Growth failure and outcome in Rett syndrome: specific growth references. - Wikidata - wikimedia - TriplyDB

Growth failure and outcome in Rett syndrome: specific growth references.

Growth failure and outcome in Rett syndrome: specific growth references.

http://www.wikidata.org/entity/Q36310174

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Rett Syndrome: Reaching for Clinical Trials Clinical Guidelines for Management of Bone Health in Rett Syndrome Based on Expert Consensus and Available Evidence MeCP2 deficiency results in robust Rett-like behavioural and motor deficits in male and female rats Preclinical research in Rett syndrome: setting the foundation for translational success.Developmental delay in Rett syndrome: data from the natural history study.Differential methylation of the micro-RNA 7b gene targets postnatal maturation of murine neuronal Mecp2 gene expression Pubertal development in Rett syndrome deviates from typical females Growth Charts for Individuals with Mucopolysaccharidosis VI (Maroteaux-Lamy Syndrome)Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome Age of diagnosis in Rett syndrome: patterns of recognition among diagnosticians and risk factors for late diagnosis.Experience of gastrostomy using a quality care framework: the example of rett syndrome The Changing Face of Survival in Rett Syndrome and MECP2-Related Disorders.Longitudinal course of epilepsy in Rett syndrome and related disorders.Progress in Rett Syndrome: from discovery to clinical trials Recent Progress in Rett Syndrome and MeCP2 Dysfunction: Assessment of Potential Treatment Options Assessment and management of nutrition and growth in Rett syndrome Effects of ω-3 PUFAs supplementation on myocardial function and oxidative stress markers in typical Rett syndrome Neurobiologically-based treatments in Rett syndrome: opportunities and challenges.Inflammatory lung disease in Rett syndrome.Development of the Tailored Rett Intervention and Assessment Longitudinal (TRIAL) database and the Rett Evaluation of Symptoms and Treatments (REST) Questionnaire.Scoliosis in Rett Syndrome: Progression, Comorbidities, and Predictors.Quantitative and qualitative insights into the experiences of children with Rett syndrome and their families.Association of human height-related genetic variants with familial short stature in Han Chinese in Taiwan.Lower incidence of fracture after IV bisphosphonates in girls with Rett syndrome and severe bone fragility.Neuroscience. Path to treat Rett syndrome.Assessment of Caregiver Inventory for Rett Syndrome.Mecp2 regulates tnfa during zebrafish embryonic development and acute inflammation.MeCP2 R168X male and female mutant mice exhibit Rett-like behavioral deficits.The MECP2 variant c.925C>T (p.Arg309Trp) causes intellectual disability in both males and females without classic features of Rett syndrome.Rett Syndrome: Coming to Terms with Treatment

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Growth failure and outcome in Rett syndrome: specific growth references.

http://www.wikidata.org/entity/Q36310174

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2012年の論文

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年學術文章

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2012年學術文章

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2012年學術文章

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Growth failure and outcome in Rett syndrome: specific growth references.

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Growth failure and outcome in Rett syndrome: specific growth references.

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Growth failure and outcome in Rett syndrome: specific growth references.

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Growth failure and outcome in Rett syndrome: specific growth references.

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Growth failure and outcome in Rett syndrome: specific growth references.

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Lauren McNair

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Steven A Skinner

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P2860

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

Rett syndrome: revised diagnostic criteria and nomenclature

Epilepsy and the natural history of Rett syndrome.

Postnatal-onset microcephaly: pathogenesis, patterns of growth, and prediction of outcome.

Growth and nutrition in Rett syndrome.

Secondary sexual characteristics and menses in young girls seen in office practice: a study from the Pediatric Research in Office Settings network.

Construction of the World Health Organization child growth standards: selection of methods for attained growth curves.

Growth charts for Down's syndrome from birth to 18 years of age.

New height, weight and head circumference charts for British children with Williams syndrome.

Do growth chart centiles need a face lift?

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