(Q37213531)

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Evaluation of current pharmacological treatment options in the management of Rett syndrome: from the present to future therapeutic alternatives

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scholarly article

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Europe PubMed Central

PMC publication ID

19 August 2017

Evaluation of current pharmacological treatment options in the management of Rett syndrome: from the present to future therapeutic alternatives (English)

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

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4

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Alan K Percy

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Europe PubMed Central

PMC publication ID

19 August 2017

author name string

Christopher A Chapleau

1

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Jane Lane

2

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Europe PubMed Central

PMC publication ID

19 August 2017

Lucas Pozzo-Miller

3

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Europe PubMed Central

PMC publication ID

19 August 2017

publication date

1 November 2013

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Europe PubMed Central

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19 August 2017

Current Clinical Pharmacology

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Europe PubMed Central

PMC publication ID

19 August 2017

8

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Europe PubMed Central

PMC publication ID

19 August 2017

4

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

358-369

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Europe PubMed Central

PMC publication ID

19 August 2017

The short-time structural plasticity of dendritic spines is altered in a model of Rett syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

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A TrkB small molecule partial agonist rescues TrkB phosphorylation deficits and improves respiratory function in a mouse model of Rett syndrome

1 reference

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6 September 2017

7,8-dihydroxyflavone exhibits therapeutic efficacy in a mouse model of Rett syndrome

1 reference

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Clinical severity and quality of life in children and adolescents with Rett syndrome

1 reference

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Genome-wide activity-dependent MeCP2 phosphorylation regulates nervous system development and function

1 reference

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6 September 2017

Isogenic pairs of wild type and mutant induced pluripotent stem cell (iPSC) lines from Rett syndrome patients as in vitro disease model

1 reference

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Brain-derived neurotrophic factor in patients with Huntington's disease

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Rett syndrome: exploring the autism link

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6 September 2017

Neuronal maturation defect in induced pluripotent stem cells from patients with Rett syndrome

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6 September 2017

Ex vivo treatment with a novel synthetic aminoglycoside NB54 in primary fibroblasts from Rett syndrome patients suppresses MECP2 nonsense mutations

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6 September 2017

Vitamin D deficiency is prevalent in girls and women with Rett syndrome

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6 September 2017

Complexities of Rett syndrome and MeCP2

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Synaptic determinants of rett syndrome.

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6 September 2017

Isolation of MECP2-null Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivation

1 reference

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Antiepileptic drug interactions - principles and clinical implications

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Potential therapeutic uses of BDNF in neurological and psychiatric disorders

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6 September 2017

Autonomic dysfunction with mutations in the gene that encodes methyl-CpG-binding protein 2: insights into Rett syndrome

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6 September 2017

Network hyperexcitability in hippocampal slices from Mecp2 mutant mice revealed by voltage-sensitive dye imaging.

1 reference

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6 September 2017

Experimental models of Rett syndrome based on Mecp2 dysfunction.

1 reference

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6 September 2017

Epigenetic modification of the FMR1 gene in fragile X syndrome is associated with differential response to the mGluR5 antagonist AFQ056.

1 reference

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6 September 2017

Rett syndrome: revised diagnostic criteria and nomenclature

1 reference

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6 September 2017

Readthrough of nonsense mutations in Rett syndrome: evaluation of novel aminoglycosides and generation of a new mouse model

1 reference

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6 September 2017

Rett syndrome diagnostic criteria: lessons from the Natural History Study

1 reference

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6 September 2017

Toward fulfilling the promise of molecular medicine in fragile X syndrome

1 reference

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6 September 2017

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

1 reference

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6 September 2017

Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes

1 reference

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Linking Molecules to Mood: New Insight Into the Biology of Depression

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6 September 2017

Deoxygedunin, a natural product with potent neurotrophic activity in mice

1 reference

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6 September 2017

Drug- and non-drug-associated QT interval prolongation

1 reference

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Proton pump inhibitor use, hip fracture, and change in bone mineral density in postmenopausal women: results from the Women's Health Initiative

1 reference

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6 September 2017

Epilepsy and the natural history of Rett syndrome.

1 reference

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6 September 2017

Variable phenotypic expression of a MECP2 mutation in a family.

1 reference

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6 September 2017

A selective TrkB agonist with potent neurotrophic activities by 7,8-dihydroxyflavone.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

N-acetylserotonin activates TrkB receptor in a circadian rhythm

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Longevity in Rett syndrome: analysis of the North American Database

1 reference

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Profile of mecasermin for the long-term treatment of growth failure in children and adolescents with severe primary IGF-1 deficiency

1 reference

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6 September 2017

Pharmaceuticals targeting nonsense mutations in genetic diseases: progress in development

1 reference

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6 September 2017

Dendritic spine pathologies in hippocampal pyramidal neurons from Rett syndrome brain and after expression of Rett-associated MECP2 mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Mecp2 deficiency decreases bone formation and reduces bone volume in a rodent model of Rett syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Breathing disorders in Rett syndrome: progressive neurochemical dysfunction in the respiratory network after birth

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions

1 reference

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Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Bdnf overexpression in hippocampal neurons prevents dendritic atrophy caused by Rett-associated MECP2 mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

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Ampakines cause sustained increases in brain-derived neurotrophic factor signaling at excitatory synapses without changes in AMPA receptor subunit expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Breathing dysfunction in Rett syndrome: understanding epigenetic regulation of the respiratory network

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

MeCP2, a key contributor to neurological disease, activates and represses transcription

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

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Severe congenital encephalopathy caused by MECP2 null mutations in males: central hypoxia and reduced neuronal dendritic structure.

1 reference

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Low-energy femoral shaft fractures associated with alendronate use.

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Differential regulation of central BDNF protein levels by antidepressant and non-antidepressant drug treatments

1 reference

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PTC124 is an orally bioavailable compound that promotes suppression of the human CFTR-G542X nonsense allele in a CF mouse model

1 reference

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6 September 2017

Role for metabotropic glutamate receptor 5 (mGluR5) in the pathogenesis of fragile X syndrome

1 reference

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6 September 2017

Correction of fragile X syndrome in mice.

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6 September 2017

Selective cerebral volume reduction in Rett syndrome: a multiple-approach MR imaging study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Brain-derived neurotrophic factor expression and respiratory function improve after ampakine treatment in a mouse model of Rett syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Modifying IGF1 activity: an approach to treat endocrine disorders, atherosclerosis and cancer

1 reference

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Melatonin and its receptors: a new class of sleep-promoting agents.

1 reference

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6 September 2017

Seizures in Rett syndrome: an overview from a one-year calendar study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Reversal of neurological defects in a mouse model of Rett syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Aminoglycoside-induced translational read-through in disease: overcoming nonsense mutations by pharmacogenetic therapy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Transient receptor potential channels as novel effectors of brain-derived neurotrophic factor signaling: potential implications for Rett syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Enhanced anxiety and stress-induced corticosterone release are associated with increased Crh expression in a mouse model of Rett syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Dysregulation of brain-derived neurotrophic factor expression and neurosecretory function in Mecp2 null mice

1 reference

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6 September 2017

ACC/AHA/ESC 2006 Guidelines for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death: a report of the American College of Cardiology/American Heart Association Task Force and the European Society of Cardiolo

1 reference

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6 September 2017

Fluoxetine and cocaine induce the epigenetic factors MeCP2 and MBD1 in adult rat brain

1 reference

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6 September 2017

Cardiac disease and Rett syndrome

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6 September 2017

Genomic DNA methylation: the mark and its mediators

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6 September 2017

The association between behavior and genotype in Rett syndrome using the Australian Rett Syndrome Database.

1 reference

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6 September 2017

Clinical trial design to evaluate the effects of drugs on cardiac repolarization: current state of the art.

1 reference

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6 September 2017

Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2.

1 reference

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6 September 2017

Rett syndrome: model of neurodevelopmental disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Postnatal loss of methyl-CpG binding protein 2 in the forebrain is sufficient to mediate behavioral aspects of Rett syndrome in mice

1 reference

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6 September 2017

Therapeutic implications of the mGluR theory of fragile X mental retardation

1 reference

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6 September 2017

Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome

1 reference

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6 September 2017

Insulin-like growth factor system in amyotrophic lateral sclerosis

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6 September 2017

Bone mass and turnover in women with epilepsy on antiepileptic drug monotherapy

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6 September 2017

The mGluR theory of fragile X mental retardation

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Phenotypic manifestations of MECP2 mutations in classical and atypical Rett syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Developmental expression of methyl-CpG binding protein 2 is dynamically regulated in the rodent brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

DNA Methylation-Related Chromatin Remodeling in Activity-Dependent Bdnf Gene Regulation

1 reference

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6 September 2017

Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Rett syndrome. Current status and new vistas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

The expression of methyl CpG binding factor MeCP2 correlates with cellular differentiation in the developing rat brain and in cultured cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Transcriptional profiling of a mouse model for Rett syndrome reveals subtle transcriptional changes in the brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Mutant mouse models of insulin-like growth factor actions in the central nervous system

1 reference

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6 September 2017

Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

A decade of molecular studies of fragile X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Safety of non-antiarrhythmic drugs that prolong the QT interval or induce torsade de pointes: an overview

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Gene expression profiling in postmortem Rett Syndrome brain: differential gene expression and patient classification.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Adverse effects of antiepileptic drugs on bone structure: epidemiology, mechanisms and therapeutic implications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Growth and nutrition in Rett syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Dendritic anomalies in disorders associated with mental retardation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Genetic and physical mapping of a gene encoding a methyl CpG binding protein, Mecp2, to the mouse X chromosome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Selective dendritic alterations in the cortex of Rett syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

6 September 2017

Aminoglycoside-mediated partial suppression of MECP2 nonsense mutations responsible for Rett syndrome in vitro

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

14 September 2017

Patients with Rett syndrome sustain low-energy fractures

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

14 September 2017

Rett syndrome: North American database

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

14 September 2017

Early defects of GABAergic synapses in the brain stem of a MeCP2 mouse model of Rett syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

14 September 2017

p75 and Trk: a two-receptor system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

14 September 2017

Rett syndrome microglia damage dendrites and synapses by the elevated release of glutamate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

28 September 2017

Signal transduction mechanism of insulin and insulin-like growth factor-1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

28 September 2017

The role of the insulin-like growth factors in the central nervous system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

28 September 2017

Adult neural function requires MeCP2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

26 June 2018

Exogenous brain-derived neurotrophic factor rescues synaptic dysfunction in Mecp2-null mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

26 June 2018

Oral treatment with desipramine improves breathing and life span in Rett syndrome mouse model

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

26 June 2018

Differential actions of acute and chronic citalopram on the rodent hypothalamic-pituitary-adrenal axis response to acute restraint stress

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

26 June 2018

Serum melatonin kinetics and long-term melatonin treatment for sleep disorders in Rett syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

26 June 2018

Sleep dysfunction in Rett syndrome: a trial of exogenous melatonin treatment.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

26 June 2018

Aberrant sleep patterns in children with the Rett syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

26 June 2018

Epilepsy treatment in Rett syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

3 September 2018

Valproate and risk of fracture in Rett syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

3 September 2018

Efficacy of levetiracetam in the treatment of drug-resistant Rett syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

3 September 2018

Suppression of nonsense mutations in Rett syndrome by aminoglycoside antibiotics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

3 September 2018

Atypical fractures of the femoral diaphysis in postmenopausal women taking alendronate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

3 September 2018

Early determinants of fractures in Rett syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

3 September 2018

Treatment with desipramine improves breathing and survival in a mouse model for Rett syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

3 September 2018

FXYD1 is an MeCP2 target gene overexpressed in the brains of Rett syndrome patients and Mecp2-null mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

3 September 2018

The digestive system and nutritional considerations for individuals with Rett syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

3 September 2018

Osteoporosis in Rett syndrome: A study on normal values.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

3 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

3 September 2018

The impact of MECP2 mutations in the expression patterns of Rett syndrome patients.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

3 September 2018

The Rett Syndrome Behaviour Questionnaire (RSBQ): refining the behavioural phenotype of Rett syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

3 September 2018

Bone histomorphometry in three females with Rett syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

3 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

3 September 2018

Expression pattern of the Rett syndrome gene MeCP2 in primate prefrontal cortex.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

3 September 2018

Osteopenia in Rett syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

3 September 2018

Rett syndrome: 3-D confocal microscopy of cortical pyramidal dendrites and afferents.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3789853

3 September 2018

Neuropathology of Rett syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/24050745

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A randomized, prospective, comparison study of polyethylene glycol 3350 without electrolytes and milk of magnesia for children with constipation and fecal incontinence

1 reference

https://pubmed.ncbi.nlm.nih.gov/24050745

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pervasive neuroanatomic abnormalities of the brain in three cases of Rett's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/24050745

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of fragile X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/24050745

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/24050745

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurodegenerative disease: BDNF copycats

1 reference

https://pubmed.ncbi.nlm.nih.gov/24050745

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microscopic Observations of the Brain in Rett Syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/24050745

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oropharyngeal dysfunction and gastroesophageal dysmotility are present in girls and women with Rett syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/24050745

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiorespiratory challenges in Rett's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/24050745

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Electrocardiographic findings in Rett syndrome: an explanation for sudden death?

1 reference

https://pubmed.ncbi.nlm.nih.gov/24050745

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DXA measurements in rett syndrome reveal small bones with low bone mass

1 reference

https://pubmed.ncbi.nlm.nih.gov/24050745

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.2174/15748847113086660069

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

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