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The oligogenic model of amyotrophic lateral sclerosis; phenotypes of three Tunisian families.
Sghaier, Ikram; Kacem, Imen; Ticozzi, Nicola; Mrabet, Saloua; Paverelli, Silvia; Abida, Youssef; Ratti, Antonia; Silani, Vincenzo; Gouider, Riadh.
Afiliação
  • Sghaier I; Neurology Department, LR18SP03, Clinical Investigation Center (CIC) "Neurosciences and Mental Health", Razi Hospital, Tunis, Tunisia.
  • Kacem I; Neurology Department, LR18SP03, Clinical Investigation Center (CIC) "Neurosciences and Mental Health", Razi Hospital, Tunis, Tunisia.
  • Ticozzi N; Faculty of Medicine of Tunis, University Tunis El Manar, Tunis, Tunisia.
  • Mrabet S; Department of Neurology and Laboratory of Neuroscience, Istituto Auxologico Italiano, IRCCS, Milano, Italy.
  • Paverelli S; Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Milano, Italy.
  • Abida Y; Neurology Department, LR18SP03, Clinical Investigation Center (CIC) "Neurosciences and Mental Health", Razi Hospital, Tunis, Tunisia.
  • Ratti A; Faculty of Medicine of Tunis, University Tunis El Manar, Tunis, Tunisia.
  • Silani V; Department of Neurology and Laboratory of Neuroscience, Istituto Auxologico Italiano, IRCCS, Milano, Italy.
  • Gouider R; Neurology Department, LR18SP03, Clinical Investigation Center (CIC) "Neurosciences and Mental Health", Razi Hospital, Tunis, Tunisia.
Clin Genet ; 102(6): 555-556, 2022 12.
Article em En | MEDLINE | ID: mdl-36028943

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esclerose Lateral Amiotrófica Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Clin Genet Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Tunísia

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esclerose Lateral Amiotrófica Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Clin Genet Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Tunísia