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Screening for Fabry disease in unknown origin axonal polyneuropathy: to do or not to do, this is the question!
Rota, Eugenia; Grandis, Marina; Di Sapio, Alessia; Ghiglione, Elisabetta; Fiorentino, Pietro; Repetto, Alessandra; Giliberto, Claudia; Gemelli, Chiara; Morelli, Nicola; Schenone, Angelo; Cocito, Dario.
Afiliación
  • Rota E; Neurology Unit, ASL Alessandria (AL), Via E. Raggio 12, 15067, Novi Ligure, AL, Italy. eugenia.rota.md@gmail.com.
  • Grandis M; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics and Maternal Infantile Sciences, University of Genoa, Genoa, Italy.
  • Di Sapio A; IRCCS Policlinico San Martino Hospital, Genoa, Italy.
  • Ghiglione E; Neurology Unit, Regina Montis Regalis Hospital, ASL CN1, Mondovì, CN, Italy.
  • Fiorentino P; Neurology Unit, ASL Alessandria (AL), Via E. Raggio 12, 15067, Novi Ligure, AL, Italy.
  • Repetto A; Neurology Unit, ASL Alessandria (AL), Via E. Raggio 12, 15067, Novi Ligure, AL, Italy.
  • Giliberto C; Neurology Unit, ASL Alessandria (AL), Via E. Raggio 12, 15067, Novi Ligure, AL, Italy.
  • Gemelli C; Neurology Unit, Regina Montis Regalis Hospital, ASL CN1, Mondovì, CN, Italy.
  • Morelli N; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics and Maternal Infantile Sciences, University of Genoa, Genoa, Italy.
  • Schenone A; Neurology and Radiology Unit, Guglielmo da Saliceto Hospital, AUSLPC, Piacenza, PC, Italy.
  • Cocito D; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics and Maternal Infantile Sciences, University of Genoa, Genoa, Italy.
Orphanet J Rare Dis ; 15(1): 216, 2020 08 20.
Article en En | MEDLINE | ID: mdl-32819406

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 2_ODS3 Problema de salud: 2_muertes_prematuras_enfermedades_notrasmisibles Asunto principal: Polineuropatías / Enfermedad de Fabry / Enfermedades del Sistema Nervioso Periférico Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Female / Humans / Male Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2020 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 2_ODS3 Problema de salud: 2_muertes_prematuras_enfermedades_notrasmisibles Asunto principal: Polineuropatías / Enfermedad de Fabry / Enfermedades del Sistema Nervioso Periférico Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Female / Humans / Male Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2020 Tipo del documento: Article País de afiliación: Italia
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