Periventricular nodular heterotopia in 22q11.2 deletion and frontal lobe migration
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T. Kiehl | T. Krings | A. Bassett | E. Chow | D. Andrade | A. Rezazadeh | E. Bercovici
[1] T. Kiehl,et al. Periventricular nodular heterotopia and bilateral intraventricular xanthogranulomas in 22q11.2 deletion syndrome , 2017 .
[2] Robert G. Wither,et al. 22q11.2 deletion syndrome lowers seizure threshold in adult patients without epilepsy , 2017, Epilepsia.
[3] Duan Xu,et al. Extensive migration of young neurons into the infant human frontal lobe , 2016, Science.
[4] E. Illingworth,et al. Cortical Development Requires Mesodermal Expression of Tbx1, a Gene Haploinsufficient in 22q11.2 Deletion Syndrome , 2016, Cerebral cortex.
[5] H. Yoo,et al. Epilepsy and Other Neuropsychiatric Manifestations in Children and Adolescents with 22q11.2 Deletion Syndrome , 2015, Journal of clinical neurology.
[6] J. Winkler,et al. 47 patients with FLNA associated periventricular nodular heterotopia , 2015, Orphanet Journal of Rare Diseases.
[7] A. LaMantia,et al. Ranbp1, Deleted in DiGeorge/22q11.2 Deletion Syndrome, is a Microcephaly Gene That Selectively Disrupts Layer 2/3 Cortical Projection Neuron Generation. , 2015, Cerebral cortex.
[8] Daniele Merico,et al. Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome , 2015, G3: Genes, Genomes, Genetics.
[9] Brian Chung,et al. Practical guidelines for managing adults with 22q11.2 deletion syndrome , 2015, Genetics in Medicine.
[10] Timo Krings,et al. Hippocampal Malrotation is Associated with Chromosome 22q11.2 Microdeletion , 2013, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.
[11] M. Henneke,et al. West syndrome, microcephaly, grey matter heterotopia and hypoplasia of corpus callosum due to a novel ARFGEF2 mutation , 2013, Journal of Medical Genetics.
[12] H. Sarnat,et al. Radial microcolumnar cortical architecture: maturational arrest or cortical dysplasia? , 2013, Pediatric neurology.
[13] A. LaMantia,et al. Cxcr4 regulation of interneuron migration is disrupted in 22q11.2 deletion syndrome , 2012, Proceedings of the National Academy of Sciences.
[14] Danko D. Georgiev,et al. Deficits in transcriptional regulators of cortical parvalbumin neurons in schizophrenia. , 2012, The American journal of psychiatry.
[15] P. Fergelot,et al. Atypical male and female presentations of FLNA-related periventricular nodular heterotopia. , 2012, European journal of medical genetics.
[16] T. Yu,et al. FLNA genomic rearrangements cause periventricular nodular heterotopia , 2012, Neurology.
[17] R. Kucherlapati,et al. Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse model. , 2011, Human molecular genetics.
[18] Mitchel S. Berger,et al. Corridors of Migrating Neurons in Human Brain and Their Decline during Infancy , 2011, Nature.
[19] K. Devriendt,et al. Practical guidelines for managing patients with 22q11.2 deletion syndrome. , 2011, The Journal of pediatrics.
[20] H. van Bokhoven,et al. Periventricular Heterotopia in Common Microdeletion Syndromes , 2010, Molecular Syndromology.
[21] Anthony-Samuel LaMantia,et al. Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome , 2009, Proceedings of the National Academy of Sciences.
[22] M. Lequin,et al. Movement disorder and neuronal migration disorder due to ARFGEF2 mutation , 2009, neurogenetics.
[23] B. Aouizerate,et al. Meta-Analysis of Brain Volume Changes in Obsessive-Compulsive Disorder , 2009, Biological Psychiatry.
[24] A. Bassett,et al. Schizophrenia and 22q11.2 deletion syndrome , 2008, Current psychiatry reports.
[25] A. Frigessi,et al. Regional thinning of the cerebral cortex in schizophrenia: Effects of diagnosis, age and antipsychotic medication , 2008, Schizophrenia Research.
[26] Arthur W Toga,et al. Relationships between IQ and regional cortical gray matter thickness in healthy adults. , 2007, Cerebral cortex.
[27] Arthur W Toga,et al. Cerebral Cortex Advance Access published October 20, 2006 Mapping Cortical Thickness in Children with 22q11.2 Deletions , 2022 .
[28] Josemir W Sander,et al. Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations. , 2006, Brain : a journal of neurology.
[29] Jean Gotman,et al. The role of periventricular nodular heterotopia in epileptogenesis. , 2005, Brain : a journal of neurology.
[30] E. Zackai,et al. Increased prevalence of unprovoked seizures in patients with a 22q11.2 deletion , 2004, American journal of medical genetics. Part A.
[31] Lorenzo D Botto,et al. A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population. , 2003, Pediatrics.
[32] Marianna D. Eddy,et al. Regionally localized thinning of the cerebral cortex in schizophrenia , 2003, Schizophrenia Research.
[33] G. Abecasis,et al. Genetic variation in the 22q11 locus and susceptibility to schizophrenia , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[34] C. Beasley,et al. Selective deficits in prefrontal cortical GABAergic neurons in schizophrenia defined by the presence of calcium-binding proteins , 2002, Biological Psychiatry.
[35] Paul Maruff,et al. The cognitive neuropsychiatric approach to investigating the neurobiology of schizophrenia and other disorders. , 2002, Journal of psychosomatic research.
[36] Renzo Guerrini,et al. Bilateral periventricular nodular heterotopia due to filamin 1 gene mutation: widespread glomeruloid microvascular anomaly and dysplastic cytoarchitecture in the cerebral cortex , 2002, Acta Neuropathologica.
[37] N W Wood,et al. Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females. , 2001, Human molecular genetics.
[38] I. Scheffer,et al. Periventricular nodular heterotopia in patients with filamin-1 gene mutations: neuroimaging findings , 2000, Pediatric Radiology.
[39] M. Owen,et al. High rates of schizophrenia in adults with velo-cardio-facial syndrome (VCFS) , 1999, Schizophrenia Research.
[40] Y. Sitoh,et al. Neuroimaging in epilepsy , 1998, Journal of magnetic resonance imaging : JMRI.
[41] I. Scheffer,et al. Periventricular Heterotopia: An X-Linked Dominant Epilepsy Locus Causing Aberrant Cerebral Cortical Development , 1996, Neuron.
[42] C. Iani,et al. Age‐Related Cortical Thickness Reduction in Non‐Demented Down's Syndrome Subjects , 2016, Journal of neuroimaging : official journal of the American Society of Neuroimaging.
[43] D J Mikulis,et al. Neuropathologic features in adults with 22q11.2 deletion syndrome. , 2009, Cerebral cortex.
[44] C. Walsh,et al. Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex , 2004, Nature Genetics.