Zobrazeno 1 - 10
of 2 941
pro vyhledávání: '"J, Pardo"'
Autor:
G. Ortega Suero, M.J. Abenza Abildúa, C. Serrano Munuera, I. Rouco Axpe, F.J. Arpa Gutiérrez, A.D. Adarmes Gómez, F.J. Rodríguez de Rivera, B. Quintans Castro, I. Posada Rodríguez, A. Vadillo Bermejo, Á. Domingo Santos, E. Blanco Vicente, I. Infante Ceberio, J. Pardo Fernández, E. Costa Arpín, C. Painous Martí, J.E. Muñoz García, P. Mir Rivera, F. Montón Álvarez, L. Bataller Alberola, J. Gascón Bayarri, C. Casasnovas Pons, V. Vélez Santamaría, A. López de Munain, G. Fernández-Eulate, J. Gazulla Abío, I. Sanz Gallego, L. Rojas Bartolomé, Ó. Ayo Martín, T. Segura Martín, C. González Mingot, M. Baraldés Rovira, R. Sivera Mascaró, E. Cubo Delgado, A. Echavarría Íñiguez, F. Vázquez Sánchez, M. Bártulos Iglesias, M.T. Casadevall Codina, E.M. Martínez Fernández, C. Labandeira Guerra, B. Alemany Perna, A. Carvajal Hernández, C. Fernández Moreno, M. Palacín Larroy, N. Caballol Pons, A. Ávila Rivera, F.J. Navacerrada Barrero, R. Lobato Rodríguez, M.J. Sobrido Gómez
Publikováno v:
Neurología (English Edition), Vol 38, Iss 6, Pp 379-386 (2023)
Introduction: Ataxia and hereditary spastic paraplegia are rare neurodegenerative syndromes. We aimed to determine the prevalence of these disorders in Spain in 2019. Patients and methods: We conducted a cross-sectional, multicentre, retrospective, d
Externí odkaz:
https://doaj.org/article/000cf9e7ad444bf8b554d5da8889bfaf
Autor:
G. Ortega Suero, M.J. Abenza Abildúa, C. Serrano Munuera, I. Rouco Axpe, F.J. Arpa Gutiérrez, A.D. Adarmes Gómez, F.J. Rodríguez de Rivera, B. Quintans Castro, I. Posada Rodríguez, A. Vadillo Bermejo, Á. Domingo Santos, E. Blanco Vicente, I. Infante Ceberio, J. Pardo Fernández, E. Costa Arpín, C. Painous Martí, J.E. Muñoz, P. Mir Rivera, F. Montón Álvarez, L. Bataller Alberola, J. Gascón Bayarri, C. Casasnovas Pons, V. Vélez Santamaría, A. López de Munain, G. Fernández-Eulate, J. Gazulla Abío, I. Sanz Gallego, L. Rojas Bartolomé, Ó. Ayo Martín, T. Segura Martín, C. González Mingot, M. Baraldés Rovira, R. Sivera Mascaró, E. Cubo Delgado, A. Echavarría Íñiguez, F. Vázquez Sánchez, M. Bártulos Iglesias, M.T. Casadevall Codina, E.M. Martínez Fernández, C. Labandeira Guerra, B. Alemany Perna, A. Carvajal Hernández, C. Fernández Moreno, M. Palacín Larroy, N. Caballol Pons, A. Ávila Rivera, F.J. Navacerrada Barrero, R. Lobato Rodríguez, M.J. Sobrido Gómez
Publikováno v:
Neurología, Vol 38, Iss 6, Pp 379-386 (2023)
Resume: Introducción: Las ataxias (AT) y paraparesias espásticas hereditarias (PEH) son síndromes neurodegenerativos raros. Nos proponemos conocer la prevalencia de las AT y PEH en España en 2019. Pacientes y métodos: Estudio transversal, multic
Externí odkaz:
https://doaj.org/article/399b955469194b76933f9adc5b6c7e9d
Autor:
L. I. Muñoz-Manchado, F. González-Saiz, J. I. Pérez-Revuelta, N. Laherrán-Cantera, R. J. Pardo-Velasco
Publikováno v:
European Psychiatry, Vol 66, Pp S446-S446 (2023)
Introduction Resistant schizophrenia is a schizophrenia subtype characterized by a non-ability to respond to an appropriate antipsychotic treatment in dosage and duration by the patients. These patients show a lower prognostic and symptomatology. The
Externí odkaz:
https://doaj.org/article/ad45c072c8ed4cad9eac283f0ed8c7bc
Publikováno v:
Analele Asociatiei Profesionale a Geografilor din Romania, Vol 12, Iss 12, Pp 5-27 (2021)
Unused industrial sites recovered for tourism in Spain have become one of the most visible aspects of tourist trends for several decades. Their basically local dimension has managed to boost the economy in the areas hit in the past by deindustrializa
Externí odkaz:
https://doaj.org/article/b294ac8d74004e3a8bdeaa95050611c4
Autor:
M. Cebey-López, M. J. Currás-Tuala, J. Gómez-Rial, I. Rivero-Calle, J. Pardo-Seco, R. Mendez-Gallart, S. Pischedda, A. Gómez-Carballa, R. Barral-Arca, A. Justicia-Grande, S. Viz-Lasheras, C. Rodríguez-Tenreiro, R. Gómez, A. Salas, F. Martinón-Torres
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundProgressive osseous heteroplasia (POH) is an ultrarare genetic disorder characterized by an inactivating mutation in the GNAS gene that causes heterotopic ossification. Inhibition of the mammalian target of the rapamycin (mTOR) signalling p
Externí odkaz:
https://doaj.org/article/739d029c73ca497da3f84a32bf92c5c3
Autor:
Hoz, Carlos J Pardo-De la1 (AUTHOR) cjpardodelahoz@gmail.com, Magain, Nicolas2 (AUTHOR), Piatkowski, Bryan3 (AUTHOR), Cornet, Luc2,4 (AUTHOR), Forno, Manuela Dal5 (AUTHOR), Carbone, Ignazio6 (AUTHOR), Miadlikowska, Jolanta1 (AUTHOR), Lutzoni, François1 (AUTHOR)
Publikováno v:
Systematic Biology. May2023, Vol. 72 Issue 3, p694-712. 19p.
Autor:
Maria J. Rodriguez, MD, Sebastian Gallo-Bernal, MD, Camilo A. Calixto, MD, Libardo Medina, MD, Elkin J. Pardo, MD, Mónica Ocampo González, MD
Publikováno v:
JACC: Case Reports, Vol 3, Iss 1, Pp 34-38 (2021)
Coronary artery fistulas are rare coronary abnormalities. Most of these fistulas have a congenital origin, and only a few are acquired. We report the case of a patient with late-acquired multiple coronary fistulas secondary to a stab wound, diagnosed
Externí odkaz:
https://doaj.org/article/c70c4bbca4cf4418ae778e797da13729
Publikováno v:
IEEE Access, Vol 9, Pp 138215-138224 (2021)
In recent years, there have been very important advances in graphic computing and technology related to the capture and representation of real objects in both 2 and 3 dimensions. One of these technologies is virtual reality, which can be incorporated
Externí odkaz:
https://doaj.org/article/d0015382635543fda2c015fb3b9ffb5e
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Autor:
Roberto Velasco, Santiago Mintegi, Carles Luaces, Mercedes de la Torre, Sebastià González, Javier Benito, Paula Vázquez, Izaskun Olaciregui, Carmen Campos, Sandra Moya, Andrés González, Carmen Vázquez, Olga Serrano, Carlos M. Angelats, Ramón Fernández, Jerónimo J. Pardo, Ester Castellarnau, Esther Ballester, Lizar Aguirre, Abel Martínez, Neus Pociello, Maria A. García, Miriam Gutiérrez, Pau Ventosa
Publikováno v:
Anales de Pediatría, Vol 93, Iss 2, Pp 124-127 (2020)
Externí odkaz:
https://doaj.org/article/6fbb3c276a8444ab834ed1b52bc609de