Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Pedro De Mingo"'
Publikováno v:
DIGITUM. Depósito Digital Institucional de la Universidad de Murcia
instname
instname
Tesis-Universidad de Murcia.
MEDICINA ESPINARDO. DEPOSITO. MU-Tesis 625.
Consulte la tesis en: BCA. GENERAL. DEPOSITO. T.M-1916.
MEDICINA ESPINARDO. DEPOSITO. MU-Tesis 625.
Consulte la tesis en: BCA. GENERAL. DEPOSITO. T.M-1916.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a5a732354e45312e71730d1cbd8ce613
http://hdl.handle.net/10201/33273
http://hdl.handle.net/10201/33273
Autor:
Mesones Peral, Jesús Enrique
Publikováno v:
DIGITUM. Depósito Digital Institucional de la Universidad de Murcia
instname
instname
Tesis-Universidad de Murcia.
MEDICINA ESPINARDO. DEPOSITO. MU-Tesis 764.
Consulte la tesis en: BCA. GENERAL. ARCHIVO UNIVERSITARIO. T.M. 2680.
MEDICINA ESPINARDO. DEPOSITO. MU-Tesis 764.
Consulte la tesis en: BCA. GENERAL. ARCHIVO UNIVERSITARIO. T.M. 2680.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::ab6a41b42e31fba75d69cd9913c5de67
http://hdl.handle.net/10201/31019
http://hdl.handle.net/10201/31019
Autor:
Emilio Geijo-Barrientos, Carlos Pastore-Olmedo, Pedro De Mingo, Miguel Blanquer, Joaquín Gómez Espuch, Francisca Iniesta, Natalia García Iniesta, Ana García-Hernández, Carlos Martín-Estefanía, Laura Barrios, José M. Moraleda, Salvador Martínez
Publikováno v:
Frontiers in Neuroscience, Vol 14 (2020)
BackgroundPreclinical studies suggest that stem cells may be a valuable therapeutic tool in amyotrophic lateral sclerosis (ALS). As it has been demonstrated that there are molecular changes at the end-plate during the early stages of motorneuron dege
Externí odkaz:
https://doaj.org/article/b4e8183a3e894de5bf2e18c2d1a7dffe
Autor:
Inmaculada Pérez-Sánchez, Juan Ramón Gimeno-Blanes, Guillermo Glover, Maria Elisa Nicolas Rocamora, María Sabater-Molina, Fuensanta Escudero, Pedro de Mingo Casado
Publikováno v:
Current Gene Therapy. 18:246-251
Duchenne muscular dystrophy is a disorder with variable expression caused by framedisrupting mutations in the dystrophin gene. It is characterized by progressive muscle weakness and dilated cardiomyopathy. In-frame dystrophin mutations cause a clinic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d5306bbb7adc03bad8bd40809cc809e
https://doi.org/10.2174/1566523218666180709125346
https://doi.org/10.2174/1566523218666180709125346
Autor:
Julia Guardiola, Francisco José Ruiz-López, Vicenta Saez, Francisca Iniesta, Pedro De Mingo, Miguel Blanquer, Joaquín Gómez-Espuch, Javier López-San Román, Virginia Izura, Salvador Martinez, José M. Moraleda
Publikováno v:
Respiratory Physiology & Neurobiology. 221:54-58
The safety of autologous bone marrow mononuclear cells (ABMNC) intraspinal infusion in amyotrophic lateral sclerosis (ALS) patients was evaluated considering breathing and sleep patterns. Patients between 20 and 65 years old were eligible if they had
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c836c7769fa67f1130a59cca0ba8f21
https://doi.org/10.1016/j.resp.2015.11.007
https://doi.org/10.1016/j.resp.2015.11.007
Autor:
Elena, Martínez-Cayuelas, Eduardo, Martínez-Salcedo, Helena, Alarcón-Martínez, Alberto, Puche-Mira, Rosario, Domingo-Jiménez, Pedro, de Mingo-Casado, Cristina, Serrano-García
Publikováno v:
Revista de neurologia. 60(7)
Hirayama disease is a rare children's muscular atrophy that affects young Asian males, with muscular atrophy usually in one of the upper limbs that progresses slowly and later stabilises. It is diagnosed by means of electromyographic/electroneurograp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::92a798c3e8ffa62c6e9dd99384e73556
https://pubmed.ncbi.nlm.nih.gov/25806480
https://pubmed.ncbi.nlm.nih.gov/25806480
Autor:
Salvador Martinez, Francisca Iniesta, Andrés Sánchez-Salinas, José Meca-Lallana, Ramón Villaverde, Maria Juliana Majado, Laura Vivancos, Javier Gil de Bernabé López, María Teresa Pardo Sáez, José M. Moraleda, Miguel A. Pérez-Espejo, Miguel Blanquer, Carmen Antúnez, Julia Guardiola, Pedro de la Rosa, José María García Santos, Juan F. Martínez-Lage, Silvia Torres del Río, Francisco José Ruiz-López, Rafael Carles, Pedro De Mingo, Joaquín Hernández, Virginia Izura, Patricia Bleda, Judith Jiménez, Joaquín Gómez-Espuch
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
Martínez, Salvador [et al.]
The objective of this article is to assess the safety of intraspinal infusion of autologous bone marrow mononuclear cells (BMNCs) and, ultimately, to look for histopathological signs of cellular neurotrophism in amyo
The objective of this article is to assess the safety of intraspinal infusion of autologous bone marrow mononuclear cells (BMNCs) and, ultimately, to look for histopathological signs of cellular neurotrophism in amyo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97647a1c488101e8536aff2e4e1aef13
http://hdl.handle.net/10261/67580
http://hdl.handle.net/10261/67580
Autor:
María Luisa Martínez-Navarro, Manuel Amorin-Díaz, Andres Fernández Barreiro, José Meca-Lallana, Pedro de Mingo-Casado
Publikováno v:
Clinical therapeutics. 32(6)
Background: Treatment with interferon-β (IFN-β) has been related to worsening of muscle spasticity in patients with multiple sclerosis (MS). However, there are no specific data on the effects of glatiramer acetate (GA) on spasticity. Objective: The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::421cdc2b3b460f4f09b738f265017f93
https://pubmed.ncbi.nlm.nih.gov/20637960
https://pubmed.ncbi.nlm.nih.gov/20637960
Autor:
Patricia Bleda, José María García Santos, Francisco José Ruíz López, Joaquín Gómez Espuch, Juan F. Martínez-Lage, Maria Juliana Majado, Villaverde Ramón, María Vicenta Sáez, Pedro de Mingo, Francisca Iniesta, José M. Moraleda, Miguel Ángel Pérez Espejo, Laura Vivancos, Rafael Carles, Virginia Izura, Andrés Sánchez Salinas, Miguel Blanquer, Salvador Martinez
Publikováno v:
Blood. 118:4393-4393
Abstract 4393 Background: Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease, characterised by loss of motoneurons (mns), and it has no cure. Cell therapy has neurotrophic effects in animal models and has been proposed as a dise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c41c7fb45d37bb8bec2a1291a7280f6f
https://doi.org/10.1182/blood.v118.21.4393.4393
https://doi.org/10.1182/blood.v118.21.4393.4393
Autor:
Blanquer, Miguel, Moraleda, Jose M., Iniesta, Francisca, Gómez-Espuch, Joaquín, Meca-Lallana, José, Villaverde, Ramón, Pérez-Espejo, Miguel Ángel, Ruíz-López, Francisco José, Santos, José María García, Bleda, Patricia, Izura, Virginia, Sáez, María, De Mingo, Pedro, Vivancos, Laura, Carles, Rafael, Jiménez, Judith, Hernández, Joaquín, Guardiola, Julia, Del Rio, Silvia Torres, Antúnez, Carmen
Publikováno v:
Stem Cells; Jun2012, Vol. 30 Issue 6, p1277-1285, 9p