Cargando…

Copy Number Variations in Children with Tourette Syndrome: Systematic Investigation in a Clinical Setting

Tourette syndrome (TS) is a neurodevelopmental disturbance with heterogeneous and not completely known etiology. Clinical and molecular appraisal of affected patients is mandatory for outcome amelioration. The current study aimed to understand the molecular bases underpinning TS in a vast cohort of...

Descripción completa

Detalles Bibliográficos
Autores principales:	Saia, Federica, Prato, Adriana, Saccuzzo, Lucia, Madia, Francesca, Barone, Rita, Fichera, Marco, Rizzo, Renata
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2023
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9956985/ https://www.ncbi.nlm.nih.gov/pubmed/36833427 http://dx.doi.org/10.3390/genes14020500

Ejemplares similares

Use of Nutritional Supplements Based on L-Theanine and Vitamin B6 in Children with Tourette Syndrome, with Anxiety Disorders: A Pilot Study
por: Rizzo, Renata, et al.
Publicado: (2022)

Symptoms compatible with long COVID in an Italian pediatric cohort of Tourette patients with and without SARS‑CoV‑2 infection: a short-term follow-up assessment
por: Prato, Adriana, et al.
Publicado: (2023)

A Randomized Controlled Trial Comparing Videoconference vs. Face-to-Face Delivery of Behavior Therapy for Youths With Tourette Syndrome in the Time of COVID-19
por: Prato, Adriana, et al.
Publicado: (2022)

Incidence of Autism Spectrum Disorder in Youths Affected by Gilles de la Tourette Syndrome Based on Data from a Large Single Italian Clinical Cohort
por: Gulisano, Mariangela, et al.
Publicado: (2020)

Functional tic-like behaviours during the COVID-19 pandemic: Follow-up over 12 months
por: Prato, Adriana, et al.
Publicado: (2023)

Novel malformations: Chiari type 1 and hydrocephalus in Zhu‐Tokita‐Takenouchi‐Kim syndrome and novel SON variants
por: Pavone, Piero, et al.
Publicado: (2022)

Investigation of modifier genes within copy number variations in Rett syndrome
por: Artuso, Rosangela, et al.
Publicado: (2011)

New Copy Number Variations in Schizophrenia
por: Magri, Chiara, et al.
Publicado: (2010)

Investigation of Copy Number Variation in Children with Conotruncal Heart Defects
por: Campos, Carla Marques Rondon, et al.
Publicado: (2015)

A Multicentric Brazilian Investigative Study of Copy Number Variations in Patients with Congenital Anomalies and Intellectual Disability
por: Ceroni, J. R. M., et al.
Publicado: (2018)

Copy number variations and cancer
por: Shlien, Adam, et al.
Publicado: (2009)

Copy number variations and stroke
por: Colaianni, Valeria, et al.
Publicado: (2016)

Copy Number Variations and Schizophrenia
por: Szecówka, Kamila, et al.
Publicado: (2022)

Copy Number Variation and Osteoporosis
por: Lovšin, Nika
Publicado: (2023)

Copy-number-variation and copy-number-alteration region detection by cumulative plots
por: Li, Wentian, et al.
Publicado: (2009)

De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis
por: Wang, Sheng, et al.
Publicado: (2018)

Analysis of copy number variations and possible candidate genes in spontaneous abortion by copy number variation sequencing
por: Bai, Wei, et al.
Publicado: (2023)

Diagnostic implications of genetic copy number variation in epilepsy plus
por: Coppola, Antonietta, et al.
Publicado: (2019)

Genomic characteristics of cattle copy number variations
por: Hou, Yali, et al.
Publicado: (2011)

MSX2 copy number increase and craniosynostosis: copy number variation detected by array comparative genomic hybridization
por: de Oliveira Pelegrino, Karla, et al.
Publicado: (2012)

Copy number variation in African Americans
por: McElroy, Joseph P, et al.
Publicado: (2009)

Copy number variation goes clinical
por: Le Caignec, Cédric, et al.
Publicado: (2009)

Copy number variation in Parkinson's disease
por: Toft, Mathias, et al.
Publicado: (2010)

Copy number variation in the bovine genome
por: Fadista, João, et al.
Publicado: (2010)

Copy Number Variation in Thai Population
por: Suktitipat, Bhoom, et al.
Publicado: (2014)

Copy Number Variation in the Horse Genome
por: Ghosh, Sharmila, et al.
Publicado: (2014)

Copy number variations among silkworms
por: Zhao, Qian, et al.
Publicado: (2014)

Copy number variation in bipolar disorder
por: Green, E K, et al.
Publicado: (2016)

Copy number variation and neuropsychiatric illness
por: Rees, Elliott, et al.
Publicado: (2021)

Copy Number Variations in Neuropsychiatric Disorders
por: Büki, Gergely, et al.
Publicado: (2023)

Plasmodium copy number variation scan: gene copy numbers evaluation in haploid genomes
por: Beghain, Johann, et al.
Publicado: (2016)

Investigation of Complement Component C4 Copy Number Variation in Human Longevity
por: Flachsbart, Friederike, et al.
Publicado: (2014)

Investigation on combined copy number variation sequencing and cytogenetic karyotyping for prenatal diagnosis
por: Zhang, Jinman, et al.
Publicado: (2021)

Investigation of Copy Number Variation in South African Patients With Congenital Heart Defects
por: Saacks, Nicole A., et al.
Publicado: (2022)

Copy number variations in candidate genomic regions confirm genetic heterogeneity and parental bias in Hirschsprung disease
por: Lantieri, Francesca, et al.
Publicado: (2019)

Copy number variation in the susceptibility to systemic lupus erythematosus
por: Barbosa, Fernanda Bueno, et al.
Publicado: (2018)

An initial comparative map of copy number variations in the goat (Capra hircus) genome
por: Fontanesi, Luca, et al.
Publicado: (2010)

Copy Number Variation Regions Differing in Segregation Patterns Span Different Sets of Genes
por: Arias, Katherine D., et al.
Publicado: (2023)

Copy Number Variation Mapping and Genomic Variation of Autochthonous and Commercial Turkey Populations
por: Strillacci, Maria G., et al.
Publicado: (2019)

Increased DNA Copy Number Variation Mosaicism in Elderly Human Brain
por: Villela, Darine, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_ag3sqal40kq0kpp3ihne2oflmf