Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Jose César Milisenda"'
Autor:
Yuji Hosono, Brandon Sie, Iago Pinal-Fernandez, Katherine Pak, Christopher A Mecoli, Maria Casal-Dominguez, Blake M Warner, Mariana J Kaplan, Jemima Albayda, Sonye Danoff, Thomas E Lloyd, Julie J Paik, Eleni Tiniakou, Rohit Aggarwal, Chester V Oddis, Siamak Moghadam-Kia, Carmelo Carmona-Rivera, Jose César Milisenda, Josep Maria Grau-Junyent, Albert Selva-O'Callaghan, Lisa Christopher-Stine, H Benjamin Larman, Andrew Lee Mammen
Publikováno v:
Annals of the Rheumatic Diseases. 82:246-252
ObjectivesIn dermatomyositis (DM), autoantibodies are associated with unique clinical phenotypes. For example, anti-TIF1γ autoantibodies are associated with an increased risk of cancer. The purpose of this study was to discover novel DM autoantibodi
Autor:
Judith Cantó‐Santos, Laura Valls‐Roca, Ester Tobías, Francesc Josep García‐García, Mariona Guitart‐Mampel, Anna Esteve‐Codina, Beatriz Martín‐Mur, Mercedes Casado, Rafael Artuch, Estel Solsona‐Vilarrasa, José Carlos Fernandez‐Checa, Carmen García‐Ruiz, Carles Rentero, Carlos Enrich, Pedro J. Moreno‐Lozano, José César Milisenda, Francesc Cardellach, Josep M. Grau‐Junyent, Glòria Garrabou
Publikováno v:
Journal of Cachexia, Sarcopenia and Muscle, Vol 14, Iss 2, Pp 964-977 (2023)
Abstract Background Inclusion body myositis (IBM) is an inflammatory myopathy clinically characterized by proximal and distal muscle weakness, with inflammatory infiltrates, rimmed vacuoles and mitochondrial changes in muscle histopathology. There is
Externí odkaz:
https://doaj.org/article/0f82886d569447a682acbe705f05bfcc
Autor:
Adriana Pané, Marcos Carrasco-Serrano, Camila Milad, Pere Leyes, Pedro Juan Moreno-Lozano, Roser Ventura, José Cesar Milisenda, Francesc Josep García-García, Glòria Garrabou, Judit García-Villoria, Rosa Maria López-Galera, Antonia Ribes, Josep Maria Grau-Junyent, Maria de Talló Forga-Visa, Cristina Montserrat-Carbonell, on behalf of PKU.CAT Consortium
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 23, p 7452 (2023)
Phenylketonuria (PKU) is the most frequent of the congenital errors of amino acid (AA) metabolism worldwide. It leads to the accumulation of the essential AA phenylalanine (Phe) and it is associated with severe neurological defects. The early diagnos
Externí odkaz:
https://doaj.org/article/24c38b1677484fd3bf1a41dbcc37b23e
Autor:
Sandra Muñoz-Braceras, Iago Pinal-Fernandez, Maria Casal-Dominguez, Katherine Pak, José César Milisenda, Shajia Lu, Massimo Gadina, Faiza Naz, Gustavo Gutierrez-Cruz, Stefania Dell’Orso, Jiram Torres-Ruiz, Josep Maria Grau-Junyent, Albert Selva-O’Callaghan, Julie J. Paik, Jemima Albayda, Lisa Christopher-Stine, Thomas E. Lloyd, Andrea M. Corse, Andrew L. Mammen
Publikováno v:
Cells, Vol 12, Iss 17, p 2198 (2023)
Dermatomyositis (DM), antisynthetase syndrome (AS), immune-mediated necrotizing myopathy (IMNM), and inclusion body myositis (IBM) are four major types of idiopathic inflammatory myopathy (IIM). Muscle biopsies from each type of IIM have unique trans
Externí odkaz:
https://doaj.org/article/430bca4e170c4fd7ba24d5229acce44e
Autor:
Judith Cantó-Santos, Laura Valls-Roca, Ester Tobías, Clara Oliva, Francesc Josep García-García, Mariona Guitart-Mampel, Félix Andújar-Sánchez, Anna Esteve-Codina, Beatriz Martín-Mur, Joan Padrosa, Raquel Aránega, Pedro J. Moreno-Lozano, José César Milisenda, Rafael Artuch, Josep M. Grau-Junyent, Glòria Garrabou
Publikováno v:
Antioxidants, Vol 12, Iss 8, p 1639 (2023)
Inclusion body myositis (IBM) is an acquired inflammatory myopathy affecting proximal and distal muscles that leads to weakness in patients over 50. It is diagnosed based on clinical and histological findings in muscle related to inflammation, degene
Externí odkaz:
https://doaj.org/article/0544446c413446e08d5fb26deb02142b
Autor:
Miriam Mayor-Echave-Sustaeta, Ana Matas-García, Ernesto Belmonte, José César Milisenda, Laura Morata, Javier Marco-Hernández
Publikováno v:
Medicina Clínica Práctica, Vol 4, Iss , Pp 100304- (2021)
Externí odkaz:
https://doaj.org/article/d49d5eeafd134bc8a3a8e77f221d6bd0
Autor:
Xavier Tomas, Diana Esteller, Juan Carlos Soler-Perromat, Lledó Cabedo, Jaime Isern-Kebschull, José César Milisenda
Publikováno v:
Medicina Clínica Práctica, Vol 4, Iss 3, Pp 100243- (2021)
Externí odkaz:
https://doaj.org/article/dea582b971774c93a5e5fdd06266d91b
Autor:
Diana Luz Juárez-Flores, Ingrid González-Casacuberta, Mario Ezquerra, María Bañó, Francesc Carmona-Pontaque, Marc Catalán-García, Mariona Guitart-Mampel, Juan José Rivero, Ester Tobias, Jose Cesar Milisenda, Eduard Tolosa, Maria Jose Marti, Ruben Fernández-Santiago, Francesc Cardellach, Constanza Morén, Glòria Garrabou
Publikováno v:
Journal of Translational Medicine, Vol 16, Iss 1, Pp 1-13 (2018)
Abstract Background Mutations in leucine rich repeat kinase 2 (LRRK2) are the most common cause of familial Parkinson’s disease (PD). Mitochondrial and autophagic dysfunction has been described as etiologic factors in different experimental models
Externí odkaz:
https://doaj.org/article/3b6607831b0d40529dfd25c7ca31b6a1
Autor:
Marc Catalán-García, Francesc Josep García-García, Pedro J. Moreno-Lozano, Gema Alcarraz-Vizán, Adrià Tort-Merino, José César Milisenda, Judith Cantó-Santos, Tamara Barcos-Rodríguez, Francesc Cardellach, Albert Lladó, Anna Novials, Glòria Garrabou, Josep M. Grau-Junyent
Publikováno v:
Journal of Clinical Medicine, Vol 9, Iss 5, p 1446 (2020)
Sporadic inclusion body myositis (sIBM) is an inflammatory myopathy associated, among others, with mitochondrial dysfunction. Similar molecular features are found in Alzheimer’s disease (AD) and Type 2 Diabetes Mellitus (T2DM), underlying potential
Externí odkaz:
https://doaj.org/article/f0c5d34edfdd4dcbabfdded9ffa91702