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Akademický článek
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Akademický článek
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Publikováno v:
Revista de neurologia. 73(4)
Joubert syndrome is produced by an alteration of the ciliary proteins essential for the structure and function of neurons and organs such as the kidneys, liver, sight, and hearing. Some 34 mutations are currently known.Calculate the incidence / preva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b9c87ff32ca019d005464ecd921c4661
https://pubmed.ncbi.nlm.nih.gov/35484703
https://pubmed.ncbi.nlm.nih.gov/35484703
Publikováno v:
Revista de neurologia. 71(10)
Epileptic status represents the most frequent neurological emergency in pediatrics. Prolonged febrile seizures represent the most common etiology. Our objective is to update its epidemiology and analyze its evolutionary consequences.Observational ana
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a950ec677fc081fec267f779fd7c7ce5
https://pubmed.ncbi.nlm.nih.gov/33145747
https://pubmed.ncbi.nlm.nih.gov/33145747
Autor:
L, Aguilera-Nieto, J, Ferrero-Turrión, M D, Mora-Ramírez, R, Calvo-Medina, C, Ruiz-García, J M, Ramos-Fernández
Publikováno v:
Revista de neurologia. 71(2)
Dyskinesia of the ADCY5 mutation is a rare movement-onset disorder in childhood. It is characterized by isolated chorea movements or associated with myoclonus and dystonia affecting the limbs, neck and face. The low number of patients and families st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0675e4231485f8cca4ce80e24ef183ee
https://pubmed.ncbi.nlm.nih.gov/32627162
https://pubmed.ncbi.nlm.nih.gov/32627162
Autor:
Ana María García-Cabrera, M V Maestre-Sanchez, F. de la Portilla, R. M. Jimenez-Rodriguez, Francisco Javier Padillo-Ruiz, Jorge Manuel Vázquez-Monchul, A Araujo-Miguez, M. L. Reyes-Díaz, I Ramallo-Solís, M Ramos-Fernández, A Jiménez-Salido, José Manuel Díaz-Pavón
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
[Aim] To assess clinical healing in patients with perianal Crohn’s disease with local intrafistular injection of autologous platelet-rich plasma.
[Method] The pilot study was conducted at a single centre between January 2013 and December 2015.
[Method] The pilot study was conducted at a single centre between January 2013 and December 2015.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77f9a4ecae07161bc9c0d3f01844b04d
http://hdl.handle.net/10261/213973
http://hdl.handle.net/10261/213973
Autor:
F, de la Portilla, A, Jiménez-Salido, A, Araujo-Miguez, M V, Maestre-Sanchez, M L, Reyes-Diaz, I, Ramallo-Solís, M, Ramos-Fernández, J M, Vázquez-Monchul, A M, García-Cabrera, R M, Jimenez-Rodríguez, J M, Díaz-Pavón, F J, Padillo-Ruiz
Publikováno v:
Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract. 24(12)
To assess clinical healing in patients with perianal Crohn's disease with local intrafistular injection of autologous platelet-rich plasma.The pilot study was conducted at a single centre between January 2013 and December 2015. Autologous platelet-ri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3d56829ff35412e47b8755786b0d685a
https://pubmed.ncbi.nlm.nih.gov/31823319
https://pubmed.ncbi.nlm.nih.gov/31823319
Publikováno v:
Revista de Neurología. 73:115
Introduccion. El sindrome de Joubert se produce por una alteracion de las proteinas ciliares esenciales para la estructura y la funcion de neuronas y organos como los rinones, el higado, la retina y el oido. Se conocen unas 34 mutaciones en la actual
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c70d615950e7812670c0361ffd75e15e
https://doi.org/10.33588/rn.7304.2021066
https://doi.org/10.33588/rn.7304.2021066
Publikováno v:
Revista de Neurología. 71:365
Introduccion. El estado epileptico representa la emergencia neurologica mas frecuente en pediatria. Las convulsiones febriles prolongadas representan la etiologia mas frecuente. Nuestro objetivo es actualizar su epidemiologia y analizar sus consecuen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9775f217cd5882cdcaaf965d26162785
https://doi.org/10.33588/rn.7110.2020306
https://doi.org/10.33588/rn.7110.2020306
Autor:
J Ferrero-Turrión, J M Ramos-Fernández, M D Mora-Ramírez, R. Calvo-Medina, C Ruiz-García, L Aguilera-Nieto
Publikováno v:
Revista de Neurología. 71:69
Introduccion. La discinesia de la mutacion ADCY5 es un raro trastorno del movimiento de inicio en la infancia. Se caracteriza por movimientos coreicos aislados o asociados a mioclonias y distonias que afectan a las extremidades, el cuello y la cara.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd676c9760bf1516ec2ffa9ad3afa197
https://doi.org/10.33588/rn.7102.2020154
https://doi.org/10.33588/rn.7102.2020154