ArticleNeurology(R) neuroimmunology & neuroinflammation2017
Paraneoplastic cerebellar degeneration associated with anti-ITPR1 antibodies.
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In one paragraph
Article in Neurology(R) neuroimmunology & neuroinflammation, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.8field-weighted citation impact, top 16% of its field
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
13 citing papers in PubMed, 31 citations in OpenAlex.
- Brain atrophy in autoimmune encephalitis: epidemiology, pathophysiology, clinical manifestations, treatment, and prognosis-an update.Journal of neurology · 2025Review
- Consensus Paper: Latent Autoimmune Cerebellar Ataxia (LACA).Cerebellum (London, England) · 2024Article
- Autoimmune cerebellar ataxia associated with anti-Purkinje cells antibodies: the next frontier of neuroimmunology.Annals of translational medicine · 2023Review
- Rare Etiologies in Immune-Mediated Cerebellar Ataxias: Diagnostic Challenges.Brain sciences · 2022Review
- Inositol 1,4,5-trisphosphate receptor type 1 autoantibody (ITPR1-IgG/anti-Sj)-associated autoimmune cerebellar ataxia, encephalitis and peripheral neuropathy: review of the literature.Journal of neuroinflammation · 2022Review
- Homer-3 Antibody Disease: A Potentially Treatable MSA-C Mimic.Movement disorders clinical practice · 2022Article
- Update on Paraneoplastic Cerebellar Degeneration.Brain sciences · 2021Review
- Paraneoplastic encephalomyeloradiculits with multiple autoantibodies against ITPR-1, GFAP and MOG: case report and literature review.Neurological research and practice · 2021Article
- Are Antibody Panels Under-Utilized in Movement Disorders Diagnosis? Yes.Movement disorders clinical practice · 2021Article
- Update in Autoimmune Movement Disorders: Newly Described Antigen Targets in Autoimmune and Paraneoplastic Cerebellar Ataxia.Frontiers in neurology · 2021Review
- Immunological Bases of Paraneoplastic Cerebellar Degeneration and Therapeutic Implications.Frontiers in immunology · 2020Review
- ITPR1 autoimmunity: Frequency, neurologic phenotype, and cancer association.Neurology(R) neuroimmunology & neuroinflammation · 2018Article
- Pragmatic Treatment of Stiff Person Spectrum Disorders.Movement disorders clinical practiceReview
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
12 authors at 1 institution in 1 country.
Giulia BerzeroAP-HP Pitié-Salpêtrière (G.B., C.D., J.-Y.D., D.P.), Service de Neurologie Mazarin, Paris, France; Neuroscience Consortium (G.B.), University of Pavia, Monza Policlinico and Pavia Mondino, Italy; Nuffield Department of Clinical Neurosciences (Y.H.), John Radcliffe Hospital, University of Oxford, United Kingdom; Institute of Experimental Immunology (L.K., M.S.), affiliated to Euroimmun AG, Lübeck, Germany; AP-HP Pitié-Salpêtrière (D.L.), Service de Neuroradiologie; Département de Chirurgie Oncologique (V.F.); Département de Biologie des Tumeurs (B.B.), Service Génétique, Institut Curie, Paris; Centre National de Référence pour les Syndromes Neurologiques Paranéoplasiques (J.H.), Hospices Civils de Lyon, Institut NeuroMyoGene INSERM U1217/CNRS UMR 5310, Université de Lyon, France; and Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) (F.G.), Service of Neurology, Hospital Clinic, Barcelona, Spain.
Yael HacohenAP-HP Pitié-Salpêtrière (G.B., C.D., J.-Y.D., D.P.), Service de Neurologie Mazarin, Paris, France; Neuroscience Consortium (G.B.), University of Pavia, Monza Policlinico and Pavia Mondino, Italy; Nuffield Department of Clinical Neurosciences (Y.H.), John Radcliffe Hospital, University of Oxford, United Kingdom; Institute of Experimental Immunology (L.K., M.S.), affiliated to Euroimmun AG, Lübeck, Germany; AP-HP Pitié-Salpêtrière (D.L.), Service de Neuroradiologie; Département de Chirurgie Oncologique (V.F.); Département de Biologie des Tumeurs (B.B.), Service Génétique, Institut Curie, Paris; Centre National de Référence pour les Syndromes Neurologiques Paranéoplasiques (J.H.), Hospices Civils de Lyon, Institut NeuroMyoGene INSERM U1217/CNRS UMR 5310, Université de Lyon, France; and Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) (F.G.), Service of Neurology, Hospital Clinic, Barcelona, Spain.
Lars KomorowskiAP-HP Pitié-Salpêtrière (G.B., C.D., J.-Y.D., D.P.), Service de Neurologie Mazarin, Paris, France; Neuroscience Consortium (G.B.), University of Pavia, Monza Policlinico and Pavia Mondino, Italy; Nuffield Department of Clinical Neurosciences (Y.H.), John Radcliffe Hospital, University of Oxford, United Kingdom; Institute of Experimental Immunology (L.K., M.S.), affiliated to Euroimmun AG, Lübeck, Germany; AP-HP Pitié-Salpêtrière (D.L.), Service de Neuroradiologie; Département de Chirurgie Oncologique (V.F.); Département de Biologie des Tumeurs (B.B.), Service Génétique, Institut Curie, Paris; Centre National de Référence pour les Syndromes Neurologiques Paranéoplasiques (J.H.), Hospices Civils de Lyon, Institut NeuroMyoGene INSERM U1217/CNRS UMR 5310, Université de Lyon, France; and Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) (F.G.), Service of Neurology, Hospital Clinic, Barcelona, Spain.
Madeleine ScharfAP-HP Pitié-Salpêtrière (G.B., C.D., J.-Y.D., D.P.), Service de Neurologie Mazarin, Paris, France; Neuroscience Consortium (G.B.), University of Pavia, Monza Policlinico and Pavia Mondino, Italy; Nuffield Department of Clinical Neurosciences (Y.H.), John Radcliffe Hospital, University of Oxford, United Kingdom; Institute of Experimental Immunology (L.K., M.S.), affiliated to Euroimmun AG, Lübeck, Germany; AP-HP Pitié-Salpêtrière (D.L.), Service de Neuroradiologie; Département de Chirurgie Oncologique (V.F.); Département de Biologie des Tumeurs (B.B.), Service Génétique, Institut Curie, Paris; Centre National de Référence pour les Syndromes Neurologiques Paranéoplasiques (J.H.), Hospices Civils de Lyon, Institut NeuroMyoGene INSERM U1217/CNRS UMR 5310, Université de Lyon, France; and Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) (F.G.), Service of Neurology, Hospital Clinic, Barcelona, Spain.
Caroline DehaisAP-HP Pitié-Salpêtrière (G.B., C.D., J.-Y.D., D.P.), Service de Neurologie Mazarin, Paris, France; Neuroscience Consortium (G.B.), University of Pavia, Monza Policlinico and Pavia Mondino, Italy; Nuffield Department of Clinical Neurosciences (Y.H.), John Radcliffe Hospital, University of Oxford, United Kingdom; Institute of Experimental Immunology (L.K., M.S.), affiliated to Euroimmun AG, Lübeck, Germany; AP-HP Pitié-Salpêtrière (D.L.), Service de Neuroradiologie; Département de Chirurgie Oncologique (V.F.); Département de Biologie des Tumeurs (B.B.), Service Génétique, Institut Curie, Paris; Centre National de Référence pour les Syndromes Neurologiques Paranéoplasiques (J.H.), Hospices Civils de Lyon, Institut NeuroMyoGene INSERM U1217/CNRS UMR 5310, Université de Lyon, France; and Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) (F.G.), Service of Neurology, Hospital Clinic, Barcelona, Spain.
Delphine LeclercqAP-HP Pitié-Salpêtrière (G.B., C.D., J.-Y.D., D.P.), Service de Neurologie Mazarin, Paris, France; Neuroscience Consortium (G.B.), University of Pavia, Monza Policlinico and Pavia Mondino, Italy; Nuffield Department of Clinical Neurosciences (Y.H.), John Radcliffe Hospital, University of Oxford, United Kingdom; Institute of Experimental Immunology (L.K., M.S.), affiliated to Euroimmun AG, Lübeck, Germany; AP-HP Pitié-Salpêtrière (D.L.), Service de Neuroradiologie; Département de Chirurgie Oncologique (V.F.); Département de Biologie des Tumeurs (B.B.), Service Génétique, Institut Curie, Paris; Centre National de Référence pour les Syndromes Neurologiques Paranéoplasiques (J.H.), Hospices Civils de Lyon, Institut NeuroMyoGene INSERM U1217/CNRS UMR 5310, Université de Lyon, France; and Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) (F.G.), Service of Neurology, Hospital Clinic, Barcelona, Spain.
Virginie FourchotteAP-HP Pitié-Salpêtrière (G.B., C.D., J.-Y.D., D.P.), Service de Neurologie Mazarin, Paris, France; Neuroscience Consortium (G.B.), University of Pavia, Monza Policlinico and Pavia Mondino, Italy; Nuffield Department of Clinical Neurosciences (Y.H.), John Radcliffe Hospital, University of Oxford, United Kingdom; Institute of Experimental Immunology (L.K., M.S.), affiliated to Euroimmun AG, Lübeck, Germany; AP-HP Pitié-Salpêtrière (D.L.), Service de Neuroradiologie; Département de Chirurgie Oncologique (V.F.); Département de Biologie des Tumeurs (B.B.), Service Génétique, Institut Curie, Paris; Centre National de Référence pour les Syndromes Neurologiques Paranéoplasiques (J.H.), Hospices Civils de Lyon, Institut NeuroMyoGene INSERM U1217/CNRS UMR 5310, Université de Lyon, France; and Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) (F.G.), Service of Neurology, Hospital Clinic, Barcelona, Spain.
Bruno BuecherAP-HP Pitié-Salpêtrière (G.B., C.D., J.-Y.D., D.P.), Service de Neurologie Mazarin, Paris, France; Neuroscience Consortium (G.B.), University of Pavia, Monza Policlinico and Pavia Mondino, Italy; Nuffield Department of Clinical Neurosciences (Y.H.), John Radcliffe Hospital, University of Oxford, United Kingdom; Institute of Experimental Immunology (L.K., M.S.), affiliated to Euroimmun AG, Lübeck, Germany; AP-HP Pitié-Salpêtrière (D.L.), Service de Neuroradiologie; Département de Chirurgie Oncologique (V.F.); Département de Biologie des Tumeurs (B.B.), Service Génétique, Institut Curie, Paris; Centre National de Référence pour les Syndromes Neurologiques Paranéoplasiques (J.H.), Hospices Civils de Lyon, Institut NeuroMyoGene INSERM U1217/CNRS UMR 5310, Université de Lyon, France; and Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) (F.G.), Service of Neurology, Hospital Clinic, Barcelona, Spain.
Jérôme HonnoratAP-HP Pitié-Salpêtrière (G.B., C.D., J.-Y.D., D.P.), Service de Neurologie Mazarin, Paris, France; Neuroscience Consortium (G.B.), University of Pavia, Monza Policlinico and Pavia Mondino, Italy; Nuffield Department of Clinical Neurosciences (Y.H.), John Radcliffe Hospital, University of Oxford, United Kingdom; Institute of Experimental Immunology (L.K., M.S.), affiliated to Euroimmun AG, Lübeck, Germany; AP-HP Pitié-Salpêtrière (D.L.), Service de Neuroradiologie; Département de Chirurgie Oncologique (V.F.); Département de Biologie des Tumeurs (B.B.), Service Génétique, Institut Curie, Paris; Centre National de Référence pour les Syndromes Neurologiques Paranéoplasiques (J.H.), Hospices Civils de Lyon, Institut NeuroMyoGene INSERM U1217/CNRS UMR 5310, Université de Lyon, France; and Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) (F.G.), Service of Neurology, Hospital Clinic, Barcelona, Spain.
Francesc GrausAP-HP Pitié-Salpêtrière (G.B., C.D., J.-Y.D., D.P.), Service de Neurologie Mazarin, Paris, France; Neuroscience Consortium (G.B.), University of Pavia, Monza Policlinico and Pavia Mondino, Italy; Nuffield Department of Clinical Neurosciences (Y.H.), John Radcliffe Hospital, University of Oxford, United Kingdom; Institute of Experimental Immunology (L.K., M.S.), affiliated to Euroimmun AG, Lübeck, Germany; AP-HP Pitié-Salpêtrière (D.L.), Service de Neuroradiologie; Département de Chirurgie Oncologique (V.F.); Département de Biologie des Tumeurs (B.B.), Service Génétique, Institut Curie, Paris; Centre National de Référence pour les Syndromes Neurologiques Paranéoplasiques (J.H.), Hospices Civils de Lyon, Institut NeuroMyoGene INSERM U1217/CNRS UMR 5310, Université de Lyon, France; and Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) (F.G.), Service of Neurology, Hospital Clinic, Barcelona, Spain.
Jean-Yves DelattreAP-HP Pitié-Salpêtrière (G.B., C.D., J.-Y.D., D.P.), Service de Neurologie Mazarin, Paris, France; Neuroscience Consortium (G.B.), University of Pavia, Monza Policlinico and Pavia Mondino, Italy; Nuffield Department of Clinical Neurosciences (Y.H.), John Radcliffe Hospital, University of Oxford, United Kingdom; Institute of Experimental Immunology (L.K., M.S.), affiliated to Euroimmun AG, Lübeck, Germany; AP-HP Pitié-Salpêtrière (D.L.), Service de Neuroradiologie; Département de Chirurgie Oncologique (V.F.); Département de Biologie des Tumeurs (B.B.), Service Génétique, Institut Curie, Paris; Centre National de Référence pour les Syndromes Neurologiques Paranéoplasiques (J.H.), Hospices Civils de Lyon, Institut NeuroMyoGene INSERM U1217/CNRS UMR 5310, Université de Lyon, France; and Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) (F.G.), Service of Neurology, Hospital Clinic, Barcelona, Spain.
Dimitri PsimarasAP-HP Pitié-Salpêtrière (G.B., C.D., J.-Y.D., D.P.), Service de Neurologie Mazarin, Paris, France; Neuroscience Consortium (G.B.), University of Pavia, Monza Policlinico and Pavia Mondino, Italy; Nuffield Department of Clinical Neurosciences (Y.H.), John Radcliffe Hospital, University of Oxford, United Kingdom; Institute of Experimental Immunology (L.K., M.S.), affiliated to Euroimmun AG, Lübeck, Germany; AP-HP Pitié-Salpêtrière (D.L.), Service de Neuroradiologie; Département de Chirurgie Oncologique (V.F.); Département de Biologie des Tumeurs (B.B.), Service Génétique, Institut Curie, Paris; Centre National de Référence pour les Syndromes Neurologiques Paranéoplasiques (J.H.), Hospices Civils de Lyon, Institut NeuroMyoGene INSERM U1217/CNRS UMR 5310, Université de Lyon, France; and Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) (F.G.), Service of Neurology, Hospital Clinic, Barcelona, Spain.
University of Pavia · IT
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