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Familial dysautonomia: Frequent, prolonged and severe hypoxemia during wakefulness and sleep

Genetic variation in the HTR1A gene and sudden infant death syndrome

Familial dysautonomia: Frequent, prolonged and severe hypoxemia during wakefulness and sleep

Debra E. Weese-Mayer, Anna S. Kenny, Heather L. Bennett, Jan-Marino Ramirez, Sue E. Leurgans

Precursors of cardiorespiratory events in infants detected by home memory monitor

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

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

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

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

Darius A Loghmanee, Debra E Weese-Mayer

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

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

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

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

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

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

Sudden Infant Death Syndrome: review of implicated genetic factors.

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

Congenital Central Hypoventilation Syndrome

Sudden Infant Death Syndrome