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期刊名:Journal of neurodevelopmental disorders

缩写:J NEURODEV DISORD

ISSN:1866-1947

e-ISSN:1866-1955

IF/分区:4.0/Q1

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共收录本刊相关文章索引566
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Elizabeth I Pierpont,Erica Kesin Richmond,Leonard Abbeduto et al. Elizabeth I Pierpont et al.
Fragile X syndrome (FXS) is the most common inherited cause of intellectual disability. Although language delays are frequently observed in FXS, neither the longitudinal course of language development nor its cognitive predictors are well u...
Frank H Bloomfield Frank H Bloomfield
Many aspects of postnatal development are influenced by events before birth, including cognitive and language development. An adverse intrauterine environment, for example secondary to poor maternal nutritional status, multiple pregnancy, o...
Silvia Paracchini Silvia Paracchini
Recent advances in the field of language-related disorders have led to the identification of candidate genes for specific language impairment (SLI) and dyslexia. Replication studies have been conducted in independent samples including popul...
Cindi G Flores,Gregory Valcante,Steve Guter et al. Cindi G Flores et al.
Restricted and repetitive behavior (RRB) is a group of heterogeneous maladaptive behaviors. RRB is one of the key diagnostic features of autism spectrum disorders (ASDs) and also commonly observed in Prader-Willi syndrome (PWS). In this stu...
Lisa A Croen,Susan L Connors,Marilyn Matevia et al. Lisa A Croen et al.
This study aims to investigate the association between prenatal exposure to terbutaline and other β2 adrenergic receptor (B2AR) agonists and autism spectrum disorders (ASDs). The methodology used is a case-control study among children born...
Elisabeth M Dykens,Evon Lee,Elizabeth Roof Elisabeth M Dykens
Prader-Willi syndrome (PWS) is well-known for its genetic and phenotypic complexities. Caused by a lack of paternally derived imprinted material on chromosome 15q11-q13, individuals with PWS have mild to moderate intellectual disabilities, ...
Dennis Drayna,Changsoo Kang Dennis Drayna
Stuttering is a common but poorly understood speech disorder. Evidence accumulated over the past several decades has indicated that genetic factors are involved, and genetic linkage studies have begun to identify specific chromosomal loci a...
Silvia De Rubeis,Claudia Bagni Silvia De Rubeis
The Fragile X syndrome (FXS) is a leading cause of intellectual disability (ID) and autism. The disease is caused by mutations or loss of the Fragile X Mental Retardation Protein (FMRP), an RNA-binding protein playing multiple functions in ...
Rebecca Christine Knickmeyer,Marsha Davenport Rebecca Christine Knickmeyer
Turner syndrome (TS) is one of the most common sex chromosome abnormalities. Affected individuals often show a unique pattern of cognitive strengths and weaknesses and are at increased risk for a number of other neurodevelopmental condition...
Toru Takumi Toru Takumi
Autism is a neurodevelopmental disorder that manifests in childhood as social behavioral abnormalities, such as abnormal social interaction, impaired communication, and restricted interest or behavior. Of the known causes of autism, duplica...