Zobrazeno 1 - 10
of 14
pro vyhledávání: '"David Moreno-Martinez"'
Publikováno v:
Medicine. 49:248-251
Publikováno v:
Molecular Genetics and Metabolism. 138:107229
Dysregulation of invariant natural killer T cells levels in a large cohort of Fabry disease patients
Publikováno v:
Molecular Genetics and Metabolism. 138:107257
Autor:
Daniel Moreno-Martinez, Maria Camprodon-Gomez, Sara Lucas-Del-Pozo, David Moreno-Martinez, Jorge Hernandez-Vara
Publikováno v:
Mov Disord Clin Pract
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::680b4f666de941495721ca768c0eae8a
https://europepmc.org/articles/PMC8414495/
https://europepmc.org/articles/PMC8414495/
Autor:
Daniel Moreno-Martinez, Manju A. Kurian, David Moreno-Martinez, Jennifer Friedman, Jorge Hernandez-Vara, Sara Lucas-Del-Pozo, Maria Camprodon-Gomez
Publikováno v:
Mov Disord Clin Pract
Autor:
Elena Arranz Canales, Elisenda Cortès-Saladelafont, Elena Martín-Hernández, Ricardo Gil Sánchez, Guillem Pintos-Morell, Javier Blasco-Alonso, Mónica A. López Rodríguez, David Moreno-Martinez, Encarna Guillén-Navarro, María Juliana Ballesta-Martínez, María Teresa García-Silva, María L. Couce, Pilar Quijada-Fraile, Montserrat Morales Conejo, Salvador García Morillo, Marc Moltó-Abad
Publikováno v:
ORPHANET JOURNAL OF RARE DISEASES
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Orphanet Journal of Rare Diseases
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
Scientia
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Orphanet Journal of Rare Diseases
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
Scientia
Background Mucopolysaccharidosis (MPS) IVA or Morquio A syndrome is a progressive and disabling disease characterized by a deficiency of the enzyme N-acetylgalactosamine-6-sulphate sulphatase. Its clinical presentation is very heterogeneous and poorl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6dcee367364b7e6201af39a9a13745d3
https://fundanet.iislafe.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=15195
https://fundanet.iislafe.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=15195
Autor:
Alessandro P. Burlina, Mark Thomas, Alison Muir, Michael West, Aleš Linhart, Sandro Feriozzi, Joan Fletcher, Ana Jovanovic, James C. Moon, R. Giugliani, João Paulo Oliveira, Juan Politei, Raphael Schiffmann, Michael Mauer, Daniel G. Bichet, Olivier Lidove, Guillem Pintos-Morell, Christiane Auray-Blais, Alberto Ortiz, Patricio Aguiar, Duncan Cole, Mathias Beck, Perry M. Elliott, Camilla Tøndel, Derralynn Hughes, David Moreno-Martinez, Albina Nowak, Mirjam Langeveld, Andrew Talbot, Einar Svarstad, David G. Warnock, Christoph Kampmann, Paula Rozenfeld, Ulla Feldt-Rasmussen
Publikováno v:
Molecular Genetics and Metabolism
Molecular Genetics and Metabolism, Elsevier, 2021, 132 (4), pp.234-243. ⟨10.1016/j.ymgme.2021.02.001⟩
Moreno-Martinez, D, Aguiar, P, Auray-Blais, C, Beck, M, Bichet, D G, Burlina, A, Cole, D, Elliott, P, Feldt-Rasmussen, U, Feriozzi, S, Fletcher, J, Giugliani, R, Jovanovic, A, Kampmann, C, Langeveld, M, Lidove, O, Linhart, A, Mauer, M, Moon, J C, Muir, A, Nowak, A, Oliveira, J P, Ortiz, A, Pintos-Morell, G, Politei, J, Rozenfeld, P, Schiffmann, R, Svarstad, E, Talbot, A S, Thomas, M, Tøndel, C, Warnock, D, West, M L & Hughes, D A 2021, ' Standardising clinical outcomes measures for adult clinical trials in Fabry disease : A global Delphi consensus ', Molecular Genetics and Metabolism, vol. 132, no. 4, pp. 234-243 . https://doi.org/10.1016/j.ymgme.2021.02.001
Molecular genetics and metabolism, 132(4), 234-243. Academic Press Inc.
Molecular Genetics and Metabolism, Elsevier, 2021, 132 (4), pp.234-243. ⟨10.1016/j.ymgme.2021.02.001⟩
Moreno-Martinez, D, Aguiar, P, Auray-Blais, C, Beck, M, Bichet, D G, Burlina, A, Cole, D, Elliott, P, Feldt-Rasmussen, U, Feriozzi, S, Fletcher, J, Giugliani, R, Jovanovic, A, Kampmann, C, Langeveld, M, Lidove, O, Linhart, A, Mauer, M, Moon, J C, Muir, A, Nowak, A, Oliveira, J P, Ortiz, A, Pintos-Morell, G, Politei, J, Rozenfeld, P, Schiffmann, R, Svarstad, E, Talbot, A S, Thomas, M, Tøndel, C, Warnock, D, West, M L & Hughes, D A 2021, ' Standardising clinical outcomes measures for adult clinical trials in Fabry disease : A global Delphi consensus ', Molecular Genetics and Metabolism, vol. 132, no. 4, pp. 234-243 . https://doi.org/10.1016/j.ymgme.2021.02.001
Molecular genetics and metabolism, 132(4), 234-243. Academic Press Inc.
International audience; Background: Recent years have witnessed a considerable increase in clinical trials of new investigational agents for Fabry disease (FD). Several trials investigating different agents are currently in progress; however, lack of
Autor:
Lucia Lavalle, Guillem Pintos-Morell, Uma Ramaswami, David Moreno-Martinez, Sara Lucas-Del-Pozo, Derralynn Hughes
Publikováno v:
Molecular Genetics and Metabolism. 129:S113-S114
Autor:
Karenth Milena, Rodríguez-Córdoba, Agreda-Soto, Sofia, Sebastián, Giraldo-Ocampo, David, Moreno-Martínez, Carolina, Pustovrh-María
Publikováno v:
In Placenta May 2022 122:19-19
Autor:
David Moreno-Martinez, Sara Lucas-Del-Pozo, Marc Moltó-Abad, Ariadna Tigri-Santiña, Carles Lorenzo-Bosquet, Guillem Pintos-Morell, Jorge Hernández-Vara
Publikováno v:
Molecular Genetics and Metabolism. 129:S102