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A Patient with Corticobasal Syndrome and Progressive Non-Fluent Aphasia (CBS-PNFA), with Variants in ATP7B, SETX, SORL1, and FOXP1 Genes.
Gaweda-Walerych, Katarzyna; Sitek, Emilia J; Borczyk, Malgorzata; Narozanska, Ewa; Brockhuis, Bogna; Korostynski, Michal; Schinwelski, Michal; Sieminski, Mariusz; Slawek, Jaroslaw; Zekanowski, Cezary.
Afiliación
  • Gaweda-Walerych K; Department of Neurogenetics and Functional Genomics, Mossakowski Medical Research Institute, Polish Academy of Sciences, 02-106 Warsaw, Poland.
  • Sitek EJ; Laboratory of Clinical Neuropsychology, Neurolinguistics and Neuropsychotherapy, Division of Neurological and Psychiatric Nursing, Faculty of Health Sciences, Medical University of Gdansk, 80-211 Gdansk, Poland.
  • Borczyk M; Neurology Department, St. Adalbert Hospital, Copernicus PL, 80-462 Gdansk, Poland.
  • Narozanska E; Laboratory of Pharmacogenomics, Department of Molecular Pharmacology, Maj Institute of Pharmacology Polish Academy of Sciences, 31-343 Krakow, Poland.
  • Brockhuis B; Neurology Department, St. Adalbert Hospital, Copernicus PL, 80-462 Gdansk, Poland.
  • Korostynski M; Department of Nuclear Medicine, Faculty of Health Sciences, Medical University of Gdansk, 80-214 Gdansk, Poland.
  • Schinwelski M; Laboratory of Pharmacogenomics, Department of Molecular Pharmacology, Maj Institute of Pharmacology Polish Academy of Sciences, 31-343 Krakow, Poland.
  • Sieminski M; Neurology Department, St. Adalbert Hospital, Copernicus PL, 80-462 Gdansk, Poland.
  • Slawek J; Neurocentrum Miwomed, 80-207 Gdansk, Poland.
  • Zekanowski C; Division of Neurological and Psychiatric Nursing, Faculty of Health Sciences, Medical University of Gdansk, 80-211 Gdansk, Poland.
Genes (Basel) ; 13(12)2022 12 14.
Article en En | MEDLINE | ID: mdl-36553628

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Afasia / Apraxias / Degeneración Corticobasal / Degeneración Hepatolenticular Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Genes (Basel) Año: 2022 Tipo del documento: Article País de afiliación: Polonia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Afasia / Apraxias / Degeneración Corticobasal / Degeneración Hepatolenticular Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Genes (Basel) Año: 2022 Tipo del documento: Article País de afiliación: Polonia