(Q33915713)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10964075%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

title

Does a peculiar EEG pattern exist also for FRAXE mental retardation? (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10964075%20AND%20SRC:MED&resulttype=core&format=json

Sebastiano Antonino Musumeci

9 November 2019

author

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10964075%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Carmela Scuderi

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10964075%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Raffaele Ferri

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10964075%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Guido Anello

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10964075%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Maurizio Elia

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10964075%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Roberto Salluzzo

1 reference

ORCID Public Data File 2021

author name string

R Salluzzo

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10964075%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

P Bosco

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10964075%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

publication date

1 September 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10964075%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

published in

Clinical Neurophysiology

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10964075%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

volume

111

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10964075%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

issue

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10964075%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

page(s)

1632-1636

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10964075%20AND%20SRC:MED&resulttype=core&format=json

Nucleus basalis magnocellularis and hippocampus are the major sites of FMR-1 expression in the human fetal brain.

9 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1388-2457%2800%2900367-9

7 January 2021

Cognitive, behavioral, and neuroanatomical assessment of two unrelated male children expressing FRAXE.

1 reference

https://api.crossref.org/works/10.1016%2FS1388-2457%2800%2900367-9

7 January 2021

Clinical, cytogenetic, and molecular analysis of three families with FRAXE

1 reference

https://api.crossref.org/works/10.1016%2FS1388-2457%2800%2900367-9

7 January 2021

Fragile X mental retardation protein: nucleocytoplasmic shuttling and association with somatodendritic ribosomes

1 reference

https://api.crossref.org/works/10.1016%2FS1388-2457%2800%2900367-9

7 January 2021

BIT-mapped somatosensory evoked potentials in the fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1388-2457%2800%2900367-9

7 January 2021

Identification of the FRAXE fragile site in two families ascertained for X linked mental retardation

1 reference

https://api.crossref.org/works/10.1016%2FS1388-2457%2800%2900367-9

7 January 2021

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

1 reference

https://api.crossref.org/works/10.1016%2FS1388-2457%2800%2900367-9

7 January 2021

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.

1 reference

https://api.crossref.org/works/10.1016%2FS1388-2457%2800%2900367-9

7 January 2021

Screening for FMR1 and FMR2 mutations in 222 individuals from Spanish special schools: identification of a case of FRAXE-associated mental retardation.

1 reference

https://api.crossref.org/works/10.1016%2FS1388-2457%2800%2900367-9

7 January 2021

FRAXE and mental retardation

1 reference

https://api.crossref.org/works/10.1016%2FS1388-2457%2800%2900367-9

7 January 2021

Amplification of the Xq28 FRAXE repeats: extreme phenotype variability?

1 reference

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7 January 2021

Population screening at the FRAXA and FRAXE loci: molecular analyses of boys with learning difficulties and their mothers.

1 reference

https://api.crossref.org/works/10.1016%2FS1388-2457%2800%2900367-9

7 January 2021

The role of size, sequence and haplotype in the stability of FRAXA and FRAXE alleles during transmission

1 reference

https://api.crossref.org/works/10.1016%2FS1388-2457%2800%2900367-9

7 January 2021

Fragile-X syndrome: a particular epileptogenic EEG pattern

1 reference

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7 January 2021

Evoked spikes and giant somatosensory evoked potentials in a patient with fragile-X syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS1388-2457%2800%2900367-9

7 January 2021

Epilepsy and EEG findings in males with fragile X syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS1388-2457%2800%2900367-9

7 January 2021

Specific sequences in the fragile X syndrome protein FMR1 and the FXR proteins mediate their binding to 60S ribosomal subunits and the interactions among them

1 reference

https://api.crossref.org/works/10.1016%2FS1388-2457%2800%2900367-9

7 January 2021

Characterisation of a new rare fragile site easily confused with the fragile X

1 reference

https://api.crossref.org/works/10.1016%2FS1388-2457%2800%2900367-9

7 January 2021

Simple tandem DNA repeats and human genetic disease

1 reference

https://api.crossref.org/works/10.1016%2FS1388-2457%2800%2900367-9

7 January 2021