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Tytuł:
Lesion volume and spike frequency on EEG impact perfusion values in focal cortical dysplasia: a pediatric arterial spin labeling study.
Autorzy:
Gennari AG; Department of Neuropediatrics, University Children's Hospital Zurich, 75, 8032, Zurich, Switzerland.; MR-Research Centre, University Children's Hospital Zurich, Zurich, Switzerland.
Bicciato G; Department of Neuropediatrics, University Children's Hospital Zurich, 75, 8032, Zurich, Switzerland.; Department of Neurology, University Hospital Zurich, Zurich, Switzerland.
Lo Biundo SP; Department of Neuropediatrics, University Children's Hospital Zurich, 75, 8032, Zurich, Switzerland.
Kottke R; Department of Radiology, University Children's Hospital Zurich, Zurich, Switzerland.
Stefanos-Yakoub I; Department of Neuropediatrics, University Children's Hospital Zurich, 75, 8032, Zurich, Switzerland.
Cserpan D; Department of Neuropediatrics, University Children's Hospital Zurich, 75, 8032, Zurich, Switzerland.
O'Gorman Tuura R; MR-Research Centre, University Children's Hospital Zurich, Zurich, Switzerland.; University of Zurich, Zurich, Switzerland.; Children's Research Centre, University Children's Hospital Zurich, Zurich, Switzerland.
Ramantani G; Department of Neuropediatrics, University Children's Hospital Zurich, 75, 8032, Zurich, Switzerland. .; University of Zurich, Zurich, Switzerland. .; Children's Research Centre, University Children's Hospital Zurich, Zurich, Switzerland. .
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Źródło:
Scientific reports [Sci Rep] 2024 Mar 31; Vol. 14 (1), pp. 7601. Date of Electronic Publication: 2024 Mar 31.
Typ publikacji:
Journal Article
MeSH Terms:
Focal Cortical Dysplasia*
Epilepsy*/diagnostic imaging
Epilepsies, Partial*
Humans ; Child ; Spin Labels ; Electroencephalography/methods ; Magnetic Resonance Imaging/methods ; Perfusion
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Deep histopathology genotype-phenotype analysis of focal cortical dysplasia type II differentiates between the GATOR1-altered autophagocytic subtype IIa and MTOR-altered migration deficient subtype IIb.
Autorzy:
Honke J; Department of Neuropathology, Universitätsklinikum Erlangen, FAU Erlangen-Nürnberg, Erlangen, Germany.; Partner of the European Reference Network (ERN) EpiCARE, Barcelona, Spain.
Hoffmann L; Department of Neuropathology, Universitätsklinikum Erlangen, FAU Erlangen-Nürnberg, Erlangen, Germany.; Partner of the European Reference Network (ERN) EpiCARE, Barcelona, Spain.
Coras R; Department of Neuropathology, Universitätsklinikum Erlangen, FAU Erlangen-Nürnberg, Erlangen, Germany.; Partner of the European Reference Network (ERN) EpiCARE, Barcelona, Spain.
Kobow K; Department of Neuropathology, Universitätsklinikum Erlangen, FAU Erlangen-Nürnberg, Erlangen, Germany.; Partner of the European Reference Network (ERN) EpiCARE, Barcelona, Spain.
Leu C; Genomic Medicine Institute, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, 44195, USA.; Charles Shor Epilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, USA.; Department of Clinical and Experimental Epilepsy, Institute of Neurology, University College London, London, UK.; Department of Neurology, McGovern Medical School, UTHealth Houston, University of Texas, Houston, USA.
Pieper T; Center for Pediatric Neurology, Neurorehabilitation, and Epileptology, Schoen-Clinic, Vogtareuth, Germany.
Hartlieb T; Center for Pediatric Neurology, Neurorehabilitation, and Epileptology, Schoen-Clinic, Vogtareuth, Germany.; Research Institute for Rehabilitation, Transition, and Palliation, Paracelsus Medical University, Salzburg, Austria.
Bien CG; Department of Epileptology (Krankenhaus Mara), Medical School, Bielefeld University, Bielefeld, Germany.
Woermann F; Department of Epileptology (Krankenhaus Mara), Medical School, Bielefeld University, Bielefeld, Germany.
Cloppenborg T; Department of Epileptology (Krankenhaus Mara), Medical School, Bielefeld University, Bielefeld, Germany.
Kalbhenn T; Department of Epileptology (Krankenhaus Mara), Medical School, Bielefeld University, Bielefeld, Germany.; Department of Neurosurgery (Evangelisches Klinikum Bethel), Medical School, Bielefeld University, Bielefeld, Germany.
Gaballa A; Department of Epileptology (Krankenhaus Mara), Medical School, Bielefeld University, Bielefeld, Germany.
Hamer H; Partner of the European Reference Network (ERN) EpiCARE, Barcelona, Spain.; Epilepsy Center, Universitätsklinikum Erlangen, FAU Erlangen-Nürnberg, Erlangen, Germany.
Brandner S; Department of Neurosurgery, Universitätsklinikum Erlangen, FAU Erlangen-Nürnberg, Erlangen, Germany.
Rössler K; Department of Neurosurgery, Medical University of Vienna, Vienna General Hospital, Vienna, Austria.
Dörfler A; Department of Neuroradiology, Universitätsklinikum Erlangen, FAU Erlangen-Nürnberg, Erlangen, Germany.
Rampp S; Department of Neurosurgery, Universitätsklinikum Erlangen, FAU Erlangen-Nürnberg, Erlangen, Germany.; Department of Neuroradiology, Universitätsklinikum Erlangen, FAU Erlangen-Nürnberg, Erlangen, Germany.
Lemke JR; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Center for Rare Diseases, University of Leipzig Medical Center, Leipzig, Germany.
Baldassari S; Inserm, CNRS, APHP, Institut du Cerveau - Paris Brain Institute - ICM, Hôpital de La Pitié Salpêtrière, Sorbonne Université, Paris, France.
Baulac S; Inserm, CNRS, APHP, Institut du Cerveau - Paris Brain Institute - ICM, Hôpital de La Pitié Salpêtrière, Sorbonne Université, Paris, France.
Lal D; Genomic Medicine Institute, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, 44195, USA.; Charles Shor Epilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, USA.; Stanley Center for Psychiatric Research, Broad Institute of Harvard and M.I.T, Cambridge, MA, 02142, USA.; Cologne Center for Genomics (CCG), Medical Faculty of the University of Cologne, University Hospital of Cologne, 50931, Cologne, Germany.; Department of Clinical and Experimental Epilepsy, Institute of Neurology, University College London, London, UK.; Department of Neurology, McGovern Medical School, UTHealth Houston, University of Texas, Houston, USA.
Nürnberg P; Cologne Center for Genomics (CCG), Medical Faculty of the University of Cologne, University Hospital of Cologne, 50931, Cologne, Germany.
Blümcke I; Department of Neuropathology, Universitätsklinikum Erlangen, FAU Erlangen-Nürnberg, Erlangen, Germany. .; Partner of the European Reference Network (ERN) EpiCARE, Barcelona, Spain. .; Stanley Center for Psychiatric Research, Broad Institute of Harvard and M.I.T, Cambridge, MA, 02142, USA. .
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Źródło:
Acta neuropathologica communications [Acta Neuropathol Commun] 2023 Nov 09; Vol. 11 (1), pp. 179. Date of Electronic Publication: 2023 Nov 09.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Focal Cortical Dysplasia*
Epilepsy*/genetics
Drug Resistant Epilepsy*
Malformations of Cortical Development*/genetics
Child ; Humans ; TOR Serine-Threonine Kinases/genetics ; GTPase-Activating Proteins/genetics ; Genotype
SCR Disease Name:
Focal cortical dysplasia of Taylor
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Limbic network co-localization predicts pharmacoresistance in dysplasia-related epilepsy.
Autorzy:
Cohen NT; Center for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, DC, USA.
Chang P; Center for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, DC, USA.
Gholipour T; Center for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, DC, USA.
Oluigbo C; Center for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, DC, USA.
Vezina LG; Center for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, DC, USA.
Xie H; Center for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, DC, USA.
Zhang A; Division of Biostatistics and Study Methodology, Children's National Research Institute, Washington, DC, USA.
Gaillard WD; Center for Neuroscience Research, Children's National Hospital, The George Washington University School of Medicine, Washington, DC, USA.
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Źródło:
Annals of clinical and translational neurology [Ann Clin Transl Neurol] 2023 Nov; Vol. 10 (11), pp. 2161-2165. Date of Electronic Publication: 2023 Sep 12.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural
MeSH Terms:
Focal Cortical Dysplasia*
Epilepsy*/drug therapy
Epilepsy*/etiology
Child ; Humans ; Seizures ; Logistic Models ; Odds Ratio
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
WNT pathway in focal cortical dysplasia compared to perilesional nonlesional tissue in refractory epilepsies.
Autorzy:
Marinowic DR; Brain Institute of Rio Grande do Sul (BraIns), Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil. .; Graduate Program in Medicine and Health Sciences, Medical School, Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil. .; Graduate Program in Medicine, Pediatrics and Child Health, Medical School, Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil. .; Graduate Program in Biomedical Gerontology, Medical School, Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil. .
Zanirati GG; Brain Institute of Rio Grande do Sul (BraIns), Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil.; Graduate Program in Medicine, Pediatrics and Child Health, Medical School, Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil.
Xavier FAC; Brain Institute of Rio Grande do Sul (BraIns), Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil.; Graduate Program in Medicine and Health Sciences, Medical School, Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil.
Varella FJ; Brain Institute of Rio Grande do Sul (BraIns), Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil.; Graduate Program in Medicine, Pediatrics and Child Health, Medical School, Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil.
Azevedo SPDC; Brain Institute of Rio Grande do Sul (BraIns), Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil.
Ghilardi IM; Brain Institute of Rio Grande do Sul (BraIns), Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil.; Graduate Program in Medicine, Pediatrics and Child Health, Medical School, Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil.
Pereira-Neto NG; Epilepsy Surgery Program, São Lucas Hospital, Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil.
Koff MAE; Epilepsy Surgery Program, São Lucas Hospital, Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil.
Paglioli E; Epilepsy Surgery Program, São Lucas Hospital, Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil.
Palmini A; Brain Institute of Rio Grande do Sul (BraIns), Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil.; Epilepsy Surgery Program, São Lucas Hospital, Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil.
Abreu JG; Biomedical Science Institute - Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Machado DC; Brain Institute of Rio Grande do Sul (BraIns), Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil.; Graduate Program in Medicine and Health Sciences, Medical School, Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil.; Graduate Program in Biomedical Gerontology, Medical School, Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil.
da Costa JC; Brain Institute of Rio Grande do Sul (BraIns), Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil.; Graduate Program in Medicine and Health Sciences, Medical School, Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil.; Graduate Program in Biomedical Gerontology, Medical School, Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil.
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Źródło:
BMC neurology [BMC Neurol] 2023 Sep 26; Vol. 23 (1), pp. 338. Date of Electronic Publication: 2023 Sep 26.
Typ publikacji:
Journal Article
MeSH Terms:
Drug Resistant Epilepsy*/genetics
Drug Resistant Epilepsy*/surgery
Focal Cortical Dysplasia*
Humans ; Child ; Wnt Signaling Pathway/genetics ; beta Catenin ; Seizures
SCR Disease Name:
Focal cortical dysplasia of Taylor
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Expression of Cytoskeletal Proteins (GFAP, Vimentin), Proapoptotic Protein (Caspase-3) and Protective Protein (S100) in the Epileptic Focus in Adults and Children with Drug-Resistant Temporal Lobe Epilepsy Associated with Focal Cortical Dysplasia.
Autorzy:
Sitovskaya D; Polenov Neurosurgical Institute-Branch of Almazov National Medical Research Centre, 197341 St. Petersburg, Russia.; Department of Pathology with a Course of Forensic Medicine Named after D.D. Lochov, St. Petersburg State Pediatric Medical University, 194100 St. Petersburg, Russia.
Zabrodskaya Y; Polenov Neurosurgical Institute-Branch of Almazov National Medical Research Centre, 197341 St. Petersburg, Russia.; Department of Pathology, Mechnikov North-West State Medical University, 191015 St. Petersburg, Russia.
Parshakov P; International Laboratory of Intangible-Driven Economy, National Research University Higher School of Economics, 614070 Perm, Russia.
Sokolova T; Polenov Neurosurgical Institute-Branch of Almazov National Medical Research Centre, 197341 St. Petersburg, Russia.
Kudlay D; Department of Pharmacology, Institute of Pharmacy, I.M. Sechenov First Moscow State Medical University, 119991 Moscow, Russia.; NRC Institute of Immunology FMBA of Russia, 115552 Moscow, Russia.
Starshinova A; Polenov Neurosurgical Institute-Branch of Almazov National Medical Research Centre, 197341 St. Petersburg, Russia.
Samochernykh K; Polenov Neurosurgical Institute-Branch of Almazov National Medical Research Centre, 197341 St. Petersburg, Russia.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2023 Sep 23; Vol. 24 (19). Date of Electronic Publication: 2023 Sep 23.
Typ publikacji:
Journal Article
MeSH Terms:
Epilepsy, Temporal Lobe*/metabolism
Focal Cortical Dysplasia*
Epilepsy*/metabolism
Drug Resistant Epilepsy*
Humans ; Adult ; Child ; Vimentin/genetics ; Vimentin/metabolism ; Cytoskeletal Proteins/metabolism ; Apoptosis Regulatory Proteins/metabolism ; Caspase 3/metabolism ; Temporal Lobe/metabolism ; Glial Fibrillary Acidic Protein/metabolism ; Retrospective Studies
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Automatic Detection of Focal Cortical Dysplasia Using MRI: A Systematic Review.
Autorzy:
Jiménez-Murillo D; Grupo de investigación Máquinas Inteligentes y Reconocimiento de Patrones, Instituto Tecnológico Metropolitano, Medellín 050013, Colombia.
Castro-Ospina AE; Grupo de investigación Máquinas Inteligentes y Reconocimiento de Patrones, Instituto Tecnológico Metropolitano, Medellín 050013, Colombia.
Duque-Muñoz L; Grupo de investigación Máquinas Inteligentes y Reconocimiento de Patrones, Instituto Tecnológico Metropolitano, Medellín 050013, Colombia.
Martínez-Vargas JD; GIDITIC, Universidad EAFIT, Medellín 050022, Colombia.
Suárez-Revelo JX; Grupo de Investigación en Imágenes Médicas SURA, Ayudas Diagnósticas SURA, Carrera 48 # 26-50, Piso 2, Medellín 050021, Colombia.
Vélez-Arango JM; Grupo de Investigación en Imágenes Médicas SURA, Ayudas Diagnósticas SURA, Carrera 48 # 26-50, Piso 2, Medellín 050021, Colombia.
de la Iglesia-Vayá M; Biomedical Imaging Unit FISABIO-CIPF, Foundation for the Promotion of the Research in Healthcare and Biomedicine (FISABIO), Avda. de Catalunya, 21, 46020 Valencia, Spain.; Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM-G23), 28029 Madrid, Spain.
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Źródło:
Sensors (Basel, Switzerland) [Sensors (Basel)] 2023 Aug 10; Vol. 23 (16). Date of Electronic Publication: 2023 Aug 10.
Typ publikacji:
Systematic Review; Journal Article; Review
MeSH Terms:
Focal Cortical Dysplasia*
Humans ; Magnetic Resonance Imaging ; Neuroimaging ; Brain ; Software
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Identifying cellular markers of focal cortical dysplasia type II with cell-type deconvolution and single-cell signatures.
Autorzy:
Galvão IC; Department of Translational Medicine, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.; The Brazilian Institute of Neuroscience and Neurotechnology (BRAINN), Campinas, Brazil.
Kandratavicius L; Department of Pathology, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.; The Brazilian Institute of Neuroscience and Neurotechnology (BRAINN), Campinas, Brazil.
Messias LA; Department of Translational Medicine, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.; The Brazilian Institute of Neuroscience and Neurotechnology (BRAINN), Campinas, Brazil.
Athié MCP; Department of Translational Medicine, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.; The Brazilian Institute of Neuroscience and Neurotechnology (BRAINN), Campinas, Brazil.
Assis-Mendonça GR; Department of Pathology, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.; The Brazilian Institute of Neuroscience and Neurotechnology (BRAINN), Campinas, Brazil.
Alvim MKM; Department of Neurology, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, SP, Brazil.; The Brazilian Institute of Neuroscience and Neurotechnology (BRAINN), Campinas, Brazil.
Ghizoni E; Department of Neurology, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, SP, Brazil.; The Brazilian Institute of Neuroscience and Neurotechnology (BRAINN), Campinas, Brazil.
Tedeschi H; Department of Neurology, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, SP, Brazil.; The Brazilian Institute of Neuroscience and Neurotechnology (BRAINN), Campinas, Brazil.
Yasuda CL; Department of Neurology, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, SP, Brazil.; The Brazilian Institute of Neuroscience and Neurotechnology (BRAINN), Campinas, Brazil.
Cendes F; Department of Neurology, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, SP, Brazil.; The Brazilian Institute of Neuroscience and Neurotechnology (BRAINN), Campinas, Brazil.
Vieira AS; Department of Structural and Functional Biology, Institute of Biology, University of Campinas (UNICAMP), Campinas, Brazil.; The Brazilian Institute of Neuroscience and Neurotechnology (BRAINN), Campinas, Brazil.
Rogerio F; Department of Pathology, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.; The Brazilian Institute of Neuroscience and Neurotechnology (BRAINN), Campinas, Brazil.
Lopes-Cendes I; Department of Translational Medicine, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil.; The Brazilian Institute of Neuroscience and Neurotechnology (BRAINN), Campinas, Brazil.
Veiga DFT; Department of Translational Medicine, School of Medical Sciences, University of Campinas (UNICAMP), Campinas, Brazil. .; The Brazilian Institute of Neuroscience and Neurotechnology (BRAINN), Campinas, Brazil. .
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Źródło:
Scientific reports [Sci Rep] 2023 Aug 16; Vol. 13 (1), pp. 13321. Date of Electronic Publication: 2023 Aug 16.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Focal Cortical Dysplasia*
Malformations of Cortical Development, Group I*
Humans ; Gliosis ; Neuroglia
SCR Disease Name:
Focal cortical dysplasia of Taylor
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
The specific DNA methylation landscape in focal cortical dysplasia ILAE type 3D.
Autorzy:
Wang DD; Department of Pathology, Xuanwu Hospital, Capital Medical University, No. 45, Changchun Street, Xicheng District, Beijing, 100053, China.; Clinical Research Center for Epilepsy, Capital Medical University, Beijing, 100053, China.; National Center for Neurological Disorders, Beijing, 100053, China.
Katoch M; Department of Neuropathology, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
Jabari S; Department of Neuropathology, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
Blumcke I; Department of Neuropathology, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
Blumenthal DB; Biomedical Network Science Lab, Department of Artificial Intelligence in Biomedical Engineering, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
Lu DH; Department of Pathology, Xuanwu Hospital, Capital Medical University, No. 45, Changchun Street, Xicheng District, Beijing, 100053, China.; Clinical Research Center for Epilepsy, Capital Medical University, Beijing, 100053, China.; National Center for Neurological Disorders, Beijing, 100053, China.
Coras R; Department of Neuropathology, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
Wang YJ; Department of Pathology, Xuanwu Hospital, Capital Medical University, No. 45, Changchun Street, Xicheng District, Beijing, 100053, China.; Clinical Research Center for Epilepsy, Capital Medical University, Beijing, 100053, China.; National Center for Neurological Disorders, Beijing, 100053, China.
Shi J; Department of Neurosurgery, Tsinghua University Yuquan Hospital, Beijing, 100049, China.
Zhou WJ; Department of Neurosurgery, Tsinghua University Yuquan Hospital, Beijing, 100049, China.
Kobow K; Department of Neuropathology, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany. .
Piao YS; Department of Pathology, Xuanwu Hospital, Capital Medical University, No. 45, Changchun Street, Xicheng District, Beijing, 100053, China. .; Clinical Research Center for Epilepsy, Capital Medical University, Beijing, 100053, China. .; National Center for Neurological Disorders, Beijing, 100053, China. .
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Źródło:
Acta neuropathologica communications [Acta Neuropathol Commun] 2023 Aug 09; Vol. 11 (1), pp. 129. Date of Electronic Publication: 2023 Aug 09.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Focal Cortical Dysplasia*
Malformations of Cortical Development*/diagnostic imaging
Malformations of Cortical Development*/genetics
Epilepsy*/genetics
Drug Resistant Epilepsy*/pathology
Child ; Young Adult ; Humans ; Child, Preschool ; Retrospective Studies ; DNA Methylation ; Magnetic Resonance Imaging
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Identifying important factors for successful surgery in patients with lateral temporal lobe epilepsy.
Autorzy:
Kim JR; Department of Neurology, Neuroscience Center, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Jo H; Department of Neurology, Neuroscience Center, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Park B; Biomedical Statistics Center, Research Institute for Future Medicine, Samsung Medical Center, Seoul, South Korea.
Park YH; Department of Neurology, Neuroscience Center, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.; Department of Health Sciences and Technology, SAIHST, Sungkyunkwan University, Seoul, South Korea.; Department of Intelligent Precision Healthcare Convergence, Sungkyunkwan University, Suwon, South Korea.
Chung YH; Department of Neurology, Neuroscience Center, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Shon YM; Department of Neurology, Neuroscience Center, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.; Department of Health Sciences and Technology, SAIHST, Sungkyunkwan University, Seoul, South Korea.
Seo DW; Department of Neurology, Neuroscience Center, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Hong SB; Department of Neurology, Neuroscience Center, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Hong SC; Department of Neurosurgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Seo SW; Department of Neurology, Neuroscience Center, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.; Biomedical Statistics Center, Research Institute for Future Medicine, Samsung Medical Center, Seoul, South Korea.; Department of Health Sciences and Technology, SAIHST, Sungkyunkwan University, Seoul, South Korea.; Department of Intelligent Precision Healthcare Convergence, Sungkyunkwan University, Suwon, South Korea.
Joo EY; Department of Neurology, Neuroscience Center, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
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Źródło:
PloS one [PLoS One] 2023 Jun 29; Vol. 18 (6), pp. e0288054. Date of Electronic Publication: 2023 Jun 29 (Print Publication: 2023).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Epilepsy, Temporal Lobe*/diagnostic imaging
Epilepsy, Temporal Lobe*/surgery
Focal Cortical Dysplasia*
Humans ; Cerebral Cortical Thinning ; Retrospective Studies ; Seizures
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Ictal Bradycardia and Asystole in Sleep-Related Hypermotor Epilepsy: A Study of 200 Patients.
Autorzy:
Muccioli, Lorenzo (AUTHOR)
Bruschi, Giulia (AUTHOR)
Ferri, Lorenzo (AUTHOR)
Scarabello, Anna (AUTHOR)
Taruffi, Lisa (AUTHOR)
Di Vito, Lidia (AUTHOR)
Mostacci, Barbara (AUTHOR)
Provini, Federica (AUTHOR)
Calandra-Buonaura, Giovanna (AUTHOR)
Tinuper, Paolo (AUTHOR)
Licchetta, Laura (AUTHOR)
Bisulli, Francesca (AUTHOR)
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Źródło:
Journal of Clinical Medicine. Mar2024, Vol. 13 Issue 6, p1767. 12p.
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
An integrated genetic analysis of epileptogenic brain malformed lesions.
Autorzy:
Fujita A; Department of Human Genetics, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-Ku, Yokohama, 236-0004, Japan.
Kato M; Department of Pediatrics, Showa University School of Medicine, Tokyo, 142-8666, Japan.
Sugano H; Department of Neurosurgery, Epilepsy Center, Juntendo University, Tokyo, 113-8421, Japan.
Iimura Y; Department of Neurosurgery, Epilepsy Center, Juntendo University, Tokyo, 113-8421, Japan.
Suzuki H; Department of Neurosurgery, Epilepsy Center, Juntendo University, Tokyo, 113-8421, Japan.
Tohyama J; Department of Child Neurology, National Hospital Organization Nishiniigata Chuo Hospital, Niigata, 950-2085, Japan.
Fukuda M; Department of Functional Neurosurgery, Epilepsy Center, National Hospital Organization Nishiniigata Chuo Hospital, Niigata, 950-2085, Japan.
Ito Y; Department of Functional Neurosurgery, Epilepsy Center, National Hospital Organization Nishiniigata Chuo Hospital, Niigata, 950-2085, Japan.
Baba S; Department of Child Neurology, Comprehensive Epilepsy Center, Seirei Hamamatsu General Hospital, Hamamatsu, 430-8558, Japan.
Okanishi T; Division of Child Neurology, Department of Brain and Neurosciences, Faculty of Medicine, Tottori University, Yonago, 683-8503, Japan.
Enoki H; Department of Pediatrics, Kawasaki Medical School, Kurashiki, 701-0192, Japan.
Fujimoto A; Comprehensive Epilepsy Center, Seirei Hamamatsu General Hospital, Hamamatsu, 430-8558, Japan.
Yamamoto A; Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo, 060-8543, Japan.
Kawamura K; Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo, 060-8543, Japan.
Kato S; Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo, 060-8543, Japan.
Honda R; Department of Pediatrics, National Hospital Organization Nagasaki Medical Center, Omura, 856-8562, Japan.
Ono T; Epilepsy Center, National Hospital Organization Nagasaki Medical Center, Omura, 856-8562, Japan.
Shiraishi H; Department of Pediatrics, Hokkaido University Graduate School of Medicine, Sapporo, 060-8638, Japan.
Egawa K; Department of Pediatrics, Hokkaido University Graduate School of Medicine, Sapporo, 060-8638, Japan.
Shirai K; Department of Pediatrics, Tsuchiura Kyodo General Hospital, Tsuchiura, 300-0028, Japan.
Yamamoto S; Department of Neurosurgery, Tsuchiura Kyodo General Hospital, Tsuchiura, 300-0028, Japan.
Hayakawa I; Division of Neurology, National Center for Child Health and Development, Tokyo, 157-8535, Japan.
Kawawaki H; Department of Pediatric Neurology, Children's Medical Center, Osaka City General Hospital, Osaka, 534-0021, Japan.
Saida K; Department of Human Genetics, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-Ku, Yokohama, 236-0004, Japan.
Tsuchida N; Department of Human Genetics, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-Ku, Yokohama, 236-0004, Japan.; Department of Rare Disease Genomics, Yokohama City University Hospital, Yokohama, 236-0004, Japan.
Uchiyama Y; Department of Human Genetics, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-Ku, Yokohama, 236-0004, Japan.; Department of Rare Disease Genomics, Yokohama City University Hospital, Yokohama, 236-0004, Japan.
Hamanaka K; Department of Human Genetics, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-Ku, Yokohama, 236-0004, Japan.
Miyatake S; Department of Human Genetics, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-Ku, Yokohama, 236-0004, Japan.; Department of Clinical Genetics, Yokohama City University Hospital, Yokohama, 236-0004, Japan.
Mizuguchi T; Department of Human Genetics, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-Ku, Yokohama, 236-0004, Japan.
Nakashima M; Department of Human Genetics, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-Ku, Yokohama, 236-0004, Japan.; Department of Biochemistry, Hamamatsu University School of Medicine, Hamamatsu, 431-3192, Japan.
Saitsu H; Department of Human Genetics, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-Ku, Yokohama, 236-0004, Japan.; Department of Biochemistry, Hamamatsu University School of Medicine, Hamamatsu, 431-3192, Japan.
Miyake N; Department of Human Genetics, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-Ku, Yokohama, 236-0004, Japan.; Department of Human Genetics, Research Institute, National Center for Global Health and Medicine, Tokyo, 162-8655, Japan.
Kakita A; Department of Pathology, Brain Research Institute, Niigata University, Niigata, 951-8585, Japan.
Matsumoto N; Department of Human Genetics, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-Ku, Yokohama, 236-0004, Japan. .
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Źródło:
Acta neuropathologica communications [Acta Neuropathol Commun] 2023 Mar 02; Vol. 11 (1), pp. 33. Date of Electronic Publication: 2023 Mar 02.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Nervous System Malformations*
Malformations of Cortical Development, Group I*/genetics
Brain Neoplasms*
Focal Cortical Dysplasia*
Humans ; Brain
SCR Disease Name:
Focal cortical dysplasia of Taylor
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
The clinico-pathological characterisation of focal cortical dysplasia type IIb genetically defined by MTOR mosaicism.
Autorzy:
Wang Y; Department of Pathology, Xuanwu Hospital, Capital Medical University, Beijing, China.; Clinical Research Center for Epilepsy, Capital Medical University, Beijing, China.; National Center for Neurological Disorders, Beijing, China.
Yu T; Clinical Research Center for Epilepsy, Capital Medical University, Beijing, China.; National Center for Neurological Disorders, Beijing, China.; Beijing Institute of Functional Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China.; Department of Functional Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China.
Blümcke I; Department of Neuropathology, University Hospital Erlangen, Erlangen, Germany.
Cai Y; Clinical Research Center for Epilepsy, Capital Medical University, Beijing, China.; National Center for Neurological Disorders, Beijing, China.; Department of Neurobiology and Clinical Biobank, Xuanwu Hospital, Capital Medical University, Beijing, China.
Sun K; Clinical Research Center for Epilepsy, Capital Medical University, Beijing, China.; National Center for Neurological Disorders, Beijing, China.; Beijing Institute of Functional Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China.; Department of Functional Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China.
Gao R; Clinical Research Center for Epilepsy, Capital Medical University, Beijing, China.; National Center for Neurological Disorders, Beijing, China.; Beijing Institute of Functional Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China.; Department of Functional Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China.
Wang Y; Department of Pathology, Xuanwu Hospital, Capital Medical University, Beijing, China.; Clinical Research Center for Epilepsy, Capital Medical University, Beijing, China.; National Center for Neurological Disorders, Beijing, China.
Fu Y; Department of Pathology, Xuanwu Hospital, Capital Medical University, Beijing, China.; Clinical Research Center for Epilepsy, Capital Medical University, Beijing, China.; National Center for Neurological Disorders, Beijing, China.
Wang W; Clinical Research Center for Epilepsy, Capital Medical University, Beijing, China.; National Center for Neurological Disorders, Beijing, China.; Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Wang Y; Clinical Research Center for Epilepsy, Capital Medical University, Beijing, China.; National Center for Neurological Disorders, Beijing, China.; Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.; Beijing Key Laboratory of Neuromodulation, Beijing, China.; Center of Epilepsy, Institute of Sleep and Consciousness Disorders, Beijing Institute for Brain Disorders, Capital Medical University, Beijing, China.
Zhang G; Clinical Research Center for Epilepsy, Capital Medical University, Beijing, China.; National Center for Neurological Disorders, Beijing, China.; Beijing Institute of Functional Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China.; Department of Functional Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China.
Piao Y; Department of Pathology, Xuanwu Hospital, Capital Medical University, Beijing, China.; Clinical Research Center for Epilepsy, Capital Medical University, Beijing, China.; National Center for Neurological Disorders, Beijing, China.
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Źródło:
Neuropathology and applied neurobiology [Neuropathol Appl Neurobiol] 2023 Feb; Vol. 49 (1), pp. e12874.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Malformations of Cortical Development*/genetics
Focal Cortical Dysplasia*
Epilepsy*/pathology
Humans ; Mosaicism ; Retrospective Studies ; TOR Serine-Threonine Kinases/metabolism
SCR Disease Name:
Focal cortical dysplasia of Taylor
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Identification of genetic characteristics in pediatric epilepsy with focal cortical dysplasia type 2 using deep whole-exome sequencing.
Autorzy:
Xu Y; Department of Neurology and Epilepsy Center, Children's Hospital of Fudan University, Shanghai, China.
Zhao R; Department of Neurosurgery, Children's Hospital of Fudan University, Shanghai, China.
Wang M; Department of Neurosurgery, Children's Hospital of Fudan University, Shanghai, China.
Wang XH; Department of Neurology and Epilepsy Center, Children's Hospital of Fudan University, Shanghai, China.
Wang Y; Department of Neurology and Epilepsy Center, Children's Hospital of Fudan University, Shanghai, China.
Li H; Department of Neurosurgery, Children's Hospital of Fudan University, Shanghai, China.
Ma YY; Department of Pathology, Children's Hospital of Fudan University, Shanghai, China.
Wu BB; Center for Molecular Medicine, Pediatrics Research Institute, Children's Hospital of Fudan University, Shanghai, China.
Zhou YF; Department of Neurology and Epilepsy Center, Children's Hospital of Fudan University, Shanghai, China.
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Źródło:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2022 Dec; Vol. 10 (12), pp. e2086. Date of Electronic Publication: 2022 Nov 07.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Focal Cortical Dysplasia*
Epilepsy*/genetics
Epilepsies, Partial*
Child ; Humans ; Exome Sequencing ; Mutation ; TOR Serine-Threonine Kinases/genetics ; TOR Serine-Threonine Kinases/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Characterisation of a novel [F]FDG brain PET database and combination with a second database for optimising detection of focal abnormalities, using focal cortical dysplasia as an example.
Autorzy:
Jin, Sameer Omer (AUTHOR)
Mérida, Inés (AUTHOR)
Stavropoulos, Ioannis (AUTHOR)
Elwes, Robert D. C. (AUTHOR)
Lam, Tanya (AUTHOR)
Guedj, Eric (AUTHOR)
Girard, Nadine (AUTHOR)
Costes, Nicolas (AUTHOR)
Hammers, Alexander (AUTHOR)
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Źródło:
EJNMMI Research. 11/15/2023, Vol. 13 Issue 1, p1-15. 15p.
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
A deep learning-based histopathology classifier for Focal Cortical Dysplasia.
Autorzy:
Vorndran, Jörg (AUTHOR)
Neuner, Christoph (AUTHOR)
Coras, Roland (AUTHOR)
Hoffmann, Lucas (AUTHOR)
Geffers, Simon (AUTHOR)
Honke, Jonas (AUTHOR)
Herms, Jochen (AUTHOR)
Roeber, Sigrun (AUTHOR)
Hamer, Hajo (AUTHOR)
Brandner, Sebastian (AUTHOR)
Hartlieb, Till (AUTHOR)
Pieper, Tom (AUTHOR)
Kudernatsch, Manfred (AUTHOR)
Bien, Christian G. (AUTHOR)
Kalbhenn, Thilo (AUTHOR)
Simon, Matthias (AUTHOR)
Adle-Biassette, Homa (AUTHOR)
Cienfuegos, Jesús (AUTHOR)
Di Giacomo, Roberta (AUTHOR)
Garbelli, Rita (AUTHOR)
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Źródło:
Neural Computing & Applications. Jun2023, Vol. 35 Issue 17, p12775-12792. 18p.
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Acquisition and Analysis of Excised Neocortex from Pediatric Patients with Focal Cortical Dysplasia Using Mesoscale Diffusion MRI.
Autorzy:
Fountain, Chandler (AUTHOR)
Ghuman, Harmanvir (AUTHOR)
Paldino, Michael (AUTHOR)
Tamber, Mandeep (AUTHOR)
Panigrahy, Ashok (AUTHOR)
Modo, Michel (AUTHOR)
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Źródło:
Diagnostics (2075-4418). May2023, Vol. 13 Issue 9, p1529. 23p.
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Wyświetlanie 1-20 z 2487

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