ArticleCells2020
Cerebral MRI and Clinical Findings in Children with
Article in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
What it found
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Who cites it
12 citing papers in PubMed, 18 citations in OpenAlex.
- Fetal magnetic resonance imaging features of syndromic megalencephaly: a systematic review of imaging-genotype associations.Pediatric radiology · 2026Review
- Macrocephaly and Characteristic MRI Findings as Early Clues to a Hereditary Overgrowth Syndrome.Cureus · 2026Article
- Neurodevelopmental and Neurologic Manifestations ofNeurology. Genetics · 2025Review
- Extracranial arteriovenous malformations: towards etiology-based therapeutic management.The Journal of clinical investigation · 2025Review
- A Newborn with Cleft Palate Associated with PTEN Hamartoma Tumor Syndrome.Clinics and practice · 2025Article
- PTEN hamartoma tumor syndrome: Clinical and genetic characterization in pediatric patients.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2024Article
- Exploring the neurological features of individuals with germline PTEN variants: A multicenter study.Annals of clinical and translational neurology · 2024Article
- Formation of a de novo intracranial arteriovenous fistula in a child with PTEN hamartoma tumor syndrome.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2022Article
- PTEN hamartoma tumor syndrome in childhood and adolescence-a comprehensive review and presentation of the German pediatric guideline.Molecular and cellular pediatrics · 2022Review
- Identification of the clinical and neuroimaging characteristics in children with neuromyelitis optica spectrum disorders: a case series.Translational pediatrics · 2021Article
- Review of PP2A Tumor Biology and Antitumor Effects of PP2A Inhibitor LB100 in the Nervous System.Cancers · 2021Review
- Fetal Megalencephaly with Cortical Dysplasia at 18 Gestational Weeks Related to Paternal UPD Mosaicism withGenes · 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
7 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
background
methodsWe retrospectively studied radiological and clinical data of pediatric patients who were presented in our hospital between 2013 and 2019 in whom
resultsWe included 27 pediatric patients (18 male) in the analysis. All patients were macrocephalic. Of these, 19 patients had received at least one cMRI scan. In 18 subjects variations were detected: enlarged perivascular spaces (EPVS; in 18), white matter abnormalities (in seven) and less frequently additional pathologies. Intellectual ability was variable. Most patients exhibited developmental delay in motor skills, but normal intelligence.
conclusioncMRI elucidates EPVS and white matter abnormalities in a high prevalence in children with PHTS and might therefore aid as a diagnostic feature to establish an earlier diagnosis of PHTS in childhood.
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Registered trials
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.