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Genetic mimics of cerebral palsy.
Pearson, Toni S; Pons, Roser; Ghaoui, Roula; Sue, Carolyn M.
Affiliation
  • Pearson TS; Department of Neurology, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Pons R; First Department of Pediatrics, National and Kapodistrian University of Athens, Aghia Sofia Hospital, Athens, Greece.
  • Ghaoui R; Department of Neurology, Royal Adelaide Hospital, Adelaide, South Australia, Australia.
  • Sue CM; Department of Neurogenetics, Kolling Institute, Royal North Shore Hospital and University of Sydney, St Leonards, NSW, Australia.
Mov Disord ; 34(5): 625-636, 2019 05.
Article in En | MEDLINE | ID: mdl-30913345
Subject(s)
Cerebral Palsy/diagnosis; Diagnosis, Differential; Movement Disorders/diagnosis; Adenylyl Cyclases/genetics; Ataxia/physiopathology; Ataxia Telangiectasia/diagnosis; Ataxia Telangiectasia/genetics; Ataxia Telangiectasia/physiopathology; Ataxia Telangiectasia/therapy; Brain/diagnostic imaging; Brain Diseases, Metabolic, Inborn/diagnosis; Brain Diseases, Metabolic, Inborn/genetics; Brain Diseases, Metabolic, Inborn/physiopathology; Brain Diseases, Metabolic, Inborn/therapy; Carbohydrate Metabolism, Inborn Errors/diagnosis; Carbohydrate Metabolism, Inborn Errors/genetics; Carbohydrate Metabolism, Inborn Errors/physiopathology; Carbohydrate Metabolism, Inborn Errors/therapy; Cerebral Palsy/physiopathology; Chorea/physiopathology; Creatine/deficiency; Creatine/genetics; Dyskinesias/diagnosis; Dyskinesias/genetics; Dyskinesias/physiopathology; Dyskinesias/therapy; Dystonia/physiopathology; Folic Acid Deficiency/diagnosis; Folic Acid Deficiency/genetics; Folic Acid Deficiency/physiopathology; Folic Acid Deficiency/therapy; GTP-Binding Protein alpha Subunits, Gi-Go/genetics; Humans; Hyperargininemia/diagnosis; Hyperargininemia/genetics; Hyperargininemia/physiopathology; Hyperargininemia/therapy; Lesch-Nyhan Syndrome/diagnosis; Lesch-Nyhan Syndrome/genetics; Lesch-Nyhan Syndrome/physiopathology; Lesch-Nyhan Syndrome/therapy; Magnetic Resonance Imaging; Mental Retardation, X-Linked/diagnosis; Mental Retardation, X-Linked/genetics; Mental Retardation, X-Linked/physiopathology; Mental Retardation, X-Linked/therapy; Monosaccharide Transport Proteins/deficiency; Monosaccharide Transport Proteins/genetics; Movement Disorders/genetics; Movement Disorders/physiopathology; Movement Disorders/therapy; Multiple Carboxylase Deficiency/diagnosis; Multiple Carboxylase Deficiency/genetics
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cerebral Palsy / Diagnosis, Differential / Movement Disorders Type of study: Diagnostic_studies / Prognostic_studies Language: En Journal: Mov Disord Journal subject: NEUROLOGIA Year: 2019 Document type: Article Affiliation country:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cerebral Palsy / Diagnosis, Differential / Movement Disorders Type of study: Diagnostic_studies / Prognostic_studies Language: En Journal: Mov Disord Journal subject: NEUROLOGIA Year: 2019 Document type: Article Affiliation country: