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Showing 97 - 108 of 212 results
Publication

Congenital central hypoventilation syndrome: Neurocognitive functioning in school age children†

Frank A. Zelko, Debra E. Weese-Mayer, Elizabeth M. Berry-Kravis, Michael N. Nelson, Sue E. Leurgans

Publication

Medullary serotonin defects and respiratory dysfunction in sudden infant death syndrome.

David S. Paterson, Debra E. Weese-Mayer, Gerard Hilaire

Publication

Congenital central hypoventilation syndrome from past to future: Model for translational and transitional autonomic medicine

Debra E. Weese-Mayer, Casey M. Rand, Darius A. Loghmanee, Elizabeth M. Berry-Kravis, Isabella Ceccherini, Larry J. Jennings, Pallavi P. Patwari

Publication

Sudden infant death syndrome (SIDS) in African Americans : polymorphisms in the gene encoding the stress peptide pituitary adenylate cyclase-activating polypeptide (PACAP)

Kevin J Cummings, Cameron Goldie, Cherise Klotz, Debra E Weese-Mayer, Elizabeth M Berry-Kravis, Margaret E Cooper, Mary L Marazita, N Torben Bech-Hansen, Richard JA Wilson, Rose Tobias, Wei-Qiao Liu

Publication

Later-onset congenital central hypoventilation syndrome due to a heterozygous 24-polyalanine repeat expansion mutation in the PHOX2B gene.

Gabriela M Repetto, Casey M Rand, Debra E Weese-Mayer, Elizabeth M Berry-Kravis, Lili Zhou, Raul J Corrales, Selim G Abara

Publication

HTR2A variation and sudden infant death syndrome: a case–control analysis

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

Publication

Congenital central hypoventilation syndrome (CCHS) and sudden infant death syndrome (SIDS): Kindred disorders of autonomic regulation

Debra E. Weese-Mayer, Casey M. Rand, Elizabeth M. Berry-Kravis, Isabella Ceccherini

Publication

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Publication

Autonomic dysregulation in young girls with Rett Syndrome during nighttime in-home recordings.

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