CDKL5 deficiency entails sleep apneas in mice.

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Sleep in neurological disorders, sleep apnea, sleep duration and body weight.Heterozygous CDKL5 Knockout Female Mice Are a Valuable Animal Model for CDKL5 Disorder.

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CDKL5 deficiency entails sleep apneas in mice.

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2017 nî lūn-bûn

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CDKL5 deficiency entails sleep apneas in mice.

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CDKL5 deficiency entails sleep apneas in mice.

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CDKL5 deficiency entails sleep apneas in mice.

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CDKL5 deficiency entails sleep apneas in mice.

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Alessandro Silvani

http://www.w3.org/2001/XMLSchema#string

Alice Valli

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Chiara Berteotti

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Rocchina Viggiano

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Sara Alvente

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Stefano Bastianini

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Viviana Lo Martire

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P2860

CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome

Disruption of the serine/threonine kinase 9 gene causes severe X-linked infantile spasms and mental retardation

The CDKL5 disorder is an independent clinical entity associated with early-onset encephalopathy

Prevalence and onset of comorbidities in the CDKL5 disorder differ from Rett syndrome

Accurate discrimination of the wake-sleep states of mice using non-invasive whole-body plethysmography.

Mapping pathological phenotypes in a mouse model of CDKL5 disorder

Cardiorespiratory anomalies in mice lacking CB1 cannabinoid receptors.

Respiratory and sleep disorders in female children with atypical Rett syndrome caused by mutations in the CDKL5 gene.

Breathing dysfunctions associated with impaired control of postinspiratory activity in Mecp2-/y knockout mice.

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495-497

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scholarly article

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10.1111/JSR.12512

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Elisabetta Ciani

Giovanna Zoccoli

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2017-02-23T00:00:00Z

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P698

28230307

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CDKL5 deficiency entails sleep apneas in mice.

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P2860

P2860

CDKL5 deficiency entails sleep apneas in mice.

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