Pages that link to "Q56232753"

The following pages link to Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopment (Q56232753):

Displaying 41 items.

• An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21 (Q24614022) (← links)
• Genes and brain malformations associated with abnormal neuron positioning (Q26779045) (← links)
• Genetic Basis of Brain Malformations (Q28076998) (← links)
• Genetic malformations of cortical development (Q28242257) (← links)
• Malformations of cortical development and epilepsy (Q30635675) (← links)
• Magnetic resonance imaging: role in the understanding of cerebral malformations (Q30667222) (← links)
• Mapping form and function in the human brain: the emerging field of functional neuroimaging in cortical malformations (Q30886913) (← links)
• Genetics of the polymicrogyria syndromes. (Q30988607) (← links)
• Cortical malformations and epilepsy: Role of MR imaging (Q31075837) (← links)
• Current concepts of polymicrogyria (Q33536491) (← links)
• Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patients (Q33808435) (← links)
• The syndrome of perisylvian polymicrogyria with congenital arthrogryposis (Q33926324) (← links)
• Epilepsy and genetic malformations of the cerebral cortex (Q34386806) (← links)
• Mechanisms of cerebral cortical patterning in mice and humans (Q34425400) (← links)
• Brain malformations, epilepsy, and infantile spasms (Q34663411) (← links)
• Bilateral frontoparietal polymicrogyria, Lennox-Gastaut syndrome, and GPR56 gene mutations (Q34743162) (← links)
• Malformations of cortical development: clinical features and genetic causes (Q35188898) (← links)
• Electromagnetic function of polymicrogyric cortex in congenital bilateral perisylvian syndrome (Q35572555) (← links)
• Malformations of cortical development: burdens and insights from important causes of human epilepsy (Q35615140) (← 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)
• A locus for bilateral perisylvian polymicrogyria maps to Xq28 (Q37216122) (← links)
• Autosomal recessive bilateral frontal polymicrogyria with ectopia lentis and chorioretinal dystrophy (Q37345579) (← links)
• Developments in Molecular Genetic Diagnostics: An Update for the Pediatric Epilepsy Specialist (Q37863822) (← links)
• A locus for bilateral occipital polymicrogyria maps to chromosome 6q16-q22. (Q38901909) (← links)
• Ictal technetium-99 m ethyl cysteinate dimer single-photon emission tomographic findings in epileptic patients with polymicrogyria syndromes: a subtraction of ictal-interictal SPECT coregistered to MRI study. (Q46837739) (← links)
• Neuroimaging findings in Pallister-Killian syndrome (Q47904955) (← links)
• Quantitative MRI detects abnormalities in relatives of patients with epilepsy and malformations of cortical development (Q48002289) (← links)
• Bilateral frontal polymicrogyria and epilepsy in a patient with Turner mosaicism: a case report (Q48248821) (← links)
• Pattern of congenital brain malformations at a referral hospital in Saudi Arabia: an MRI study (Q48625331) (← links)
• Cognitive functioning in bilateral perisylvian polymicrogyria (BPP): clinical and radiological correlations. (Q48935194) (← links)
• Congenital bilateral perisylvian syndrome with pituitary hypoplasia and ectopic neurohypophysis (Q49214518) (← links)
• Characterization of the linguistic profile of a family with Perisylvian Syndrome (Q52029774) (← links)
• Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2. (Q54987240) (← links)
• Neuroimaging findings in macrocephaly-capillary malformation: a longitudinal study of 17 patients. (Q55045687) (← links)
• Voxel-based morphometry and intellectual assessment in patients with congenital bilateral perisylvian syndrome (Q56232648) (← links)
• Malformations of cortical development and epilepsy (Q56232687) (← links)
• Sodium Channel SCN3A (Na1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development (Q57039803) (← links)
• (Q57086649) (redirect page) (← links)
• (Q61876994) (redirect page) (← links)
• Developmental Dynamic Dysphasia: Are Bilateral Brain Abnormalities a Signature of Inefficient Neural Plasticity? (Q91710214) (← links)