Cargando…

Use of the Griffiths mental development scale-Chinese in the assessment of children with autism spectrum disorder and global developmental delay/intellectual disability

The Griffiths Mental Development Scale-Chinese (GDS-C) is used in China to assess the development of children from birth to 8 years of age. Language disorders are a common symptom of autism spectrum disorder (ASD) and global developmental delay (GDD)/intellectual disability (ID). There is a need to...

Descripción completa

Detalles Bibliográficos
Autores principales:	Wang, Hui, Du, Yu, Mao, Zhenghuan, Che, Yueping, Li, Haifeng, Ding, Li, Jin, Huiying
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Lippincott Williams & Wilkins 2021
Materias:	6200
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8021334/ https://www.ncbi.nlm.nih.gov/pubmed/33787650 http://dx.doi.org/10.1097/MD.0000000000025407

Ejemplares similares

A case of West syndrome and global developmental delay in a child with a heterozygous mutation in the TBL1XR1 gene: A case report
por: Wu, Xiao-Hui, et al.
Publicado: (2023)

Exon 21 deletion in the OPHN1 gene in a family with syndromic X-linked intellectual disability: Case report
por: Bogliş, Alina, et al.
Publicado: (2020)

Weight status in individuals with autism spectrum disorder: A study protocol for systematic review and meta-analysis
por: Xie, Xue-Ni, et al.
Publicado: (2019)

Correlation analysis of expression of CC and CXC chemokines in children with autism spectrum disorder
por: Peng, Guangyang, et al.
Publicado: (2021)

A Developmental Profile of Children With Autism Spectrum Disorder in China Using the Griffiths Mental Development Scales
por: Li, Hong-Hua, et al.
Publicado: (2020)

Identification of target hub genes and construction of a novel miRNA regulatory network in autism spectrum disorder by integrated analysis
por: Zhu, Jinyi, et al.
Publicado: (2023)

Low Rates of Genetic Testing in Children With Developmental Delays, Intellectual Disability, and Autism Spectrum Disorders
por: Peabody, John, et al.
Publicado: (2015)

A nonsense mutation in the CUL3 gene in a Chinese patient with autism spectrum disorder and epilepsy: A case report
por: Qian, Meijia, et al.
Publicado: (2022)

Can probiotic supplements improve the symptoms of autism spectrum disorder in children?: A protocol for systematic review and meta analysis
por: Feng, Kai, et al.
Publicado: (2021)

Association between congenital heart disease and autism spectrum disorders: A protocol for a systematic review and meta-analysis
por: Ma, Dan, et al.
Publicado: (2023)

Editorial: Developmental delay and intellectual disability
por: Banerjee, Santasree, et al.
Publicado: (2022)

Effects of social stories intervention for children and adolescents with autism spectrum disorders: A protocol for a systematic review and meta-analysis of randomized controlled trials
por: Chen, Tingting, et al.
Publicado: (2020)

Analysis of potential biomarkers and immune infiltration in autism based on bioinformatics analysis
por: Cao, Wenjun, et al.
Publicado: (2023)

A novel 1p33p32.2 deletion involving SCP2, ORC1, and DAB1 genes in a patient with craniofacial dysplasia, short stature, developmental delay, and leukoencephalopathy: A case report
por: Jiang, Maoying, et al.
Publicado: (2020)

YWHAZ variation causes intellectual disability and global developmental delay with brain malformation
por: Wan, Rui-Ping, et al.
Publicado: (2022)

Chromosomal microarray analysis of 410 Han Chinese patients with autism spectrum disorder or unexplained intellectual disability and developmental delay
por: Liu, Yi, et al.
Publicado: (2022)

Evaluation of Individuals with Non-Syndromic Global Developmental Delay and Intellectual Disability
por: AlMutiri, Rowim, et al.
Publicado: (2023)

Prenatal, perinatal, and postnatal factors associated with autism: A meta-analysis
por: Wang, Chengzhong, et al.
Publicado: (2017)

Genetic testing in patients with global developmental delay / intellectual disabilities. A review
por: MICLEA, DIANA, et al.
Publicado: (2015)

Relationship Between Developmental Dislocation of the Hip in Infant and Acetabular Dysplasia at Skeletal Maturity
por: Okano, Kunihiko, et al.
Publicado: (2015)

Epidemiological investigation and ultrasonic diagnosis of developmental dysplasia of the hip in Chinese infants: A large multi-center cohort study
por: Xu, Na, et al.
Publicado: (2022)

De novo variants in EBF3 are associated with hypotonia, developmental delay, intellectual disability, and autism
por: Tanaka, Akemi J., et al.
Publicado: (2017)

Pedobarographic Analysis Following Pemberton's Pericapsular Osteotomy for Unilateral Developmental Dysplasia of the Hip: An Observational Study
por: Xu, Chao, et al.
Publicado: (2015)

The Periosteal Autografts Transplantation for Cartilage Defects of the Hip in Older Children With Developmental Dysplasia as an Adjunctive Procedure
por: Du, Ming-Hua, et al.
Publicado: (2016)

Importance and usage of chromosomal microarray analysis in diagnosing intellectual disability, global developmental delay, and autism; and discovering new loci for these disorders
por: Ceylan, Ahmet Cevdet, et al.
Publicado: (2018)

Chromosomal Microarray Testing in 42 Korean Patients with Unexplained Developmental Delay, Intellectual Disability, Autism Spectrum Disorders, and Multiple Congenital Anomalies
por: Lee, Sun Ho, et al.
Publicado: (2017)

Retrospective observational study comparing the international hip dysplasia institute classification with the Tonnis classification of developmental dysplasia of the hip
por: Miao, Mingyuan, et al.
Publicado: (2017)

Porencephaly in an Italian neonate with foetal alcohol spectrum disorder: A case report
por: Mencarelli, Annalisa, et al.
Publicado: (2020)

Genomic diagnosis for children with intellectual disability and/or developmental delay
por: Bowling, Kevin M., et al.
Publicado: (2017)

Prevalence and Developmental Profiles of Autism Spectrum Disorders in Children With Global Developmental Delay
por: Shan, Ling, et al.
Publicado: (2022)

Clinical characteristic and risk factors of recurrent sexual abuse and delayed reported sexual abuse in childhood
por: Hu, Mei-Hua, et al.
Publicado: (2018)

Magnetic resonance imaging evaluation of the labrum to predict acetabular development in developmental dysplasia of the hip: A STROBE compliant study
por: Shirai, Yasuhiro, et al.
Publicado: (2017)

Thriving in Youth with Autism Spectrum Disorder and Intellectual Disability
por: Weiss, Jonathan A., et al.
Publicado: (2015)

Psychopathology in Adults with Autism Spectrum Disorder and Intellectual Disability
por: Mccarthy, J.
Publicado: (2022)

Broad-spectrum Antibiotic Plus Metronidazole May Not Prevent the Deterioration of Necrotizing Enterocolitis From Stage II to III in Full-term and Near-term Infants: A Propensity Score-matched Cohort Study
por: Luo, Li-Juan, et al.
Publicado: (2015)

A delayed diagnosis of catecholaminergic polymorphic ventricular tachycardia with a mutant of RYR2 at c.7580T>G for 6 years in a 9-year-old child
por: Duan, Hongyu, et al.
Publicado: (2018)

Genetic factors and the risk of drug-resistant epilepsy in young children with epilepsy and neurodevelopment disability: A prospective study and updated meta-analysis
por: Lin, Chien-Heng, et al.
Publicado: (2021)

Effect of delayed palivizumab administration on respiratory syncytial virus infection-related hospitalisation: A retrospective, observational study
por: Kamori, Akiko, et al.
Publicado: (2021)

Motor proficiency differences among students with intellectual disabilities, autism, and developmental disability
por: Jeoung, Bogja
Publicado: (2018)

Clinical Case Report of Expansive Laminoplasty for Cervical Myelopathy Due to Both Disc Herniation and Developmental Cervical Spinal Canal Stenosis in Older Adolescents
por: Zhou, Hua, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_2a9s25nj7ghshl5535k2thkf9f