Zobrazeno 1 - 10
of 74
pro vyhledávání: '"José C, Milisenda"'
Autor:
Mónica López-Rodríguez, Miguel Angel Torralba-Cabeza, Iván Pérez de Pedro, Alberto Rivera, Roi Suarez Gil, Ana Gómez-Belda, Jose Luis Patier de la Peña, Alberto de los Santos Moreno, Albert Selva-O’Callaghan, Igor Gómez Gárate, Andrés González García, Roberto Hurtado, Pablo Tutor de Ureta, Miguel Ángel Barba-Romero, José C. Milisenda, Josep M. Grau-Junyent, POMPE study group
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-8 (2023)
Abstract Background The screening of high-risk populations using dried blood spots (DBS) has allowed the rapid identification of patients with Pompe disease, mostly in Neurology departments. The aim of the study was to determine the prevalence of lat
Externí odkaz:
https://doaj.org/article/8aaa538b7b294b509d6b3b97e1ce7ac7
Autor:
Ana Matas-Garcia, José C. Milisenda, Gerard Espinosa, Míriam Cuatrecasas, Albert Selva-O’Callaghan, Josep María Grau, Sergio Prieto-González
Publikováno v:
Diagnostics, Vol 12, Iss 5, p 1200 (2022)
Dermatomyositis is a systemic vasculopathy mainly affecting skin, muscle and lung, but may affect the gastrointestinal tract. We aim to describe clinical characteristics of patients with severe gastrointestinal involvement related to dermatomyositis
Externí odkaz:
https://doaj.org/article/6bb2367118b24988b9ca854dcac39bd2
Autor:
Ana Matas-García, Alfredo Guillén-Del-Castillo, Boris Kisluk, Albert Selva-O'Callaghan, Gerard Espinosa, Sergio Prieto-González, Pedro Moreno Lozano, Glòria Garrabou, Josep María Grau-Junyent, Carmen Pilar Simeon-Aznar, José C Milisenda
Publikováno v:
Rheumatology. 62:SI82-SI90
Objective The objective of this study was to analyse the clinico–serological and histological phenotypes of patients with SSc with associated myopathy. Methods From November 2002 to September 2020, 52 patients with SSc underwent a muscle biopsy for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50acd20370480f210d00b8b9da385651
https://doi.org/10.1093/rheumatology/keac361
https://doi.org/10.1093/rheumatology/keac361
Autor:
José C Milisenda, Iago Pinal-Fernandez, Thomas E Lloyd, Josep Maria Grau-Junyent, Lisa Christopher-Stine, Andrea M Corse, Andrew L Mammen
Publikováno v:
Rheumatology.
ObjectiveDiagnostic muscle biopsies are routinely immunostained for major histocompatibility complex class I (MHC-I) protein. In this study we analysed the prevalence and patterns of MHC-I immunostaining in biopsies from patients with different types
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89b810ad5281e9556b45b8873d7769d1
https://doi.org/10.1093/rheumatology/kead052
https://doi.org/10.1093/rheumatology/kead052
Publikováno v:
Current Opinion in Rheumatology. 33:544-553
Purpose of review Necrotizing myopathy is a broad term. It includes patients with the recently described immune-mediated necrotizing myopathies (IMNM) who have specific antibodies, such as anti-hydroxy-3-methylglutaryl-CoA reductase or anti-signal re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a83ca5668d1377da9da606b339fd05b
https://doi.org/10.1097/bor.0000000000000836
https://doi.org/10.1097/bor.0000000000000836
Autor:
Josep M. Grau, Ferran Seguí, José C. Milisenda, María José Cubillas Rodríguez, Ana Matas-García, Aurora Sánchez, Glòria Garrabou, Pia Gallano, Lidia Gonzalez-Quereda
Publikováno v:
Neurological Sciences. 41:2967-2971
Anoctamin 5 (ANO5) is a putative intracellular calcium-activated chloride channel. Recessive mutations in ANO5 may present from asymptomatic hyperCKemia and exercise-induced myalgia to proximal and/or distal muscle weakness. Here we describe the clin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e01e8989e03851aab9d29492addf467
https://doi.org/10.1007/s10072-020-04453-y
https://doi.org/10.1007/s10072-020-04453-y
Autor:
Ana, Matas-García, Alfredo, Guillén-Del-Castillo, Boris, Kisluk, Albert, Selva-O'Callaghan, Gerard, Espinosa, Sergio, Prieto-González, Pedro Moreno, Lozano, Glòria, Garrabou, Josep María, Grau-Junyent, Carmen Pilar, Simeon-Aznar, José C, Milisenda
Publikováno v:
Rheumatology (Oxford, England).
To analyze the clinico-serological and histological phenotype of patients with systemic sclerosis (SSc) with associated myopathy.From November 2002 to September 2020, 52 patients with SSc underwent a muscle biopsy for suspected myopathy. We establish
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1608eb68cd3870fb2d50543f838d2332
https://pubmed.ncbi.nlm.nih.gov/35713496
https://pubmed.ncbi.nlm.nih.gov/35713496
Autor:
Albert Selva O'Callaghan, José C. Milisenda, Iago Pinal-Fernandez, Josep M. Grau, Ana Matas García, Cristina Jou
Publikováno v:
Medicina Clínica. 153:437-440
Background and objectives Sporadic inclusion body myositis (sIBM) diagnosis is frequently delayed or confused with another class of disorders, and misdiagnosis is common. Sometimes, we have problems diagnosing an sIBM in the early stages or predictin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52ffac34367bab834d9ab316ab1428e2
https://doi.org/10.1016/j.medcli.2019.04.022
https://doi.org/10.1016/j.medcli.2019.04.022
Myositis Autoantigen Expression Correlates With Muscle Regeneration but Not Autoantibody Specificity
Autor:
David R. Amici, José C. Milisenda, Assia Derfoul, Andrea M. Corse, Maria Casal-Dominguez, Lisa Christopher-Stine, Andrew L. Mammen, Julie J. Paik, Jemima Albayda, Thomas E. Lloyd, Richard M Yeker, Iago Pinal-Fernandez, Albert Selva-O'Callaghan, Cassie A. Parks, Katherine Pak, Paul H. Plotz, Josep M. Grau-Junyent
Publikováno v:
Arthritis Rheumatol
Objective Although more than a dozen myositis-specific autoantibodies (MSAs) have been identified, most patients with myositis are positive for a single MSA. The specific overexpression of a given myositis autoantigen in myositis muscle has been prop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e7b253a972ac22b6bdcbfc159ac79d4
https://doi.org/10.1002/art.40883
https://doi.org/10.1002/art.40883
Publikováno v:
Medicina Clínica (English Edition). 158:567
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::845e2f481ff893361bd585582db23280
https://doi.org/10.1016/j.medcle.2022.01.007
https://doi.org/10.1016/j.medcle.2022.01.007