Zobrazeno 1 - 6
of 6
pro vyhledávání: '"María Rabasa Pérez"'
Autor:
Victoria Cerrada, Marta García-López, Sofía Alvarez-Galeano, Ana Moreno-Izquierdo, Alejandro Lucia, María Rabasa Pérez, Joaquín Arenas, M. Esther Gallardo
Publikováno v:
Stem Cell Research, Vol 49, Iss , Pp 102108- (2020)
Peripheral blood mononuclear cells (PBMCs) from a McArdle patient carrying a homozygous mutation in the PYGM gene: c.2392 T > C; p.Trp798Arg were used for the generation of the human iPSC line, IISHDOi007-A. For the delivery of the reprogramming fact
Externí odkaz:
https://doaj.org/article/794ddd10f01b43a8bbd4a4ec8227656d
Autor:
Santiago Fernández Fernández, Javier Ricardo Pérez Sánchez, Guillermo Hernández Pérez, María Rabasa Pérez, Cristina Guijarro Castro, Guilherme Carvalho Monteiro, Valentina Vélez-Santamaría, David García-Azorín, David Ezpeleta
Publikováno v:
Journal of Clinical Neuroscience. 101:112-117
We describea series of patients with COVID-19 who presented with seizures, reported in the Spanish Society of Neurology's COVID-19 Registry. This observational, descriptive,multicentre, registry-based study includes patients with confirmed COVID-19 w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::632b1def9fba932c546396ba2f03a80c
https://doi.org/10.1016/j.jocn.2022.05.013
https://doi.org/10.1016/j.jocn.2022.05.013
Autor:
Inés Fernández-Barriuso, Luis A. Rodríguez de Antonio, Inés González-Suárez, María Rabasa Pérez
Publikováno v:
Multiple Sclerosis and Related Disorders
Highlights • Para-infectious myelitis can occur as a result of Sars-Cov2 infection. • Transverse myeltis and longitudinally extensive myelitis cases were most frequently reported. • Covid-19 symptoms in myelitis cases varied from asymptomatic c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81269392c47439454f52b259478be48a
Autor:
Ana Moreno-Izquierdo, Victoria Cerrada, Sofía Alvarez-Galeano, Alejandro Lucia, M. Esther Gallardo, Marta García-López, María Rabasa Pérez, Joaquín Arenas
Publikováno v:
Stem Cell Research, Vol 49, Iss, Pp 102108-(2020)
Peripheral blood mononuclear cells (PBMCs) from a McArdle patient carrying a homozygous mutation in the PYGM gene: c.2392 T > C; p.Trp798Arg were used for the generation of the human iPSC line, IISHDOi007-A. For the delivery of the reprogramming fact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06d5ebdba6dd39361fb34f7030868401
http://www.sciencedirect.com/science/article/pii/S1873506120304098
http://www.sciencedirect.com/science/article/pii/S1873506120304098
Autor:
Diana Cantero, Juan Francisco Gonzalo Martínez, Cristina Domínguez-González, María Rabasa Pérez, Eduard Gallardo, Cinta Lleixà, Yolanda Ruano, Aurelio Hernández-Laín
Publikováno v:
Journal of the neurological sciences. 394
Introduction: Sarcoglycanopathies (LGMD 2C 2F) are a subgroup of limb-girdle muscular dystrophies (LGMD), caused by mutations in sarcoglycan genes. They usually have a childhood onset and rapidly progressive course with loss of ability to walk over 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6d893242a8e07167c7e25f63f78c038
https://pubmed.ncbi.nlm.nih.gov/30218921
https://pubmed.ncbi.nlm.nih.gov/30218921
Publikováno v:
Journal of the Neurological Sciences. 358:475-476
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b38575642d30395d1118a32afc9dd93
https://doi.org/10.1016/j.jns.2015.08.032
https://doi.org/10.1016/j.jns.2015.08.032