ArticleNeuroImage. Clinical2018
Open access · goldAbstract read
In one paragraph
Article in NeuroImage. Clinical, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 2 of them syntheses that pooled it.
0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 2 pooled it
2.5field-weighted citation impact, top 11% 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
30 citing papers in PubMed, 2 syntheses or guidelines pooled it, 44 citations in OpenAlex.
- The cognitive profile of hereditary spastic paraplegia: a systematic review of the literature.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2025Pooled it
- The Intersection of Genetics and Neuroimaging: A Systematic Review of Imaging Genetics in Neurological Disease for Personalized Treatment.Journal of molecular neuroscience : MN · 2025Pooled it
- Hereditary spastic paraplegia (HSP) gene 11 (Spg11) attenuates lipid accumulation in myeloid cells and neuroinflammation in the midbrain without affecting α-synuclein pathology.Journal of neuroinflammation · 2026Article
- Early Detection of Central Nervous System Involvement in ATTRv Using Multimodal MRI and Cognitive Assessments.European journal of neurology · 2026Article
- Spinal cord cross sign: a potential marker for hereditary spastic paraplegia type 5.Neuroradiology · 2025Observational
- Sensory Dysfunction in ALS and Other Motor Neuron Diseases: Clinical Relevance, Histopathology, Neurophysiology, and Insights from Neuroimaging.Biomedicines · 2025Review
- Review
- Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients.Acta neuropathologica · 2024Article
- Metabolite profile in hereditary spastic paraplegia analyzed using magnetic resonance spectroscopy: a cross-sectional analysis in a longitudinal study.Frontiers in neuroscience · 2024Article
- Clinically approved immunomodulators ameliorate behavioral changes in a mouse model of hereditary spastic paraplegia type 11.Frontiers in neuroscience · 2024Article
- Hereditary spastic paraplegia: Novel insights into the pathogenesis and management.SAGE open medicine · 2024Review
- Movement disorders in hereditary spastic paraplegias.Arquivos de neuro-psiquiatria · 2023Review
- Outcome Measures and Biomarkers for Clinical Trials in Hereditary Spastic Paraplegia: A Scoping Review.Genes · 2023Article
- Clinical analysis in patients withFrontiers in neurology · 2023Article
- Article
- Genetic landscape of early-onset dementia in Hungary.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2022Article
- Neuropsychology and MRI correlates of neurodegeneration in SPG11 hereditary spastic paraplegia.Orphanet journal of rare diseases · 2022Article
- Systematic Analysis of Brain MRI Findings in Adaptor Protein Complex 4-Associated Hereditary Spastic Paraplegia.Neurology · 2021Article
- Thalamic atrophy in patients with pure hereditary spastic paraplegia type 4.Journal of neurology · 2021Article
- Spinal Cord Gray and White Matter Damage in Different Hereditary Spastic Paraplegia Subtypes.AJNR. American journal of neuroradiology · 2021Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
13 authors at 6 institutions in 2 countries.
Ingrid FaberDepartment of Neurology, University of Campinas (UNICAMP), Campinas, Brazil.
Alberto Rolim Muro MartinezDepartment of Neurology, University of Campinas (UNICAMP), Campinas, Brazil.
Thiago Junqueira Ribeiro de RezendeDepartment of Neurology, University of Campinas (UNICAMP), Campinas, Brazil.
Carlos Roberto MartinsDepartment of Neurology, University of Campinas (UNICAMP), Campinas, Brazil.
Melina Pazian MartinsDepartment of Neurology, University of Campinas (UNICAMP), Campinas, Brazil.
Charles Marques LourençoDepartment of Neurology, University of São Paulo (USP-RP), Ribeirão Preto, Brazil.
Wilson MarquesDepartment of Neurology, University of São Paulo (USP-RP), Ribeirão Preto, Brazil.
Celeste MontecchianiLaboratorio di Neurogenetica, Centro Europeo di Ricerca sul Cervello (CERC) - Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Santa Lucia, Rome, Italy.
Antonio OrlacchioLaboratorio di Neurogenetica, Centro Europeo di Ricerca sul Cervello (CERC) - Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Santa Lucia, Rome, Italy; Dipartimento di Scienze Chirurgiche e Biomediche, Università di Perugia, Perugia, Italy.
Jose Luiz PedrosoDepartment of Neurology, Federal University of São Paulo (UNIFESP), São Paulo, Brazil.
Orlando Graziani Povoas BarsottiniDepartment of Neurology, Federal University of São Paulo (UNIFESP), São Paulo, Brazil.
Íscia Lopes-CendesDepartment of Medical Genetics, University of Campinas (UNICAMP), Campinas, Brazil.
Marcondes Cavalcante FrançaDepartment of Neurology, University of Campinas (UNICAMP), Campinas, Brazil. Electronic address: mcfrancajr@uol.com.br.
Universidade Estadual de Campinas (UNICAMP) · BRUniversidade Federal de São Paulo · BRIstituti di Ricovero e Cura a Carattere Scientifico · ITUniversidade de Ribeirão Preto · BRUniversidade de São Paulo · BRUniversity of Perugia · IT
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
MutationAdolescentAdultBasal GangliaDiffusion Tensor ImagingFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedNeuroimagingNeuropsychological TestsProteinsSpastic Paraplegia, HereditaryWhite MatterYoung AdultProteinsSPG11 protein, humanACE-R, Addenbrooke's Cognitive Examination RevisedALS, amyotrophic lateral sclerosisCA, cord areaCE, cord eccentricityCMAP, compound muscle action potentialComplicated hereditary spastic paraplegiaCST, corticospinal tractDTI, diffusion tensor imagingFA, fractional anisotropyGM, grey matterGrey matterHSP, hereditary spastic paraplegiaLH, left hemisphereMD, mean diffusivityMOCA, Montreal cognitive assessmentMotor neuron disorderNPI, neuropsychiatric inventoryPNP, sensory-motor polyneuropathyPNS, peripheral nervous systemRH, right hemisphereROI, region of interestSC, spinal cordSNAP, sensory nerve action potentialSPG11Spinal cordSPRS, Spastic Paraplegia Rating ScaleSTS, cortex adjacent to the superior temporal sulcusThinning of the corpus callosumWES, whole exome sequencingWhite matterWM, white matter
Identifiers
What OpenQuestion holds
Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390
Registered trials
None linked
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.