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Intrathecal IgG synthesis: marker of progression in multiple sclerosis patients

Autor: Guillermo Izquierdo, Juan Luis Ruiz-Peña, J M Gata, G Navarro, M. D. Paramo, García-Moreno Jm, Gamero Ma, S Angulo

Publikováno v: Acta Neurologica Scandinavica. 105:158-163

Objectives We study the power of IgG synthesis value as a marker of disease activity in multiple sclerosis (MS). Material and methods Link index was calculated in 202 MS patients. Time between first, second and third attack and progression index (PI)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::cb6e13210dfb4ad048aa626a11c173f0
https://doi.org/10.1034/j.1600-0404.2002.1o009.x

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Differential cognitive impairment for diverse forms of multiple sclerosis

Autor: Pablo Duque, Guillermo Izquierdo, Encarnacion Vaquero, Gamero Ma, Manuel Vázquez-Marrufo, Javier J. Gonzalez-Rosa, Monica Borges, Carlos M. Gómez

Publikováno v: idUS. Depósito de Investigación de la Universidad de Sevilla
instname
BMC Neuroscience, Vol 7, Iss 1, p 39 (2006)
BMC Neuroscience

Background Cognitive impairment is a common feature in multiple sclerosis (MS) patients and occurs in 60% of all cases. Unfortunately, neurological examination does not always agree with the neuropsychological evaluation in determining the cognitive

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1222947daf956ff169a43e188cd6f41b
https://hdl.handle.net/10668/817

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Quality certification, firm performance and organizational structre in spanish hotel industry

Autor: Pertusa Ortega, Eva María, Tarí Guilló, Juan José, Pereira Moliner, Jorge, Molina Azorín, José Francisco, López Gamero, Mª Dolores

Publikováno v: UPCommons. Portal del coneixement obert de la UPC
Universitat Politècnica de Catalunya (UPC)
Intangible Capital; 2013: Vol.: 9 Núm.: 1

Objeto: La certificación en calidad puede ayudar a las empresas a mejorar su eficiencia y sus resultados. El objetivo de este artículo es analizar las diferencias entre los hoteles certificados y no certificados con relación al desarrollo de prác

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::7c344f183af58441ac6abab09c6953df
http://hdl.handle.net/2099/13253

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Placebo effect characteristics observed in a single, international, longitudinal study in Huntington's disease

Autor: Cubo, E, González, M, del Puerto, I, de Yébenes, Jg, Arconada, Of, Gabriel Galán, Jm, Ehdi, Sg, Zangerl, A, Seppi, K, Wenning, G, Poewe, W, Foeldy, D, Auff, E, Schober, T, Wenzel, K, Ott, E, Walli, J, Leblhuber, F, Dürr, A, Bloch, F, Messouak, O, Tallaksen, C, Dubois, B, Guillamo, Js, Bachoud Lévi, Ac, Engles, A, Krystkowiak, P, Destée, A, Memin, A, Thibaut Tanchou, S, Pasquier, F, Azulay, Jp, Demonet, Jf, Galitzky, M, Rascol, O, Mollion, H, Broussolle, E, Madigand, M, Lallement, F, Goizet, C, Tison, F, Arguillère, S, Viallet, F, Bakchine, S, Khoris, J, Pages, M, Camu, W, Resch, F, Hannequin, D, Durif, F, Saudeau, D, Autret, A, Andrich, J, Saft, C, Kraus, Ph, Przuntek, H, Ecker, D, Kramer, B, Landwehrmeyer, Gb, Ludolph, Ac, Priller, J, Meierkord, H, Kuznik, D, Dose, M, Squitieri, F, Albanese, A, Abbruzzese, Giovanni, Filla, A, van de Warrenburg, B, de Jong, D, Kremer, H, van Vugt, J, Grimbergen, Y, Roos, R, Gawel, M, Janik, P, Kowalczys, H, Pilczuk, B, Kwiecinski, H, Świat, M, Ochudło, S, Modestowicz, R, Niezgoda, A, Łukasik, M, Lukasik, M, García Ruiz, P, Descals, Am, Rojo, A, Fontán, A, Hernández, J, Cantarero, S, Fanjul, S, Alegre, J, Roldán, Sg, Mateo, D, Burguera, Ja, Solis, P, Calopa, M, Jaumà, S, Bas, J, Tolosa, E, Muñoz, Je, Gámez, J, Cervera, C, Zarranz, Jj, Lezcano, E, Gómez, Jc, Chacón, J, Dinca, L, Gamero, Ma, Redondo, L, Castro, A, Sesar, A, López del Val, J, López, E, Ríos, C, Castillio, V, Burgunder, Jm, Nirkko, A, Kälin, A, Vingerhoets, F, Wider, C.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3710::a9bdc3672ae61d9166ab914534506595
http://hdl.handle.net/11567/772905

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Weight loss in Huntington disease increases with higher CAG repeat number

Autor: Aziz, Na, van der Burg, Jm, Landwehrmeyer, Gb, Brundin, P, Stijnen, T, Ehdi, Sg, Roos, Ra, Zangerl, A, Seppi, K, Wenning, G, Poewe, W, Foeldy, D, Auff, E, Schober, T, Wenzel, K, Ott, E, Walli, J, Leblhuber, F, Dürr, A, Bloch, F, Messouak, O, Tallaksen, C, Dubois, B, Guillamo, Js, Bachoud Lévi, Ac, Engles, A, Krystkowiak, P, Destée, A, Memin, A, Thibaut Tanchou, S, Pasquier, F, Azulay, Jp, Demonet, Jf, Galitzky, M, Rascol, O, Mollion, H, Broussolle, E, Madigand, M, Lallement, F, Goizet, C, Tison, F, Arguillère, S, Viallet, F, Bakchine, S, Khoris, J, Pages, M, Camu, W, Resch, F, Hannequin, D, Durif, F, Saudeau, D, Autret, A, Andrich, J, Saft, C, Kraus, Ph, Przuntek, H, Ecker, D, Kramer, B, Ludolph, Ac, Priller, J, Meierkord, H, Kuznik, D, Dose, M, Squitieri, F, Albanese, A, Abbruzzese, Giovanni, Filla, A, van de Warrenburg, B, de Jong, D, Kremer, H, van Vugt, J, Grimbergen, Y, Roos, R, Gawel, M, Janik, P, Kowalczys, H, Pilczuk, B, Kwiecinski, H, Swiat, M, Ochudło, S, Modestowicz, R, Niezgoda, A, Łukasik, M, Garcia de Yébenes, J, García Ruiz, P, Martínez Descals, A, Rojo, A, Fontán, A, Hernández, J, Cantarero, S, Fanjul, S, Alegre, J, Giménez Roldán, S, Mateo, D, Burguera, Ja, Solis, P, Calopa, M, Jaumà, S, Bas, J, Tolosa, E, Muñoz, Je, Gámez, J, Cervera, C, Zarranz, Jj, Lezcano, E, Gómez, Jc, Chacón, J, Dinca, L, Gamero, Ma, Redondo, L, Castro, A, Sesar, A, López del Val, J, López, E, Ríos, C, Castillio, V, Burgunder, Jm, Nirkko, A, Kälin, A, Vingerhoets, F, Wider, C.

Huntington disease (HD) is a hereditary neurodegenerative disorder caused by an expanded number of CAG repeats in the huntingtin gene. A hallmark of HD is unintended weight loss, the cause of which is unknown. In order to elucidate the underlying mec

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20e5a04814e3611a0b3b4fc135c6f95c
http://hdl.handle.net/11588/476413

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Variable expression of cerebral cavernous malformations in carriers of a premature termination codon in exon 17 of the Krit1 gene

Autor: García-Moreno Jm, Guillermo Izquierdo, Gamero Ma, Francisca Solano, Miguel Lucas, Alzenire F Costa

Publikováno v: BMC Neurology
BMC Neurology, Vol 3, Iss 1, p 5 (2003)

Background Cerebral cavernous malformations (CCM) present as either sporadic or autosomal dominant conditions with incomplete penetrance of symptoms. Differences in genetic and environmental factors might be minimized among first-degree relatives. We

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b70760c00581cf36bda98a7a9e24a1b
https://doi.org/10.1186/1471-2377-3-5

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