Pages that link to "Q33808435"
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The following pages link to Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patients (Q33808435):
Displaying 50 items.
- RTTN mutations link primary cilia function to organization of the human cerebral cortex (Q24297843) (← links)
- A developmental and genetic classification for malformations of cortical development: update 2012 (Q26858999) (← links)
- Genetic Basis of Brain Malformations (Q28076998) (← links)
- Polymicrogyria-associated epilepsy: a multicenter phenotypic study from the Epilepsy Phenome/Genome Project (Q30411527) (← links)
- Structural abnormalities in patients with insular/peri-insular epilepsy: spectrum, frequency, and pharmacoresistance (Q30652287) (← links)
- Polymicrogyria: a common and heterogeneous malformation of cortical development (Q30828370) (← links)
- Malformations of Cortical Development: From Postnatal to Fetal Imaging (Q31133197) (← links)
- The Prevalence of Malformations of Cortical Development in a Pediatric Hereditary Hemorrhagic Telangiectasia Population. (Q31153252) (← links)
- Malformations of cortical development: genetic mechanisms and diagnostic approach (Q31162335) (← links)
- Polymicrogyria: pathology, fetal origins and mechanisms. (Q34109022) (← links)
- Gabapentin attenuates hyperexcitability in the freeze-lesion model of developmental cortical malformation (Q34266645) (← links)
- Polymicrogyria includes fusion of the molecular layer and decreased neuronal populations but normal cortical laminar organization (Q35041227) (← links)
- Morphological and functional aspects of progenitors perturbed in cortical malformations (Q35077279) (← links)
- What disorders of cortical development tell us about the cortex: one plus one does not always make two (Q35115582) (← links)
- Malformations of cortical development: clinical features and genetic causes (Q35188898) (← links)
- Germline recessive mutations in PI4KA are associated with perisylvian polymicrogyria, cerebellar hypoplasia and arthrogryposis (Q35693908) (← links)
- Characterisation of mutations of the phosphoinositide-3-kinase regulatory subunit, PIK3R2, in perisylvian polymicrogyria: a next-generation sequencing study (Q36354683) (← links)
- Scalp EEG does not predict hemispherectomy outcome (Q36443341) (← links)
- Glutamate biosensor imaging reveals dysregulation of glutamatergic pathways in a model of developmental cortical malformation (Q36614897) (← links)
- A case of Bilateral Perisylvian Syndrome with reading disability (Q36645961) (← links)
- Expanding the spectrum of TUBA1A-related cortical dysgenesis to Polymicrogyria (Q36686747) (← links)
- Polymicrogyria and congenital parvovirus b19 infection (Q36842710) (← links)
- Midbrain-hindbrain malformations in patients with malformations of cortical development and epilepsy: a series of 220 patients (Q37453568) (← links)
- Quantification and discrimination of abnormal sulcal patterns in polymicrogyria (Q37463653) (← links)
- Surgical management of medically refractory epilepsy in patients with polymicrogyria. (Q37587197) (← links)
- Pontine malformation, undecussated pyramidal tracts, and regional polymicrogyria: a new syndrome (Q37646995) (← links)
- Abnormal development of the human cerebral cortex. (Q37803421) (← links)
- Recent advances in the genetic etiology of brain malformations (Q38116442) (← links)
- The wide spectrum of tubulinopathies: what are the key features for the diagnosis? (Q38214584) (← links)
- Mapping genetic influences on cortical regionalization (Q39464664) (← links)
- Polymicrogyric Cortex may Predispose to Seizures via Abnormal Network Topology: An fMRI Connectomics Study (Q40112015) (← links)
- Cortical Clefts and Cortical Bumps: A Continuous Spectrum (Q41071795) (← links)
- Ultra-high-field MR imaging in polymicrogyria and epilepsy (Q41299267) (← links)
- Venous pattern of polymicrogyria detected by susceptibility weighted imaging (SWI). (Q42073211) (← links)
- Whole-exome sequencing of a unique brain malformation with periventricular heterotopia, cingulate polymicrogyria and midbrain tectal hyperplasia. (Q42517953) (← links)
- Overlapping cortical malformations and mutations in TUBB2B and TUBA1A. (Q42519980) (← links)
- Zika virus associated microcephaly/micrencephaly-fetal brain imaging in comparison with neuropathology (Q42999899) (← links)
- Intracranial evaluation of the epileptogenic zone in regional infrasylvian polymicrogyria (Q43874593) (← links)
- Phosphorus magnetic resonance spectroscopy in malformations of cortical development (Q43973877) (← links)
- Homozygous truncating mutation of the KBP gene, encoding a KIF1B-binding protein, in a familial case of fetal polymicrogyria (Q44309455) (← links)
- Proposal for a magnetic resonance imaging protocol for the detection of epileptogenic lesions at early outpatient stages. (Q45210359) (← links)
- Neurodevelopmental abnormalities in children with PHACE syndrome (Q45838673) (← links)
- A review of structural brain abnormalities in Pallister-Killian syndrome (Q47266509) (← links)
- Stereoelectroencephalography and surgical outcome in polymicrogyria-related epilepsy: A multicentric study. (Q47741685) (← links)
- Bilateral frontoparietal polymicrogyria (Q48449990) (← links)
- Second-Trimester Sonographic Diagnosis of Polymicrogyria (Q48495063) (← links)
- Social competence following pediatric stroke: contributions of brain insult and family environment (Q48650758) (← links)
- The histopathology of polymicrogyria: a series of 71 brain autopsy studies (Q50577595) (← links)
- A de novo 1.4-Mb deletion at 21q22.11 in a boy with developmental delay. (Q52647144) (← links)
- Relationships Between Morphologic and Functional Patterns in the Polymicrogyric Cortex. (Q52680074) (← links)