(Q33702137)

28 July 2017

title

Repeated insulin-like growth factor 1 treatment in a patient with rett syndrome: a single case study (English)

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28 July 2017

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14

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28 July 2017

Giorgio Pini

1

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28 July 2017

M Flora Scusa

2

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28 July 2017

Alberto Benincasa

3

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28 July 2017

Ilaria Bottiglioni

4

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28 July 2017

Laura Congiu

5

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28 July 2017

Cyrus Vadhatpour

6

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28 July 2017

Anna Maria Romanelli

7

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28 July 2017

Ilaria Gemo

8

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28 July 2017

Chetti Puccetti

9

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28 July 2017

Rachel McNamara

10

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28 July 2017

Seán O'Leary

11

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28 July 2017

Aiden Corvin

12

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28 July 2017

Michael Gill

13

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28 July 2017

publication date

3 June 2014

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28 July 2017

published in

Frontiers in pediatrics

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28 July 2017

volume

2

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28 July 2017

page(s)

52

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Safety, pharmacokinetics, and preliminary assessment of efficacy of mecasermin (recombinant human IGF-1) for the treatment of Rett syndrome

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042280

Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042280

Changing the perspective on early development of Rett syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042280

IGF1 as a Potential Treatment for Rett Syndrome: Safety Assessment in Six Rett Patients

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042280

Adult neural function requires MeCP2.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042280

Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042280

The story of Rett syndrome: from clinic to neurobiology

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042280

Reversal of neurological defects in a mouse model of Rett syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042280

Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042280

MeCP2 expression and function during brain development: implications for Rett syndrome's pathogenesis and clinical evolution

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042280

Rett syndrome: a comprehensive review of the literature

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042280

The disease progression of Mecp2 mutant mice is affected by the level of BDNF expression

21 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.3389%2FFPED.2014.00052

Level of S100B protein, neuron specific enolase, orexin A, adiponectin and insulin-like growth factor in serum of pediatric patients suffering from sleep disorders with or without epilepsy

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.3389%2FFPED.2014.00052

Laron syndrome. First report from Greece

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24918098

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.3389/FPED.2014.00052

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28 July 2017

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28 July 2017

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