Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Emilio Fernández-Álvarez"'
Paediatric Movement Disorders is a relatively new and exciting field of Child Neurology. The present book represents the outcome of an international symposium, organized as a forum for exchange between both adult and child neurologists. The contribut
Autor:
Emilio Fernández Álvarez
Publikováno v:
Cuadernos de Música Iberoamericana; Vol 17 (2008); 23-60
Cuadernos de Música Iberoamericana; Vol. 17 (2008); 23-60
Revistas Científicas Complutenses
Universidad Complutense de Madrid (UCM)
Cuadernos de Música Iberoamericana, Vol 17, Iss 0, Pp 23-60 (2008)
Cuadernos de Música Iberoamericana; Vol. 17 (2008); 23-60
Revistas Científicas Complutenses
Universidad Complutense de Madrid (UCM)
Cuadernos de Música Iberoamericana, Vol 17, Iss 0, Pp 23-60 (2008)
This article is the first attempt at reconstructing the life and works of the composer José María de los Reyes Francesconi y Suffó, focusing on his Madrilenian period (1804-1809). Based on the study of documents held at the Biblioteca Nacional and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::917049b97b4021fe71edeb5964e459d0
https://revistas.ucm.es/index.php/CMIB/article/view/61137
https://revistas.ucm.es/index.php/CMIB/article/view/61137
Autor:
Emilio Fernández Álvarez
Publikováno v:
REVISTA DE NEUROLOGIA
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
Gracias a la aplicacion de modernas tecnicas como la siguiente secuenciacion (next-generation sequencing) en el estudio de encefalopatias aparentemente no heredadas ha sido posible descubrir mutaciones patogenas de novo en genes insospechados y defin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d139e2dc358cb9c7393f2f609c1926cd
http://fundanet.fsjd.org/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=14671
http://fundanet.fsjd.org/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=14671
Autor:
Rafael Artuch, Jaume Campistol, Maite García Silva, Bru Cormand, Mercè Pineda, Belén Pérez Dueñas, Lisbeth Birk Møller, Inés Carilho, Angeles Ruiz, Eduardo López Laso, M. Ribasés, Aida Ormazabal, Angels Garcia Cazorla, Clara Barbot, Emilio Fernández Álvarez
Publikováno v:
Medicina Clínica. 127:81-85
BACKGROUND AND OBJECTIVE: In the last few years, it has been described inborn errors of neurotransmitter and pterin metabolism and defects in folate and glucose transport across blood brain barrier. All these defects are classified as rare diseases a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5668d887ef0b715947bf0275d2a34b12
https://doi.org/10.1157/13090262
https://doi.org/10.1157/13090262
Autor:
J. Soler, María Canals, Emilio Fernández Álvarez, Juan José Vázquez, J. C. de Agustin, Dolores Rodríguez-Arnao
Publikováno v:
European Journal of Pediatric Surgery. 9:236-241
INTRODUCTION Innovative surgical and pharmacological therapeutic measures in short-bowel syndrome (SBS) are constantly changing the prognosis of this devastating condition. The aim of this paper is to present our most recent experience in the treatme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c7e1a9149ecc73d03f80139e330b052
https://doi.org/10.1055/s-2008-1072252
https://doi.org/10.1055/s-2008-1072252
Autor:
Mercedes, Serrano, Mónica, Rebollo, Christel, Depienne, Agnès, Rastetter, Emilio, Fernández-Álvarez, Jordi, Muchart, Loreto, Martorell, Rafael, Artuch, José A, Obeso, Belén, Pérez-Dueñas
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 27(10)
Thiamine transporter-2 deficiency, a condition resulting from mutations in the SLC19A3 gene, has been described in patients with subacute dystonia and striatal necrosis. The condition responds extremely well to treatment with biotin and has thus been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::70de93fdb60e1cdeea6c2325d7b7cbcd
https://pubmed.ncbi.nlm.nih.gov/22777947
https://pubmed.ncbi.nlm.nih.gov/22777947
Movement disorders in children: a clinical update with video recordings covers a wide range of disease conditions that are characterized by involuntary movements possibly associated with signs of more diffuse dysfunction of the nervous system.These i
Autor:
Emilio Fernández Álvarez
Publikováno v:
Revista de Neurología. 40:S075
Pacientes y metodos. Se recogen 16 casos de trastornos del movimiento de origen funcional en ninos y adolescentes menores de 18 anos. Corresponden al 2,4% de una serie personal de trastornos del movimiento en sujetos menores de 18 anos. Resultados. L
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64581477937c8636c89c5cb9b709da95
https://doi.org/10.33588/rn.40s01.2005086
https://doi.org/10.33588/rn.40s01.2005086
Autor:
Emilio Fernández Álvarez
Publikováno v:
Revista de Neurología. 36:54
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d01bc0ce75a39863eb2aed280385eed
https://doi.org/10.33588/rn.36s1.2003060
https://doi.org/10.33588/rn.36s1.2003060