Secondary medical diagnosis in fragile X syndrome with and without autism spectrum disorder. - Wikidata - awgldk - TriplyDB

Secondary medical diagnosis in fragile X syndrome with and without autism spectrum disorder.

Secondary medical diagnosis in fragile X syndrome with and without autism spectrum disorder.

http://www.wikidata.org/entity/Q55490353

about

What can we learn about autism from studying fragile X syndrome?Advances in the treatment of fragile X syndrome The genetic and neurobiologic compass points toward common signaling dysfunctions in autism spectrum disorders The contribution of inhibitory interneurons to circuit dysfunction in Fragile X Syndrome Fragile X syndrome: A review of clinical management Premutation in the Fragile X Mental Retardation 1 (FMR1) Gene Affects Maternal Zn-milk and Perinatal Brain Bioenergetics and Scaffolding.Fragile X: leading the way for targeted treatments in autism.Resilience to audiogenic seizures is associated with p-ERK1/2 dephosphorylation in the subiculum of Fmr1 knockout mice.Fragile X: a family of disorders.Epilepsy and Autism.Early identification of autism in fragile X syndrome: a review.Broad clinical involvement in a family affected by the fragile X premutation.Understanding relationships between autism, intelligence, and epilepsy: a cross-disorder approach.Increased prevalence of seizures in boys who were probands with the FMR1 premutation and co-morbid autism spectrum disorder.Fragile X and autism: Intertwined at the molecular level leading to targeted treatments.Autoimmune disease in mothers with the FMR1 premutation is associated with seizures in their children with fragile X syndrome Consistency between research and clinical diagnoses of autism among boys and girls with fragile X syndrome.Molecular Advances Leading to Treatment Implications for Fragile X Premutation Carriers Impact of acamprosate on plasma amyloid-β precursor protein in youth: a pilot analysis in fragile X syndrome-associated and idiopathic autism spectrum disorder suggests a pharmacodynamic protein marker.Cardiac autonomic regulation in autism and Fragile X syndrome: a review.Parent-delivered touchscreen intervention for children with fragile X syndrome.Regulation of molecular pathways in the Fragile X Syndrome: insights into Autism Spectrum Disorders Reading and phonological skills in boys with fragile X syndrome FMR1 premutation and full mutation molecular mechanisms related to autism.Identification of expanded alleles of the FMR1 Gene in the CHildhood Autism Risks from Genes and Environment (CHARGE) study.eIF4E/Fmr1 double mutant mice display cognitive impairment in addition to ASD-like behaviors.Fragile X syndrome: causes, diagnosis, mechanisms, and therapeutics.Motor abilities of children diagnosed with fragile X syndrome with and without autism Clinical report: a male with Down syndrome, fragile X syndrome, and autism.Autism spectrum disorders: the quest for genetic syndromes.Public Health Literature Review of Fragile X Syndrome.Comorbidity of intellectual disability confounds ascertainment of autism: implications for genetic diagnosis.Origins of epilepsy in fragile X syndrome.Association of fragile X syndrome, Robertsonian translocation (13, 22) and autism in a child.The Emergence of Effortful Control in Young Boys With Fragile X Syndrome.Emotion recognition and visual-scan paths in Fragile X syndrome.

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Secondary medical diagnosis in fragile X syndrome with and without autism spectrum disorder.

http://www.wikidata.org/entity/Q55490353

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2008 nî lūn-bûn

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Secondary medical diagnosis in ...... hout autism spectrum disorder.

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American Journal of Medical Genetics

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Secondary medical diagnosis in ...... thout autism spectrum disorder

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Catalina García-Nonell

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David Hessl

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Emily Marvin

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Eugenia Rigau Ratera

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Flora Tassone

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Michele Y Ono

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Randi J Hagerman

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Susan Harris

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P2860

Specific Genetic Disorders and Autism: Clinical Contribution Towards their Identification

Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking duplicons

Molecular and cognitive predictors of the continuum of autistic behaviours in fragile X

A marker X chromosome

Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism

Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2

Neurobiology of autism.

Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype

Chromosomal abnormalities in a clinic sample of individuals with autistic disorder.

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1911-1916

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10.1002/AJMG.A.32290

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15

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Nicole Tartaglia

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5225369

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18627038

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Autism spectrum

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4097171

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