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Precursors of cardiorespiratory events in infants detected by home memory monitor

Carl E Hunt, Michael J Corwin, George Lister, Debra E Weese-Mayer, Sally L Davidson Ward, Larry R Tinsley, Michael R Neuman, Marian Willinger, Rangasamy Ramanathan, Denis Rybin

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Congenital central hypoventilation syndrome: PHOX2B genotype determines risk for sudden death.

Jerome O Gronli, Barbara A Santucci, Sue E Leurgans, Elizabeth M Berry-Kravis, Debra E Weese-Mayer

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Sudden infant death syndrome: another year of new hope but no cure.

Darius A Loghmanee, Debra E Weese-Mayer

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Sudden infant death syndrome: rare mutation in the serotonin system FEV gene.

Casey M Rand, Elizabeth M Berry-Kravis, Lili Zhou, Wenqing Fan, Debra E Weese-Mayer

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Rapid-Onset Obesity With Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation Presenting in Childhood

Diego Ize-Ludlow, Juliette A Gray, Mark A Sperling, Elizabeth M Berry-Kravis, Jeff M Milunsky, I Sadaf Farooqi, Casey M Rand, Debra E Weese-Mayer

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Vagal and sympathetic heart rate and blood pressure control in adult onset PHOX2B mutation–confirmed congenital central hypoventilation syndrome

André Diedrich, Beth A Malow, Nick A Antic, Kyoko Sato, R Doug McEvoy, Christopher J Mathias, David Robertson, Elizabeth M Berry-Kravis, Debra E Weese-Mayer

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Sudden Infant Death Syndrome: review of implicated genetic factors.

Debra E Weese-Mayer, Michael J Ackerman, Mary L Marazita, Elizabeth M Berry-Kravis

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Autonomic nervous system dysregulation: breathing and heart rate perturbation during wakefulness in young girls with Rett syndrome.

Debra E Weese-Mayer, Steven P Lieske, Christina M Boothby, Anna S Kenny, Heather L Bennett, Jean M Silvestri, Jan-Marino Ramirez

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Facial phenotype in children and young adults with PHOX2B-determined congenital central hypoventilation syndrome: quantitative pattern of dysmorphology.

Emily S Todd, Seth M Weinberg, Elizabeth M Berry-Kravis, Jean M Silvestri, Anna S Kenny, Casey M Rand, Lili Zhou, Brion S Maher, Mary L Marazita, Debra E Weese-Mayer

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Precursors of cardiorespiratory events in infants detected by home memory monitor

Congenital central hypoventilation syndrome: PHOX2B genotype determines risk for sudden death.

Sudden infant death syndrome: another year of new hope but no cure.

Sudden infant death syndrome: rare mutation in the serotonin system FEV gene.

Rapid-Onset Obesity With Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation Presenting in Childhood

Vagal and sympathetic heart rate and blood pressure control in adult onset PHOX2B mutation–confirmed congenital central hypoventilation syndrome

Sudden Infant Death Syndrome: review of implicated genetic factors.

Autonomic nervous system dysregulation: breathing and heart rate perturbation during wakefulness in young girls with Rett syndrome.

Characterization of dermatoglyphics in PHOX2B-confirmed congenital central hypoventilation syndrome.

Pediatric Autonomic Disorders

Nicotine metabolizing genes GSTT1 and CYP1A1 in sudden infant death syndrome

Facial phenotype in children and young adults with PHOX2B-determined congenital central hypoventilation syndrome: quantitative pattern of dysmorphology.

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