Characterisation of breathing and associated central autonomic dysfunction in the Rett disorder - Wikidata - awgldk - TriplyDB

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

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

http://www.wikidata.org/entity/Q35270725

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Pathogenesis of lethal cardiac arrhythmias in Mecp2 mutant mice: implication for therapy in Rett syndrome Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice Illness Severity, Social and Cognitive Ability, and EEG Analysis of Ten Patients with Rett Syndrome Treated with Mecasermin (Recombinant Human IGF-1).Rett Syndrome: Reaching for Clinical Trials Insulin-Like Growth Factor 1 and Related Compounds in the Treatment of Childhood-Onset Neurodevelopmental Disorders Prevalence and onset of comorbidities in the CDKL5 disorder differ from Rett syndrome Clinical Guidelines for Management of Bone Health in Rett Syndrome Based on Expert Consensus and Available Evidence Autonomic cardiovascular control in methyl-CpG-binding protein 2 (Mecp2) deficient mice MeCP2 deficiency results in robust Rett-like behavioural and motor deficits in male and female rats Manipulations of MeCP2 in glutamatergic neurons highlight their contributions to Rett and other neurological disorders Female Mecp2(+/-) mice display robust behavioral deficits on two different genetic backgrounds providing a framework for pre-clinical studies.Brain activity mapping in Mecp2 mutant mice reveals functional deficits in forebrain circuits, including key nodes in the default mode network, that are reversed with ketamine treatment.Morphological and functional reversal of phenotypes in a mouse model of Rett syndrome.Preclinical research in Rett syndrome: setting the foundation for translational success.Cardiovascular regulation in the period preceding vasovagal syncope in conscious humans.Autonomic breathing abnormalities in Rett syndrome: caregiver perspectives in an international database study.Effect of Sarizotan, a 5-HT1a and D2-like receptor agonist, on respiration in three mouse models of Rett syndrome Effects of sedation on auditory brainstem response in Rett syndrome.Respiratory phenotypes are distinctly affected in mice with common Rett syndrome mutations MeCP2 T158A and R168X.Effects of weekly low-frequency rTMS on autonomic measures in children with autism spectrum disorder.Respiratory rhythm generation in vivo.Seizures in Rett syndrome: an overview from a one-year calendar study Annotation: Rett syndrome: recent progress and implications for research and clinical practice.Separate respiratory phenotypes in methyl-CpG-binding protein 2 (Mecp2) deficient mice.Clinical manifestations and stages of Rett syndrome.Cardiac autonomic regulation in autism and Fragile X syndrome: a review.Habituation without NMDA Receptor-Dependent Desensitization of Hering-Breuer Apnea Reflex in a Mecp2 Mutant Mouse Model of Rett Syndrome MeCP2 is critical within HoxB1-derived tissues of mice for normal lifespan Treatment of cardiac arrhythmias in a mouse model of Rett syndrome with Na+-channel-blocking antiepileptic drugs.Clinical variability in Rett syndrome.Impaired CO2 sensitivity of astrocytes in a mouse model of Rett syndrome.Paradoxical physiological responses to propranolol in a Rett syndrome patient: a case report The relationship of Rett syndrome and MECP2 disorders to autism.Post-inspiratory discharges are the centrepiece of respiratory disrhythmia in a gene knockout model of Rett syndrome.Physiological correlates of social avoidance behavior in children and adolescents with fragile x syndrome.Progressive Changes in a Distributed Neural Circuit Underlie Breathing Abnormalities in Mice Lacking MeCP2.The association between behavior and genotype in Rett syndrome using the Australian Rett Syndrome Database.Brain-derived neurotrophic factor enhances fetal respiratory rhythm frequency in the mouse preBötzinger complex in vitro.An optogenetic mouse model of rett syndrome targeting on catecholaminergic neurons.Evaluation of current pharmacological treatment options in the management of Rett syndrome: from the present to future therapeutic alternatives.

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

http://www.wikidata.org/entity/Q35270725

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Archives of Disease in Childhood

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Characterisation of breathing ...... sfunction in the Rett disorder

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Al-Rawas S

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Apartopoulos F

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Engerström IW

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P2860

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

Role of medulla oblongata in generation of sympathetic and vagal outflows.

Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females.

Recent insights into hyperventilation from the study of Rett syndrome.

The location of descending fibres to sympathetic preganglionic vasomotor and sudomotor neurons in man.

Hyperventilation in the awake state: potentially treatable component of Rett syndrome.

The neuropathology of Rett syndrome--overview 1994.

Abnormal expression of microtubule-associated protein 2 (MAP-2) in neocortex in Rett syndrome.

Immaturity of medullary cardiorespiratory neurones leading to inappropriate autonomic reactions as a likely cause of sudden death in Rett's syndrome.

Temporal response patterns of the human sinus node to brief carotid baroreceptor stimuli.

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