Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Paul Alejandro Méndez"'
Autor:
Leydy Katherin Duque Suárez, Gerardo Quintana López, Paola Ximena Coral Alvarado, Paul Alejandro Méndez Patarroyo, Helena Groot deRestrepo, Valeriano López-Segura
Publikováno v:
Translational Medicine Communications, Vol 3, Iss 1, Pp 1-10 (2018)
Abstract Background Autoimmune diseases are syndromes characterized by an immune response against self-antigens. They are complex pathologies associated with a variety of genetic determinants, but these genes cannot fully explain the aetiology of aut
Externí odkaz:
https://doaj.org/article/b45be9fd71ad4c0a8cfd985386bb0cdb
Autor:
Hernán Darío Páez, Gerardo Quintana, Leidy Paola Prada, Paola Coral, Paul Alejandro Méndez, Fabio Andrés García
Publikováno v:
Revista Colombiana de Reumatología (English Edition). 26:63-67
Polyarteritis nodosa is part of the primary systemic vasculitis that specifically compromises vessels of medium caliber, and can affect virtually any organ. The diagnosis of this disease is based on clinical criteria, such as pain and weakness in the
Autor:
Hernán Darío Páez, Leidy Paola Prada, Paul Alejandro Méndez, Gerardo Quintana, Fabio Andrés García, Paola Coral
Publikováno v:
Revista Colombiana de Reumatología. 26:63-67
Resumen La poliarteritis nodosa hace parte de las vasculitis sistemicas primarias, especificamente compromete vasos de mediano calibre pudiendo afectar virtualmente a cualquier organo. El diagnostico de esta enfermedad se basa en criterios clinicos,
Autor:
Jose Fernando Molina, Paola Coral-Alvarado, Gerardo Quintana López, Jorge Alberto Galindo Díaz, Philippe Chalem, Paul Alejandro Méndez Patarroyo, Gerardo Muñetón López
Publikováno v:
Rheumatology. 54:104-112
OBJECTIVE The aim of this study was to design and validate LupusCol, an instrument for the evaluation of health-related quality of life (HRQoL) in Colombian adult patients with SLE. METHODS Items and domains of the initial instrument were defined. Pr
Autor:
Ricard Cervera, Gustavo Aroca, Paul Alejandro Méndez Patarroyo, Gerardo Quintana, Paola Coral-Alvarado, Antonio Iglesias-Gamarra, Philippe Chalem, Ariel Iván Ruiz
Publikováno v:
Autoimmunity Reviews. 9:750-755
Background In clinical practice, it is sometimes difficult to diagnose a relapse in patients suffering from systemic lupus erythematosus (SLE) and lupus nephritis (LN) having potential complications, including renal failure and death. Some immunologi
Autor:
José Félix Restrepo, Samanda Adriana Rojas, Federico Rondón, Álvaro Sánchez Contreras, Antonio Iglesias-Gamarra, Pablo Lorenzana, Paul Alejandro Méndez Patarroyo, Alejandro Manosalva
Publikováno v:
Journal of clinical rheumatology : practical reports on rheumaticmusculoskeletal diseases. 10(6)
Patients with Hashimoto thyroiditis may have neurologic manifestations that have been described in the literature for some decades now; these include psychiatric disorders, abnormal movements, and simulation of cerebrovascular events. Nuclear magneti
Autor:
Antonio Iglesias-Gamarra, Álvaro Sánchez Contreras, Paul Alejandro Méndez Patarroyo, Adriana Rojas-Villarraga, José Félix Restrepo
Publikováno v:
Journal of clinical rheumatology : practical reports on rheumaticmusculoskeletal diseases. 12(2)
BACKGROUND Paget disease of bone has an unknown etiology, having complex pathogenesis leading to increased bone resorption in the first phase and an excess of bone formation with more advanced disease. The disease has been associated to white ancestr
Autor:
Rojas-Villarraga, Adriana, Patarroyo, Paul Alejandro Méndez, Contreras, Alvaro Sánchez, Restrepo, José Félix, Iglesias-Gamarra, Antonio
Publikováno v:
Journal of Clinical Rheumatology; April 2006, Vol. 12 Issue: 2 p57-60, 4p
Autor:
Sánchez Contreras, Alvaro, Rojas, Samanda Adriana, Manosalva, Alejandro, Patarroyo, Paul Alejandro Méndez, Lorenzana, Pablo, Restrepo, Jose Félix, Iglesias-Gamarra, Antonio, Rondon, Federico
Publikováno v:
Journal of Clinical Rheumatology; December 2004, Vol. 10 Issue: 6 p339-343, 5p
Autor:
Antonio Iglesias-Gamarra, Paul Alejandro Méndez Patarroyo, José Félix Restrepo, Eric L. Matteson, Samanda Adriana Rojas, Federico Rondón
Publikováno v:
Journal of Autoimmune Diseases
Introduction Idiopathic systemic vasculitis represents a group of clinical entities having non-specific etiology with the common characteristic of acute or chronic inflammatory compromise of the small and large vessels walls, associated with fibrinoi