Brief Report: Functional MRI of a Patient with 7q11.23 Duplication Syndrome and Autism Spectrum Disorder
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V. Napolioni | G. Merla | M. Piccirilli | P. Prontera | D. Serino | B. Caldini | L. Scarponi | M. Muti | E. Donti | Paolo Prontera | Domenico Serino | Bernardo Caldini | Laura Scarponi | Giuseppe Merla | Giuseppe Testa | Marco Muti | Valerio Napolioni | Giovanni Mazzotta | Massimo Piccirilli | Emilio Donti | Giuseppe Testa | Giovanni Mazzotta
[1] A. Mencarelli,et al. Aicardi Syndrome Associated with Autosomal Genomic Imbalance: Coincidence or Evidence for Autosomal Inheritance with Sex-Limited Expression? , 2013, Molecular Syndromology.
[2] Martha E Shenton,et al. MRI amygdala volume in Williams Syndrome. , 2011, Research in developmental disabilities.
[3] K. Malisza,et al. Functional magnetic resonance imaging of facial information processing in children with autistic disorder, attention deficit hyperactivity disorder and typically developing controls , 2011, International journal of adolescent medicine and health.
[4] L. Welberg. Autism: The importance of getting the dose right , 2011, Nature Reviews Neuroscience.
[5] Kathryn Roeder,et al. Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism , 2011, Neuron.
[6] Boris Yamrom,et al. Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders , 2011, Neuron.
[7] P. Teale,et al. Brain size and brain/intracranial volume ratio in major mental illness , 2010, BMC psychiatry.
[8] Nicola Brunetti-Pierri,et al. Copy number variants at Williams–Beuren syndrome 7q11.23 region , 2010, Human Genetics.
[9] Timothy A Keller,et al. The nature of brain dysfunction in autism: functional brain imaging studies , 2010, Current opinion in neurology.
[10] B. V. van Bon,et al. Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome. , 2009, European journal of medical genetics.
[11] R. Cerini,et al. Dysmorphic features, simplified gyral pattern and 7q11.23 duplication reciprocal to the Williams-Beuren deletion , 2008, European Journal of Human Genetics.
[12] Andreas Meyer-Lindenberg,et al. Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour , 2006, Nature Reviews Neuroscience.
[13] S. Scherer,et al. Severe expressive-language delay related to duplication of the Williams-Beuren locus. , 2005, The New England journal of medicine.
[14] Abraham Z. Snyder,et al. A unified approach for morphometric and functional data analysis in young, old, and demented adults using automated atlas-based head size normalization: reliability and validation against manual measurement of total intracranial volume , 2004, NeuroImage.
[15] J. Denie,et al. Supravalvular Aortic Stenosis , 1958, Circulation.
[16] D. Hedges,et al. Amygdala volume in adults with posttraumatic stress disorder: a meta-analysis. , 2009, The Journal of neuropsychiatry and clinical neurosciences.
[17] R. Guerrini,et al. Cortical dysplasia of the left temporal lobe might explain severe expressive-language delay in patients with duplication of the Williams–Beuren locus , 2007, European Journal of Human Genetics.