Long-Term Outcome of a Series of Patients With Narcolepsy Type 1 and Comorbidity With Immunopathological and Autoimmune Diseases

Autor: Francisco J. Martinez-Orozco, Miguel Fernandez-Arquero, Jose L. Vicario, Laura Lillo-Triguero, Elena Ameyugo, Rosa Peraita-Adrados

Publikováno v: Journal of clinical medicine research. 14(8)

The aim of this study was to evaluate the long-term outcome of our series of narcolepsy type 1 (NT1) patients with comorbid autoimmune diseases (ADs) and other immunopathological diseases (IDs), focusing on the incidence of new ADs and IDs in this sa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa1735e180839cd0711ad7bd33f00376
https://pubmed.ncbi.nlm.nih.gov/36128006

Corticospinal tract and motor cortex degeneration in pure hereditary spastic paraparesis type 4 (SPG4)

Autor: Manuel Desco, Juan A Guzmán-De-Villoria, María-Jesús Sobrido, Daniel Martín de Blas, Luis Marcos-Vidal, Yasser Alemán-Gómez, Francisco Grandas, Agustín Lage-Castellanos, Susanna Carmona, Andrés Ordoñez Ugalde, José Luis Muñoz-Blanco, Irene Catalina, Laura Lillo, Beatriz Quintáns, Francisco J. Navas-Sánchez, Alberto Fernández-Pena

Publikováno v: Amyotrophic lateral sclerosisfrontotemporal degeneration. 23(1-2)

Objective: SPG4 is an autosomal dominant pure form of hereditary spastic paraplegia (HSP) caused by mutations in the SPAST gene. HSP is considered an upper motor neuron disorder characterized by progressive retrograde degeneration, or "dying-back" ph

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3dc626674de5fee4f740465dba70066
https://pubmed.ncbi.nlm.nih.gov/34894929

Thalamic atrophy in patients with pure hereditary spastic paraplegia type 4

Autor: Yasser Alemán-Gómez, Andrés Ordóñez-Ugalde, Manuel Desco, Beatriz Quintáns, Francisco Grandas, Susanna Carmona, María-Jesús Sobrido, Julia Romero, Francisco J. Navas-Sánchez, Pilar Fernández-García, Luis Marcos-Vidal, Julio Pardo, Laura Lillo, Alberto Fernández-Pena, Irene Catalina, Daniel Martín de Blas, Juan A Guzmán-De-Villoria, José Luis Muñoz-Blanco

Publikováno v: Journal of Neurology

SPG4 is an autosomal dominant pure form of hereditary spastic paraplegia (HSP) caused by mutations in the SPAST gene. HSP is considered an upper motor neuron disorder characterized by progressive spasticity and weakness of the lower limbs caused by d

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b2f20f283daf8db2ac325066a9e1bd9

A new incidence peak of childhood narcolepsy type 1 in 2013:a new perspective on the role of influenza virus?

Autor: Claudio L. Bassetti, Teresa Paiva, Johannes Mathis, Laura Lillo-Triguero, Yves Dauvilliers, Aleksandra Wierzbicka, Elena Antelmi, Jari K. Gool, António Martins da Silva, Mauro Manconi, Markku Partinen, Geert Mayer, Birgit Högl, Gert Jan Lammers, Rafael del Rio-Villegas, Lucie Barateau, Christian R. Baumann, Zhongxing Zhang, Pablo Medrano-Martínez, Corina Gorban, Eva Feketeova, Karel Sonka, José Haba-Rubio, Alex Iranzo, Rolf Fronczek, Joan Santamaria, Fabio Pizza, Rosa Peraita-Adrados, Francesca Canellas, Ramin Khatami, Sebastiaan Overeem, Peter Young, Carole Pesenti, Carles Gaig, Michel Lecendreux, Raphael Heinzer, Giuseppe Plazzi

Increased incidence rates of narcolepsy type 1 (NT1) after the 2009-2010 H1N1 influenza pandemic (pH1N1) have been reported world-wide. While some European countries found an association between the NT1 increase and H1N1 vaccination Pandemrix, report

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ef33c630e8a9cb182272556ebf7213c

Exploring the clinical features of narcolepsy type 1 versus narcolepsy type 2 from European Narcolepsy Network database with machine learning

Autor: Aleksandra Wierzbicka, Fabio Pizza, Francesca Canellas, António Martins da Silva, Rosa Peraita-Adrados, Ramin Khatami, Teresa Paiva, Laura Lillo-Triguero, Peter Young, Mauro Manconi, Joan Santamaria, Carles Gaig, Birgit Högl, Yves Dauvilliers, Elena Antelmi, Lucie Barateau, Alex Iranzo, Gianina Luca, Markku Partinen, Michel Lecendreux, Johannes Mathis, Geert Mayer, Carole Pesenti, Raphael Heinzer, Zhongxing Zhang, Pablo Medrano-Martínez, Claudio L. Bassetti, Giuseppe Plazzi, Christian R. Baumann, Gert Jan Lammers, Eva Feketeova, Karel Sonka, José Haba-Rubio, Rafael del Rio-Villegas, Corina Gorban, Sebastiaan Overeem, Rolf Fronczek

Publikováno v: Scientific reports, vol. 8, no. 1, pp. 10628
Scientific Reports
Scientific Reports, 8(1):10628. Nature Publishing Group
Scientific Reports, 8
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Scientific Reports, Nature Publishing Group, 2018, 8 (1), pp.10628. ⟨10.1038/s41598-018-28840-w⟩
Zhang, Zhongxing; Mayer, Geert; Dauvilliers, Yves; Plazzi, Giuseppe; Pizza, Fabio; Fronczek, Rolf; Santamaria, Joan; Partinen, Markku; Overeem, Sebastiaan; Peraita-Adrados, Rosa; da Silva, Antonio Martins; Sonka, Karel; Rio-Villegas, Rafael del; Heinzer, Raphael; Wierzbicka, Aleksandra; Young, Peter; Högl, Birgit; Bassetti, Claudio; Manconi, Mauro; Feketeova, Eva; ... (2018). Exploring the clinical features of narcolepsy type 1 versus narcolepsy type 2 from European Narcolepsy Network database with machine learning. Scientific Reports, 8(1), p. 10628. Nature Publishing Group 10.1038/s41598-018-28840-w
Scientific Reports, Vol 8, Iss 1, Pp 1-11 (2018)
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid

Narcolepsy is a rare life-long disease that exists in two forms, narcolepsy type-1 (NT1) or type-2 (NT2), but only NT1 is accepted as clearly defined entity. Both types of narcolepsies belong to the group of central hypersomnias (CH), a spectrum of p

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afbeb0c33337f191883b91c2cc18e206
https://doi.org/10.1038/s41598-018-28840-w