Zobrazeno 1 - 10 of 47 pro vyhledávání: '"F, Apollo"'
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Coexistence of variants in TBK1 and in other ALS-related genes elucidates an oligogenic model of pathogenesis in sporadic ALS
Autor: Marcella Zollino, Giuseppe Marangi, Paolo Niccolò Doronzio, Nilo Riva, Dante Lamberti, Stefania Scarlino, Amelia Conte, Daniela Bernardo, Laura Pozzi, Christian Lunetta, Giulia Bisogni, Mario Sabatelli, Sara Patrizi, Tommaso Russo, Serena Lattante, F. Apollo
Publikováno v: Neurobiology of aging. 84
Variants in tank-binding kinase 1 (TBK1) are responsible for a significant proportion of amyotrophic lateral sclerosis (ALS) cases. In the present study, we analyzed variants in TBK1 extracted by targeted sequencing of 32 genes in a group of 406 Ital
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55ff6d51f4f11d2bfb528cab7d70351a
https://pubmed.ncbi.nlm.nih.gov/31000212
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The international classification of the epilepsies and epileptic syndromes
Autor: Ettore Beghi, F. Apollo, Giuseppe Rinaldi, Michele Zarrelli, Michele Germano, Piero Di Viesti, P. Simone
Publikováno v: Epilepsy Research. 41:223-234
An algorithm has been structured as a guided reading of the international league against epilepsy (ILAE) syndromic classification to be used in clinical practice by less experienced physicians in newly diagnosed patients. The algorithm followed the o
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::51892e5a00a333456c0e9f518ebb69f6
https://doi.org/10.1016/s0920-1211(00)00147-9
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6
Morbidity in patients with epilepsy: type and complications: a European cohort study
Autor: Francesco Pisani, U. Runge, C.A. Defanti, Raffaele Manni, Antonio Gambardella, L. Moltrasio, Luigi Maria Specchio, S. Giubergia, M. Nikanorowa, N. Zanotta, E. Steuernagel, Peter Wolf, Giancarla Oteri, E. Ferreira, Gaetano Zaccara, S. Giovanni Rotondo, A.E.H. Sonnen, J. Griet, C. van Heijden, A. David, G. Castelnovo, R. Murelli, S. A. Gromov, L. Antonini, A. Mascarini, Barbara Frigeni, Giuliano Avanzini, T. Talvik, L. Mapelli, P. Zagnoni, F. Arienti, R. Thorbecke, E. Fiordelli, Elena Belousova, V. Mikhailov, Graziella Bogliun, Clara Tonini, Carlo Andrea Galimberti, Ettore Beghi, Nicola Specchio, Cesare Maria Cornaggia, M.C.T.F.M. de Krom, M.W.C. van den Broek, Mariska van den Broek, L. V. Lipatova, S.W. Brown, T. Levart, Umberto Aguglia, J.M. Lopes-Lima, H. Coyle, E. Boati, W. A. Hauser, N. Zupancic, Michele Zarrelli, A. Beilmann, Nr Alderley Edge, Messina C.E. Cavestro, P. Di Viesti, Concetta Russo, Mirco Cosottini, F. Apollo, E. Breviario, I.M. Ravnik, M.P. Pasolini, J.N. Loeber, Massimiliano Beghi, E. Biagi, P. Beleza, A. Tartara, P. Pinto
Publikováno v: Epilepsia. 45(1)
Summary: Purpose: To investigate the risk of illnesses in a cohort of patients with epilepsy and in matched nonepilepsy controls, by type and complications. Methods: A total of 951 children and adults with idiopathic, cryptogenic, or remote symptomat
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39c21dd60b9e81295e51df9212b460f5
https://pubmed.ncbi.nlm.nih.gov/14692910
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Arterial hypertension as a risk factor for chronic symmetric polyneuropathy
Autor: Di Viesti P, F. Apollo, Michele Zarrelli, Ettore Beghi, L. Amoruso, P. Simone
Publikováno v: Journal of epidemiology and biostatistics. 6(5)
OBJECTIVE To assess whether arterial hypertension (AH) is an independent risk factor for chronic symmetric polyneuropathy (CSP) in the elderly. BACKGROUND A strong relationship has been detected between AH and distal symmetric polyneuropathy in insul
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a073a9ab45ea29754bc12004338752c
https://pubmed.ncbi.nlm.nih.gov/11822730
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The international classification of the epilepsies and epileptic syndromes. An algorithm for its use in clinical practice
Autor: G, Rinaldi, M M, Zarrelli, E, Beghi, F, Apollo, M, Germano, P D, Viesti, P, Simone
Publikováno v: Epilepsy research. 41(3)
An algorithm has been structured as a guided reading of the international league against epilepsy (ILAE) syndromic classification to be used in clinical practice by less experienced physicians in newly diagnosed patients. The algorithm followed the o
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c3e6b5f396decef46c064f8d0b1e04e6
https://pubmed.ncbi.nlm.nih.gov/10962213
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[Central core disease. Report of 2 cases in adults]
Autor: M, Bisceglia, S, Fusilli, F, Apollo, V, Attino, P, Simone
Publikováno v: Pathologica. 91(6)
"Central core disease" (CCD) is a rare disease of infancy and childhood and represents the prototypic member of a group of muscular disorders known as "congenital, benign (non progressive) myopathies". It is very uncommon to diagnose cases affected b
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::210c05d48501355ee8ea41f656fef90b
https://pubmed.ncbi.nlm.nih.gov/10783639
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Myasthenia gravis during interferon alfa therapy
Autor: M.T. Palmisani, F. Apollo, Amelia Evoli, Serenella Servidei, Anna Paola Batocchi, Pietro Attilio Tonali
Patients treated with interferon alfa can develop autoantibodies and autoimmune diseases. We describe two patients who developed myasthenia gravis with abnormal levels of serum anti-acetylcholine receptor antibodies during interferon alfa-2b treatmen
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b55d308143be5d3bc34122df47007591
http://hdl.handle.net/10807/19016
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