Zobrazeno 1 - 10
of 108
pro vyhledávání: '"Maria Luisa Martínez"'
Autor:
Óscar Fernández Fernández, Lucienne Costa-Frossard, Maria Luisa Martínez Ginés, Paloma Montero Escribano, José María Prieto González, Lluís Ramió-Torrentà, Yolanda Aladro, Ana Alonso Torres, Elena Álvarez Rodríguez, Andrés Labiano-Fontcuberta, Lamberto Landete Pascual, Ambrosio Miralles Martínez, Ester Moral Torres, Pedro Oliva-Nacarino
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
IntroductionThe Spasticity-Plus Syndrome (SPS) in multiple sclerosis (MS) refers to a combination of spasticity and other signs/symptoms such as spasms, cramps, bladder dysfunction, tremor, sleep disorder, pain, and fatigue. The main purpose is to de
Externí odkaz:
https://doaj.org/article/60412756c06b4332b1107302498e9bb2
Autor:
Antonio Portoles, Julián Benito-León, Jordi A Matias-Guiu, Jorge Matias-Guiu, Julio Prieto, Javier González-Rosa, Miguel Ángel Hernández, Maria Luisa Martínez-Ginés, Natalia Pérez-Macías, Iván Padrón
Publikováno v:
BMJ Open, Vol 14, Iss 1 (2024)
Introduction Fatigue is one of the most disabling symptoms of multiple sclerosis (MS), and effective treatments are lacking. Amantadine is one of the most used treatments, although its efficacy is under debate. Transcranial magnetic stimulation (TMS)
Externí odkaz:
https://doaj.org/article/77832c52d3de4cf3b40aca1b0b088cba
Autor:
Oscar Fernandez, Lucienne Costa-Frossard, Maria Luisa Martínez-Ginés, Paloma Montero, Jose María Prieto-González, Lluís Ramió-Torrentà
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Background: Multiple sclerosis (MS) treatment has radically improved over the last years; however, MS symptom management is still challenging. The novel Spasticity-Plus syndrome was conceptualized to frame several spasticity-related symptoms that can
Externí odkaz:
https://doaj.org/article/b83f8a3a99f94975b3b75a69f16eb915
Autor:
Ana Navas, Ricard Ferrer, Maria Luisa Martínez, Gemma Gomà, Gisela Gili, Jordi Masip, David Suárez, Antonio Artigas
Publikováno v:
Annals of Intensive Care, Vol 8, Iss 1, Pp 1-9 (2018)
Abstract Background Septic shock is a leading cause of death in critical patients. In patients with gram-negative septic shock, hemoperfusion with polymyxin B aims to remove endotoxins from plasma. We analyzed the clinical and biological response to
Externí odkaz:
https://doaj.org/article/e8a2ffdb39d247cd9eda348950dbe294
Autor:
Francisco Hernansanz Iglesias, Clara Alavedra Celada, Carmen Berbel Navarro, Lidia Palau Morales, Núria Albi Visus, Cristina Cobo Valverde, Vanessa Matias Dorado, Maria Luisa Martínez Muñoz, Carles Blay Pueyo, Esther Limón Ramírez, Raimon Milà Villaroel, Núria Montellà Jordana, Josep Maria Bonet Simó
Publikováno v:
International Journal of Integrated Care, Vol 18, Iss 2 (2018)
Background: Chronicity, and particularly complex care needs for people with chronic diseases is one of the main challenges of health systems. Objective: To determine the population prevalence of people with chronic diseases and complex care needs and
Externí odkaz:
https://doaj.org/article/17a57f20bd8a436b89ebd244f31cbd4c
Autor:
María Encarnación Gómez Sánchez, Fernando de Manueles Marcos, Maria Luisa Martínez Martínez, Roberto Vera Berón, Jose Manuel Azaña Défez
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 91, Iss 5 suppl 1, Pp 111-113 (2016)
Abstract Acral persistent papular mucinosis (APPM) is a rare subtype of localized lichen myxedematosus. It consists of small papules localized exclusively on the back of the hands, wrists and extensor aspects of distal forearms with no other clinical
Externí odkaz:
https://doaj.org/article/02fb65a2387d41c3b1d5aa3d40719687
Los registros de enfermedades en la investigación epidemiológica de las enfermedades raras en España
Autor:
Óscar Zurriaga Lloréns, Carmen Martínez García, Vanessa Arizo Luque, Maria José Sánchez Pérez, Julián Mauro Ramos Aceitero, Maria José García Blasco, Maria José Ferrari Arroyo, Lilisbeth Perestelo Pérez, Enrique Ramalle Gómara, Maria Luisa Martínez Frias, Manuel Posada de la Paz
Publikováno v:
Revista Española de Salud Pública, Vol 80, Iss 3, Pp 249-257 (2006)
Fundamento: En el caso de las enfermedades raras existen dificultades para utilizar herramientas como los registros de enfermedades. El objetivo de este trabajo es describir la situación de los registros sobre enfermedades raras en España. Mét
Externí odkaz:
https://doaj.org/article/68031bf71d7f41f6a655336ce9716106
Autor:
María Encarnación Gómez Sánchez, Maria Luisa Martínez Martínez, Jose Luis Agudo Mena, Luis Iñiguez De Onzoño Martín
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 92, Iss 5 suppl 1, Pp 113-114 (2017)
Abstract Osteoma cutis or cutaneous ossification is a rare entity characterized by the formation of bone in the skin. We present an isolated primary osteoma cutis located on the palm, an atypical location.
Externí odkaz:
https://doaj.org/article/bf6eaa83e20041439388f673dc0d51fa
Autor:
Maria Clara Bonaglia, Roberto Giorda, Silvana Beri, Cristina De Agostini, Francesca Novara, Marco Fichera, Lucia Grillo, Ornella Galesi, Annalisa Vetro, Roberto Ciccone, Maria Teresa Bonati, Sabrina Giglio, Renzo Guerrini, Sara Osimani, Susan Marelli, Claudio Zucca, Rita Grasso, Renato Borgatti, Elisa Mani, Cristina Motta, Massimo Molteni, Corrado Romano, Donatella Greco, Santina Reitano, Anna Baroncini, Elisabetta Lapi, Antonella Cecconi, Giulia Arrigo, Maria Grazia Patricelli, Chiara Pantaleoni, Stefano D'Arrigo, Daria Riva, Francesca Sciacca, Bernardo Dalla Bernardina, Leonardo Zoccante, Francesca Darra, Cristiano Termine, Emanuela Maserati, Stefania Bigoni, Emanuela Priolo, Armand Bottani, Stefania Gimelli, Frederique Bena, Alfredo Brusco, Eleonora di Gregorio, Irene Bagnasco, Ursula Giussani, Lucio Nitsch, Pierluigi Politi, Maria Luisa Martinez-Frias, Maria Luisa Martínez-Fernández, Nieves Martínez Guardia, Anna Bremer, Britt-Marie Anderlid, Orsetta Zuffardi
Publikováno v:
PLoS Genetics, Vol 7, Iss 7, p e1002173 (2011)
In this study, we used deletions at 22q13, which represent a substantial source of human pathology (Phelan/McDermid syndrome), as a model for investigating the molecular mechanisms of terminal deletions that are currently poorly understood. We charac
Externí odkaz:
https://doaj.org/article/5c43355a53914e768e4abdfa928036cf
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