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Berry-Kravis, Elizabeth

One or more keywords matched the following items that are connected to Berry-Kravis, Elizabeth

Item Type	Name
Concept	Autonomic Nervous System
Concept	Autonomic Nervous System Diseases
Academic Article	Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b.
Academic Article	Sudden infant death syndrome: case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development.
Academic Article	Congenital central hypoventilation syndrome: PHOX2B genotype determines risk for sudden death.
Academic Article	Congenital central hypoventilation syndrome: neurocognitive functioning in school age children.
Academic Article	Congenital Central Hypoventilation Syndrome: Neurocognition Already Reduced in Preschool-Aged Children.
Academic Article	Absence of mutations in HCRT, HCRTR1 and HCRTR2 in patients with ROHHAD.
Academic Article	Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation (ROHHAD): exome sequencing of trios, monozygotic twins and tumours.
Academic Article	Monozygotic twins discordant for ROHHAD phenotype.
Academic Article	Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation: analysis of hypothalamic and autonomic candidate genes.
Academic Article	Autonomic regulation in fragile X syndrome.
Academic Article	Congenital central hypoventilation syndrome from past to future: model for translational and transitional autonomic medicine.
Academic Article	HTR2A variation and sudden infant death syndrome: a case-control analysis.
Academic Article	Congenital central hypoventilation syndrome (CCHS) and sudden infant death syndrome (SIDS): kindred disorders of autonomic regulation.
Academic Article	Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation presenting in childhood.
Academic Article	Adult identified with congenital central hypoventilation syndrome--mutation in PHOX2b gene and late-onset CHS.
Academic Article	Genetics of congenital central hypoventilation syndrome: lessons from a seemingly orphan disease.

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Autonomic Nervous System