterini Giannakopoulou, Stergios Gatzonis, Roser Maria Pons, Antigoni Papavasiliou, Vasiliki Vartela, Maria Bonou, Genovefa Kolovou, Constantina Aggeli, Aikaterini Christidi, Flora Bacopoulou, Dimitris Tousoulis, Sophie Mavrogeni
Publikováno v:
Journal of Clinical Medicine, Vol 11, Iss 14, p 4009 (2022)
Heart failure (HF) patients frequently develop brain deficits that lead to cognitive dysfunction (CD), which may ultimately also affect survival. There is an important interaction between brain and heart that becomes crucial for survival in patients
Externí odkaz:
https://doaj.org/article/9155e903cfb44e05bec8466ec009914c
Autor:
Emmanuel Kanavakis, Maria Svingou, Roser-Maria Pons, Sophia Kitsiou-Tzeli, Kyriaki Kekou, Christalena Sofocleous, Dimitris Petichakis, George K. Papadimas, Pelagia Vorgia, Artemis Gika
Publikováno v:
Molecular and cellular probes. 30(4)
Dystrophinopathies are allelic X-linked myopathies caused by large deletions/duplications or small lesions along the DMD gene. An unexpected dynamic trinucleotide (GAA) expansion, ranging from ∼59 to 82 pure GAA repeats, within the DMD intron 62, w