Seizures in Fragile X Syndrome: Characteristics and Comorbid Diagnoses (Q34143566)

31 July 2017

title

Seizures in fragile X syndrome: characteristics and comorbid diagnoses (English)

1 reference

31 July 2017

Seizures in Fragile X Syndrome: Characteristics and Comorbid Diagnoses (English)

1 reference

https://api.crossref.org/works/10.1352/1944-7558-115.6.461

2 August 2024

1 reference

severity of illness index

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20945999

2 August 2024

2

Melissa Raspa

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20945999

2 August 2024

6

Donald B. Bailey

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20945999

2 August 2024

author name string

Elizabeth Berry-Kravis

1

1 reference

31 July 2017

Lisa Loggin-Hester

3

1 reference

31 July 2017

Ellen Bishop

4

1 reference

31 July 2017

David Holiday

5

1 reference

31 July 2017

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20945999

2 August 2024

publication date

1 November 2010

1 reference

full work available at URL

31 July 2017

http://meridian.allenpress.com/ajidd/article-pdf/115/6/461/2024316/1944-7558-115_6_461.pdf

file format

Portable Document Format

1 reference

https://api.crossref.org/works/10.1352/1944-7558-115.6.461

American Journal on Intellectual and Developmental Disabilites

2 August 2024

published in

1 reference

31 July 2017

volume

115

1 reference

31 July 2017

issue

6

1 reference

31 July 2017

page(s)

461-472

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From mRNP trafficking to spine dysmorphogenesis: the roots of fragile X syndrome

31 July 2017

cites work

1

1 reference

https://api.crossref.org/works/10.1352/1944-7558-115.6.461

Co-occurring conditions associated with FMR1 gene variations: findings from a national parent survey.

2 August 2024

3

1 reference

https://api.crossref.org/works/10.1352/1944-7558-115.6.461

Lamotrigine therapy for autistic disorder: a randomized, double-blind, placebo-controlled trial

2 August 2024

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1 reference

https://api.crossref.org/works/10.1352/1944-7558-115.6.461

A pilot open label, single dose trial of fenobam in adults with fragile X syndrome.

2 August 2024

7

1 reference

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Prolonged epileptiform discharges induced by altered group I metabotropic glutamate receptor-mediated synaptic responses in hippocampal slices of a fragile X mouse model.

2 August 2024

8

1 reference

https://api.crossref.org/works/10.1352/1944-7558-115.6.461

Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits

2 August 2024

9

1 reference

https://api.crossref.org/works/10.1352/1944-7558-115.6.461

Autistic spectrum disorder: evaluating a possible contributing or causal role of epilepsy

2 August 2024

10

1 reference

https://api.crossref.org/works/10.1352/1944-7558-115.6.461

The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation

2 August 2024

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1 reference

https://api.crossref.org/works/10.1352/1944-7558-115.6.461

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

2 August 2024

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1 reference

https://api.crossref.org/works/10.1352/1944-7558-115.6.461

Local protein synthesis and spine morphogenesis: Fragile X syndrome and beyond.

2 August 2024

14

1 reference

https://api.crossref.org/works/10.1352/1944-7558-115.6.461

The fragile X prevalence paradox

2 August 2024

15

1 reference

https://api.crossref.org/works/10.1352/1944-7558-115.6.461

Origins of epilepsy in fragile X syndrome

2 August 2024

16

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https://api.crossref.org/works/10.1352/1944-7558-115.6.461

Advances in the treatment of fragile X syndrome

2 August 2024

17

1 reference

https://api.crossref.org/works/10.1352/1944-7558-115.6.461

Altered synaptic plasticity in a mouse model of fragile X mental retardation

2 August 2024

18

1 reference

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Epilepsy and fragile X gene mutations

2 August 2024

20

1 reference

https://api.crossref.org/works/10.1352/1944-7558-115.6.461

Brain-derived neurotrophic factor rescues synaptic plasticity in a mouse model of fragile X syndrome

2 August 2024

21

1 reference

https://api.crossref.org/works/10.1352/1944-7558-115.6.461

The autism-epilepsy connection

2 August 2024

22

1 reference

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Reduced cortical synaptic plasticity and GluR1 expression associated with fragile X mental retardation protein deficiency.

2 August 2024

23

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Differences in the clinical presentation of Trisomy 21 with and without autism

2 August 2024

24

1 reference

https://api.crossref.org/works/10.1352/1944-7558-115.6.461

Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome.

2 August 2024

25

1 reference

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Epilepsy and fragile X syndrome: a follow-up study

2 August 2024

26

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Epilepsy and EEG findings in males with fragile X syndrome.

2 August 2024

27

1 reference

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Benign childhood epilepsy with centrotemporal spikes and the focal sharp wave trait is not linked to the fragile X region

2 August 2024

28

1 reference

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Can sodium valproate improve learning in children with epileptiform bursts but without clinical seizures?

2 August 2024

29

1 reference

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Epilepsy and EEG findings in 18 males with fragile X syndrome

2 August 2024

30

1 reference

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The Role of Epilepsy and Epileptiform EEGs in Autism Spectrum Disorders

2 August 2024

31

1 reference

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Epileptic encephalopathies and their relationship to developmental disorders: do spikes cause autism?

2 August 2024

32

1 reference

https://api.crossref.org/works/10.1352/1944-7558-115.6.461

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

2 August 2024

33

1 reference

https://api.crossref.org/works/10.1352/1944-7558-115.6.461

Multiple Gq-coupled receptors converge on a common protein synthesis-dependent long-term depression that is affected in fragile X syndrome mental retardation.

2 August 2024

34

1 reference

https://api.crossref.org/works/10.1352/1944-7558-115.6.461

Fragile X mental retardation protein is necessary for neurotransmitter-activated protein translation at synapses

2 August 2024

35

1 reference

https://api.crossref.org/works/10.1352/1944-7558-115.6.461

2 August 2024

Identifiers

1 reference

release_ry32ygfkjvgadgotnvdvmohg3i

31 July 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ry32ygfkjvgadgotnvdvmohg3i

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference