Pages that link to "Q34513420"
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The following pages link to Gray matter heterotopia (Q34513420):
Displaying 41 items.
- Progress towards a cellular neurobiology of reading disability (Q30475697) (← links)
- Magnetic resonance imaging: role in the understanding of cerebral malformations (Q30667222) (← links)
- Periventricular nodular heterotopia: report of a pediatric series (Q30700496) (← links)
- Disorders of cortical formation: MR imaging features. (Q31170078) (← links)
- Congenital malformations of the brain (Q33391697) (← links)
- Radiosurgery for the treatment of dominant hemisphere periventricular heterotopia and intractable epilepsy in a series of three patients (Q34115019) (← links)
- Reelin' in Genes for Cortical Dysplasia (Q35524626) (← links)
- Malformations of cortical development: burdens and insights from important causes of human epilepsy (Q35615140) (← links)
- Assessment of gray matter heterotopia by magnetic resonance imaging (Q35886354) (← links)
- Incidental Findings and Normal Anatomical Variants on MRI of the Brain in Adults for Primary Headaches (Q36308243) (← links)
- Absences in adult seizure disorders (Q36344188) (← links)
- Developmental differences of the major forebrain commissures in lissencephalies (Q37257104) (← links)
- Gray matter volumes and cognitive ability in the epileptogenic brain malformation of periventricular nodular heterotopia (Q37291978) (← links)
- Bilateral subependymal heterotopia, ventriculomegaly and cerebellar asymmetry: fetal MRI findings of a rare association of brain anomalies (Q37464318) (← links)
- Association of periventricular nodular heterotopia with posterior fossa cyst: a prenatal case series. (Q41726875) (← links)
- Autopsy case of multiple anomalies with hypoplastic cerebrum, eyes, and endocrine organs, mimicking Micro syndrome (Q41922141) (← links)
- Alpha-[11C]methyl-L-tryptophan uptake in patients with periventricular nodular heterotopia and epilepsy (Q43451254) (← links)
- High-resolution 3-T MR imaging of the temporal part of the caudate tail in children. (Q45905564) (← links)
- Neuronal migration defect: a case of subcortical heterotopia in a California sea lion (Q46057434) (← links)
- Role of SOX2 mutations in human hippocampal malformations and epilepsy (Q47219057) (← links)
- Quantitative MRI detects abnormalities in relatives of patients with epilepsy and malformations of cortical development (Q48002289) (← links)
- Evaluation of Subependymal Gray Matter Heterotopias on Fetal MRI. (Q48101718) (← links)
- Concurrent neurodegenerative pathologies in periventricular nodular heterotopia (Q48121120) (← links)
- Automated morphometric magnetic resonance imaging analysis for the detection of periventricular nodular heterotopia (Q48204441) (← links)
- Periventricular nodular heterotopia on prenatal ultrasound and magnetic resonance imaging (Q48295700) (← links)
- IMAGING DIAGNOSIS-MAGNETIC RESONANCE IMAGING OF A NEURONAL HETEROTOPIA IN THE BRAIN OF A CAT. (Q48413462) (← links)
- Hemimegalencephalic appearance of normal hemisphere in unilateral heterotopia and absent corpus callosum (Q48450996) (← links)
- Subcortical laminar (band) heterotopia (Q48914651) (← links)
- Like father, like son: periventricular nodular heterotopia and nonverbal learning disorder (Q49033863) (← links)
- Nodular heterotopia: a neuropathological study of 24 patients undergoing surgery for drug-resistant epilepsy (Q49063803) (← links)
- Cervical meningocele associated with subependymal nodular heterotopia (Q51802354) (← links)
- Voxel-based 3D MRI analysis helps to detect subtle forms of subcortical band heterotopia. (Q51899488) (← links)
- De novo and inherited private variants in MAP1B in periventricular nodular heterotopia. (Q54534163) (← links)
- Comprehensive behavioral analysis of mice deficient in Rapgef2 and Rapgef6, a subfamily of guanine nucleotide exchange factors for Rap small GTPases possessing the Ras/Rap-associating domain. (Q55299963) (← links)
- Grey matter heterotopia: what EEG-fMRI can tell us about epileptogenicity of neuronal migration disorders (Q57041936) (← links)
- Neuropsychiatric symptoms and diagnosis of grey matter heterotopia: A case-based reflection (Q57651732) (← links)
- Pathologic characteristics of the cortical dysplasias (Q77381444) (← links)
- [Partial corpus callosum agenesis] (Q81153471) (← links)
- Malformations of cortical development (Q88794931) (← links)
- ECE2 regulates neurogenesis and neuronal migration during human cortical development (Q90616642) (← links)
- Hypothalamic hamartoma, gray matter heterotopia and polymicrogyria in a boy: a case report and literature review (Q97871440) (← links)