IGF1 as a Potential Treatment for Rett Syndrome: Safety Assessment in Six Rett Patients (Q42049161)

15 October 2017

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

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15 October 2017

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11

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15 October 2017

12

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15 October 2017

Giorgio Pini

1

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15 October 2017

Maria Flora Scusa

2

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15 October 2017

Laura Congiu

3

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15 October 2017

Alberto Benincasa

4

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15 October 2017

Paolina Morescalchi

5

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15 October 2017

Ilaria Bottiglioni

6

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15 October 2017

Pietro Di Marco

7

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15 October 2017

Paolo Borelli

8

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15 October 2017

Ubaldo Bonuccelli

9

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15 October 2017

Andrea Della-Chiesa

10

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15 October 2017

13 June 2012

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Autism Research & Treatment

15 October 2017

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15 October 2017

2012

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15 October 2017

679801

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Creative Commons Attribution 3.0 Unported

15 October 2017

start time

1 January 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

cites work

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FOXG1 is responsible for the congenital variant of Rett syndrome

5 June 2018

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Diagnostic criteria for the Zappella variant of Rett syndrome (the preserved speech variant).

5 June 2018

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The role of recombinant human insulin-like growth factor-I in treating children with short stature

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Insulin-like growth factor 1 (IGF-1) mediates the effects of enriched environment (EE) on visual cortical development.

5 June 2018

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Reversal of neurological defects in a mouse model of Rett syndrome

5 June 2018

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Gene expression changes and molecular pathways mediating activity-dependent plasticity in visual cortex

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Insulin-like growth factor-1 promotes neuronal glucose utilization during brain development and repair processes

5 June 2018

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5 June 2018

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Characterisation of breathing and associated central autonomic dysfunction in the Rett disorder

5 June 2018

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5 June 2018

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Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice

5 June 2018

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A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

5 June 2018

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Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

5 June 2018

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Electroencephalographical study of the Rett syndrome with special reference to the monorhythmic theta activities in adult patients.

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Epilepsy in Rett syndrome: association between phenotype and genotype, and implications for practice.

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Epilepsy treatment in Rett syndrome

17 August 2018

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Early-onset seizure variant of Rett syndrome: definition of the clinical diagnostic criteria.

17 August 2018

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High prevalence of biochemical acromegaly in primary care patients with elevated IGF-1 levels

17 August 2018

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Methyl CpG-binding protein 2 (a mutation of which causes Rett syndrome) directly regulates insulin-like growth factor binding protein 3 in mouse and human brains.

17 August 2018

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

17 August 2018

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Assessment of the maturity-related brainstem functions reveals the heterogeneous phenotypes and facilitates clinical management of Rett syndrome

17 August 2018

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17 August 2018

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Effect of insulinlike growth factor-1 treatment in children with cystic fibrosis

17 August 2018

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Medium-term open label trial of L-carnitine in Rett syndrome.

17 August 2018

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Osteopenia in Rett syndrome

17 August 2018

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Insulin-like growth factors cross the blood-brain barrier

17 August 2018

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Long-term treatment with recombinant insulin-like growth factor (IGF)-I in children with severe IGF-I deficiency due to growth hormone insensitivity

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12 December 2020

Cardiorespiratory challenges in Rett's syndrome

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12 December 2020

Clinical and electroencephalographic effects of folinic acid treatment in Rett syndrome patients

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12 December 2020

Rett syndrome: a suggested staging system for describing impairment profile with increasing age towards adolescence

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12 December 2020

Changes in serum insulin-like growth factor I (IGF-I) and IGF-binding protein-3 levels during growth hormone treatment in prepubertal short children born small for gestational age

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12 December 2020

Rett syndrome: analysis of deaths in the British survey

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12 December 2020

Therapy for 6.5-7.5 years with recombinant insulin-like growth factor I in children with growth hormone insensitivity syndrome: a clinical research center study

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12 December 2020

Osteoblast-specific knockout of the insulin-like growth factor (IGF) receptor gene reveals an essential role of IGF signaling in bone matrix mineralization

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12 December 2020

Identifiers

DOI

10.1155/2012/679801

1 reference

15 October 2017

1 reference

15 October 2017

1 reference