(Q34462975)

2 August 2017

A pilot controlled trial of insulin-like growth factor-1 in children with Phelan-McDermid syndrome (English)

1 reference

Erratum: A pilot controlled trial of insulin-like growth factor-1 in children with Phelan-McDermid syndrome

2 August 2017

1 reference

corrigendum / erratum

1 reference

10.1186/S13229-015-0025-0

DOI

12 July 2019

http://api.crossref.org/works?select=update-to&filter=doi:10.1186/S13229-015-0025-0

author

Joseph Buxbaum

11

1 reference

2 August 2017

Teresa Tavassoli

8

0 references

Latha Soorya

10

object named as

Latha Soorya

1 reference

2 August 2017

4

Danielle Halpern

1 reference

2 August 2017

5

Yitzchak Frank

1 reference

2 August 2017

6

David Grodberg

1 reference

2 August 2017

7

Robert Rapaport

1 reference

2 August 2017

Alexander Kolevzon

1

1 reference

2 August 2017

Lauren Bush

2

1 reference

2 August 2017

A Ting Wang

3

1 reference

2 August 2017

William Chaplin

9

1 reference

2 August 2017

12 December 2014

1 reference

2 August 2017

1 reference

2 August 2017

5

1 reference

2 August 2017

1

1 reference

2 August 2017

54

1 reference

https://scigraph.springernature.com/pub.10.1186/2040-2392-5-54

2 August 2017

0 references

cites work

Differences in white matter reflect atypical developmental trajectory in autism: A Tract-based Spatial Statistics study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

SHANK3 haploinsufficiency: a "common" but underdiagnosed highly penetrant monogenic cause of autism spectrum disorders

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

Insulin-like growth factor-1 rescues synaptic and motor deficits in a mouse model of autism and developmental delay

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

Neuropsychopathology in 7 Patients with the 22q13 Deletion Syndrome: Presence of Bipolar Disorder and Progressive Loss of Skills

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

Defects in translational regulation contributing to human cognitive and behavioral disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

Protein interactome reveals converging molecular pathways among autism disorders

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

A model for neural development and treatment of Rett syndrome using human induced pluripotent stem cells

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

22q13.3 deletion syndrome: clinical and molecular analysis using array CGH

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

Neurobehavioral profile and brain imaging study of the 22q13.3 deletion syndrome in childhood

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

Structural variation of chromosomes in autism spectrum disorder

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

Contribution of SHANK3 mutations to autism spectrum disorder

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

6 July 2018

The postsynaptic density

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

Identification of a recurrent breakpoint within the SHANK3 gene in the 22q13.3 deletion syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

Molecular and phenotypic characterization of ring chromosome 22

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

Molecular characterisation of patients with subtelomeric 22q abnormalities using chromosome specific array-based comparative genomic hybridisation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrum

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

6 July 2018

22q13 deletion syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

Varieties of repetitive behavior in autism: comparisons to mental retardation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

Clinical, cytogenetic, and molecular characterization of seven patients with deletions of chromosome 22q13.3

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

The aberrant behavior checklist: a behavior rating scale for the assessment of treatment effects.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4326443

Novel de novo SHANK3 mutation in autistic patients

6 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-5-54

Structural neural phenotype of autism: preliminary evidence from a diffusion tensor imaging study using tract-based spatial statistics

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-5-54

Brain activation in sedated children: auditory and visual functional MR imaging

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-5-54

Speech delay in children: a functional MR imaging study

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-5-54

Intranasal insulin to improve developmental delay in children with 22q13 deletion syndrome: an exploratory clinical trial.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-5-54

Dose-dependent effect of risperidone treatment in a case of 22q13.3 deletion syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-5-54

The effects of propofol on cerebral blood flow velocity and cerebral oxygen extraction during cardiopulmonary bypass

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25685306

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/2040-2392-5-54

1 reference

Dimensions Publication ID

2 August 2017

0 references

1 reference

2 August 2017

1 reference