Zobrazeno 1 - 10
of 120
pro vyhledávání: '"Ignacio Pascual-Pascual"'
Autor:
Richard S. Finkel, Monique M. Ryan, Samuel Ignacio Pascual Pascual, John W. Day, Eugenio Mercuri, Darryl C. De Vivo, Richard Foster, Jacqueline Montes, Juliana Gurgel‐Giannetti, Drew MacCannell, Zdenek Berger
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 9, Iss 6, Pp 819-829 (2022)
Abstract Objective The long‐term favorable safety profile of nusinersen provides an opportunity to consider a higher dose. We report on the relationships between nusinersen cerebrospinal fluid (CSF) exposure, biomarker levels, and clinical efficacy
Externí odkaz:
https://doaj.org/article/0511be6ebada4f91a7caec4dbaa8c369
Autor:
Candela Machuca, Angel Vilches, Eleonora Clemente, Samuel Ignacio Pascual-Pascual, Arantxa Bolinches-Amorós, Ana Artero Castro, Carmen Espinos, Marian Leon, Pavla Jendelova, Slaven Erceg
Publikováno v:
Stem Cell Research, Vol 33, Iss , Pp 166-170 (2018)
The human iPSC cell line, CARS-FiPS4F1 (ESi064-A), derived from dermal fibroblast from the apparently healthy carrier of the mutation of the gene SACSIN, was generated by non-integrative reprogramming technology using OCT3/4, SOX2, CMYC and KLF4 repr
Externí odkaz:
https://doaj.org/article/6099d90be0f440dab9874731f3220b0f
Autor:
Candela Machuca Arellano, Angel Vilches, Eleonora Clemente, Samuel Ignacio Pascual-Pascual, Arantxa Bolinches-Amorós, Ana Artero Castro, Carmen Espinos, Marian Leon Rodriguez, Pavla Jendelova, Slaven Erceg
Publikováno v:
Stem Cell Research, Vol 31, Iss , Pp 249-252 (2018)
The human iPSC cell line, ARS-FiPS4F1 (ESi063-A), derived from dermal fibroblast from the patient autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) caused by mutations on the gene SACSIN, was generated by non-integrative reprogrammin
Externí odkaz:
https://doaj.org/article/0e4c7322f2a443f193c4de107a9fca4b
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
María Vázquez López, Pedro Castro de Castro, Nuria Gil Villanueva, Andrés José Alcaraz Romero, Samuel Ignacio Pascual Pascual
Publikováno v:
Anales de Pediatría, Vol 88, Iss 3, Pp 167-169 (2018)
Externí odkaz:
https://doaj.org/article/29220b2112274898bacacc92e3ca7b40
Autor:
María Vázquez López, Pedro Castro de Castro, Nuria Gil Villanueva, Andrés José Alcaraz Romero, Samuel Ignacio Pascual Pascual
Publikováno v:
Anales de Pediatría (English Edition), Vol 88, Iss 3, Pp 167-169 (2018)
Externí odkaz:
https://doaj.org/article/a1c9d68081b042fdb106aadc0a9298ca
Autor:
Ana Méndez-Echevarría, María Belén Caminoa, Teresa del Rosal, Inmaculada Casas, Francisco Pozo, Samuel Ignacio Pascual-Pascual, Mar García-Romero, Carmen Cámara, Cristina Calvo
Publikováno v:
Viruses, Vol 13, Iss 5, p 867 (2021)
Background: The impact of respiratory virus infection in patients diagnosed with ataxia-telangiectasia (A-T) has not been well studied. Methods: A prospective case control study was performed at a National Reference Unit for Primary Immunodeficiency
Externí odkaz:
https://doaj.org/article/1506ee36f2354af29fd67e0fbfd08c14
Autor:
Gloria Tapias, Mar García-Romero, Carlos Crespo, Maribel Cuesta, Carles Forné, Samuel Ignacio Pascual-Pascual
Publikováno v:
Farmacia Hospitalaria, Vol 40, Iss 5, Pp 412-426 (2016)
Objective: Cost-minimization analysis of onabotulinumtoxinA and abobotulinumtoxinA, taking into account the real dose administered to children with spasticity associated with dynamic equinus foot deformity due to cerebral palsy. Method: A single cent
Externí odkaz:
https://doaj.org/article/67ef647875d8414788beadb40524bdb2
Autor:
Irene Pulido-Valdeolivas, David Gómez-Andrés, Juan Andrés Martín-Gonzalo, Irene Rodríguez-Andonaegui, Javier López-López, Samuel Ignacio Pascual-Pascual, Estrella Rausell
Publikováno v:
PLoS ONE, Vol 13, Iss 3, p e0192345 (2018)
The Hereditary Spastic Paraplegias (HSP) are a group of heterogeneous disorders with a wide spectrum of underlying neural pathology, and hence HSP patients express a variety of gait abnormalities. Classification of these phenotypes may help in monito
Externí odkaz:
https://doaj.org/article/ca2c1267bd714f989a1a792a8015683b
Autor:
Walter Strobl, Tim Theologis, Reinald Brunner, Serdar Kocer, Elke Viehweger, Ignacio Pascual-Pascual, Richard Placzek
Publikováno v:
Toxins, Vol 7, Iss 5, Pp 1629-1648 (2015)
Botulinum toxin A (BoNT-A) is considered a safe and effective therapy for children with cerebral palsy (CP), especially in the hands of experienced injectors and for the majority of children. Recently, some risks have been noted for children with Gro
Externí odkaz:
https://doaj.org/article/1d91e312a21248e9ab2764ace4cb9fe3